J. Inazawa

J. Inazawa, S. Kosuda, H. Tsuda, 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Expression of cIAP-1 correlates with nodal metastasis in squamous cell carcinoma of the tongue.

J. Inazawa, H. Tsuda, I. Imoto, 2008, International journal of oral and maxillofacial surgery.

Nuclear expression of cIAP-1, an apoptosis inhibiting protein, predicts lymph node metastasis and poor patient prognosis in head and neck squamous cell carcinomas.

J. Inazawa, H. Tsuda, I. Imoto, 2005, Cancer letters.

Molecular cloning of a novel non-receptor tyrosine kinase, HYL (hematopoietic consensus tyrosine-lacking kinase).

J. Inazawa, A. Iwama, T. Suda, 1994, Oncogene.

Laboratory of DNA Information Analysis Laboratory of Sequence Analysis Laboratory of Genome Database

J. Inazawa, K. Kozaki, J. Inazawa, 2018 .

Genetic or epigenetic silencing of low density lipoprotein receptor‐related protein 1B expression in oral squamous cell carcinoma

J. Inazawa, I. Imoto, T. Nakagawa, 2006, Cancer science.

Transcriptional Regulation of the CLC-K1 Promoter by myc-Associated Zinc Finger Protein and Kidney-Enriched Krüppel-Like Factor, a Novel Zinc Finger Repressor

J. Inazawa, K. Yokoyama, F. Marumo, 2000, Molecular and Cellular Biology.

A transcriptional variant of the LC3A gene is involved in autophagy and frequently inactivated in human cancers

J. Inazawa, T. Kawano, H. Bai, 2012, Oncogene.

Assignment of the human myeloperoxidase gene (MPO) to bands q21.3----q23 of chromosome 17.

J. Inazawa, M. Taniwaki, S. Misawa, 1989, Cytogenetics and cell genetics.

Assignment of the human granulocyte colony-stimulating factor receptor gene (CSF3R) to chromosome 1 at region p35-p34.3.

J. Inazawa, S. Nagata, R. Fukunaga, 1991, Genomics.

The Clinical Significance of Aurora-A/STK15/BTAK Expression in Human Esophageal Squamous Cell Carcinoma

J. Inazawa, M. Imamura, T. Kan, 2005, Clinical Cancer Research.

Significant impact of miRNA–target gene networks on genetics of human complex traits

M. Kanai, Y. Okada, Toshihiro Tanaka, 2016, Scientific Reports.

Heterozygous deletion at 14q22.1–q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

J. Inazawa, A. Hata, I. Imoto, 2008, American journal of medical genetics. Part A.

Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family.

Y. Nakamura, S. Inoue, J. Inazawa, 1995, Genomics.

Genomic organization, sequence and chromosomal localization of the mouse Tbr2 gene and a comparative study with Tbr1.

J. Inazawa, M. Ueno, K. Nakashima, 2000, Gene.

Lysosomal-Associated Protein Multispanning Transmembrane 5 Gene (LAPTM5) Is Associated with Spontaneous Regression of Neuroblastomas

S. Ichinose, J. Inazawa, I. Imoto, 2009, PloS one.

Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q.

Y. Nakamura, J. Inazawa, T. Tokino, 1996, Cancer research.

Mild prominence of the Sylvian fissure in a Bainbridge‐Ropers syndrome patient with a novel frameshift variant in ASXL3

J. Inazawa, T. Kaname, K. Yanagi, 2017, Clinical case reports.

ANA, a novel member of Tob/BTG1 family, is expressed in the ventricular zone of the developing central nervous system

J. Inazawa, S. Matsuda, Tadashi Yamamoto, 1998, Oncogene.

Massive computational identification of somatic variants in exonic splicing enhancers using The Cancer Genome Atlas

J. Inazawa, K. Tanimoto, T. Muramatsu, 2019, Cancer medicine.

SKI and MEL1 Cooperate to Inhibit Transforming Growth Factor-β Signal in Gastric Cancer Cells*

J. Inazawa, K. Miyazono, M. Matsuoka, 2009, Journal of Biological Chemistry.

Mammalian occludin in epithelial cells: its expression and subcellular distribution.

J. Inazawa, M. Itoh, K. Fujimoto, 1997, European journal of cell biology.

SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processing

S. Ichinose, J. Inazawa, J. Kudoh, 2011, EMBO molecular medicine.

Identification and characterization of transforming growth factor beta‐induced in circulating tumor cell subline from pancreatic cancer cell line

J. Inazawa, Taku Sato, M. Tanabe, 2018, Cancer science.

Increase of bone marrow-derived secretory lineage epithelial cells during regeneration in the human intestine.

H. Okano, J. Inazawa, T. Hibi, 2005, Gastroenterology.

The human homologue of the murine Llglh gene (LLGL) maps within the Smith-Magenis syndrome region in 17p11.2.

Y. Nakamura, J. Inazawa, N. Takahashi, 1996, Cytogenetics and cell genetics.

γ-Glutamylcyclotransferase as a novel immunohistochemical biomarker for the malignancy of esophageal squamous tumors.

J. Inazawa, T. Kawano, Y. Eishi, 2014, Human pathology.

Significance of Akt activation and AKT gene increases in soft tissue tumors.

J. Inazawa, Y. Oda, Y. Dobashi, 2014, Human pathology.

Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous‐cell carcinoma

J. Inazawa, H. Tsuda, I. Imoto, 2008, Cancer science.

Frequent methylation-associated silencing of a candidate tumor-suppressor, CRABP1, in esophageal squamous-cell carcinoma

J. Inazawa, K. Tanaka, T. Kawano, 2007, Oncogene.

Diverse involvement of isoforms and gene aberrations of Akt in human lung carcinomas

J. Inazawa, Y. Dobashi, H. Matsubara, 2015, Cancer science.

ACTN4 gene amplification and actinin‐4 protein overexpression drive tumour development and histological progression in a high‐grade subset of ovarian clear‐cell adenocarcinomas

Tesshi Yamada, J. Inazawa, H. Tsuda, 2012, Histopathology.

Detection of chromosomal aneusomy by fluorescence in situ hybridization in fine‐needle aspirates from breast tumors

J. Inazawa, M. Watatani, Y. Miyoshi, 2000, Cancer.

Abstract 2080: miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma

J. Inazawa, I. Imoto, S. Arii, 2010 .

Fibroblast growth factor signals regulate transforming growth factor‐β‐induced endothelial‐to‐myofibroblast transition of tumor endothelial cells via Elk1

Hiroshi I. Suzuki, J. Inazawa, K. Miyazono, 2019, Molecular oncology.

Structure and chromosomal localization of the human stromal cell-derived factor 1 (SDF1) gene.

J. Inazawa, T. Honjo, T. Shinohara, 1995, Genomics.

HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome

J. Inazawa, K. Ihara, Kyoko Watanabe, 2011, Journal of Human Genetics.

Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation

J. Inazawa, Y. Goto, I. Imoto, 2010, Journal of Human Genetics.

Clinicopathological significance of WT1 expression in ovarian cancer: a possible accelerator of tumor progression in serous adenocarcinoma

J. Inazawa, H. Tsuda, O. Matsubara, 2007, Virchows Archiv.

Publisher Correction: miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein

J. Inazawa, K. Tanimoto, J. Inoue, 2018, Scientific Reports.

miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein

J. Inazawa, K. Tanimoto, J. Inoue, 2018, Scientific Reports.

Breakpoint junction of interstitial homozygous deletion at chromosome 2q33 in a small cell lung carcinoma.

J. Yokota, T. Kohno, J. Inazawa, 1996, DNA research : an international journal for rapid publication of reports on genes and genomes.

Identification of a novel fusion gene in a pre‐B acute lymphoblastic leukemia with t(1;19)(q23;p13)

J. Inazawa, I. Imoto, Y. Kaneko, 2004, Cancer science.

Induction of mdl/EAT, Bd-2 Related Gene, byRetinoicAcidor HeatShock in the Human Embryonal Carcinoma Cells, NCR-G3

J. Inazawa, S. Imai, A. Umezawa, 1996 .

cDNA cloning, genomic structure and chromosomal mapping of the mouse glucuronyltransferase-S involved in the biosynthesis of the HNK-1 carbohydrate epitope.

J. Inazawa, S. Oka, T. Kawasaki, 2002, Gene.

Frequent Silencing of Low Density Lipoprotein Receptor-Related Protein 1B (LRP1B) Expression by Genetic and Epigenetic Mechanisms in Esophageal Squamous Cell Carcinoma

K. Chin, J. Gray, S. Hirohashi, 2004, Cancer Research.

DEK oncoprotein regulates transcriptional modifiers and sustains tumor initiation activity in high-grade neuroendocrine carcinoma of the lung

S. Hirohashi, F. Hosoda, J. Inazawa, 2010, Oncogene.

Overexpression of SMYD2 relates to tumor cell proliferation and malignant outcome of esophageal squamous cell carcinoma.

J. Inazawa, H. Tsuda, I. Imoto, 2009, Carcinogenesis.

ASSOCIATION OF KALLIKREIN 5-OVEREXPRESSION WITH INVASIVENESS OF URINARY BLADDER CARCINOMA CELLS

J. Inazawa, Y. Mizutani, T. Miki, 2008 .

Multiplex PCR/liquid chromatography assay for screening of subtelomeric rearrangements.

J. Inazawa, R. Kosaki, K. Kosaki, 2007, Genetic testing.

Association of KLK5 overexpression with invasiveness of urinary bladder carcinoma cells

J. Inazawa, Y. Mizutani, T. Miki, 2007, Cancer science.

Genomic loss and epigenetic silencing of very-low-density lipoprotein receptor involved in gastric carcinogenesis

S. Hirohashi, J. Inazawa, H. Tsuda, 2006, Oncogene.

Identification of target genes within an amplicon at 14q12‐q13 in esophageal squamous cell carcinoma

Y. Nakamura, J. Inazawa, I. Imoto, 2001, Genes, chromosomes & cancer.

Copy number alterations in urothelial carcinomas: their clinicopathological significance and correlation with DNA methylation alterations

F. Hosoda, T. Shibata, J. Inazawa, 2010, Carcinogenesis.

The Whole Nucleotide Sequence and Chromosomal Localization of the Gene for Human Metabotropic Glutamate Receptor Subtype 6

S. Nakanishi, T. Hashimoto, J. Inazawa, 1997, The European journal of neuroscience.

FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes.

J. Inazawa, H. Nishino, H. Ueyama, 1996, Cytogenetics and cell genetics.

Establishment of a cell line from a malignant rhabdoid tumor of the liver lacking the function of two tumor suppressor genes, hSNF5/INI1 and p16.

J. Inazawa, I. Imoto, H. Moritake, 2005, Cancer genetics and cytogenetics.

High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs.

Y. Nakamura, J. Inazawa, T. Abe, 1995, Genomics.

Germline mutation of the RET proto-oncogene in children with total intestinal aganglionosis.

J. Inazawa, D. Ichikawa, T. Kimura, 1997, Journal of Pediatric Surgery.

NF-κB Inducing Kinase, a Central Signaling Component of the Non-Canonical Pathway of NF-κB, Contributes to Ovarian Cancer Progression

J. Inazawa, I. Imoto, T. Kiyono, 2014, PloS one.

Esophageal squamous cell carcinoma developed 11 years after allogeneic bone marrow transplantation for acute lymphatic leukemia.

J. Inazawa, Y. Tokairin, T. Kawano, 2013, Japanese journal of clinical oncology.

Radiation sensitivities of 31 human oesophageal squamous cell carcinoma cell lines

J. Inazawa, S. Ban, Koji Watanabe, 2005, International journal of experimental pathology.

Different drug sensitivity in two neuroblastoma cell lines established from the same patient before and after chemotherapy

J. Inazawa, S. Tsuchida, T. Sugimoto, 1991, International journal of cancer.

Down‐regulation of SKP2 induces apoptosis in lung‐cancer cells

J. Inazawa, Takashi Takahashi, T. Fujisawa, 2003, Cancer science.

Loss of material from chromosome arm 1p during malignant progression of meningioma revealed by fluorescent in Situ hybridization

J. Inazawa, T. Abe, S. Ueda, 1998, Cancer.

Assignment of the human Fas antigen gene (Fas) to 10q24.1.

J. Inazawa, S. Nagata, T. Abe, 1992, Genomics.

Molecular cloning of a human transmembrane-type protein tyrosine phosphatase and its expression in gastrointestinal cancers.

J. Inazawa, H. Noguchi, T. Uchida, 1994, The Journal of biological chemistry.

Alteration in Copy Numbers of Genes as a Mechanism for Acquired Drug Resistance

J. Inazawa, A. Tomida, T. Tsuruo, 2004, Cancer Research.

Myelomonocytic crisis with t(5;17) and a p53 mutation in a patient with chronic myelogenous leukemia

J. Inazawa, S. Misawa, H. Nakai, 1994, American journal of hematology.

BST-1, a surface molecule of bone marrow stromal cell lines that facilitates pre-B-cell growth.

J. Inazawa, T. Hirano, T. Kaisho, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Molecular cloning and chromosomal assignment of the human brain-type phosphodiesterase I/nucleotide pyrophosphatase gene (PDNP2).

J. Inazawa, K. Sano, N. Nishimura, 1995, Genomics.

Human arylhydrocarbon receptor repressor (AHRR) gene: genomic structure and analysis of polymorphism in endometriosis

J. Inazawa, I. Imoto, J. Mimura, 2001, Journal of Human Genetics.

Grb10/GrbIR as an in vivo substrate of Tec tyrosine kinase

U. Ikeda, J. Inazawa, M. Kasuga, 1998, Genes to cells : devoted to molecular & cellular mechanisms.

Cell culture in esophageal squamous cell carcinoma and the association with molecular markers.

J. Inazawa, I. Imoto, M. Imamura, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

Expression of catalase and myeloperoxidase genes in hydrogen peroxide-resistant HL-60 cells.

J. Inazawa, T. Abe, K. Hashinaka, 1991, DNA and cell biology.

Amplification and over‐expression of the AIB1 nuclear receptor co‐activator gene in primary gastric cancers

Yusuke Nakamura, J. Inazawa, C. Sakakura, 2000, International journal of cancer.

cDNA cloning and chromosomal localization of the human ciliary neurotrophic factor gene

J. Inazawa, T. Deguchi, H. Misawa, 1995, Neuroscience Letters.

The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation.

K. Yamakawa, Masahiro Ito, Yusuke Nakamura, 2002, American journal of human genetics.

Assignment of cardiac homeobox gene CSX to human chromosome 5q34.

J. Inazawa, R. Nagai, Y. Yazaki, 1995, Genomics.

22q13 microduplication in two patients with common clinical manifestations: A recognizable syndrome?

J. Inazawa, I. Imoto, N. Okamoto, 2007, American journal of medical genetics. Part A.

Successful Imatinib Treatment of Cardiac Involvement of FIP1L1-PDGFRA-Positive Chronic Eosinophilic Leukemia Followed by Severe Hepatotoxicity

J. Inazawa, O. Miura, A. Arai, 2007, International journal of hematology.

A novel metalloprotease/disintegrin–like gene at 17q21.3 is somatically rearranged in two primary breast cancers

T. Katagiri, J. Inazawa, M. Emi, 1993, Nature genetics.

Overexpressed NF-kappaB-inducing kinase contributes to the tumorigenesis of adult T-cell leukemia and Hodgkin Reed-Sternberg cells.

J. Inazawa, Y. Iwasaki, T. Masuda, 2008, Blood.

Overexpressed NF- (cid:1) B–inducing kinase contributes to the tumorigenesis of adult T-cell leukemia and Hodgkin Reed-Sternberg cells

J. Inazawa, Y. Iwasaki, T. Masuda, 2008 .

Structural analysis of the gene encoding RP58, a sequence-specific transrepressor associated with heterochromatin.

J. Inazawa, M. Kasai, R. Ishida, 2000, Gene.

Molecular Cloning , Characterization , and Chromosomal Localization of a Novel Protein-Tyrosine Phosphatase , HPTPq

J. Inazawa, Y. Yazaki, J. Nishida, 2002 .

Concurrent targeting of MAP3K3 and BRD4 by miR-3140-3p overcomes acquired resistance to BET inhibitors in neuroblastoma cells

J. Inazawa, K. Tanimoto, J. Inoue, 2021, Molecular therapy. Nucleic acids.

miR-1293, a Candidate for miRNA-Based Cancer Therapeutics, Simultaneously Targets BRD4 and the DNA Repair Pathway.

J. Inazawa, H. Harada, K. Tanimoto, 2020, Molecular therapy : the journal of the American Society of Gene Therapy.

Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel

J. Inazawa, K. Moriyama, S. Hirose, 2019, Journal of Human Genetics.

Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1.

K. Mitsuya, M. Oshimura, J. Inazawa, 1995, Genomics.

Chromosomal mapping of the human smooth muscle actin gene (enteric type, ACTA3) to 2p13.1 and molecular nature of the hindIII polymorphism.

J. Inazawa, H. Nishino, H. Ueyama, 1995, Genomics.

Detection of an i(17q) chromosome by fluorescent in situ hybridization with a chromosome 17 alpha satellite DNA probe.

J. Inazawa, M. Taniwaki, S. Misawa, 1992, Cancer genetics and cytogenetics.

Human Fas ligand: gene structure, chromosomal location and species specificity.

J. Inazawa, T. Abe, M. Tanaka, 1994, International immunology.

High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridization.

Y. Nakamura, J. Inazawa, T. Abe, 1993, Genomics.

Identical deletion at 14q13.3 including PAX9 and NKX2-1 in siblings from mosaicism of unaffected parent

J. Inazawa, I. Morisaki, M. Yagi, 2015, Journal of Human Genetics.

MECP2 Duplication Syndrome in Male Patients with Severe Mental Retardation and Intractable Epilepsy

J. Inazawa, Y. Goto, J. Tohyama, 2010 .

Isolation and mapping of a human gene (RPD3L1) that is homologous to RPD3, a transcription factor in Saccharomyces cerevisiae.

Y. Furukawa, Y. Nakamura, T. Akiyama, 1996, Cytogenetics and cell genetics.

CLINICAL REPORT Neuroradiologic Features of CASK Mutations

J. Inazawa, H. Arai, N. Okamoto, 2010 .

Structure of the gene for human transglutaminase 1.

J. Inazawa, T. Abe, H. Doi, 1992, The Journal of biological chemistry.

Chromosomal localization and cDNA sequence of human BTEB, a GC box binding protein

M. Oshimura, J. Inazawa, Y. Fujii‐Kuriyama, 1993, Somatic cell and molecular genetics.

p53 gene mutation is not directly related to tumoricidal effects of preoperative radiochemohyperthermia therapy for rectal cancers

J. Inazawa, D. Ichikawa, M. Shirasu, 1996, Journal of surgical oncology.

Molecular cloning of a human RP105 homologue and chromosomal localization of the mouse and human RP105 genes (Ly64 and LY64).

J. Inazawa, N. Copeland, D. Gilbert, 1996, Genomics.

Assignment of the human mitochondrial NADP(+)-specific isocitrate dehydrogenase (IDH2) gene to 15q26.1 by in situ hybridization.

T. Huh, J. Inazawa, B. Song, 1996, Genomics.

Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia

J. Inazawa, M. Sanada, I. Imoto, 2009, Journal of Human Genetics.

The unbalanced 1;7 translocation in de novo myelodysplastic syndrome and its clinical implication

J. Inazawa, M. Taniwaki, S. Misawa, 1990, Cancer.

Cytogenetic studies in 32 patients with myelodysplastic syndrome: insights to specific chromosomal abnormalities and prognosis.

J. Inazawa, M. Taniwaki, S. Misawa, 1987, Japanese journal of clinical oncology.

Frequent deletions of material from chromosome arm 1p in oligodendroglial tumors revealed by double‐target fluorescence in situ hybridization and microsatellite analysis

Y. Nakamura, J. Inazawa, Y. Arakawa, 1995, Genes, chromosomes & cancer.

N-ras mutation and karyotypic evolution are closely associated with leukemic transformation in myelodysplastic syndrome.

J. Inazawa, M. Taniwaki, H. Kaneko, 1994, Leukemia.

Amendment history : Erratum ( August 2006 ) Early G 2 / M checkpoint failure as a molecular mechanism underlying etoposide-induced chromosomal aberrations

J. Inazawa, M. Nagasawa, S. Mizutani, 2018 .

Early G2/M checkpoint failure as a molecular mechanism underlying etoposide-induced chromosomal aberrations.

J. Inazawa, M. Nagasawa, S. Mizutani, 2005, The Journal of clinical investigation.

Assignment of the human mitochondrial NAD+ -specific isocitrate dehydrogenase alpha subunit (IDH3A) gene to 15q25.1-->q25.2by in situ hybridization.

T. Huh, J. Inazawa, B. Song, 1996, Genomics.

Cloning and chromosomal mapping of human glucuronyltransferase involved in biosynthesis of the HNK-1 carbohydrate epitope.

J. Inazawa, Y. Mitsumoto, S. Oka, 2000, Genomics.

High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes.

A. Tanigami, Y. Nakamura, J. Inazawa, 1994, Cytogenetics and cell genetics.

Chromosomal localization of the protein tyrosine phosphatase G1 gene and characterization of the aberrant transcripts in human colon cancer cells

J. Inazawa, F. Itoh, K. Imai, 1994, FEBS letters.

Chromosomal Assignment of the Gene for Protein Tyrosine Phosphatase HPTPδ

J. Inazawa, M. Ogimoto, T. Katagiri, 1993, Japanese journal of cancer research : Gann.

Precise localization of the human gene encoding cell adhesion kinase β (CAKβ/PYK2) to chromosome 8 at p21.1 by fluorescence in situ hybridization

N. Kakazu, J. Inazawa, T. Abe, 1996, Human Genetics.

Genomic structure and chromosomal localization of the gene encoding translin, a recombination hotspot binding protein.

J. Inazawa, M. Kasai, K. Aoki, 1997, Genomics.

Proceedings of the schistosome genome project.

D. Johnston, D. Rollinson, J. Inazawa, 1997, Memorias do Instituto Oswaldo Cruz.

Assignment of the human calpastatin gene (CAST) to chromosome 5 at region q14----q22.

N. Shimizu, S. Minoshima, J. Inazawa, 1990, Cytogenetics and cell genetics.

Fluorescence in situ hybridization analysis of chromosomal localization of three human cytochrome P450 2C genes (CYP2C8, 2C9, and 2C10) at 10q24.1

H. Yamazaki, J. Inazawa, T. Shimada, 1994, Japanese Journal of Human Genetics.

Identification of a novel gene, GASC1, within an amplicon at 9p23-24 frequently detected in esophageal cancer cell lines.

Y. Nakamura, S. Sugano, J. Inazawa, 2000, Cancer research.

Expression and chromosomal assignment of PTPH1 gene encoding a cytosolic protein tyrosine phosphatase homologous to cytoskeletal‐associated proteins

J. Inazawa, F. Itoh, K. Imai, 1993, International journal of cancer.

Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion

J. Inazawa, A. Hata, R. Kosaki, 2012, Journal of Human Genetics.

The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD).

J. Inazawa, K. Omura, T. Amagasa, 2004, American journal of human genetics.

Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor

J. Inazawa, I. Imoto, H. Hosoi, 2004, Journal of Human Genetics.

Homozygous deletion in a neuroblastoma cell line defined by a high‐density STS map spanning human chromosome band 1p36

J. Inazawa, J. Takita, E. Soeda, 2001, Genes, chromosomes & cancer.

Isolation and characterization of a novel secretory protein, stromal cell-derived factor-2 (SDF-2) using the signal sequence trap method.

J. Inazawa, T. Honjo, T. Nakano, 1996, Gene.

The CASK gene harbored in a deletion detected by array‐CGH as a potential candidate for a gene causative of X‐linked dominant mental retardation

O. Migita, J. Inazawa, A. Hata, 2008, American journal of medical genetics. Part A.

Chromosomes and Clinical Features in 6 Cases of Gliomas

J. Inazawa, T. Abe, M. Fujimoto, 1991 .

Distribution of breakpoint within the breakpoint cluster region (bcr) in chronic myelogenous leukemia with a complex philadelphia chromosome translocation

J. Inazawa, M. Taniwaki, S. Misawa, 1989, American journal of hematology.

Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy

J. Inazawa, K. Kojima, J. Inoue, 2019, Molecular therapy. Nucleic acids.

Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome

J. Inazawa, K. Masuda, I. Imoto, 2015, PloS one.

Human dihydrolipoamide succinyltransferase: cDNA cloning and localization on chromosome 14q24.2-q24.3.

J. Inazawa, T. Miyata, S. Ohta, 1993, Biochimica et biophysica acta.

Familial nasal NK/T‐cell lymphoma and pesticide use

J. Inazawa, T. Hongyo, K. Aozasa, 2001, American journal of hematology.

The oncogenic role of GASC1 in chemically induced mouse skin cancer

J. Inazawa, H. Nagase, K. Fujiwara, 2015, Mammalian Genome.

Involvement of cyclin D3 in liver metastasis of colorectal cancer, revealed by genome-wide copy-number analysis

J. Inazawa, H. Tsuda, S. Okabe, 2005, Laboratory Investigation.

Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations

Yusuke Nakamura, T. Morizono, T. Tsunoda, 2010, Nature Genetics.

Cloning, expression and chromosomal localization of a novel gene for protein tyrosine phosphatase (PTP-U2) induced by various differentiation-inducing agents.

J. Inazawa, T. Tsuruo, H. Seimiya, 1995, Oncogene.

Genomic alterations in primary gastric cancers analyzed by comparative genomic hybridization and clinicopathological factors.

Y. Nakamura, J. Inazawa, C. Sakakura, 2000, Hepato-gastroenterology.

Causal Relationship between the Loss of RUNX3 Expression and Gastric Cancer

S. Itohara, J. Inazawa, A. Kaneda, 2002, Cell.

Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese

T. Kawaguchi, Toshihiro Tanaka, J. Inazawa, 2018, Scientific Reports.

Frequent inactivation of a putative tumor suppressor, angiopoietin-like protein 2, in ovarian cancer.

S. Hirohashi, J. Inazawa, T. Kasamatsu, 2008, Cancer research.

YAP is a candidate oncogene for esophageal squamous cell carcinoma.

J. Inazawa, T. Kawano, H. Tsuda, 2011, Carcinogenesis.

Comparative genomic hybridization of squamous cell carcinoma of the esophagus: The possible involvement of the DP1 gene in the 13q34 amplicon

J. Inazawa, Y. Nakamura, Y. Fukuda, 1999, Genes, chromosomes & cancer.

miR-152 is a tumor suppressor microRNA that is silenced by DNA hypermethylation in endometrial cancer.

J. Inazawa, I. Imoto, D. Aoki, 2011, Cancer research.

DNA amplification and expression of FADD in oral squamous cell carcinoma.

J. Inazawa, K. Omura, Y. Nakajima, 2009, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization

T Takahashi, J. Inazawa, C. Sakakura, 1999, Genes, chromosomes & cancer.

Screening of DNA copy‐number aberrations in gastric cancer cell lines by array‐based comparative genomic hybridization

Hidetaka Mochizuki, Hitoshi Tsuda, J. Inazawa, 2005, Cancer science.

Identification of BAIAP2 (BAI-associated protein 2), a novel human homologue of hamster IRSp53, whose SH3 domain interacts with the cytoplasmic domain of BAI1

Y. Nakamura, Y. Taketani, J. Inazawa, 1999, Cytogenetic and Genome Research.

Activation of B‐Myb by E2F1 in hepatocellular carcinoma

J. Inazawa, M. Taniwaki, T. Okanoue, 2008, Hepatology research : the official journal of the Japan Society of Hepatology.

Induction of mcl1/EAT, Bcl-2 related gene, by retinoic acid or heat shock in the human embryonal carcinoma cells, NCR-G3.

J. Inazawa, J. Hata, S. Imai, 1996, Cell structure and function.

Chromosomal translocation, t(1;11)(q12;p15), in an extragonadal immature teratoma.

J. Inazawa, T. Abe, S. Ueda, 1997, Cancer Genetics and Cytogenetics.

Reprimo, a New Candidate Mediator of the p53-mediated Cell Cycle Arrest at the G2 Phase*

T. Taniguchi, J. Inazawa, E. Oda, 2000, The Journal of Biological Chemistry.

TERC identified as a probable target within the 3q26 amplicon that is detected frequently in non-small cell lung cancers.

J. Inazawa, I. Imoto, T. Iizasa, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

A Novel Amplicon at 9p23‐24 in Squamous Cell Carcinoma of the Esophagus That Lies Proximal to GASC1 and Harbors NFIB

M. Oka, J. Inazawa, I. Imoto, 2001, Japanese journal of cancer research : Gann.

An improved rapid procedure for fluorescence in situ hybridization that is applicable to intraoperative cancer cytodiagnosis.

J. Inazawa, C. Sakakura, K. Koide, 2000, Cancer letters.

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.

Y. Fukushima, N. Niikawa, J. Inazawa, 1996, Human molecular genetics.

Reconstitution of IKATP: An Inward Rectifier Subunit Plus the Sulfonylurea Receptor

J. Inazawa, L. Aguilar-Bryan, S. Seino, 1995, Science.

Tumor‐suppressive microRNA silenced by tumor‐specific DNA hypermethylation in cancer cells

J. Inazawa, K. Kozaki, 2012, Cancer science.

PIK3CA mutation is an oncogenic aberration at advanced stages of oral squamous cell carcinoma

J. Inazawa, H. Tsuda, I. Imoto, 2006, Cancer science.

PIK 3 CA mutation is an oncogenic aberration at advanced stages of oral squamous cell carcinoma

J. Inazawa, H. Tsuda, I. Imoto, 2006 .

Potential for reversing miR-634-mediated cytoprotective processes to improve efficacy of chemotherapy against oral squamous cell carcinoma

J. Inazawa, H. Harada, J. Inoue, 2022, Molecular therapy oncolytics.

Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers

J. Inazawa, M. Emi, I. Imoto, 2002, Japanese journal of cancer research : Gann.

Genomic landscape of a mouse model of diffuse-type gastric adenocarcinoma

S. Ishikawa, D. Komura, J. Inazawa, 2021, Gastric Cancer.

Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors.

Y. Nakamura, J. Inazawa, R. Kudo, 1993, Cancer research.

Receptor tyrosine kinase amplification is predictive of distant metastasis in patients with oral squamous cell carcinoma

S. Ishikawa, J. Inazawa, H. Katoh, 2017, Cancer science.

A complete Not I restriction map covering the entire long arm of human chromosome 11

N. Kakazu, F. Hosoda, J. Inazawa, 1997, Genes to cells : devoted to molecular & cellular mechanisms.

Bipolar affective disorder associated with β-thalassemia minor

J. Inazawa, T. Nakajima, H. Harada, 1995, Biological Psychiatry.

Identification of a novel gene, MASL1, within an amplicon at 8p23.1 detected in malignant fibrous histiocytomas by comparative genomic hybridization.

Y. Nakamura, T. Fujiwara, J. Inazawa, 1999, Cancer research.

Molecular cloning and characterization of human caspase-activated DNase.

J. Inazawa, H. Toh, S. Nagata, 1998, Proceedings of the National Academy of Sciences of the United States of America.

PH Domain-Only Protein PHLDA3 Is a p53-Regulated Repressor of Akt

Tsutomu Ohta, Shuichi Tsutsumi, Hiroyuki Aburatani, 2009, Cell.

Genome-Wide Association Study of Breast Cancer in the Japanese Population

Yusuke Nakamura, T. Katagiri, Y. Miki, 2013, PloS one.

An expression profile of genes in human retina and isolation of a complementary DNA for a novel rod photoreceptor protein.

J. Inazawa, K. Okubo, S. Kinoshita, 1997, Investigative ophthalmology & visual science.

The Suppression of Aurora-A/STK15/BTAK Expression Enhances Chemosensitivity to Docetaxel in Human Esophageal Squamous Cell Carcinoma

S. Tsunoda, J. Inazawa, Y. Shimada, 2007, Clinical Cancer Research.

The Suppression of Aurora-A / STK 15 / BTAK Expression Enhances Chemosensitivity to Docetaxel in Human Esophageal Squamous Cell Carcinoma

J. Inazawa, Y. Sakai, Y. Hashimoto, 2007 .

Structural Organization and Chromosomal Assignment of the Human obese Gene (*)

K. Nakao, N. Tamura, J. Inazawa, 1995, The Journal of Biological Chemistry.

A Simple G-Banding Technique Adaptable for Fluorescent in situ Hybridization (FISH) and Physical Ordering of Human Renin (REN) and Catepsin E (CTSE) Genes by Multi-Color FISH.

J. Inazawa, T. Abe, T. Ariyama, 1993 .

Molecular cloning of a novel apoptosis-related gene, human Nap1 (NCKAP1), and its possible relation to Alzheimer disease.

Y. Sakaki, I. Kanazawa, J. Inazawa, 2000, Genomics.

Detection and isolation of a novel human gene located on Xp11.2-p11.4 that escapes X-inactivation using a two-dimensional DNA mapping method.

K. Nakai, A. Fujiyama, J. Inazawa, 1998, Genomics.

A novel gene in the chromosomal region for juvenile myoclonic epilepsy on 6p12 encodes a brain-specific lysosomal membrane protein.

K. Yamakawa, K. Agarwala, J. Inazawa, 2001, Biochemical and biophysical research communications.

miR-544a induces epithelial-mesenchymal transition through the activation of WNT signaling pathway in gastric cancer.

J. Inazawa, H. Uetake, K. Kozaki, 2015, Carcinogenesis.

Genetic diagnosis of cancer

Y. Nakamura, J. Inazawa, 1998, International Journal of Clinical Oncology.

Chromosomal aberrations in colorectal cancers and liver metastases analyzed by comparative genomic hybridization

J. Inazawa, C. Sakakura, H. Taniguchi, 2001, International journal of cancer.

Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15

J. Inazawa, M. Taketo, R. Kanezaki, 2000, Oncogene.

Integrated genomic and functional analyses reveal glyoxalase I as a novel metabolic oncogene in human gastric cancer

F. Hosoda, J. Inazawa, Y. Arai, 2014, Oncogene.

miR-509-5p and miR-1243 increase the sensitivity to gemcitabine by inhibiting epithelial-mesenchymal transition in pancreatic cancer

J. Inazawa, D. Ichikawa, E. Otsuji, 2017, Scientific Reports.

Isolation and chromosomal localization of the human cone cGMP phosphodiesterase gamma cDNA (PDE6H).

J. Inazawa, K. Okubo, S. Kinoshita, 1996, Genomics.

Isolation and characterization of a novel gene deleted in DiGeorge syndrome.

N. Niikawa, J. Inazawa, H. Kurahashi, 1995, Human molecular genetics.

Resequencing and copy number analysis of the human tyrosine kinase gene family in poorly differentiated gastric cancer.

Yusuke Nakamura, S. Hirohashi, F. Hosoda, 2009, Carcinogenesis.

Cloning and characterization of an interstitial deletion at chromosome 11p15 in a sporadic breast cancer.

Y. Nakamura, J. Inazawa, K. Takita, 1992, Human molecular genetics.

Physical Ordering of Three Polymorphic DNA Markers Spanning the Regions Containing a Tumor Suppressor Gene of Renal Cell Carcinoma by Three‐color Fluorescent in situ Hybridization

J. Inazawa, T. Abe, T. Ariyama, 1992, Japanese journal of cancer research : Gann.

A case of incomplete DiGeorge syndrome associated with partial monosomy 22q11.1 due to maternal 14;22 translocation

J. Inazawa, K. Hamaoka, S. Tsuda, 1989, Japanese Journal of Human Genetics.

Unfavorable prognostic factors associated with high frequency of microsatellite instability and comparative genomic hybridization analysis in endometrial cancer.

J. Inazawa, I. Imoto, D. Aoki, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

Deletion mapping on chromosome 1p in well-differentiated gastric cancer.

Y. Nakamura, J. Inazawa, T. Nakajima, 1996, British Journal of Cancer.

Comparative genomic hybridization (CGH)‐arrays pave the way for identification of novel cancer‐related genes

J. Inazawa, I. Imoto, Issei Imoto, 2004, Cancer science.

Array‐based comparative genomic hybridization analysis of high‐grade neuroendocrine tumors of the lung

S. Hirohashi, F. Hosoda, T. Shibata, 2005, Cancer science.

Frequent silencing of DBC1 is by genetic or epigenetic mechanisms in non-small cell lung cancers.

S. Hirohashi, T. Shibata, J. Inazawa, 2005, Human molecular genetics.

Amplification and overexpression of SKP2 are associated with metastasis of non-small-cell lung cancers to lymph nodes.

J. Inazawa, T. Iizasa, T. Fujisawa, 2004, The American journal of pathology.

Genetic Classification of Lung Adenocarcinoma Based on Array-Based Comparative Genomic Hybridization Analysis: Its Association with Clinicopathologic Features

S. Hirohashi, F. Hosoda, T. Shibata, 2005, Clinical Cancer Research.

TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas

Masakazu Ueda, J. Inazawa, M. Emi, 2002, Hepatology.

Frequent silencing of protocadherin 17, a candidate tumour suppressor for esophageal squamous cell carcinoma.

J. Inazawa, T. Kawano, H. Kawachi, 2010, Carcinogenesis.

PRTFDC1, a possible tumor-suppressor gene, is frequently silenced in oral squamous-cell carcinomas by aberrant promoter hypermethylation

J. Inazawa, N. Kamata, I. Imoto, 2007, Oncogene.

Promoter hypermethylation contributes to frequent inactivation of a putative conditional tumor suppressor gene connective tissue growth factor in ovarian cancer.

S. Hirohashi, J. Inazawa, T. Kasamatsu, 2007, Cancer research.

Frequent silencing of the candidate tumor suppressor PCDH20 by epigenetic mechanism in non-small-cell lung cancers.

S. Hirohashi, F. Hosoda, T. Shibata, 2006, Cancer research.

Cancers Small-Cell Lung − by Epigenetic Mechanism in Non PCDH 20 Frequent Silencing of the Candidate Tumor Suppressor

S. Hirohashi, F. Hosoda, T. Shibata, 2006 .

Advances in Brief Frequent Silencing of Low Density Lipoprotein Receptor-Related Protein 1 B ( LRP 1 B ) Expression by Genetic and Epigenetic Mechanisms in Esophageal Squamous Cell Carcinoma

K. Chin, J. Gray, S. Hirohashi, 2004 .

Identification of CpG islands hypermethylated in human lung cancer by the arbitrarily primed-PCR method

J. Yokota, T. Kohno, J. Inazawa, 1998, Human Genetics.

Integrative genome‐wide analyses reveal the transcriptional aberrations in Japanese esophageal squamous cell carcinoma

T. Noda, S. Mori, J. Inazawa, 2021, Cancer science.

A novel target gene, SKP2, within the 5p13 amplicon that is frequently detected in small cell lung cancers.

S. Hirohashi, J. Inazawa, Takashi Takahashi, 2002, The American journal of pathology.

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia

J. Inazawa, T. Amino, H. Mizusawa, 2007, Journal of Human Genetics.

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan

I. Kanazawa, J. Inazawa, I. Imoto, 2003, Journal of Human Genetics.

Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma

Y. Miyagi, Y. Kamatani, Y. Okada, 2016, Nature Communications.

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies

Y. Fukushima, J. Inazawa, S. Saitoh, 2011, Journal of Human Genetics.

Identification of ZASC1 encoding a Krüppel-like zinc finger protein as a novel target for 3q26 amplification in esophageal squamous cell carcinomas.

J. Inazawa, I. Imoto, M. Imamura, 2003, Cancer research.

Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines: Possible Involvement of the ATF3 and CENPF Genes in the 1q32 Amplicon

Yusuke Nakamura, Yutaka Shimada, Masayuki Imamura, 2000, Japanese journal of cancer research : Gann.

Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system

Tatsuhiko Tsunoda, Daichi Shigemizu, Teruaki Konishi, 2016, Oncotarget.

Genetic profile of hepatocellular carcinoma revealed by array-based comparative genomic hybridization: identification of genetic indicators to predict patient outcome.

S. Hirohashi, F. Hosoda, T. Shibata, 2005, Journal of hepatology.

The hypusine cascade promotes cancer progression and metastasis through the regulation of RhoA in squamous cell carcinoma

S. Imoto, J. Inazawa, R. Yamaguchi, 2016, Oncogene.

ASK1 and ASK2 differentially regulate the counteracting roles of apoptosis and inflammation in tumorigenesis

Hiromi Nakamura, S. Kōzuma, Y. Taketani, 2009, The EMBO journal.

Expression and Gene Amplification of Actinin-4 in Invasive Ductal Carcinoma of the Pancreas

S. Hirohashi, J. Inazawa, H. Tsuda, 2008, Clinical Cancer Research.

Actinin-4 expression in ovarian cancer: a novel prognostic indicator independent of clinical stage and histological type

J. Inazawa, H. Tsuda, M. Takano, 2007, Modern Pathology.

miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein

J. Inazawa, K. Tanimoto, J. Inoue, 2018, Scientific Reports.

Genome‐wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage

S. Hirohashi, F. Hosoda, T. Shibata, 2010, Cancer science.

Genome-wide DNA methylation profiles in both precancerous conditions and clear cell renal cell carcinomas are correlated with malignant potential and patient outcome

S. Hirohashi, F. Hosoda, T. Shibata, 2008, Carcinogenesis.

A novel human RasGAP‐like gene that maps within the prostate cancer susceptibility locus at chromosome 1q25

J. Inazawa, T. Maeda, M. Asaka, 1998, FEBS letters.

A novel amplification target, DUSP26, promotes anaplastic thyroid cancer cell growth by inhibiting p38 MAPK activity

J. Inazawa, M. Emi, I. Imoto, 2007, Oncogene.

Cell Death and Survival The Impact of miRNA-Based Molecular Diagnostics and Treatment of NRF 2-Stabilized Tumors

J. Inazawa, T. Kawano, K. Omura, 2014 .

Structure and Expression of the Ah Receptor Repressor Gene*

J. Inazawa, Y. Fujii‐Kuriyama, Y. Matsuda, 2001, The Journal of Biological Chemistry.

Molecular Cytogenetic Analysis of 17 Renal Cancer Cell Lines: Increased Copy Number at 5q31‐33 in Cell Lines from Nonpapillary Carcinomas

Yusuke Nakamura, J. Inazawa, Mitsuaki Yoshida, 2000, Japanese journal of cancer research : Gann.

Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11–p12: LRRC1, GCLC, KIAA0057 and CLIC5

Antonio V. Delgado-Escueta, Julia N. Bailey, M. T. Medina, 2002, Epilepsy Research.

Genomic copy‐number alterations of MYC and FHIT genes are associated with survival in esophageal squamous‐cell carcinoma

J. Inazawa, T. Kawano, Y. Eishi, 2012, Cancer science.

Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population

Y. Kamatani, Yusuke Nakamura, T. Katagiri, 2019, Scientific Reports.

Alpha‐smooth‐muscle actin and desmin expressions in human neuroblastoma cell lines

A. Gown, J. Inazawa, H. Hosoi, 1991, International journal of cancer.

Promoter analysis and chromosomal mapping of human EBAG9 gene.

S. Inoue, J. Inazawa, M. Emi, 2000, Biochemical and biophysical research communications.

CD44 is a potential target of amplification within the 11p13 amplicon detected in gastric cancer cell lines

J. Inazawa, I. Imoto, K. Yanagihara, 2000, Genes, chromosomes & cancer.

Potential of tumor-suppressive miR-596 targeting LGALS3BP as a therapeutic agent in oral cancer.

J. Inazawa, T. Amagasa, M. Furuta, 2013, Carcinogenesis.

Elevated expression levels of NCOA3, TOP1, and TFAP2C in breast tumors as predictors of poor prognosis

Hideaki Kurioka, Takahiro Oka, J. Inazawa, 2003, Cancer.

Identification of cIAP1 as a candidate target gene within an amplicon at 11q22 in esophageal squamous cell carcinomas.

J. Inazawa, H. Tsuda, M. Ohki, 2001, Cancer research.

Overexpression of PDZK1 within the 1q12-q22 amplicon is likely to be associated with drug-resistance phenotype in multiple myeloma.

J. Inazawa, M. Taniwaki, S. Shimizu, 2004, The American journal of pathology.

Association of 17q21-q24 gain in ovarian clear cell adenocarcinomas with poor prognosis and identification of PPM1D and APPBP2 as likely amplification targets.

J. Inazawa, I. Imoto, D. Aoki, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

Overexpression of NF-κB inducing kinase underlies constitutive NF-κB activation in lung cancer cells.

J. Inazawa, A. Hasegawa, I. Imoto, 2010, Lung cancer.

ERM, a PEA3 Subfamily of Ets Transcription Factors, Can Cooperate with c-Jun (*)

J. Inazawa, T. Hirano, K. Nakajima, 1995, The Journal of Biological Chemistry.

Cytogenetic analysis of spontaneously discharged products of conception by array-based comparative genomic hybridization

O. Migita, J. Inazawa, K. Matsuoka, 2016, SpringerPlus.

Pax-5 Is Essential for κ Sterile Transcription during Igκ Chain Gene Rearrangement1

J. Inazawa, A. Kudo, Hiromu Sato, 2004, The Journal of Immunology.

Analysis of numerical aberrations in specific chromosomes by fluorescent in situ hybridization as a diagnostic tool in breast cancer

J. Inazawa, D. Ichikawa, T. Yamaguchi, 1996, Cancer.

Cloning of cDNAs encoding the human BAG1 protein and localization of the human BAG1 gene to chromosome 9p12.

J. Inazawa, K. Huebner, John Calvin Reed, 1996, Genomics.

Genome‐wide association study identifies gastric cancer susceptibility loci at 12q24.11‐12 and 20q11.21

Y. Kamatani, Yusuke Nakamura, C. Tanikawa, 2018, Cancer science.

Clonal origin of Philadelphia chromosome negative cells with trisomy 8 appearing during the course of alpha-interferon therapy for Ph positive chronic myelocytic leukemia.

N. Kakazu, Y. Nakamura, J. Inazawa, 1995, Cancer genetics and cytogenetics.

SNO is a probable target for gene amplification at 3q26 in squamous-cell carcinomas of the esophagus.

N. Nomura, J. Inazawa, I. Imoto, 2001, Biochemical and biophysical research communications.

Actinin-4 gene amplification in ovarian cancer: a candidate oncogene associated with poor patient prognosis and tumor chemoresistance

Hitoshi Tsuda, Masashi Takano, Tesshi Yamada, 2009, Modern Pathology.

Novel targets for the 18 p 11 . 3 amplification frequently observed in esophageal squamous cell carcinomas

J. Inazawa, I. Imoto, M. Imamura, 2001 .

Expression of cIAP1, a target for 11q22 amplification, correlates with resistance of cervical cancers to radiotherapy.

Masahiko Miura, Hitoshi Tsuda, Setsuo Hirohashi, 2002, Cancer research.

Expression of cIAP 1 , a Target for 11 q 22 Amplification , Correlates with Resistance of Cervical Cancers to Radiotherapy 1

S. Hirohashi, J. Inazawa, H. Tsuda, 2002 .

Molecular cloning of the breakpoint of t(11;22)(q23;q11) chromosome translocation in an adult acute myelomonocytic leukaemia

Y. Akao, T. Naoe, J. Inazawa, 1996, British journal of haematology.

Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes

J. Inazawa, M. Nagasawa, S. Mizutani, 2008, Cancer science.

Damaged epithelia regenerated by bone marrow–derived cells in the human gastrointestinal tract

J. Inazawa, T. Hibi, Y. Ikeda, 2002, Nature Medicine.

Identification of PDHX as a metabolic target for esophageal squamous cell carcinoma

J. Inazawa, H. Tsuda, T. Asakage, 2021, Cancer science.

Identification of SMURF1 as a possible target for 7q21.3‐22.1 amplification detected in a pancreatic cancer cell line by in‐house array‐based comparative genomic hybridization

S. Hirohashi, T. Shibata, J. Inazawa, 2008, Cancer science.

Isolation and mapping of a human gene (DIFF6) homologous to yeast CDC3, CDC10, CDC11, and CDC12, and mouse Diff6.

Y. Nakamura, T. Fujiwara, J. Inazawa, 1996, Cytogenetics and cell genetics.

Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese

Gary K. Chen, Hiroyuki Takahashi, Yusuke Nakamura, 2012, Nature Genetics.

Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population

Yusuke Nakamura, T. Kawaguchi, T. Tsunoda, 2010, Nature Genetics.

Potential in a single cancer cell to produce heterogeneous morphology, radiosensitivity and gene expression.

J. Inazawa, S. Ban, Y. Shimada, 2005, Journal of radiation research.

Characterization of an embryonal rhabdomyosarcoma cell line showing amplification and over‐expression of the N‐myc oncogene

A. Gown, J. Inazawa, Y. Hayashi, 1990, International journal of cancer.

Diverse responses to retinoid in morphological differentiation, tumorigenesis and n‐myc expression in human neuroblastoma sublines

J. Inazawa, T. Sugimoto, T. Matsumura, 1989, International journal of cancer.

Clinicopathologic analysis of breast carcinoma with chromosomal aneusomy detected by fluorescence in situ hybridization

J. Inazawa, Y. Miyoshi, S. Noguchi, 2001, Cancer.

IQGAP1, a negative regulator of cell-cell adhesion, is upregulated by gene amplification at 15q26 in gastric cancer cell lines HSC39 and 40A

A. Tanigami, J. Inazawa, S. Kuroda, 2001, Journal of Human Genetics.

12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population

Y. Kamatani, K. Matsuda, C. Haiman, 2019, Nature Communications.

Identification, basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP1 gene.

J. Inazawa, M. Sudol, D. Carey, 2012, Gene.

Identi fi cation , basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP 1 gene

J. Inazawa, M. Sudol, D. Carey, 2012 .

BCL2L2 is a probable target for novel 14q11.2 amplification detected in a non‐small cell lung cancer cell line

J. Inazawa, H. Tsuda, I. Imoto, 2007, Cancer science.

Overexpressed Skp2 within 5p amplification detected by array‐based comparative genomic hybridization is associated with poor prognosis of glioblastomas

T. Yoshimine, J. Inazawa, H. Tsuda, 2005, Cancer science.

PTK2 and EIF3S3 genes may be amplification targets at 8q23‐q24 and are associated with large hepatocellular carcinomas

J. Inazawa, S. Arii, K. Yasui, 2003, Hepatology.

GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines

J. Inazawa, Y. Matsuo, I. Imoto, 2003, Journal of Human Genetics.

Association of 17 q 21-q 24 Gain in Ovarian Clear Cell Adenocarcinomas with Poor Prognosis and Identification of PPM 1 D and APPBP 2 as Likely Amplification Targets 1

J. Inazawa, I. Imoto, D. Aoki, 2003 .

MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas

Yutaka Shimada, Masayuki Imamura, Masakazu Ueda, 2002, Journal of Human Genetics.

miR-655 Is an EMT-Suppressive MicroRNA Targeting ZEB1 and TGFBR2

J. Inazawa, T. Kawano, Y. Harazono, 2013, PloS one.

Cancer-associated miRNAs and their therapeutic potential

J. Inazawa, J. Inoue, 2021, Journal of Human Genetics.

Genetic Clustering of Clear Cell Renal Cell Carcinoma Based on Array-Comparative Genomic Hybridization: Its Association with DNA Methylation Alteration and Patient Outcome

S. Hirohashi, F. Hosoda, T. Shibata, 2008, Clinical Cancer Research.

Non-incidental coamplification of Myc and ERBB2, and Myc and EGFR, in gastric adenocarcinomas

J. Inazawa, H. Fujii, I. Imoto, 2007, Modern Pathology.

Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hybridization

J. Inazawa, Toshiki Mori, Y. Fukuda, 1998, Journal of Human Genetics.

DNA analysis using long-term preserved fixed cytogenetic preparations

J. Inazawa, M. Taniwaki, S. Misawa, 1988, Japanese Journal of Human Genetics.

Krüppel‐like factor 12 plays a significant role in poorly differentiated gastric cancer progression

Misao Ohki, Kengo Takeuchi, Yasuhito Arai, 2009, International journal of cancer.

Dermokine as a novel biomarker for early-stage colorectal cancer

J. Inazawa, I. Imoto, E. Otsuji, 2010, Journal of Gastroenterology.

Molecular cloning and chromosomal mapping of a bone marrow stromal cell surface gene, BST2, that may be involved in pre-B-cell growth.

J. Inazawa, T. Kaisho, T. Ochi, 1995, Genomics.

Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study

Toshihiro Tanaka, J. Inazawa, K. Moriyama, 2016, BMJ Open.

Identification of PAK4 as a putative target gene for amplification within 19q13.12‐q13.2 in oral squamous‐cell carcinoma

J. Inazawa, H. Tsuda, I. Imoto, 2009, Cancer science.

The brain finger protein gene (ZNF179), a member of the RING finger family, maps within the Smith-Magenis syndrome region at 17p11.2.

Y. Nakamura, S. Inoue, J. Inazawa, 1997, American journal of medical genetics.

Stabilization of phenotypic plasticity through mesenchymal-specific DNA hypermethylation in cancer cells

J. Inazawa, I. Imoto, T. Amagasa, 2012, Oncogene.

SIX1 promotes epithelial–mesenchymal transition in colorectal cancer through ZEB1 activation

J. Inazawa, H. Tsuda, I. Imoto, 2012, Oncogene.

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

Ellen F. Macnamara, Ryan K. Dale, Pedro P. Rocha, 2021, Science Advances.

Increased gene dosage of myelin protein zero causes Charcot‐Marie‐Tooth disease

S. Tsuji, J. Inazawa, H. Ishiura, 2012, Annals of neurology.

The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpoints

J. Inazawa, Y. Goto, I. Imoto, 2012, American journal of medical genetics. Part A.

Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation

J. Inazawa, Y. Goto, I. Imoto, 2011, Journal of Human Genetics.

Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis

J. Inazawa, Y. Goto, I. Imoto, 2010, Journal of Human Genetics.

The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separase

T. Noda, J. Inazawa, M. Yanagida, 2006, The Journal of cell biology.

miR-766-5p Targets Super-Enhancers by Downregulating CBP and BRD4

J. Inazawa, J. Inoue, T. Muramatsu, 2021, Cancer Research.

Prognostic implication of laminin-5 gamma 2 chain expression in the invasive front of colorectal cancers, disclosed by area-specific four-point tissue microarrays

H. Ueno, J. Inazawa, H. Tsuda, 2005, Laboratory Investigation.

Isolation and characterisation of lymphatic endothelial cells from lung tissues affected by lymphangioleiomyomatosis

Kenji Suzuki, J. Inazawa, Kazuhisa Takahashi, 2021, Scientific Reports.

Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia‐de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array‐based comparative genomic hybridization

J. Inazawa, S. Mizutani, I. Imoto, 2007, American journal of medical genetics. Part A.

Genetic variants in C5 and poor response to eculizumab.

J. Inazawa, K. Ando, Y. Kanakura, 2014, The New England journal of medicine.

Assignment of the human cytochrome P-450 nifedipine oxidase gene (CYP3A4) to chromosome 7 at band q22.1 by fluorescence in situ hybridization

H. Yamazaki, J. Inazawa, T. Shimada, 1992, Japanese Journal of Human Genetics.

Isolation, characterization and structural organization of the gene and pseudogene for the dihydrolipoamide succinyltransferase component of the human 2-oxoglutarate dehydrogenase complex.

J. Inazawa, S. Ohta, K. Nakano, 1994, European journal of biochemistry.

Molecular Cytogenetic Characterization of the Critical Deletion at 17p11.2 in Japanese Patients with Smith-Magenis Syndrome (SMS)

J. Inazawa, K. Hayasaka, Toshiyuki Kimura, 2003 .

POU2AF1, an amplification target at 11q23, promotes growth of multiple myeloma cells by directly regulating expression of a B-cell maturation factor, TNFRSF17

J. Inazawa, S. Iida, R. Ueda, 2008, Oncogene.

Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy

M. T. Medina, K. Yamakawa, J. Inazawa, 2006, Neuroscience Letters.

Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)

J. Inazawa, N. Okamoto, H. Osaka, 2017, PloS one.

Clinical and molecular cytogenetic characterization of two patients with non‐mutational aberrations of the FMR2 gene

J. Inazawa, S. Mizutani, I. Imoto, 2007, American journal of medical genetics. Part A.

Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation

Y. Fukushima, Y. Nakamura, J. Inazawa, 2000, Human Genetics.

Gene-expression phenotypes for vascular invasiveness of hepatocellular carcinomas.

Y. Miki, J. Inazawa, S. Arii, 2010, Surgery.

dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia

J. Inazawa, K. Imai, S. Nonoyama, 2007, American journal of medical genetics. Part A.

Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

M. Kanai, Y. Kamatani, Y. Okada, 2020, Nature Genetics.

Ploidy analysis in paraffin-embedded malignant fibrous histiocytoma by DNA cytofluorometry and flourescence in situ hybridization.

Y. Hirasawa, J. Inazawa, T. Abe, 1997, Cancer letters.

Autophagy is required for cell survival under L-asparaginase-induced metabolic stress in acute lymphoblastic leukemia cells

J. Inazawa, M. Takagi, S. Mizutani, 2017, Oncogene.

miR-634 Activates the Mitochondrial Apoptosis Pathway and Enhances Chemotherapy-Induced Cytotoxicity.

J. Inazawa, T. Kawano, K. Tanimoto, 2015, Cancer research.

Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene

T. Nakajima, T. Kodama, J. Inazawa, 1999, Journal of Human Genetics.

Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1).

J. Inazawa, Y. Nakamura, T. Tanaka, 1996, Genomics.

Structure of the human ferrochelatase gene. Exon/intron gene organization and location of the gene to chromosome 18.

J. Inazawa, T. Abe, S. Taketani, 1992, European journal of biochemistry.

An alternatively spliced isoform of transcriptional repressor ATF3 and its induction by stress stimuli.

Tsonwin Hai, J. Inazawa, I. Imoto, 2002, Nucleic acids research.

The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumors

Akira Teramoto, Hiroshi Takahashi, J. Inazawa, 2001, Journal of Human Genetics.

Improving the Efficacy of EGFR Inhibitors by Topical Treatment of Cutaneous Squamous Cell Carcinoma with miR-634 Ointment

J. Inazawa, K. Fujiwara, Katsunori Kobayashi, 2020, Molecular therapy oncolytics.

A novel amplification at 17q21-23 in ovarian cancer cell lines detected by comparative genomic hybridization.

S. Inoue, J. Inazawa, I. Imoto, 2001, Gynecologic oncology.

The tumor suppressive microRNA miR-218 targets the mTOR component Rictor and inhibits AKT phosphorylation in oral cancer.

J. Inazawa, I. Imoto, K. Omura, 2011, Cancer research.

Correlation between genetic alteration and long‐term clinical outcome of patients with oligodendroglial tumors, with identification of a consistent region of deletion on chromosome arm 1p

J. Inazawa, K. Mineura, N. Hashimoto, 2003, Cancer.

Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation.

Yusuke Nakamura, Y. Fukushima, J. Inazawa, 2000 .

Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization

Y. Nakamura, J. Inazawa, C. Sakakura, 1999, British Journal of Cancer.

Precise localization of the human gene encoding cell adhesion kinase beta (CAK beta/PYK2) to chromosome 8 at p21.1 by fluorescence in situ hybridization.

N. Kakazu, J. Inazawa, T. Sasaki, 1996, Human genetics.

Molecular alterations in AKT and its protein activation in human lung carcinomas.

J. Inazawa, Y. Dobashi, H. Matsubara, 2012, Human pathology.

Ovarian cancer therapeutic potential of glutamine depletion based on GS expression

Y. Song, J. Inazawa, N. Miyasaka, 2018, Carcinogenesis.

The Japanese Society of Pathology Guidelines on the handling of pathological tissue samples for genomic research: Standard operating procedures based on empirical analyses

Y. Miyagi, J. Inazawa, Teruhiko Yoshida, 2018, Pathology international.

Integrative array-based approach identifies MZB1 as a frequently methylated putative tumor suppressor in hepatocellular carcinoma.

J. Inazawa, I. Imoto, S. Arii, 2012, Clinical cancer research : an official journal of the American Association for Cancer Research.

Amplification on double‐minute chromosomes and partial‐tandem duplication of the MILL gene in leukemic cells of a patient with acute myelogenous leukemia

M. Seto, J. Inazawa, T. Abe, 1998, Genes, chromosomes & cancer.

Genome‐wide DNA methylation profiles in liver tissue at the precancerous stage and in hepatocellular carcinoma

S. Hirohashi, F. Hosoda, T. Shibata, 2009, International journal of cancer.

miR-432 Induces NRF2 Stabilization by Directly Targeting KEAP1

J. Inazawa, J. Inoue, Y. Nakajima, 2017, Molecular Cancer Research.

Association of over-expressed TFDP1 with progression of hepatocellular carcinomas

J. Inazawa, S. Arii, Kohichiroh Yasui, 2003, Journal of Human Genetics.

The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome

J. Inazawa, T. Taira, T. Nakagawa, 2011, BMC Neuroscience.

Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma

S. Miyano, S. Imoto, J. Inazawa, 2017, Oncotarget.

Diagnostic clinical application of two-color fluorescence in situ hybridization that detects chromosome 1 and 17 alterations to direct touch smear and liquid-based thin-layer cytologic preparations of endometrial cancers

J. Inazawa, H. Tsuda, D. Aoki, 2004, International Journal of Gynecologic Cancer.

Involvement of overexpressed wild-type BRAF in the growth of malignant melanoma cell lines

J. Inazawa, I. Imoto, A. Hirasawa, 2004, Oncogene.

Pax-5 is essential for kappa sterile transcription during Ig kappa chain gene rearrangement.

J. Inazawa, A. Kudo, Hiromu Sato, 2004, Journal of immunology.

An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers.

J. Inazawa, M. Emi, I. Imoto, 2001, American journal of medical genetics.

Aberrations of chromosomes 1 and 17 in six human osteosarcoma cell lines using double-target fluorescence in situ hybridization.

Y. Hirasawa, J. Inazawa, T. Abe, 1998, Cancer genetics and cytogenetics.

Relationship between chromosomal aberrations by fluorescence in situ hybridization and DNA ploidy by cytofluorometry in osteosarcoma.

Y. Hirasawa, J. Inazawa, T. Abe, 1999, Cancer Letters.

Genomic structure and chromosomal localization of the gene encoding TRAX, a Translin-associated factor X

J. Inazawa, M. Kasai, K. Aoki, 2000, Journal of Human Genetics.

Clinical Utility of Germline Genetic Testing in Japanese Men Undergoing Prostate Biopsy

J. Inazawa, T. Matsuda, Y. Momozawa, 2022, JNCI cancer spectrum.

Gene amplification of ESR1 in breast cancers—fact or fiction? A fluorescence in situ hybridization and multiplex ligation‐dependent probe amplification study

J. Inazawa, H. Ikeda, Y. Dobashi, 2012, The Journal of pathology.

Reexamination of chromosomal loci of human muscle actin genes by fluorescence in situ hybridization

J. Inazawa, H. Nishino, H. Ueyama, 1995, Japanese Journal of Human Genetics.

Cloning and characterization of a novel Rab-family gene, Rab36, within the region at 22q11.2 that is homozygously deleted in malignant rhabdoid tumors.

Y. Nakamura, J. Inazawa, T. Sugimoto, 1999, Biochemical and biophysical research communications.

Genomic structure and chromosomal mapping of the human Site-1 protease

T. Nakajima, K. Iwaki, T. Kodama, 2000 .

Genetically distinct and clinically relevant classification of hepatocellular carcinoma: putative therapeutic targets.

S. Hirohashi, F. Hosoda, T. Shibata, 2007, Gastroenterology.

Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome

N. Kakazu, J. Inazawa, M. Taniwaki, 1999, Genes, chromosomes & cancer.

The Tumor-Suppressive miR-497-195 Cluster Targets Multiple Cell-Cycle Regulators in Hepatocellular Carcinoma

S. Miyano, A. Niida, T. Shimamura, 2013, PloS one.

Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines

Yusuke Nakamura, M. Isobe, M. Seto, 1999, Journal of Human Genetics.

Philadelphia chromosome-negative cells with trisomy 8 after busulfan and interferon treatment of Ph1-positive chronic myelogenous leukemia.

J. Inazawa, T. Abe, Y. Miura, 1996, International journal of hematology.

HECT-type Ubiquitin Ligase ITCH Targets Lysosomal-associated Protein Multispanning Transmembrane 5 (LAPTM5) and Prevents LAPTM5-mediated Cell Death*

J. Inazawa, I. Imoto, K. Kozaki, 2011, The Journal of Biological Chemistry.

Correlation of KIT and EGFR overexpression with invasive ductal breast carcinoma of the solid‐tubular subtype, nuclear grade 3, and mesenchymal or myoepithelial differentiation

J. Inazawa, H. Tsuda, D. Morita, 2005, Cancer Science.

Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array‐based comparative genomic hybridization

J. Inazawa, S. Mizutani, I. Imoto, 2005, American journal of medical genetics. Part A.

Chromosomal localization of the human and mouse hyaluronan synthase genes.

A. Olsen, N. Doggett, J. Inazawa, 1997, Genomics.

GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12

Yusuke Nakamura, Shoichiro Tsugane, Yoichiro Kamatani, 2018, Carcinogenesis.

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis

J. Inazawa, R. Kosaki, S. Mizutani, 2007, Journal of Human Genetics.

Subcloning and characterization of highly metastatic cells derived from human esophageal squamous cell carcinoma KYSE150 cells by in vivo selection

J. Inazawa, T. Kawano, N. Fujiwara, 2017, Oncotarget.

cDNA Cloning and Chromosomal Localization of the Human Telencephalin and Its Distinctive Interaction with Lymphocyte Function-associated Antigen-1*

J. Inazawa, Y. Yoshihara, T. Mizuno, 1997, The Journal of Biological Chemistry.

Structural organization of the human oxytocin receptor gene.

J. Inazawa, C. Azuma, T. Kimura, 1994, The Journal of biological chemistry.

Suppression of MET Signaling Mediated by Pitavastatin and Capmatinib Inhibits Oral and Esophageal Cancer Cell Growth

J. Inazawa, Bo Xu, T. Muramatsu, 2020, Molecular Cancer Research.

Exosomal microRNA miR-1246 induces cell motility and invasion through the regulation of DENND2D in oral squamous cell carcinoma

J. Inazawa, K. Ueda, T. Muramatsu, 2016, Scientific Reports.

Overexpression of SMYD2 contributes to malignant outcome in gastric cancer

J. Inazawa, H. Tsuda, I. Imoto, 2014, British Journal of Cancer.

High Expression of SQSTM1/p62 Protein Is Associated with Poor Prognosis in Epithelial Ovarian Cancer

J. Inazawa, H. Tsuda, M. Takano, 2014, Acta histochemica et cytochemica.

Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line

Yoshiyuki Sakaki, Masahira Hattori, Misao Ohki, 2000, Oncogene.

Genome-Wide DNA Methylation Profiles in Renal Tumors of Various Histological Subtypes and Non-Tumorous Renal Tissues

S. Hirohashi, F. Hosoda, T. Shibata, 2011, Pathobiology.

Diagnosis and Prognostication of Ductal Adenocarcinomas of the Pancreas Based on Genome-Wide DNA Methylation Profiling by Bacterial Artificial Chromosome Array-Based Methylated CpG Island Amplification

F. Hosoda, T. Shibata, J. Inazawa, 2010, Journal of biomedicine & biotechnology.

ADAM23, a possible tumor suppressor gene, is frequently silenced in gastric cancers by homozygous deletion or aberrant promoter hypermethylation

S. Hirohashi, F. Hosoda, J. Inazawa, 2005, Oncogene.

Identification and characterization of human PKNOX2, a novel homeobox-containing gene.

J. Inazawa, I. Imoto, I Imoto, 2001, Biochemical and biophysical research communications.

Reduced Levels of ATF-2 Predispose Mice to Mammary Tumors

Koichi Nagasaki, Yoshio Miki, Shintaro Nomura, 2006, Molecular and Cellular Biology.

Neuroradiologic Features of CASK Mutations

J. Inazawa, A. Barkovich, J. Takanashi, 2010, American Journal of Neuroradiology.

Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses

N. Niikawa, Y. Nakamura, J. Inazawa, 1994, Genes, chromosomes & cancer.

Isolation and mapping of a human gene (RABL) encoding a small GTP-binding protein homologous to the Ras-related RAB gene.

Y. Nakamura, J. Inazawa, H. Han, 1996, Cytogenetics and cell genetics.

Clinical and radiological features of Japanese patients with a severe phenotype due to CASK mutations

J. Inazawa, A. Barkovich, J. Takanashi, 2012, American journal of medical genetics. Part A.

Chromosome 9q33q34 microdeletion with early infantile epileptic encephalopathy, severe dystonia, abnormal eye movements, and nephroureteral malformations.

J. Inazawa, S. Nonoyama, H. Matsumoto, 2014, Pediatric neurology.

Human Gene for β-Microseminoprotein: Its Promoter Structure and Chromosomal Localization

J. Inazawa, H. Ueyama, I. Ohkubo, 1995 .

Detection of numerical alterations of chromosomes 3, 7, 17 and X in low-grade intracystic papillary tumors of the breast by multi-color fluorescencein situ hybridization

S. Hirohashi, J. Inazawa, T. Takarabe, 1997, Breast cancer.

Detection of numerical and structural alterations and fusion of chromosomes 16 and 1 in low-grade papillary breast carcinoma by fluorescence in situ hybridization.

S. Hirohashi, J. Inazawa, H. Tsuda, 1997, The American journal of pathology.

Identification of an Efs isoform that lacks the SH3 domain and chromosomal mapping of human Efs

J. Inazawa, Terukatsu Sasaki, M. Ishino, 1997, Oncogene.

Absence in Ph-negative, M-BCR rearrangement-positive chronic myelogenous leukemia of linkage between 5' ABL and 3' M-BCR sequences in Philadelphia translocation.

J. Inazawa, S. Misawa, H. Nishigaki, 1992, Leukemia.

cDNA sequence, gene structure, and chromosomal localization of the human ATP-sensitive potassium channel, uKATP-1, gene (KCNJ8).

J. Inazawa, S. Seino, N. Inagaki, 1995, Genomics.

Genetic analysis of multifocal superficial urothelial cancers by array-based comparative genomic hybridisation

J. Inazawa, G. Tsujimoto, H. Nishiyama, 2007, British Journal of Cancer.

Augmentation of lenvatinib efficacy by topical treatment of miR-634 ointment in anaplastic thyroid cancer

J. Inazawa, Katsunori Kobayashi, T. Asakage, 2021, Biochemistry and biophysics reports.

Multi-color FISH : Application to the Simultaneous Detection of Chromosome Aberrations in Neuro-epithelial Tumor Cell Lines

J. Inazawa, D. Ichikawa, T. Matsumura, 1995 .

Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer

T. Shibata, J. Inazawa, T. Kinoshita, 2019, BMC Cancer.

Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease

A. Singleton, M. Farrer, J. Inazawa, 2006 .

A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progression.

J. Inazawa, K. Mineura, N. Hashimoto, 2003, Cancer genetics and cytogenetics.

Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)

J. Inazawa, A. Hata, I. Imoto, 2011, Human Genetics.

The human caspase-activated DNase gene (hCAD): genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locus

J. Inazawa, A. Nakagawara, S. Nagata, 1999, Journal of Human Genetics.

Down-regulation of LAPTM5 in human cancer cells

J. Inazawa, T. Kawano, J. Inoue, 2016, Oncotarget.

ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array‐based comparative genomic hybridization

J. Inazawa, H. Tsuda, I. Imoto, 2008, Cancer science.

Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.

A. Singleton, M. Farrer, J. Inazawa, 2006, Annals of neurology.

Isolation of novel genes within the amplified regions in tumors detected by comparative genomic hybridization (CGH)

J. Inazawa, 1999 .

Multistep Carcinogenesis of Esophageal Carcinoma

Yusuke Nakamura, J. Inazawa, T. Tokino, 1997 .

Assignment of the human renal dipeptidase gene (DPEP1) to band q24 of chromosome 16.

J. Inazawa, S. Misawa, K. Kashima, 1992, Cytogenetics and cell genetics.

Assignment of the human ST2 gene to chromosome 2 at q11.2

S. Tominaga, S. Tsuji, J. Inazawa, 1996, Human Genetics.

The Impact of miRNA-Based Molecular Diagnostics and Treatment of NRF2-Stabilized Tumors

J. Inazawa, T. Kawano, K. Omura, 2013, Molecular Cancer Research.

High Expression of p62 Protein Is Associated with Poor Prognosis and Aggressive Phenotypes in Endometrial Cancer.

J. Inazawa, H. Tsuda, M. Takano, 2015, The American journal of pathology.

Skp2 overexpression is a p27Kip1‐independent predictor of poor prognosis in patients with biliary tract cancers

J. Inazawa, I. Imoto, S. Arii, 2004, Cancer science.

predictor of poor prognosis in patients with biliary tract cancers

J. Inazawa, I. Imoto, S. Arii, 2004 .

A missense variant in NUF2, a component of the kinetochore NDC80 complex, causes impaired chromosome segregation and aneuploidy associated with microcephaly and short stature

J. Inazawa, H. Mitsubuchi, D. T. Uehara, 2021, Human Genetics.

Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2

Y. Nakamura, J. Inazawa, T. Tokino, 1993, Genes, chromosomes & cancer.

Imaging flow cytometry-based multiplex FISH for three IGH translocations in multiple myeloma

J. Inazawa, Toshikazu Yamaguchi, J. Kuroda, 2023, Journal of Human Genetics.

Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment

K. Yamakawa, H. Kasai, I. Graef, 2024, eLife.

Establishment and characterization of a cisplatin-resistant human neuroblastoma cell line.

A. Naganuma, J. Inazawa, T. Sawada, 1999, Anticancer research.

Surgical contribution to recurrence-free survival in patients with macrovascular-invasion-negative hepatocellular carcinoma.

Hiroshi Tanaka, Toshiaki Kurokawa, Shinji Tanaka, 2009, Journal of the American College of Surgeons.

Identification of the homozygously deleted region at chromosome 1p36.2 in human neuroblastoma.

M. Hattori, Y. Sakaki, Y. Nakamura, 2000, Medical and pediatric oncology.

Significance of GSTP1 for predicting the prognosis and chemotherapeutic efficacy in esophageal squamous cell carcinoma.

J. Inazawa, D. Ichikawa, E. Otsuji, 2013, Oncology reports.

Human ryudocan core protein: molecular cloning and characterization of the cDNA, and chromosomal localization of the gene.

J. Inazawa, J. Takamatsu, R. Rosenberg, 1993, Biochemical and biophysical research communications.

Genomic structure and mapping of human orphan receptor LXR alpha: upregulation of LXRa mRNA during monocyte to macrophage differentiation.

H. Aburatani, T. Nakajima, J. Inazawa, 2000, Journal of atherosclerosis and thrombosis.

Partial tandem duplication of GRIA3 in a male with mental retardation

J. Inazawa, I. Imoto, Zhengping Jia, 2007, American journal of medical genetics. Part A.

Frequent association of alternative splicing of NER, a nuclear hormone receptor gene in cancer tissues

Yusuke Nakamura, J. Inazawa, T. Nishihira, 1997, Oncogene.

PTPN13, a fas-associated protein tyrosine phosphatase, is located on the long arm of chromosome 4 at band q21.3.

J. Inazawa, K. Huebner, John Calvin Reed, 1996, Genomics.

Assignment of the human antizyme gene (OAZ) to chromosome 19p13.3 by fluorescence in situ hybridization.

J. Inazawa, J. F. Atkins, S. Matsufuji, 1996, Genomics.

Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer

T. Shibata, J. Inazawa, T. Kinoshita, 2019, BMC Cancer.

Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta

N. Niikawa, J. Inazawa, T. Miyamoto, 1999, Journal of Human Genetics.

The human protoporphyrinogen oxidase gene (PPOX): organization and location to chromosome 1.

H. Inokuchi, J. Inazawa, T. Abe, 1995, Genomics.

Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors.

Y. Nakamura, J. Inazawa, R. Kudo, 1993, Cancer Research.

Comparative genomic hybridization of squamous cell carcinoma of the esophagus: The possible involvement of the DP1 gene in the 13q34 amplicon

J. Inazawa, Y. Nakamura, Y. Fukuda, 1999, Genes, chromosomes & cancer.

Reciprocal t(14;19)(q32.3;q13.1) in a patient with B-cell lymphoma.

J. Inazawa, M. Taniwaki, S. Misawa, 1990, Cancer genetics and cytogenetics.

Identification of a novel Sry-related gene and its germ cell-specific expression.

J. Inazawa, N. Copeland, D. Gilbert, 1999, Nucleic acids research.

Molecular and Cellular Pathobiology the Tumor Suppressive Microrna Mir-218 Targets the Mtor Component Rictor and Inhibits Akt Phosphorylation in Oral Cancer

J. Inazawa, I. Imoto, K. Omura, 2022 .

Expanding the BBMRI-ERIC Directory into a Global Catalogue of COVID-19-Ready Collections: A Joint Initiative of BBMRI-ERIC and ISBER

T. Takagi, Toshihiro Tanaka, S. Imoto, 2020 .

BCL 2 L 2 is a probable target for novel 14 q 11 . 2 amplification detected in a non-small cell lung cancer cell line

J. Inazawa, H. Tsuda, I. Imoto, 2007 .

Squamous Cell Carcinoma Genetic and Epigenetic Mechanisms in Esophageal ) Expression by Receptor-Related Protein 1 B ( LRP 1 B Low Density Lipoprotein Frequent Silencing of Updated

K. Chin, J. Gray, S. Hirohashi, 2004 .

Assignment of the human protein tyrosine phosphatase, receptor-type, zeta (PTPRZ) gene to chromosome band 7q31.3.

J. Inazawa, M. Ogimoto, T. Katagiri, 1995, Cytogenetics and cell genetics.

Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle

J. Inazawa, M. Emi, T. Yokota, 2001, Journal of Human Genetics.

Germline mutations of the RET proto-oncogene in pedigree with MEN type 2A: DNA analysis and its implications for pediatric surgery.

J. Inazawa, I. Nishisho, T. Shimotake, 1996, Journal of pediatric surgery.

Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophy

O. Abe, S. Aoki, T. Matsukawa, 2020, Brain communications.

Molecular cloning and mapping of a human cDNA (SC5DL) encoding a protein homologous to fungal sterol-C5-desaturase.

Y. Nakamura, J. Inazawa, M. Matsushima, 1996, Cytogenetics and cell genetics.

High Expression of p62 Protein Is Associated with Poor Prognosis and Aggressive Phenotypes in Endometrial Cancer.

J. Inazawa, H. Tsuda, M. Takano, 2015, The American journal of pathology.

A BAC-based STS-content map spanning a 35-Mb region of human chromosome 1p35-p36.

F. Hosoda, J. Inazawa, Y. Arai, 2001, Genomics.

Human arylhydrocarbon receptor: functional expression and chromosomal assignment to 7p21.

M. Oshimura, J. Inazawa, Y. Fujii‐Kuriyama, 1994, Journal of biochemistry.

Molecular alterations in AKT and its protein activation in human lung carcinomas.

J. Inazawa, Y. Dobashi, H. Matsubara, 2012, Human pathology.

Significance of GSTP 1 for predicting the prognosis and chemotherapeutic efficacy in esophageal squamous cell carcinoma

J. Inazawa, D. Ichikawa, E. Otsuji, 2022 .

Overexpressed NF- (cid:1) B–inducing kinase contributes to the tumorigenesis of adult T-cell leukemia and Hodgkin Reed-Sternberg cells

J. Inazawa, Y. Iwasaki, T. Masuda, 2008 .

Regional chromosomal assignment of carcinoembryonic antigen gene (CEA) to chromosome 19 at band q13.2.

J. Inazawa, M. Taniwaki, S. Misawa, 1991, Cancer genetics and cytogenetics.

CARCINOEMBRYONIC ANTIGEN (CEA) FAMILY GENES ARE LOCATED ON HUMAN CHROMOSOME 19 AT BAND q13.2

J. Inazawa, T. Abe, 1990 .

Microsatellite instability is an early genetic event in myelodysplastic syndrome.

J. Inazawa, H. Kaneko, S. Misawa, 1995, Blood.

Genome‐wide DNA methylation profiles in urothelial carcinomas and urothelia at the precancerous stage

S. Hirohashi, F. Hosoda, T. Shibata, 2010, Cancer science.

miR-544a induces epithelial-mesenchymal transition through the activation of WNT signaling pathway in gastric cancer.

J. Inazawa, H. Uetake, K. Kozaki, 2015, Carcinogenesis.

ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array‐based comparative genomic hybridization

J. Inazawa, H. Tsuda, I. Imoto, 2008, Cancer Science.

Chromosome arm 20q gains and other genomic alterations in esophageal squamous cell carcinoma, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization.

J. Inazawa, C. Sakakura, A. Hagiwara, 2003, Hepato-gastroenterology.

Genome-Wide DNA Methylation Profiles in Renal Tumors of Various Histological Subtypes and Non-Tumorous Renal Tissues

S. Hirohashi, F. Hosoda, T. Shibata, 2011, Pathobiology.

Multiple Primary Cancers with Microsatellite Instability: Report of a Case

J. Inazawa, D. Ichikawa, Toshiharu Yamaguchi, 1996, Japanese journal of cancer research : Gann.

Therapeutic applications of local injection of hsa-miR-634 into canine spontaneous malignant melanoma tumors

J. Inazawa, J. Inoue, T. Hasegawa, 2023, Cancer Gene Therapy.