M. Emi

M. Becich, S. Pastorino, A. Gazdar, 2015, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations.

L. Jorde, T. Nakajima, M. Emi, 2002, American journal of human genetics.

Combined hypermethylation and chromosome loss associated with inactivation of SSI-1/SOCS-1/JAB gene in human hepatocellular carcinomas.

M. Emi, Y. S. Kim, A. Yoshimura, 2002, Cancer letters.

Inactivation of SSI-1, a JAK/STAT inhibitor, in human hepatocellular carcinomas, as revealed by two-dimensional electrophoresis.

M. Emi, N. Konishi, Y. Kim, 2001, Journal of hepatology.

Allelotyping of anaplastic thyroid carcinoma: Frequent allelic losses on 1q, 9p, 11, 17, 19p, and 22q

M. Emi, Koichi Ito, Y. Kitamura, 2000, Genes, chromosomes & cancer.

Inactivation of both alleles of the DPC4/SMAD4 gene in advanced colorectal cancers: identification of seven novel somatic mutations in tumors from Japanese patients.

M. Emi, M. Ito, H. Nagai, 1999, Mutation research.

Identification of a 1‐cM region of common deletion on 13q14 associated with human prostate cancer

M. Emi, K. Akakura, Masatoshi Watanabe, 1999 .

Characterization of liver-cirrhosis nodules by analysis of gene-expression profiles and patterns of allelic loss

M. Emi, N. Konishi, T. Tajiri, 2004, Journal of Human Genetics.

Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700s

Todd A. Johnson, T. Tsunoda, S. Pastorino, 2015, PLoS genetics.

A novel sperm-specific hypomethylation sequence is a demethylation hotspot in human hepatocellular carcinomas.

K Matsubara, M Monden, M. Emi, 1999, Gene.

Overexpressed in anaplastic thyroid carcinoma‐1 (OEATC‐1) as a novel gene responsible for anaplastic thyroid carcinoma

M. Emi, M. Nagahama, J. Akaishi, 2005, Cancer.

Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer

Yusuke Nakamura, Masahiko Onda, Fujio Kasumi, 1998, Japanese journal of cancer research : Gann.

Hypermethylation associated with inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human hepatoblastomas

Mitsutoshi Nakamura, M. Emi, N. Konishi, 2003, Journal of Human Genetics.

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

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

Association of nucleotide variations in the apolipoprotein B48 receptor gene (APOB48R) with hypercholesterolemia

T. Nakajima, M. Emi, Y. Ezura, 2005, Journal of Human Genetics.

Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers

Yusuke Nakamura, Toshihiro Tanaka, T. Tsunoda, 2004, Journal of Cancer Research and Clinical Oncology.

Mesothelioma developing in carriers of inherited genetic mutations

M. Emi, T. Nakano, G. Gaudino, 2020, Translational lung cancer research.

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

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

Overrepresentation of the EBAG9 gene at 8q23 associated with early-stage breast cancers.

Y. Nakamura, S. Inoue, M. Emi, 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.

Promoter analysis and chromosomal mapping of human EBAG9 gene.

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

Overrepresentation of the EBAG 9 Gene at 8 q 23 Associated with Early-Stage Breast Cancers 1

Yusuke Nakamura, S. Inoue, M. Emi, 2001 .

A Subset of Mesotheliomas With Improved Survival Occurring in Carriers of BAP1 and Other Germline Mutations.

S. Pastorino, M. Emi, H. Pass, 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Frequent multiplication of chromosomal region 8q24.1 associated with aggressive histologic types of breast cancers.

Y. Nakamura, M. Emi, T. Yokota, 1999, Cancer letters.

Amplification, up‐regulation and over‐expression of DVL‐1, the human counterpart of the Drosophila disheveled gene, in primary breast cancers

M. Emi, O. Kawanami, T. Shiba, 2003, Cancer science.

High-density array-CGH with targeted NGS unmask multiple noncontiguous minute deletions on chromosome 3p21 in mesothelioma

S. Pastorino, M. Emi, T. Nakano, 2016, Proceedings of the National Academy of Sciences.

Frequent Loss of Genome Gap Region in 4p16.3 Subtelomere in Early-Onset Type 2 Diabetes Mellitus

M. Emi, Y. Hinokio, H. Katagiri, 2011, Experimental diabetes research.

Segmental copy number loss of SFMBT1 gene in elderly individuals with ventriculomegaly: a community-based study.

M. Emi, T. Kawanami, Hidenori Sato, 2011, Internal medicine.

Various types of LRP5 mutations in four patients with osteoporosis‐pseudoglioma syndrome: Identification of a 7.2‐kb microdeletion using oligonucleotide tiling microarray

M. Emi, T. Shiihara, T. Matsuishi, 2010, American journal of medical genetics. Part A.

Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human matrix Gla protein (MGP) locus

M. Emi, T. Shiba, K. Tsukamoto, 1998, Journal of Human Genetics.

Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human estrogen receptor β locus

Hajime Orimo, Satoshi Inoue, S. Inoue, 1998, Journal of Human Genetics.

Detailed analysis of genetic alterations in colorectal tumors from patients with and without familial adenomatous polyposis (FAP).

M. Emi, Y. Miyoshi, J. Utsunomiya, 1993, Oncogene.

Primary structure of human salivary α-amylase gene

M. Emi, Takesada Mori, K. Matsubara, 1986 .

Sequences of cDNAs for human salivary and pancreatic α-amylases

M. Emi, K. Matsubara, G. Kōsaki, 1984 .

Risk prediction for metastasis of clear cell renal cell carcinoma using digital multiplex ligation‐dependent probe amplification

M. Emi, M. Ohmuraya, A. Kanematsu, 2021, Cancer science.

Association of the PIK3C2G gene polymorphisms with type 2 DM in a Japanese population.

M. Emi, I. Kubota, M. Muramatsu, 2005, Biochemical and biophysical research communications.

Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1‐cM Intervals on Genomic Contigs at 6q21 and 6q25.3

Yusuke Nakamura, M. Emi, S. Haga, 2000, Japanese journal of cancer research : Gann.

PTEN/MMAC1 Mutations in Hepatocellular Carcinomas: Somatic Inactivation of Both Alleles in Tumors

M. Emi, N. Konishi, T. Tajiri, 1999, Japanese journal of cancer research : Gann.

Somatic mutation of the PTEN/MMAC1 gene in breast cancers with microsatellite instability.

Y. Nakamura, M. Emi, G. Sakamoto, 1999, Cancer Letters.

Somatic Mutations of the PTEN/MMAC1 Gene in Fifteen Japanese Endometrial Cancers: Evidence for Inactivation of Both Alleles

M. Emi, Y. Sugisaki, K. Kurose, 1998, Japanese journal of cancer research : Gann.

Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray

Tatsuhiko Tsunoda, Yoshio Miki, Fujio Kasumi, 2004, Cancer science.

Association of genetic alterations on chromosome 17 and loss of hormone receptors in breast cancer.

T. Katagiri, M. Emi, S. Yasuda, 1995, British Journal of Cancer.

Copy number loss in the region of the ASPN gene in patients with acetabular dysplasia

M. Emi, E. Chosa, T. Sekimoto, 2017, Bone & joint research.

Primary structure of human pancreatic α-amylase gene: its comparison with human salivary α-amylase gene

M. Emi, Takesada Mori, N. Tomita, 1987 .

Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders

M. Emi, T. Kawanami, Hidenori Sato, 2017, BMC Medical Genetics.

Genome-wide copy number analysis in primary breast cancer

M. Emi, M. Toi, Hidenori Sato, 2012, Expert opinion on therapeutic targets.

Molecular cloning and nucleotide sequence of human pancreatic secretory trypsin inhibitor (PSTI) cDNA.

Y. Nakamura, M. Emi, K. Matsubara, 1985, Biochemical and biophysical research communications.

Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases

Y. Kamatani, Yusuke Nakamura, Y. Ohnishi, 2017, Journal of epidemiology.

Fusion of a novel gene, ELKS, to RET due to translocation t(10;12)(q11;p13) in a papillary thyroid carcinoma

M. Emi, M. Fujimori, Y. Kitamura, 1999, Genes, chromosomes & cancer.

Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers

M. Emi, O. Kawanami, I. Mikami, 2004, Journal of Human Genetics.

Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world.

N. Saitou, L. Jorde, T. Nakajima, 2004, American journal of human genetics.

Segmental copy number loss in the region of Semaphorin 4D gene in patients with acetabular dysplasia

M. Emi, E. Chosa, T. Sekimoto, 2013, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis.

M. Emi, G. Sobue, T. Kawanami, 2010, Biochemical and biophysical research communications.

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.

Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation

M. Emi, H. Ohashi, Hidenori Sato, 2011, Human Genetics.

Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypes.

M. Emi, J. Lalouel, P. Hopkins, 1991, Arteriosclerosis and thrombosis : a journal of vascular biology.

Chapter 9 – Lipoprotein(a) and Plasminogen: Linkage Analysis

M. Emi, R. Hegele, J. Lalouel, 1990 .

Genetic linkage between lipoprotein(a) phenotype and a DNA polymorphism in the plasminogen gene.

M. Emi, R. Hegele, J. Lalouel, 1988, Genomics.

A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene

M. Emi, A. Teramoto, Hiroshi Takahashi, 2000, Journal of Human Genetics.

A single nucleotide polymorphism in the CCL1 gene predicts acute exacerbations in chronic obstructive pulmonary disease.

M. Emi, I. Kubota, Y. Takeishi, 2006, American journal of respiratory and critical care medicine.

Cloning, characterization and nucleotide sequences of two cDNAs encoding human pancreatic trypsinogens.

K Matsubara, Y. Nakamura, M. Emi, 1986, Gene.

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.

Down‐regulation of members of glycolipid‐enriched membrane raft gene family, MAL and BENE, in cervical squamous cell cancers

M. Emi, K. Yoneyama, Mitsuko Hatta, 2004, The journal of obstetrics and gynaecology research.

Genetic studies of 457 breast cancers. Clinicopathologic parameters compared with genetic alterations

Yusuke Nakamura, T. Katagiri, M. Emi, 1994, Cancer.

Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 protein

N. Saitou, T. Nakajima, M. Emi, 2005, Genes and Immunity.

Tob, a novel protein that interacts with p185erbB2, is associated with anti-proliferative activity.

Y. Nakamura, M. Emi, M. Yoshida, 1996, Oncogene.

Association of a single nucleotide variant in the human tumour necrosis factor alpha promoter region with decreased bone mineral density

S. Inoue, T. Nakajima, M. Emi, 2002, Annals of human biology.

Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer

T. Nakajima, M. Emi, T. Shuin, 2005, Journal of Human Genetics.

HNF1B alterations associated with congenital anomalies of the kidney and urinary tract

M. Emi, K. Nakanishi, S. Ito, 2010, Pediatric Nephrology.

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.

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 .

Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals

T. Nakajima, M. Emi, Y. Ezura, 2001, Journal of Human Genetics.

Accuracy of genotyping for single nucleotide polymorphisms by a microarray-based single nucleotide polymorphism typing method involving hybridization of short allele-specific oligonucleotides.

M. Emi, Y. Ezura, M. Kajita, 2002, DNA research : an international journal for rapid publication of reports on genes and genomes.

The effect of genetic determinants of low density lipoprotein levels on lipoprotein (a).

M. Emi, R. Hegele, J. Lalouel, 1991, Clinical and investigative medicine. Medecine clinique et experimentale.

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.

A family with spinal anaplastic ependymoma: evidence of loss of chromosome 22q in tumor

M. Emi, T. Yokota, Koshi Matsumoto, 2003, Journal of Human Genetics.

Somatic alteration and depleted nuclear expression of BAP1 in human esophageal squamous cell carcinoma

M. Emi, M. Nagasaki, C. Ishioka, 2015, Cancer science.

Common null variant, Arg192Stop, in a G‐protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activity

M. Emi, I. Kubota, S. Koyano, 2008, Hepatology research : the official journal of the Japan Society of Hepatology.

A nonfunctioning single nucleotide polymorphism in olfactory receptor gene family is associated with the forced expiratory volume in the first second/the forced vital capacity values of pulmonary function test in a Japanese population.

M. Emi, I. Kubota, Y. Takeishi, 2007, Biochemical and biophysical research communications.

Comprehensive gene expression profiling of anaplastic thyroid cancers with cDNA microarray of 25 344 genes.

Toshihiro Tanaka, T. Tsunoda, M. Emi, 2004, Endocrine-related cancer.

Down‐regulation in Multiple Human Cancers of a Novel Gene, DMHC, from 17q25.1 That Encodes an Integral Membrane Protein

S. Sugano, M. Emi, H. Harada, 2001, Japanese journal of cancer research : Gann.

Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers

Sumio Sugano, S. Sugano, M. Emi, 2001, Journal of Human Genetics.

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

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

Three TNF α single nucleotide polymorphisms in the Japanese population

T. Nakajima, M. Emi, Y. Ezura, 2002 .

Nine novel single-nucleotide polymorphisms in the integrin β4 (ITGB4) gene in the Japanese population

M. Emi, T. Kajiwara, H. Harada, 2001, Journal of Human Genetics.

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.

M. Emi, J. Lalouel, A. Hata, 1990, The Journal of clinical investigation.

Association of estrogen receptor β (ESR2) gene polymorphism with blood pressure

Satoshi Inoue, Y. Ouchi, S. Inoue, 2000, Journal of Human Genetics.

Association of Estrogen Receptor β Gene Polymorphism with Bone Mineral Density

Y. Ouchi, S. Inoue, M. Emi, 2000 .

Identification of RAI3 as a therapeutic target for breast cancer.

M. Emi, K. Nishikawa, A. Tomura, 2005, Endocrine-related cancer.

Identification of RAI3 as a therapeutic target for breast cancer.

M. Emi, K. Nishikawa, A. Tomura, 2005, Endocrine-related cancer.

Suppressor of cytokine signalling‐1 gene silencing in acute myeloid leukaemia and human haematopoietic cell lines

M. Emi, H. Kanegane, I. Kawase, 2004, British journal of haematology.

A polymorphism of the aldehyde dehydrogenase 2 gene is a risk factor for multiple lacunar infarcts in Japanese men: the Takahata Study

M. Emi, T. Hosoya, M. Muramatsu, 2007, European journal of neurology.

Identification of a 1‐Mb common region at 16q24.1–24.2 deleted in hepatocellular carcinoma

M. Emi, T. Tajiri, S. Matsumoto, 2000, Genes, chromosomes & cancer.

Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM.

M. Emi, S. Hunt, P. Hopkins, 2008, Biochemical and biophysical research communications.

Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability

M. Emi, T. Shimada, H. Orimo, 2000, Journal of Human Genetics.

Two distinct commonly deleted regions on chromosome 13q suggest involvement of BRCA2 and retinoblastoma genes in sporadic breast carcinomas.

Y. Nakamura, M. Emi, T. Iwase, 1996, Cancer.

Identification of a I-cM region of common deletion on 13q14 associated with human prostate cancer.

M. Emi, K. Akakura, H. Ito, 1999, Genes, chromosomes & cancer.

Linkage disequilibrium analyses of natriuretic peptide precursor B locus reveal risk haplotype conferring high plasma BNP levels.

M. Emi, I. Kubota, Y. Takeishi, 2007, Biochemical and biophysical research communications.

Detailed deletion mapping of chromosome arm 3p in breast cancers: A 2‐cM region on 3p14.3‐21.1 and a 5‐cM region on 3p24.3‐25.1 commonly deleted in tumors

M. Emi, G. Sakamoto, F. Kasumi, 1997, Genes, chromosomes & cancer.

[iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI)].

M. Emi, T. Kawanami, Hidenori Sato, 2010, Rinshō shinkeigaku Clinical neurology.

A functional polymorphism of the TNF-alpha gene that is associated with type 2 DM.

M. Emi, M. Muramatsu, Hidenori Sato, 2008, Biochemical and biophysical research communications.

Upregulation and Overexpression of DVL1, the Human Counterpart of the Drosophila Dishevelled Gene, in Prostate Cancer

M. Emi, N. Konishi, M. Onda, 2005, Tumori.

Short somatic alterations at the site of copy number variation in breast cancer

T. Shibata, M. Emi, Y. Murakami, 2020, Cancer science.

Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis

Hidenori Sato, M. Emi, S. Ikegawa, 2008, Journal of Human Genetics.

Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women

M. Emi, Shuichiro Watanabe, H. Orimo, 2000, Journal of Bone and Mineral Metabolism.

Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locus

T. Nakajima, M. Emi, Y. Shirai, 1999, Journal of Human Genetics.

Three distinct commonly deleted regions of chromosome arm 16q in human primary and metastatic prostate cancers

M. Emi, T. Shiraishi, Hiroyoshi Suzuki, 1996, Genes, chromosomes & cancer.

Association of a promoter haplotype (-1542G/-525C) in the tumor necrosis factor receptor associated factor-interacting protein gene with low bone mineral density in Japanese women.

S. Inoue, M. Emi, Y. Ezura, 2003, Bone.

Association of a Haplotype (196Phe/532Ser) in the Interleukin‐1‐Receptor‐Associated Kinase (IRAK1) Gene With Low Radial Bone Mineral Density in Two Independent Populations

S. Inoue, M. Emi, Y. Ezura, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction.

M. Emi, S. Hunt, J. Lalouel, 1991, Arteriosclerosis and thrombosis : a journal of vascular biology.

Association of Molecular Variants, Haplotypes, and Linkage Disequilibrium Within the Human Vitamin D‐Binding Protein (DBP) Gene With Postmenopausal Bone Mineral Density

S. Inoue, T. Nakajima, M. Emi, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Isolation and mapping of 88 new RFLP markers on human chromosome 8.

Y. Nakamura, M. Oshimura, M. Emi, 1992, Genomics.

Analysis of the MEN1 gene in sporadic pituitary adenomas from Japanese patients.

M. Emi, Y. Kitamura, A. Teramoto, 1999, Cancer letters.

DNA alterations during multi-step development of human hepatocellular carcinomas revealed by laser capture microdissection.

M. Emi, S. Kaneko, Kenichi Kobayashi, 2003, Hepatology research : the official journal of the Japan Society of Hepatology.

Differential expression of multiple isoforms of the ELKS mRNAs involved in a papillary thyroid carcinoma

M. Emi, T. Yokota, S. Minami, 2002, Genes, chromosomes & cancer.

Hypertriglyceridemia associated with amino acid variation Asn985Tyr of theRP1 gene

M. Emi, Y. Ezura, H. Bujo, 2003, Journal of Human Genetics.

A promoter SNP (−1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia

M. Emi, S. Umemura, Y. Ezura, 2003, Journal of Human Genetics.

Osteopontin is associated with nuclear factor kappaB gene expression during tail-suspension-induced bone loss.

Masaki Noda, Hisashi Kurosawa, Muneaki Ishijima, 2006, Experimental cell research.

Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus

T. Nakajima, T. Kodama, M. Emi, 1999, Journal of Human Genetics.

A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus

M. Emi, K. Tsukamoto, Y. Shirai, 1998, Journal of Human Genetics.

Molecular analysis of TSC2/PKD1 contiguous gene deletion syndrome.

M. Emi, M. Matsuo, K. Nozu, 2011, The Kobe journal of medical sciences.

Kobe University Repository : Kernel タイトル Tit le Molecular Analysis of TSC 2 / PKD 1 Cont iguous Gene Delet ion Syndrome

M. Emi, M. Matsuo, K. Nozu, 2019 .

Allelic loss at 1p34-36 predicts poor prognosis in node-negative breast cancer.

Y. Nakamura, M. Emi, F. Akiyama, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy

M. Emi, H. Sasaki, Hidenori Sato, 2011, Molecular Brain.

Universal fluorescent labeling (UFL) method for automated microsatellite analysis.

M. Emi, T. Shiba, T. Shimada, 2002, DNA research : an international journal for rapid publication of reports on genes and genomes.

[Genetic analysis of osteoporosis susceptibility: future perspectives on genome wide analysis].

M. Emi, Y. Ezura, 2005, Clinical calcium.

Association of Multiple Nucleotide Variations in the Pituitary Glutaminyl Cyclase Gene (QPCT) With Low Radial BMD in Adult Women

S. Inoue, M. Emi, Y. Ezura, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Association of common missense changes in ELAC2 (HPC2) with prostate cancer in a Japanese case-control series

M. Skolnick, N. Camp, M. Emi, 2002, Journal of Human Genetics.

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.

A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1→q11.1

Yusuke Nakamura, M. Oshimura, M. Emi, 2004, Human Genetics.

Association of a single‐nucleotide polymorphism in the promoter region of leukemia inhibitory factor receptor gene with low bone mineral density in adult women

S. Inoue, M. Emi, Y. Ezura, 2004 .

[Cytogenetic abnormalities, genetic alterations, and applications for genetic diagnosis in breast cancer].

Y. Nakamura, M. Emi, K. Tsukamoto, 1996, Nihon rinsho. Japanese journal of clinical medicine.

Genetic association of low-density lipoprotein receptor-related protein 2 (LRP2) with plasma lipid levels.

T. Nakajima, M. Emi, H. Bujo, 2007, Journal of atherosclerosis and thrombosis.

A 3‐Mb physical map of the chromosome region 8p21.3‐p22, including a 600‐kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer, and non‐small cell lung cancer

Yusuke Nakamura, M. Oshimura, M. Emi, 1994, Genes, chromosomes & cancer.

Allelic losses on 18q21 are associated with progression and metastasis in human prostate cancer

M. Emi, H. Ito, T. Shiraishi, 1997, Genes, chromosomes & cancer.

Molecular genetic diagnosis of a family with hypercholesterolemia by a mismatched PCR-RFLP method for genotyping single base substitution of the LDL receptor gene.

M. Emi, P. Hopkins, R. Williams, 1998, Japanese heart journal.

A BglII RFLP at the lipoprotein lipase gene.

Y. Nakamura, M. Emi, R. Hegele, 1989, Nucleic acids research.

A polymorphic CA repeat sequence at the human calcitonin locus

M. Emi, K. Tsukamoto, 1998, Journal of Human Genetics.

Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia.

M. Emi, R. Hegele, J. Lalouel, 1989, The American journal of cardiology.

Structure, organization, and chromosomal mapping of the human macrophage scavenger receptor gene.

T. Kodama, M. Emi, Y. Yazaki, 1993, The Journal of biological chemistry.

Three TNFalpha single nucleotide polymorphisms in the Japanese population.

T. Nakajima, M. Emi, Y. Ezura, 2002, Annals of Human Biology.

hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction Type III dyslipoproteinemia in patients heterozygous for familial

M. Emi, S. Hunt, J. Lalouel, 2011 .

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.

RFLPs upstream of the low-density lipoprotein receptor (LDLR) gene.

Y. Nakamura, M. Emi, R. Hegele, 1988, Nucleic acids research.

Expression of human salivary alpha-amylase gene in Saccharomyces cerevisiae and its secretion using the mammalian signal sequence.

Y. Nakamura, M. Emi, A. Miyanohara, 1986, Gene.

Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus

M. Emi, T. Shiba, K. Tsukamoto, 1998, Journal of Human Genetics.

Association of common missense changes in ELAC2 (HPC2) with prostate cancer in a Japanese case-control series

M. Skolnick, N. Camp, M. Emi, 2002, Journal of Human Genetics.

Contribution of HLA genes to genetic predisposition in diffuse panbronchiolitis.

S. Kudoh, M. Emi, Y. Yazaki, 1998, American journal of respiratory and critical care medicine.

Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women

S. Inoue, M. Emi, Y. Ezura, 2005, Journal of Human Genetics.

Mutations in the BRCA1 gene in Japanese breast cancer patients

M. Skolnick, Yusuke Nakamura, T. Katagiri, 1996, Human mutation.