M. Ouchida

J. Soh, S. Toyooka, T. Mitsudomi, 2007, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Oesophageal squamous cell carcinoma may develop within a background of accumulating DNA methylation in normal and dysplastic mucosa

N. Matsubara, J. Jass, J. Murakami, 2006, Gut.

Therapy for hyperthermia‐induced seizures in Scn1a mutant rats

T. Serikawa, H. Matsui, T. Sendo, 2011, Epilepsia.

Antinociceptive effects of intrathecal landiolol injection in a rat formalin pain model.

N. Obata, S. Mizobuchi, Hirotaka Kanzaki, 2012, Acta medica Okayama.

Prevalent hyper-methylation of the CDH13 gene promoter in malignant B cell lymphomas.

M. Tanimoto, T. Yoshino, M. Harada, 2004, International journal of oncology.

Detection of codon 61 point mutations of the K-ras gene in lung and colorectal cancers by enriched PCR.

J. Soh, S. Toyooka, M. Yano, 2003, Oncology Report.

Detection of EGFR Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay

S. Toyooka, Masaki Tokumo, K. Kiura, 2006, Clinical Cancer Research.

Transforming activity of the RL‐akt gene, a c‐akt gene activated by long terminal repeat insertion in murine leukemia RL♂1 cells

K. Tsukuda, M. Tanino, E. Nakayama, 1999 .

Spinal nerve injury causes upregulation of ErbB2 and ErbB3 receptors in rat dorsal root ganglia

N. Obata, S. Mizobuchi, Hirotaka Kanzaki, 2013, Journal of pain research.

Aberrant promoter methylation of human DAB2 interactive protein (hDAB2IP) gene in lung cancers

S. Toyooka, A. Gazdar, M. Aoe, 2005, International journal of cancer.

Human RAD 17 Polymorphism at Codon 546 Is Associated with the Risk of Colorectal Cancer.

N. Matsubara, Hiromasa Yamamoto, Kaori Sasai, 2017, Acta medica Okayama.

CACNA1A variants may modify the epileptic phenotype of Dravet syndrome

Katsuhiro Kobayashi, H. Matsui, T. Nishiki, 2013, Neurobiology of Disease.

The coiled-coil domain targets human histidine domain-protein tyrosine phosphatase to late endosomes.

M. Ouchida, C. Tanase, M. Foanene, 2008 .

Gene silencing of the tyrosine phosphatase SHP1 gene by aberrant methylation in leukemias/lymphomas.

K. Hayashi, M. Tanimoto, T. Yoshino, 2002, Cancer research.

Expression changes of the neuregulin 1 isoforms in neuropathic pain model rats

N. Obata, S. Mizobuchi, Hirotaka Kanzaki, 2012, Neuroscience Letters.

Novel animal model of combined generalized and focal epilepsy

T. Mashimo, I. Ohmori, M. Ouchida, 2022, Epilepsia.

A Screening test for the prediction of Dravet syndrome before one year of age

J. Hattori, I. Ohmori, Y. Ohtsuka, 2008, Epilepsia.

Scn1a and Cacna1a mutations mutually alter their original phenotypes in rats

I. Ohmori, M. Ouchida, Kiyoka Kobayashi, 2020, Neurochemistry International.

Multifaceted Analysis of IL-23A- and/or EBI3-Including Cytokines Produced by Psoriatic Keratinocytes

M. Sakaguchi, M. Ouchida, Nahoko Tomonobu, 2021, International journal of molecular sciences.

FULL-LENGTH ORIGINAL REASARCH A screening test for the prediction of Dravet syndrome before one year of age

J. Hattori, I. Ohmori, Y. Ohtsuka, 2008 .

Proteomics‐based analysis of invasion‐related proteins in malignant gliomas

I. Date, Hirotaka Kanzaki, M. Ouchida, 2013, Neuropathology : official journal of the Japanese Society of Neuropathology.

Decoy strategy targeting the brain-derived neurotrophic factor exon I to attenuate tactile allodynia in the neuropathic pain model of rats.

N. Obata, S. Mizobuchi, Hirotaka Kanzaki, 2011, Biochemical and biophysical research communications.

T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity.

T. Furukawa, T. Ohe, J. Kurokawa, 2007, Journal of molecular and cellular cardiology.

Splicing isoform of SYT-SSX fusion protein accelerates transcriptional activity and cell proliferation.

H. Inoue, A. Yoshida, T. Ozaki, 2003, Cancer letters.

Single nucleotide polymorphism in the RAD18 gene and risk of colorectal cancer in the Japanese population.

Hiromasa Yamamoto, M. Aoe, M. Yano, 2007, Oncology reports.

The association between RAD18 Arg302Gln polymorphism and the risk of human non-small-cell lung cancer

Hiromasa Yamamoto, M. Aoe, M. Yano, 2007, Journal of Cancer Research and Clinical Oncology.

SS18 (synovial sarcoma translocation, chromosome 18)

M. Ouchida, 2011 .

Significant growth suppression of synovial sarcomas by the histone deacetylase inhibitor FK228 in vitro and in vivo.

H. Inoue, H. Sonobe, A. Yoshida, 2005, Cancer letters.

Loss or down‐regulation of HLA class I expression at the allelic level in freshly isolated leukemic blasts

M. Tanimoto, K. Matsue, A. Hiraki, 2007, Cancer science.

Allelic loss and reduced expression of the ING3, a candidate tumor suppressor gene at 7q31, in human head and neck cancers

M. Gunduz, N. Nagai, Sachio Ito, 2002, Oncogene.

Aberrant serine protease activities in atopic dermatitis.

M. Ouchida, S. Morizane, H. Nomura, 2022, Journal of dermatological science.

Increased DOI-induced wet-dog shakes in adrenocorticotropic hormone-treated rats are not affected by chronic imipramine treatment: possible involvement of enhanced 5-HT(2A)-receptor expression in the frontal cortex.

Y. Kitamura, T. Sendo, Hirotaka Kanzaki, 2008, Journal of pharmacological sciences.

Eradication of hepatitis C virus subgenomic replicon by interferon results in aberrant retinol-related protein expression.

N. Kato, H. Shiraha, A. Takaki, 2012, Acta Medica Okayama.

Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain

S. Toyokuni, T. Mashimo, I. Ohmori, 2022, Neurobiology of Disease.

Different responses to 5-fluoraouracil in mutagenicity and gene expression between two human lymphoblastoid cell lines with or without TP53 mutation.

M. Ouchida, K. Shimizu, Hiroaki Oka, 2012, Acta medica Okayama.

Rasmussen encephalitis associated with SCN1A mutation

Katsuhiro Kobayashi, H. Matsui, Y. Maegaki, 2008, Epilepsia.

Single nucleotide polymorphism at codon 133 of the RASSF1 gene is preferentially associated with human lung adenocarcinoma risk.

M. Aoe, M. Yano, N. Shimizu, 2006, Cancer letters.

VLX1570 induces apoptosis through the generation of ROS and induction of ER stress on leukemia cell lines

K. Tohyama, M. Ouchida, M. Shibakura, 2021, Cancer science.

MicroRNA-21 correlates with tumorigenesis in malignant peripheral nerve sheath tumor (MPNST) via programmed cell death protein 4 (PDCD4)

A. Yoshida, T. Ozaki, Tsuyoshi Sasaki, 2012, Journal of Cancer Research and Clinical Oncology.

Uncovering Direct Targets of MiR-19a Involved in Lung Cancer Progression

Sachio Ito, M. Ouchida, K. Shimizu, 2015, PloS one.

Frequent deletion and down-regulation of ING4, a candidate tumor suppressor gene at 12p13, in head and neck squamous cell carcinomas.

Y. Ninomiya, H. Nagatsuka, B. Cengiz, 2005, Gene.

Prognostic Value of Loss of Heterozygosity around three Candidate Tumor Suppressor Genes on Chromosome 10q in Astrocytomas

T. Tamiya, K. Terada, T. Ohmoto, 2002, Journal of Neuro-Oncology.

Deletional Mapping of 2q21-37 Region in Oral Cancer

Tomio Inoue, B. Cengiz, M. Gunduz, 2005 .

Multiple splicing variants of Naf1/ABIN-1 transcripts and their alterations in hematopoietic tumors.

M. Tanimoto, Y. Matsuo, M. Ouchida, 2006, International journal of molecular medicine.

Novel Direct Targets of miR-19a Identified in Breast Cancer Cells by a Quantitative Proteomic Approach

Hirotaka Kanzaki, Sachio Ito, M. Ouchida, 2012, PloS one.

Activated Proliferation of B-Cell Lymphomas/Leukemias with the SHP1 Gene Silencing by Aberrant CpG Methylation

K. Hayashi, T. Yoshino, T. Akagi, 2003, Laboratory Investigation.

Accumulation of Specific Epigenetic Abnormalities During Development and Progression of T Cell Leukemia/Lymphoma

D. Ennishi, M. Tanimoto, T. Yoshino, 2011 .

Single nucleotide polymorphism of the AXIN2 gene is preferentially associated with human lung cancer risk in a Japanese population.

M. Aoe, M. Yano, N. Shimizu, 2006, International journal of molecular medicine.

Identification of a candidate tumor suppressor gene RHOBTB1 located at a novel allelic loss region 10q21 in head and neck cancer

H. Nagatsuka, M. Gunduz, Sachio Ito, 2005, Journal of Cancer Research and Clinical Oncology.

A reverse transcriptase‐polymerase chain reaction assay in the diagnosis of soft tissue sarcomas

T. Ozaki, A. Kawai, T. Dan'ura, 2000, Cancer.

Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers

S. Toyooka, Y. Naomoto, S. Tanabe, 2010, Journal of Cancer Research and Clinical Oncology.

The allelic distribution of a single nucleotide polymorphism in the PDCD5 gene locus of Japanese non-small cell lung cancer patients.

J. Soh, S. Toyooka, K. Matsuo, 2008, Molecular medicine reports.

A novel WD40 repeat protein, WDC146, highly expressed during spermatogenesis in a stage-specific manner.

S. Ito, M. Ouchida, K. Shimizu, 2001, Biochemical and biophysical research communications.

Genomic structure of the human ING1 gene and tumor-specific mutations detected in head and neck squamous cell carcinomas.

S. Nishioka, M. Gunduz, M. Ouchida, 2000, Cancer research.

Advances in Brief Genomic Structure of the Human ING 1 Gene and Tumor-specific Mutations Detected in Head and Neck Squamous Cell Carcinomas 1

S. Nishioka, M. Gunduz, M. Ouchida, 2000 .

Genome-Wide Analyses on Loss of Heterozygosity in Head and Neck Squamous Cell Carcinomas

M. Gunduz, N. Nagai, Sachio Ito, 2003, Laboratory Investigation.

Aberrant Promoter Methylation in Human DAB2 Interactive Protein (hDAB2IP) Gene in Breast Cancer

S. Toyooka, H. Doihara, A. Gazdar, 2004, Clinical Cancer Research.

REIC/Dkk-3 stable transfection reduces the malignant phenotype of mouse prostate cancer RM9 cells.

M. Sakaguchi, N. Huh, K. Ochiai, 2009, International journal of molecular medicine.

Genetic seizure susceptibility underlying acute encephalopathies in childhood

Katsuhiro Kobayashi, H. Matsui, Y. Maegaki, 2010, Epilepsy Research.

Effect of Naturally Occurring E2F-4 Alterations on Transcriptional Activation and Proliferation in Transfected Cells

N. Matsubara, M. Tanino, S. Meltzer, 2001, Laboratory Investigation.

Identification of direct targets for the miR‐17‐92 cluster by proteomic analysis

Hirotaka Kanzaki, Sachio Ito, M. Ouchida, 2011, Proteomics.

Decreased expression of the SIN3A gene, a candidate tumor suppressor located at the prevalent allelic loss region 15q23 in non-small cell lung cancer.

Nobuyoshi Shimizu, Kenji Shimizu, Hiroshi Date, 2008, Lung cancer.

Tumor‐specific exon creation of the HELLS/SMARCA6 gene in non‐small cell lung cancer

S. Toyooka, H. Shigematsu, M. Yano, 2004, International journal of cancer.

Cumulative Epigenetic Abnormalities in Host Genes with Viral and Microbial Infection during Initiation and Progression of Malignant Lymphoma/Leukemia

T. Yoshino, A. Utsunomiya, M. Ouchida, 2011, Cancers.

Multi-step aberrant CpG island hyper-methylation is associated with the progression of adult T-cell leukemia/lymphoma.

K. Ohshima, M. Tanimoto, M. Matsuoka, 2010, The American journal of pathology.

MET gene amplification or EGFR mutation activate MET in lung cancers untreated with EGFR tyrosine kinase inhibitors

W. Lam, J. Minna, J. Soh, 2009, International journal of cancer.

Positive correlation between allelic loss at chromosome 14q24-31 and poor prognosis of patients with renal cell carcinoma.

H. Kumon, S. Ebara, Y. Nasu, 2004, Urology.

A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy

K. Tomizawa, Y. Mori, H. Matsui, 2008, Neurobiology of Disease.

Genetic alterations in lung adenocarcinoma with a micropapillary component.

J. Soh, S. Toyooka, S. Miyoshi, 2016, Molecular and clinical oncology.

Single nucleotide polymorphism in fibroblast growth factor receptor 4 at codon 388 is associated with prognosis in high‐grade soft tissue sarcoma

H. Inoue, A. Yoshida, T. Ozaki, 2003, Cancer.

Cyclin C interacts with steroid receptor coactivator 2 and upregulates cell cycle genes in MCF-7 cells.

G. Mellgren, M. Ouchida, Thomas Helland, 2015, Biochimica et biophysica acta.

Highly frequent allelic loss of chromosome 6q16-23 in osteosarcoma: involvement of cyclin C in osteosarcoma.

A. Yoshida, T. Ozaki, Hirotaka Kanzaki, 2006, International journal of molecular medicine.

Osteoclast-Derived Zinc Finger (OCZF) Protein With POZ Domain, a Possible Transcriptional Repressor, Is Involved in Osteoclastogenesis

A. Kukita, T. Kukita, O. Kohashi, 1999 .

Osteoclast-derived zinc finger (OCZF) protein with POZ domain, a possible transcriptional repressor, is involved in osteoclastogenesis.

A. Kukita, T. Kukita, O. Kohashi, 1999, Blood.

A CACNB4 mutation showing altered Cav2.1 function in a patient with Dravet syndrome

K. Tomizawa, H. Matsui, T. Nishiki, 2009 .

Aberrant methylation of p57KIP2 gene in lung and breast cancers and malignant mesotheliomas.

S. Toyooka, H. Doihara, M. Toyota, 2004, Oncology reports.

Cytologic changes in two cervical carcinoma cell lines after transfection of the wild‐type p53 gene

T. Iwasaka, P. Zheng, M. Ouchida, 1996, Acta obstetricia et gynecologica Scandinavica.

Epidermal growth factor receptor mutation status and adjuvant chemotherapy with uracil-tegafur for adenocarcinoma of the lung.

J. Soh, S. Toyooka, K. Matsuo, 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Paroxysmal movement disorders in severe myoclonic epilepsy in infancy

E. Oka, I. Ohmori, Y. Ohtsuka, 2003, Brain and Development.

TP53 codon 72 polymorphism is associated with pancreatic cancer risk in males, smokers and drinkers.

T. Yagi, K. Nakachi, Masao Yoshioka, 2011, Molecular medicine reports.

Genetic risk of hepatocellular carcinoma in patients with hepatitis C virus: A case control study

Shinichiro Nakamura, K. Nouso, Kazuhide Yamamoto, 2012, Journal of gastroenterology and hepatology.

Accumulation of aberrant CpG hypermethylation by Helicobacter pylori infection promotes development and progression of gastric MALT lymphoma.

K. Takata, T. Yoshino, M. Ouchida, 2009, International journal of oncology.

HD-PTP: A novel protein tyrosine phosphatase gene on human chromosome 3p21.3.

S. Toyooka, K. Tsukuda, M. Ouchida, 2000, Biochemical and biophysical research communications.

Single nucleotide polymorphisms in the EXO1 gene and risk of colorectal cancer in a Japanese population.

M. Aoe, M. Yano, N. Shimizu, 2004, Carcinogenesis.

A Missense Mutation of the Gene Encoding Voltage-Dependent Sodium Channel (Nav1.1) Confers Susceptibility to Febrile Seizures in Rats

T. Serikawa, Y. Ohno, Y. Mori, 2010, The Journal of Neuroscience.

Genetic and epigenetic alterations of BRG1 promote oral cancer development.

H. Nagatsuka, H. Tsujigiwa, M. Gunduz, 2005, International journal of oncology.

Anti-tumor effect of bisphosphonate (YM529) on non-small cell lung cancer cell lines

F. Hara, S. Toyooka, Masaki Tokumo, 2007, BMC Cancer.

Development of a novel analgesic for neuropathic pain targeting brain-derived neurotrophic factor.

H. Nakatsuka, Keita Hazama, M. Ouchida, 2020, Biochemical and biophysical research communications.

Cumulative kinetics of epigenetic abnormalities during initiation and progression of Adult T-cell Leukemia/Lymphoma (ATLL)

K. Takata, T. Yoshino, A. Utsunomiya, 2011, Retrovirology.

Methylphenidate improves learning impairments and hyperthermia‐induced seizures caused by an Scn1a mutation

H. Matsui, T. Mashimo, I. Ohmori, 2014, Epilepsia.

Analysis of All 34 Exons of the SPINK5 Gene in Japanese Atopic Dermatitis Patients.

H. Hattori, K. Tada, K. Iwatsuki, 2018, Acta medica Okayama.

Inhalation of 10% carbon dioxide rapidly terminates Scn1a mutation-related hyperthermia-induced seizures

H. Matsui, T. Nishiki, I. Ohmori, 2013, Epilepsy Research.

A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data

Katsuhiro Kobayashi, H. Yoshinaga, Toshiyuki Yamamoto, 2017, Brain and Development.

Severity dependent up-regulations of LOX-1 and MCP-1 in early sclerotic changes of common carotid arteries in spontaneously hypertensive rats

M. Shoji, N. Omori, Keiko Sato, 2004, Neurological research.

Txn1 mutation is a monogenic cause of chronic kidney disease associated with mitochondrial dysfunction in rats

S. Toyokuni, T. Mashimo, I. Ohmori, 2023, bioRxiv.

SYT, a partner of SYT-SSX oncoprotein in synovial sarcomas, interacts with mSin3A, a component of histone deacetylase complex

H. Inoue, T. Ozaki, A. Kawai, 2004, Laboratory Investigation.

Loss of tumorigenicity of Ewing's sarcoma cells expressing antisense RNA to EWS-fusion transcripts.

M. Ouchida, M. Ouchida, E. Reddy, 1995, Oncogene.

Five-aza-2′-deoxycytidine-induced hypomethylation of cholesterol 25-hydroxylase gene is responsible for cell death of myelodysplasia/leukemia cells

Y. Tohyama, K. Tohyama, M. Ouchida, 2015, Scientific Reports.

MET gene amplification or EGFR mutation activate MET in lung cancers untreated with EGFR tyrosine kinase inhibitors

W. Lam, J. Minna, J. Soh, 2009, International journal of cancer.

Functional mutation of DNA polymerase beta found in human gastric cancer--inability of the base excision repair in vitro.

T. Mukai, M. Ouchida, K. Hori, 1999, Mutation research.