H. Harada

发表

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy.

J. Towbin, M. Ackerman, T. Arimura, 2009, Journal of the American College of Cardiology.

Polymorphisms in the SOD2 and HLA-DRB1 genes are associated with nonfamilial idiopathic dilated cardiomyopathy in Japanese.

H. Nishi, H. Harada, A. Kimura, 1999, Biochemical and biophysical research communications.

Hypertrophic obstructive cardiomyopathy due to a novel T-to-A transition at codon 624 in the beta-myosin heavy chain (beta-MHC) gene possibly related to the sudden death.

F. Ohsuzu, H. Harada, A. Kimura, 1997, International journal of cardiology.

Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancer

M. Emi, T. Mukai, Y. Nakabeppu, 2003, Oncogene.

Down-regulation of a novel gene, DRLM, in human liver malignancy from 4q22 that encodes a NAP-like protein.

M. Emi, T. Yokota, Y. Ezura, 2002, Gene.

DDH245 2221..2231

S. Shirasawa, T. Sasazuki, N. Ishikawa, 2004 .

DNA typing of HLA class II genes in B-lymphoblastoid cell lines homozygous for HLA.

T. Sasazuki, H. Harada, A. Kimura, 1992, Tissue antigens.

Chapter 3 Cardiac Ankyrin Repeat Protein Gene ( ANKRD 1 ) Mutations in Hypertrophic Cardiomyopathy

J. Towbin, M. Ackerman, T. Arimura, 2010 .

Sequencing and population analysis of four novel HLA-DPA1 alleles.

T. Sasazuki, H. Harada, A. Kimura, 1992, Human immunology.

Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene.

T. Imaizumi, H. Nishi, H. Harada, 1996, Journal of cardiac failure.

Identification, tissue expression, and chromosomal position of a novel gene encoding human ubiquitin-conjugating enzyme E2-230k.

M. Emi, T. Yokota, H. Harada, 2001, Gene.

Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes: genomic structure and seven polymorphisms of the FAP-1 gene

M. Emi, H. Harada, A. Teramoto, 2002, Journal of Human Genetics.

Two novel single-nucleotide polymorphisms of the Caspase-9 (CASP9) gene in the Japanese population

M. Emi, T. Kajiwara, H. Harada, 2001, Genes and Immunity.

Human calcitonin receptor-like receptor for adrenomedullin: genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis

T. Nakajima, M. Emi, S. Umemura, 2001, Journal of Human Genetics.

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

M. Matsuzaki, T. Sasazuki, J. Choo, 1997, Nature Genetics.

Genomic structure of the human NLK (nemo-like kinase) gene and analysis of its promoter region.

M. Emi, Y. Ezura, H. Harada, 2002, Gene.

A highly polymorphic CA repeat marker at the EBAG9/RCAS1 locus on 8q23 that detected frequent multiplication in breast cancer

T. Kazui, H. Harada, M. Tsuneizumi, 2002, Annals of human biology.

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.

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

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

SNPs in the promoter of a B cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease.

S. Shirasawa, T. Sasazuki, N. Ishikawa, 2004, Human molecular genetics.

ZFAT expression in B and T lymphocytes and identification of ZFAT-regulated genes.

N. Kato, S. Shirasawa, T. Sasazuki, 2008, Genomics.

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.

A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy.

T. Imaizumi, H. Nishi, H. Harada, 1995, Circulation.

Novel missense mutation in cardiac ? myosin heavy chain gene found in a japanese patient with hypertrophic cardiomyopathy

T. Sasazuki, H. Nishi, H. Harada, 1992 .

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.

Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathy

I. Nonaka, H. Nishi, H. Harada, 2018, Journal of Human Genetics.

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.

Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy.

H. Nishi, H. Harada, A. Kimura, 2001, American heart journal.

Possible Gene Effect of a Mutant Cardiac β-Myosin Heavy Chain Gene on the Clinical Expression of Familial Hypertrophic Cardiomyopathy

T. Sasazuki, H. Nishi, H. Harada, 1994 .

Possible gene dose effect of a mutant cardiac beta-myosin heavy chain gene on the clinical expression of familial hypertrophic cardiomyopathy.

T. Sasazuki, H. Nishi, H. Harada, 1994, Biochemical and biophysical research communications.

DNA typing of HLA class II genes in Japanese patients with dilated cardiomyopathy.

T. Sasazuki, T. Imaizumi, H. Nishi, 1995, Journal of molecular and cellular cardiology.

Novel variant transthyretin gene (Ser50 to Ile) in familial cardiac amyloidosis.

T. Sasazuki, H. Nishi, H. Harada, 1992, Biochemical and biophysical research communications.

A missense mutation of cardiac beta-myosin heavy chain gene linked to familial hypertrophic cardiomyopathy in affected Japanese families.

T. Sasazuki, H. Nishi, H. Harada, 1993, Biochemical and biophysical research communications.

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.

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy.

J. Towbin, T. Arimura, A. Sato, 2009, Journal of the American College of Cardiology.