M. Satoh

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.

Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy

A. Matsumori, K. Ueda, T. Arimura, 2000, Human Genetics.

MICA gene polymorphism in Takayasu's arteritis and Buerger's disease.

Y. Yasukochi, T. Arimura, A. Kimura, 1998, International journal of cardiology.

Clinical expression in patients with hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutation.

Y. Doi, A. Kimura, H. Kitaoka, 1999, Circulation.

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

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

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene.

M Hiroe, F. Marumo, M. Hiroe, 1999, Biochemical and biophysical research communications.

Identification of MICA alleles with a long Leu-repeat in the transmembrane region and no cytoplasmic tail due to a frameshift-deletion in exon 4.

H. Inoko, K. Ueda, T. Arimura, 2001, Tissue antigens.

HLA linked with leprosy in southern China: HLA-linked resistance alleles to leprosy.

A. Kimura, M. Satoh, S. Mineshita, 1999, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

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.

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family.

W. Lee, A. Kimura, W. Lee, 1998, The American journal of cardiology.