M. Takahashi

发表

Gene expression profiling of clear cell renal cell carcinoma: Gene identification and prognostic classification

K. Furge, B. Teh, D. Rhodes, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Lack of association between dopamine D2 receptor gene Cys311 variant and schizophrenia.

S. Tsuji, O. Onodera, M. Takahashi, 1996, American journal of medical genetics.

Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia.

S. Cannon, M. Takahashi, Stephen C. Cannon, 1999, Biophysical journal.

Loss of heterozygosity at cylindromatosis gene locus, CYLD, in sporadic skin adnexal tumours.

S. Lakhani, M. Takahashi, C. Jones, 2001, Journal of clinical pathology.

Molecular etiology of idiopathic cardiomyopathy in Asian populations.

T. Hayashi, T. Arimura, A. Kimura, 2001, Journal of cardiology.

Familial gastric cancer: clinicopathological characteristics, RER phenotype and germline p53 and E-cadherin mutations.

J. Yokota, T. Kohno, A. Reeve, 1999, Carcinogenesis.

Lack of association between the Met196Arg polymorphism in the TNFR2 gene and autoimmune diseases accompanied by vasculitis including SLE in Japanese.

H. Hashimoto, M. Takahashi, N. Nishikimi, 2001, Tissue antigens.

Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function?

M. Santoro, G. Lenoir, S. Lyonnet, 1999, Human mutation.

New mutation of the myelin Po gene in a pedigree of Charcot-Marie-Tooth neuropathy type 1

K. Hayasaka, M. Takahashi, M. Kaido, 1993 .

Two cases of the caudal duplication anomaly including a discordant monozygotic twin.

R. Hofstra, A. V. van Essen, J. Baert, 2002, American journal of medical genetics.

Association of clinical features with HLA in chronic pulmonary thromboembolism

T. Kuriyama, A. Kimura, N. Tanabe, 2005, European Respiratory Journal.

14-3-3 protein eta chain gene (YWHAH) polymorphism and its genetic association with schizophrenia.

S. Tsuji, T. Kumanishi, S Igarashi, 1999, American journal of medical genetics.

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

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

Mapping of the HLA-linked genes controlling the susceptibility to Takayasu's arteritis.

H. Inoko, A. Kimura, M. Ota, 2000, International journal of cardiology.

Association study between schizophrenia and dopamine D3 receptor gene polymorphism.

S. Tsuji, Hajime Tanaka, O. Onodera, 1996, American journal of medical genetics.

Analysis of tumor necrosis factor-alpha promoter polymorphism in type 1 diabetes: HLA-B and -DRB1 alleles are primarily associated with the disease in Japanese.

T. Sasazuki, K. Hamaguchi, A. Kimura, 2000, Tissue antigens.

Mutational analysis within the 3' region of the PKD1 gene in Japanese families.

M. Komeda, K. Tsuchiya, M. Takahashi, 2001, Mutation research.

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.

Familial adult renal neoplasia

R. Kahnoski, B. Teh, D. Nicol, 2002, Journal of medical genetics.

Dominant-negative mutations of the tumor suppressor p53 relating to early onset of glioblastoma multiforme.

H. Kashiwazaki, M. Tada, H. Tonoki, 1999, Cancer research.

Somatic mutations of the APC gene in primary breast cancers.

M. Tada, K. Furuuchi, J. Hamada, 2000, The American journal of pathology.

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.

Two regions of homozygous deletion clusters at chromosome band 9p21 in human lung cancer

J. Minna, M. Yamazaki, H. Tashiro, 2000, Genes, chromosomes & cancer.

Inactivation of the PTEN/MMAC1/TEP1 gene in human lung cancers

J. Yokota, T. Kohno, M. Takahashi, 1998, Genes, chromosomes & cancer.

Physical and transcriptional map of a 311-kb segment of chromosome 18q21, a candidate lung tumor suppressor locus.

M. Yamazaki, Y. Fukuzumi, Y. Fujimori, 2001, Genomics.

Does ‘granular cell’ renal cell carcinoma exist? Molecular and histological reclassification

M. Tretiakova, N. Vogelzang, J. Sugimura, 2007, Histopathology.

Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

I. Kanazawa, G. Sobue, T. Shimohata, 1999, Human molecular genetics.

Inactivate the remaining p53 allele or the alternate p73? Preferential selection of the Arg72 polymorphism in cancers with recessive p53 mutants but not transdominant mutants.

R. Iggo, A. Hirai, M. Tada, 2001, Carcinogenesis.

cDNA microarray analysis assists in diagnosis of malignant intrarenal pheochromocytoma originally masquerading as a renal cell carcinoma

B. Teh, C. Eng, H. Kanayama, 2005, Journal of Medical Genetics.

New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.

K. Hayasaka, M. Takahashi, M. Kaido, 1993, Biochemistry and molecular biology international.

Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12–q13

S. Seal, M. Stratton, R. Siebert, 2000, Human Genetics.

carcinoma originally masquerading as a renal cell of malignant intrarenal pheochromocytoma cDNA microarray analysis assists in diagnosis and

B. Teh, H. Kanayama, S. Kagawa, 2005 .

Lack of association between LTA and LGALS2 polymorphisms and myocardial infarction in Japanese and Korean populations.

A. Kimura, M. Sawabe, T. Naruse, 2007, Tissue antigens.