T. Tanaka

发表

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

Toshihiro Tanaka, H. Saito, Y. Nakamura, 2001, Blood.

Mapping of a gene for May-Hegglin anomaly to chromosome 22q

Y. Nakamura, H. Saito, T. Kamiya, 1999, Human Genetics.

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT

S. Tsuji, Hitoshi Takahashi, H. Takahashi, 1996, Nature Genetics.

Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25.

Toshihiro Tanaka, S. Kuroda, Y. Nakamura, 2000, Stroke.

Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia.

T. Takagi, Toshihiro Tanaka, T. Tsunoda, 2001, Cancer research.

Identification and characterization of the potential promoter regions of 1031 kinds of human genes.

T. Tsunoda, T. Tanaka, Y. Suzuki, 2001, Genome research.

Prediction of sensitivity of esophageal tumors to adjuvant chemotherapy by cDNA microarray analysis of gene-expression profiles.

T Tanaka, T. Takagi, Yusuke Nakamura, 2001, Cancer research.

Growth and gene expression profile analyses of endometrial cancer cells expressing exogenous PTEN.

T. Tsunoda, Y. Nakamura, H. Kuramoto, 2001, Cancer research.

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease.

Y. Ohnishi, T. Tsunoda, Y. Nakamura, 2001, American journal of human genetics.

Suppression by citrus auraptene of phorbol ester-and endotoxin-induced inflammatory responses: role of attenuation of leukocyte activation.

Takuji Tanaka, A. Murakami, H. Ohigashi, 2000, Carcinogenesis.

Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1).

J. Inazawa, Y. Nakamura, T. Tanaka, 1996, Genomics.

Identification by cDNA microarray of genes involved in ovarian carcinogenesis.

T Tanaka, T. Takagi, Toshihiro Tanaka, 2000, Cancer research.

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

Yusuke Nakamura, Y. Yazaki, R. Nagai, 1998, Human Genetics.

Up-regulation of the ectodermal-neural cortex 1 (ENC1) gene, a downstream target of the beta-catenin/T-cell factor complex, in colorectal carcinomas.

T Tanaka, Toshihiro Tanaka, T. Tsunoda, 2001, Cancer research.

Identification of AF17 as a downstream gene of the beta-catenin/T-cell factor pathway and its involvement in colorectal carcinogenesis.

Toshihiro Tanaka, T. Tsunoda, Y. Furukawa, 2001, Cancer research.

Inhibitory effect of citrus nobiletin on phorbol ester-induced skin inflammation, oxidative stress, and tumor promotion in mice.

A. Murakami, H. Ohigashi, T. Tanaka, 2000, Cancer research.

Antiangiogenic activity of BAI1 in vivo: implications for gene therapy of human glioblastomas

Y. Nakamura, T. Tokino, S. Asano, 2006, Cancer Gene Therapy.

Suppression of tumor promoter-induced oxidative stress and inflammatory responses in mouse skin by a superoxide generation inhibitor 1'-acetoxychavicol acetate.

Takuji Tanaka, A. Murakami, H. Ohigashi, 1998, Cancer research.

A simple phenolic antioxidant protocatechuic acid enhances tumor promotion and oxidative stress in female ICR mouse skin: dose-and timing-dependent enhancement and involvement of bioactivation by tyrosinase.

Takuji Tanaka, A. Murakami, H. Ohigashi, 2000, Carcinogenesis.

Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population

R. Yamada, Y. Ohnishi, Y. Ohnishi, 2000, Human Genetics.

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome.

Y. Yazaki, Y. Nakamura, R. Nagai, 1997, Circulation.

Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population

N. Murata, R. Yamada, Y. Ohnishi, 2000, Human Genetics.

Isolation of a novel human gene, MARKL1, homologous to MARK3 and its involvement in hepatocellular carcinogenesis.

T Tanaka, T. Tsunoda, Y. Furukawa, 2001, Neoplasia.

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

Yusuke Nakamura, Toshihiro Tanaka, Y. Yazaki, 1998, Human Genetics.

Fine mapping of the Darier's disease locus on chromosome 12q.

S. Bale, G. Richard, O. Mcbride, 1994, The Journal of investigative dermatology.

Alkaline phosphatase activity in the osteoclasts induced by experimental tooth movement.

K. Noda, Y. Nakamura, Y. Kuwahara, 1991, Journal of electron microscopy.

Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method.

T. Tanaka, Y. Nakamura, J. Nishiu, 1998, Genomics.

Construction of a normalized directionally cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing.

A. Ogiwara, Y. Yazaki, Y. Nakamura, 1996, Genomics.

Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine.

Y. Ohnishi, T. Tsunoda, R. Yamada, 2000, Genome informatics. Workshop on Genome Informatics.

Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3.

Y. Nakamura, J. Nishiu, T. Tanaka, 1998, Genomics.

Characteristics of Shed Snake Skin Permeability to Indomethacin and Fatty Alcohols

N. Yata, H. Makita, Y. Nakamura, 1996, The Journal of pharmacy and pharmacology.

Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X Chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions

G. Herman, J. Parrish, A. Chatterjee, 1995, Mammalian Genome.