Toshihiro Tanaka
0000-0001-6201-9784
102 papers found
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Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25
Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population
Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population
Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene
Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population
Mapping of a gene for May-Hegglin anomaly to chromosome 22q
Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.
Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome
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
Novel mechanism of HERG current suppression in LQT2: Shift in voltage dependence of HERG inactivation
Genomic organization and mutational analysis of HERG , a gene responsible for familial long QT syndrome
Isolation and Chromosomal Mapping of the Human Homolog of Perilipin (PLIN), a Rat Adipose Tissue-Specific Gene, by Differential Display Method
Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3
Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population
Identification by differential display of eight known genes induced during in vivo intimal hyperplasia
Four Novel KVLQT1 and Four Novel HERG Mutations in Familial Long-QT Syndrome
Construction of a Normalized Directionally Cloned cDNA Library from Adult Heart and Analysis of 3040 Clones by Partial Sequencing
Molecular Cloning and Mapping of a Human cDNA for Cytosolic Malate Dehydrogenase (MDH1)
Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1
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
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