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Journal of Human Genetics|February 26, 2003
Hypermethylation associated with inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human hepatoblastomasHisaki Nagai, Tetsuji Naka, Yoshie Terada, et al.
Journal of Human Genetics|February 1, 2003
Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surfaceAritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Journal of Human Genetics|February 1, 2003
A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathyMasakazu Mimaki, Akemi Ikota, Aya Sato, et al.
Journal of Human Genetics|August 9, 2002
Relation between angiotensin-converting enzyme II genotype and atrial fibrillation in Japanese patients with hypertrophic cardiomyopathyAkiyoshi Ogimoto, Mareomi Hamada, Jun Nakura, et al.
Journal of Human Genetics|August 9, 2002
A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5Ryo Suminaga, Yasuhiro Takeshima, Kayo Adachi, et al.
Journal of Human Genetics|August 9, 2002
Characterization of a VNTR polymorphism in the coding region of the CEL geneShoko Higuchi, Yusuke Nakamura, Susumu Saito
Journal of Human Genetics|August 16, 2002
The role of vitamin D receptor gene polymorphisms in the susceptibility to prostate cancer of a southern European populationRui Medeiros, António Morais, André Vasconcelos, et al.
Journal of Human Genetics|August 16, 2002
906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese populationSusumu Saito, Aritoshi Iida, Akihiro Sekine, et al.
Journal of Human Genetics|January 11, 2003
A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigreeJiahui Xia, Hao Deng, Yong Feng, et al.
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