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The Tohoku Journal of Experimental Medicine|June 10, 2004
Sudden infant death syndrome is not associated with the mutation of PHOX2B gene, a major causative gene of congenital central hypoventilation syndromeKazuki Kijima, Ayako Sasaki, Takao Niki, et al.Plos One|June 30, 2016
Multiplex APLP System for High-Resolution Haplogrouping of Extremely Degraded East-Asian Mitochondrial DNAsTsuneo Kakuda, Hideki Shojo, Mayumi Tanaka, et al.Journal of Human Genetics|October 12, 2007
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: unequal sister chromatid exchange during paternal gametogenesisHiroko Arai, Tesshu Otagiri, Ayako Sasaki, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 12, 2008
Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylationTohru Okanishi, Yoshiaki Saito, Isao Yuasa, et al.Archives of Toxicology|June 24, 2010
Genetic variants associated with arsenic metabolism within human arsenic (+3 oxidation state) methyltransferase show wide variation across multiple populationsJunko Fujihara, Toshihiro Yasuda, Hideaki Kato, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 2006
Variation of interleukin 8 -251 A>T polymorphism in worldwide populations and intra-ethnic differences in Japanese populationsJunko Fujihara, Kuninori Shiwaku, Toshihiro Yasuda, et al.Cell Biochemistry and Function|July 19, 2008
Three single nucleotide polymorphisms leading to non-synonymous amino acid substitution in the human ribonuclease 2 and angiogenin genes exhibit markedly less genetic heterogeneity in six populationsMisuzu Ueki, Haruo Takeshita, Junko Fujihara, et al.Biochemical Genetics|January 26, 2008
Development of genotyping methods for single nucleotide polymorphism in the human pancreatic ribonuclease gene (RNASE1) and their application to population studiesMisuzu Ueki, Reiko Iida, Junko Fujihara, et al.Internal Medicine (Tokyo, Japan)|May 15, 2010
The genotypes of IL-1 beta and MMP-3 are associated with the prognosis of HCV-related hepatocellular carcinomaKinya Okamoto, Chihiro Ishida, Yuichiro Ikebuchi, et al.Bioscience Reports|April 13, 2004
Polymorphism, heteroplasmy, mitochondrial fusion and diabetesAya Sato, Hitoshi Endo, Kazuo Umetsu, et al.Pageof 9