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Biochemical and Biophysical Research Communications|August 2, 2002
Single nucleotide polymorphisms of thrifty genes for energy metabolism: evolutionary origins and prospects for intervention to prevent obesity-related diseasesYasuo Kagawa, Yoshiko Yanagisawa, Kyoko Hasegawa, et al.Electrophoresis|July 20, 2011
Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2Haruo Takeshita, Junko Fujihara, Mikiko Soejima, et al.Journal of Human Genetics|February 15, 2013
A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathyKentaro Toyota, Taeko Hashimoto, Daisuke Ogino, et al.JIMD Reports|February 23, 2013
Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass SpectrometryToshiyuki Fukao, Shinsuke Maruyama, Toshihiro Ohura, et al.Journal of Inherited Metabolic Disease|March 25, 2011
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type IMailys Guillard, Yoshinao Wada, Hana Hansikova, et al.Journal of Human Genetics|November 9, 2012
The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations, Timothy Jinam, Nao Nishida, et al.Human Mutation|October 12, 2013
De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathyHirofumi Kodera, Kazuyuki Nakamura, Hitoshi Osaka, et al.Genome Research|October 7, 2004
Mitochondrial genome variation in eastern Asia and the peopling of JapanMasashi Tanaka, Vicente M Cabrera, Ana M González, et al.Pageof 9