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Journal of Human Genetics|September 13, 2005
Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathyKazuki Kijima, Chikahiko Numakura, Tomohide Goto, et al.BMC Zoology|May 11, 2023
Complete mitochondrial genomes of three fairy shrimps from snowmelt pools in JapanTakashi Kitano, Hidenori Sato, Norihito Takahashi, et al.Gene|September 5, 2006
Origin and evolution of gene for prolactin-induced proteinTakashi Kitano, Wei Tian, Kazuo Umetsu, et al.Legal Medicine (Tokyo, Japan)|March 17, 2016
The art of traditional native PAGE: The APLP 48-ID assay for human identificationKazuo Umetsu, Isao Yuasa, Masaki Hashiyada, et al.Genomics|February 8, 2003
Evolution of the cystatin B gene: implications for the origin of its variable dodecamer tandem repeat in humansMotoki Osawa, Mika Kaneko, Hidekazu Horiuchi, et al.Forensic Science International|June 14, 2002
Molecular analysis of the human esterase D gene ESD(*)Q0(yonago) responsible for incompatibility in a Japanese paternity caseIsao Yuasa, Kazuo Umetsu, Shuichi Tsuchida, et al.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.Legal Medicine (Tokyo, Japan)|November 27, 2007
Allele frequencies of a SNP and a 27-bp deletion that are the determinant of earwax type in the ABCC11 geneTakashi Kitano, Isao Yuasa, Kentaro Yamazaki, et al.Pageof 6