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Human Mutation|August 30, 2008
Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamilyElena G Bochukova, Tony Roscioli, Dale J Hedges, et al.Gene|October 24, 2006
Different evolutionary fates of recently integrated human and chimpanzee LINE-1 retrotransposonsJungnam Lee, Richard Cordaux, Kyudong Han, et al.Analytical Biochemistry|April 4, 2003
Human DNA quantitation using Alu element-based polymerase chain reactionJerilyn A Walker, Gail E Kilroy, Jinchuan Xing, et al.Journal of Molecular Biology|April 22, 2005
Alu retrotransposition-mediated deletionPauline A Callinan, Jianxin Wang, Scott W Herke, et al.Plos Genetics|December 7, 2011
Repetitive elements may comprise over two-thirds of the human genomeA P Jason de Koning, Wanjun Gu, Todd A Castoe, et al.BMC Genomics|July 2, 2010
Mobile element scanning (ME-Scan) by targeted high-throughput sequencingDavid J Witherspoon, Jinchuan Xing, Yuhua Zhang, et al.Journal of Forensic Sciences|February 24, 2007
Human genomic DNA quantitation system, H-Quant: development and validation for use in forensic caseworkJaiprakash G Shewale, Elaine Schneida, Jonathan Wilson, et al.Gene|October 24, 2006
A SINE-based dichotomous key for primate identificationScott W Herke, Jinchuan Xing, David A Ray, et al.Analytical Biochemistry|April 25, 2003
Quantitative intra-short interspersed element PCR for species-specific DNA identificationJerilyn A Walker, David A Hughes, Bridget A Anders, et al.Genome Research|May 4, 2005
Under the genomic radar: the stealth model of Alu amplificationKyudong Han, Jinchuan Xing, Hui Wang, et al.Pageof 17