Showing results (21-30 of 59) with videos related to
Sort By:
Pageof 6
Plos One|September 3, 2014
Regionally-specified second trimester fetal neural stem cells reveals differential neurogenic programmingYiping Fan, Guillaume Marcy, Eddy S M Lee, et al.Nature|July 13, 2010
Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisitionDaniel W Bellott, Helen Skaletsky, Tatyana Pyntikova, et al.ESMO Open|November 16, 2016
NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancerKakoli Das, Xiu Bin Chan, David Epstein, et al.Ophthalmic Genetics|January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndromeStuart W Tompson, Charles Johnson, Diana Abbott, et al.American Journal of Ophthalmology|December 11, 2012
CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United StatesSing-Hui Lim, Khanh-Nhat Tran-Viet, Tammy L Yanovitch, et al.Nature Genetics|February 28, 2006
High mutation rates have driven extensive structural polymorphism among human Y chromosomesSjoerd Repping, Saskia K M van Daalen, Laura G Brown, et al.NPJ Genomic Medicine|June 25, 2019
Implementation of genomics in medical practice to deliver precision medicine for an Asian populationYasmin Bylstra, Sonia Davila, Weng Khong Lim, et al.Genomics|June 5, 2004
A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c regionSjoerd Repping, Saskia K M van Daalen, Cindy M Korver, et al.Genome Biology|September 30, 2011
First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneumWillie Yu, Waraporn Chan-On, Melissa Teo, et al.Nature Genetics|October 7, 2003
Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selectionSjoerd Repping, Helen Skaletsky, Laura Brown, et al.Pageof 6