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American Journal of Medical Genetics. Part A|September 14, 2007
WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformationsMohnish Suri, Peter Kelehan, David O'neill, et al.
Genetic Epidemiology|August 22, 2009
Genetic comparison of a Croatian isolate and CEPH European foundersPau Navarro, Véronique Vitart, Caroline Hayward, et al.
Biochemical and Biophysical Research Communications|December 21, 2004
The Wilms' tumor gene WT1 is a common marker of progenitor cells in fetal liverKeisuke Kanato, Naoki Hosen, Masashi Yanagihara, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 1, 2006
Increased expression of the 5-HT transporter confers a low-anxiety phenotype linked to decreased 5-HT transmissionKatie A Jennings, Merewyn K Loder, W John Sheward, et al.
Human Molecular Genetics|December 9, 2010
Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papillaRachel Berry, Louise Harewood, Liming Pei, et al.
American Journal of Hypertension|March 7, 2009
A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolateMaja Barbalić, Nina Smolej Narancić, Tatjana Skarić-Jurić, et al.
Human Molecular Genetics|August 1, 2013
WT1 regulates the expression of inhibitory chemokines during heart developmentVictor Velecela, Laura A Lettice, You-Ying Chau, et al.
Human Molecular Genetics|January 16, 2007
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traitsHarry Campbell, Andrew D Carothers, Igor Rudan, et al.
Nature Genetics|December 22, 2009
Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherinOfelia M Martínez-Estrada, Laura A Lettice, Abdelkader Essafi, et al.
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