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Human Molecular Genetics|August 14, 2003
Murine Denys-Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosisCharles E Patek, Stewart Fleming, Colin G Miles, et al.
Development (Cambridge, England)|February 24, 2011
Wt1 controls retinoic acid signalling in embryonic epicardium through transcriptional activation of Raldh2Juan Antonio Guadix, Adrián Ruiz-Villalba, Laura Lettice, et al.
Bio-Protocol|January 1, 2019
Notochord Injury Assays that Stimulate Transcriptional Responses in Zebrafish LarvaeZhiqiang Zeng, Juan C Lopez-Baez, Laura Lleras-Forero, et al.
The Journal of Pathology|August 5, 2003
The wt1-heterozygous mouse; a model to study the development of glomerular sclerosisAswin L Menke, Annemieke IJpenberg, Stewart Fleming, et al.
The American Journal of Pathology|April 28, 2005
Implication of Wt1 in the pathogenesis of nephrogenic failure in a mouse model of retinoic acid-induced caudal regression syndromeHerman K W Tse, Maran B W Leung, Adrian S Woolf, et al.
Frontiers in Genetics|December 7, 2013
The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traitsYoshinobu Uemoto, Ricardo Pong-Wong, Pau Navarro, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 8, 2016
Extracardiac septum transversum/proepicardial endothelial cells pattern embryonic coronary arterio-venous connectionsElena Cano, Rita Carmona, Adrián Ruiz-Villalba, et al.
G3 (Bethesda, Md.)|September 14, 2012
Uncovering networks from genome-wide association studies via circular genomic permutationClaudia P Cabrera, Pau Navarro, Jennifer E Huffman, et al.
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