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The International Journal of Developmental Biology|July 27, 2002
Diverse requirements for Notch signalling in mammalsDuncan B Sparrow, Melanie Clements, Sarah L Withington, et al.
The Journal of Cell Biology|August 1, 2007
Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivoInsa Geffers, Katrin Serth, Gavin Chapman, et al.
Human Molecular Genetics|January 13, 2011
Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axisKylie Lopes Floro, Stanley T Artap, Jost I Preis, et al.
Plos One|September 21, 2011
Complex SUMO-1 regulation of cardiac transcription factor Nkx2-5Mauro W Costa, Stella Lee, Milena B Furtado, et al.
Kidney International|January 15, 2015
Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signalingLorine J Wilkinson, Cailda S Neal, Reetu R Singh, et al.
American Journal of Medical Genetics. Part A|July 31, 2013
Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversusDuncan B Sparrow, Eissa Ali Faqeih, Bahauddin Sallout, et al.
Differentiation; Research in Biological Diversity|October 4, 2022
Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factorsDimuthu Alankarage, Annabelle Enriquez, Robert D Steiner, et al.
Nature Genetics|April 22, 2008
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivationMarnie E Blewitt, Anne-Valerie Gendrel, Zhenyi Pang, et al.
Molecular and Cellular Biology|December 16, 2003
Cited1 is required in trophoblasts for placental development and for embryo growth and survivalTristan A Rodriguez, Duncan B Sparrow, Annabelle N Scott, et al.
Human Molecular Genetics|January 22, 2013
Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6Duncan B Sparrow, Aideen McInerney-Leo, Zoran S Gucev, et al.
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