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Plos Genetics|August 17, 2005
Fog2 is required for normal diaphragm and lung development in mice and humansKate G Ackerman, Bruce J Herron, Sara O Vargas, et al.Nature|August 23, 2008
PRDM16 controls a brown fat/skeletal muscle switchPatrick Seale, Bryan Bjork, Wenli Yang, et al.Human Molecular Genetics|June 1, 2010
Genome-wide identification of mouse congenital heart disease lociAnna Kamp, Michael A Peterson, Karen L Svenson, et al.Molecular Cell|August 27, 2013
NEK8 links the ATR-regulated replication stress response and S phase CDK activity to renal ciliopathiesHyo Jei Claudia Choi, Jia-Ren Lin, Jean-Baptiste Vannier, et al.Acta Neuropathologica Communications|April 9, 2015
Amyloid accelerates tau propagation and toxicity in a model of early Alzheimer's diseaseAmy M Pooler, Manuela Polydoro, Eduardo A Maury, et al.Human Molecular Genetics|April 8, 2016
Reduction of ciliary length through pharmacologic or genetic inhibition of CDK5 attenuates polycystic kidney disease in a model of nephronophthisisHervé Husson, Sarah Moreno, Laurie A Smith, et al.Biorxiv : the Preprint Server for Biology|February 6, 2026
A Sensitized ENU Mutagenesis Screen for Thrombosis Modifiers Identifies Suppressor Variants in Non-mutagenized Parental Generations Due to Antithrombotic Selective PressuresMarisa A Brake, Audrey C Cleuren, Sydney Torres, et al.Genome Research|February 8, 2006
Utilization of a whole genome SNP panel for efficient genetic mapping in the mouseJennifer L Moran, Andrew D Bolton, Pamela V Tran, et al.American Journal of Human Genetics|October 25, 2022
Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorderReham Khalaf-Nazzal, James Fasham, Katherine A Inskeep, et al.Nature Communications|January 21, 2015
ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterningPeter G Czarnecki, George C Gabriel, Danielle K Manning, et al.Pageof 15