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Cell Cycle (Georgetown, Tex.)|May 6, 2015
Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytesNadine Kraemer, Ethiraj Ravindran, Sami Zaqout, et al.
Frontiers in Neurology|January 27, 2023
Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsySvea Horn, Magdalena Danyel, Nina Erdmann, et al.
Progress in Neurobiology|November 26, 2009
Many roads lead to primary autosomal recessive microcephalyAngela M Kaindl, Sandrine Passemard, Pavan Kumar, et al.
Wiener Klinische Wochenschrift|January 1, 1992
[Extracorporeal shock wave treatment of calcium containing gallbladder calculi]G Meiser, G Lexer, M Heinerman, et al.
Mitochondrion|July 9, 2017
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasiaGudrun Schottmann, Sylvie Picker-Minh, Jana Marie Schwarz, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|November 12, 2005
[Systemic ALlambda amyloidosis associated with vascular fragility]Martin Laimer, Karin Kaindl, Michael Emberger, et al.
Orphanet Journal of Rare Diseases|April 17, 2013
Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutationLina Issa, Katrin Mueller, Katja Seufert, et al.
Cell Research|October 23, 2020
Binding pathway determines norepinephrine selectivity for the human β1AR over β2ARXinyu Xu, Jonas Kaindl, Mary J Clark, et al.
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