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Human Molecular Genetics|January 7, 2015
CRIM1 haploinsufficiency causes defects in eye development in human and mouseFilippo Beleggia, Yun Li, Jieqing Fan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 20, 2015
Nucleoside diphosphate kinase B-activated intermediate conductance potassium channels are critical for neointima formation in mouse carotid arteriesXiao-Bo Zhou, Yu-Xi Feng, Qiang Sun, et al.
Nature Metabolism|January 28, 2026
Lamin A/C-regulated cysteine catabolic flux modulates stem cell fate through epigenome reprogrammingYinuo Wang, Haojie Shi, Janina Wittig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 22, 2014
DYT16 revisited: exome sequencing identifies PRKRA mutations in a European dystonia familyMichael Zech, Florian Castrop, Barbara Schormair, et al.
Plos One|August 1, 2017
G protein-coupled receptor kinase 2 promotes cardiac hypertrophyPhilipp Schlegel, Julia Reinkober, Eric Meinhardt, et al.
European Journal of Medical Genetics|February 4, 2014
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progressionKatrin Bürk, Frank J Kaiser, Stephanie Tennstedt, et al.
The Journal of Clinical Investigation|June 3, 2009
The natriuretic peptide/guanylyl cyclase--a system functions as a stress-responsive regulator of angiogenesis in miceMichaela Kuhn, Katharina Völker, Kristine Schwarz, et al.
Cells|October 2, 2020
Dissecting G<sub>q/11</sub>-Mediated Plasma Membrane Translocation of Sphingosine Kinase-1Kira Vanessa Blankenbach, Ralf Frederik Claas, Natalie Judith Aster, et al.
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