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The Journal of Biological Chemistry|September 6, 2000
Disruption of a single copy of the SERCA2 gene results in altered Ca2+ homeostasis and cardiomyocyte functionY Ji, M J Lalli, G J Babu, et al.
American Journal of Human Genetics|February 15, 2002
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21Xianhua Piao, Lina Basel-Vanagaite, Rachel Straussberg, et al.
The Journal of Clinical Investigation|April 1, 1994
Overexpression of apolipoprotein CII causes hypertriglyceridemia in transgenic miceN S Shachter, T Hayek, T Leff, et al.
Cell Metabolism|April 6, 2017
FGF21 Regulates Metabolism Through Adipose-Dependent and -Independent MechanismsLucas D BonDurant, Magdalene Ameka, Meghan C Naber, et al.
Brain : a Journal of Neurology|February 3, 2026
ARX mutation-associated interneuron defects provide insights into mechanisms underlying developmental epilepsiesYoungshin Lim, Shyam K Akula, Abigail K Myers, et al.
JTO Clinical and Research Reports|September 30, 2021
High-Grade Neuroendocrine Carcinoma Within a Tracheal Polyp: A Case ReportVictor Brochu, Gurdip Singh Tamber, Roni F Rayes, et al.
Pediatric Radiology|December 2, 2000
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findingsT Y Poussaint, J W Fox, W B Dobyns, et al.
Journal of Electrocardiology|April 9, 2010
Prevalence of electrocardiographic abnormalities in a middle-aged, biracial population: Coronary Artery Risk Development in Young Adults studyJoseph A Walsh, Ronald Prineas, Martha L Daviglus, et al.
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