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Human Molecular Genetics|July 19, 2015
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosisBen J Gu, Judith Field, Sébastien Dutertre, et al.
Annals of Clinical and Translational Neurology|September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsyMichael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
American Journal of Respiratory and Critical Care Medicine|August 8, 2020
Procalcitonin to Reduce Long-Term Infection-associated Adverse Events in Sepsis. A Randomized TrialEvdoxia Kyriazopoulou, Lydia Liaskou-Antoniou, George Adamis, et al.
Science Translational Medicine|September 20, 2019
Adipose tissue-derived WNT5A regulates vascular redox signaling in obesity via USP17/RAC1-mediated activation of NADPH oxidasesIoannis Akoumianakis, Fabio Sanna, Marios Margaritis, et al.
Lancet (London, England)|April 29, 2021
Miscarriage matters: the epidemiological, physical, psychological, and economic costs of early pregnancy lossSiobhan Quenby, Ioannis D Gallos, Rima K Dhillon-Smith, et al.
Analytical Biochemistry|December 19, 2023
An assessment of a biosensor system for the quantification of microcystins in freshwater cyanobacterial bloomsJustin D Chaffin, Katelyn B Barker, Sarah R Bickman, et al.
Diabetes|June 4, 2017
Hypothalamic Inflammation in Human Obesity Is Mediated by Environmental and Genetic FactorsCarina Kreutzer, Sönke Peters, Dominik M Schulte, et al.
Neurology|December 3, 2017
Clinical and molecular characterization of KCNT1-related severe early-onset epilepsyAmy McTague, Umesh Nair, Sony Malhotra, et al.
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