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Human Molecular Genetics|May 12, 2023
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defectsRebekah Tillotson, Keqin Yan, Julie Ruston, et al.American Journal of Respiratory and Critical Care Medicine|March 3, 2012
17β-Estradiol attenuates hypoxic pulmonary hypertension via estrogen receptor-mediated effectsTim Lahm, Marjorie Albrecht, Amanda J Fisher, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|October 10, 2023
Alpha-1 antitrypsin inhibits fractalkine-mediated monocyte-lung endothelial cell interactionsAndrew Mikosz, Kevin Ni, Fabienne Gally, et al.Human Genetics|June 24, 2006
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivityErica R Eichers, Muhammad M Abd-El-Barr, Richard Paylor, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|May 17, 2015
Endothelial disruptive proinflammatory effects of nicotine and e-cigarette vapor exposuresKelly S Schweitzer, Steven X Chen, Sarah Law, et al.The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
Effect of MK-386, a novel inhibitor of type 1 5 alpha-reductase, alone and in combination with finasteride, on serum dihydrotestosterone concentrations in menJ I Schwartz, A Van Hecken, P J De Schepper, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 25, 2000
Effects of ENU dosage on mouse strainsM J Justice, D A Carpenter, J Favor, et al.Neuroendocrinology|March 14, 2023
Changes in Corticotropin-Releasing Factor Receptor Type 1, Co-Expression with Tyrosine Hydroxylase and Oxytocin Neurons, and Anxiety-Like Behaviors across the Postpartum Period in MiceRose M De Guzman, Zachary J Rosinger, Krystyna A Rybka, et al.Proceedings of the National Academy of Sciences of the United States of America|April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeJonathan L Tobin, Matt Di Franco, Erica Eichers, et al.Blood|May 23, 2007
Mutations in the cofilin partner Aip1/Wdr1 cause autoinflammatory disease and macrothrombocytopeniaBenjamin T Kile, Athanasia D Panopoulos, Roslynn A Stirzaker, et al.Pageof 26