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Journal of the Association for Research in Otolaryngology : JARO|May 20, 2014
Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type CKelly A King, Sandra Gordon-Salant, Karen S Pawlowski, et al.JAMA Network Open|August 7, 2024
Neighborhood Socioeconomic Disadvantage Across the Life Course and Premature MortalityWayne R Lawrence, Anna M Kucharska-Newton, Jared W Magnani, et al.Molecular Metabolism|August 28, 2019
Cognitive dysfunction in diabetic rats is prevented by pyridoxamine treatment. A multidisciplinary investigationSarah Kassab, Paul Begley, Stephanie J Church, et al.Physical Review Letters|March 26, 2013
Catch and release of microwave photon statesYi Yin, Yu Chen, Daniel Sank, et al.Neurochemical Research|June 8, 2023
Luvadaxistat: A Novel Potent and Selective D-Amino Acid Oxidase Inhibitor Improves Cognitive and Social Deficits in Rodent Models for SchizophreniaRosa Fradley, Pascal Goetghebeur, David Miller, et al.American Journal of Human Genetics|May 23, 2000
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotypeC Bétard, A Rasquin-Weber, C Brewer, et al.Journal of the American College of Cardiology|July 18, 2015
Contractile Function During Angiotensin-II Activation: Increased Nox2 Activity Modulates Cardiac Calcium Handling via Phospholamban PhosphorylationMin Zhang, Benjamin L Prosser, Moradeke A Bamboye, et al.American Journal of Preventive Cardiology|September 6, 2021
Improving the enrollment of women and racially/ethnically diverse populations in cardiovascular clinical trials: An ASPC practice statementErin D Michos, Tina K Reddy, Martha Gulati, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 19, 2012
Audiovestibular dysfunction associated with adoptive cell immunotherapy for melanomaBradley J Seaman, Elizabeth A Guardiani, Carmen C Brewer, et al.Elife|November 9, 2021
Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.Pageof 76