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American Journal of Medical Genetics. Part A|December 25, 2009
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian populationColleen A Campbell, Charley C Della Santina, Nicole C Meyer, et al.
American Journal of Hematology|December 6, 2019
Increased mitochondrial apoptotic priming with targeted therapy predicts clinical response to re-induction chemotherapyJacqueline S Garcia, Shruti Bhatt, Geoffrey Fell, et al.
MMWR. Morbidity and Mortality Weekly Report|June 17, 2021
Emergency Department Visits for Suspected Suicide Attempts Among Persons Aged 12-25 Years Before and During the COVID-19 Pandemic - United States, January 2019-May 2021Ellen Yard, Lakshmi Radhakrishnan, Michael F Ballesteros, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy successSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Progress in Retinal and Eye Research|March 27, 2018
CRISPR-Cas9 genome engineering: Treating inherited retinal degenerationErin R Burnight, Joseph C Giacalone, Jessica A Cooke, et al.
Human Molecular Genetics|April 30, 2002
VSX1: a gene for posterior polymorphous dystrophy and keratoconusElise Héon, Alex Greenberg, Kelly K Kopp, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 22, 2001
CD6+ donor marrow T-cell depletion as the sole form of graft-versus-host disease prophylaxis in patients undergoing allogeneic bone marrow transplant from unrelated donorsR J Soiffer, E Weller, E P Alyea, et al.
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