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Ophthalmic Genetics|April 21, 2016
A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generationsAndrew Kemerley, Christina Sloan, Wanda Pfeifer, et al.Current Issues in Molecular Biology|March 27, 2024
COVID-19 Associated Cardiovascular Disease-Risks, Prevention and Management: Heart at Risk Due to COVID-19Andrew Kemerley, Abhishek Gupta, Mahesh Thirunavukkarasu, et al.Ophthalmology|September 14, 2014
Vitritis in pediatric genetic retinal disordersMaria Stunkel, Sajag Bhattarai, Andrew Kemerley, et al.Ophthalmic Genetics|July 12, 2021
Clinical albinism score, presence of nystagmus and optic nerves defects are correlated with visual outcome in patients with oculocutaneous albinismAlina V Dumitrescu, Johnny Tran, Wanda Pfeifer, et al.Cells|June 10, 2023
Role of Pellino-1 in Inflammation and Cardioprotection following Severe Sepsis: A Novel Mechanism in a Murine Severe Sepsis ModelMahesh Thirunavukkarasu, Santosh Swaminathan, Andrew Kemerley, et al.Biomaterials|August 17, 2023
Biodegradable piezoelectric skin-wound scaffoldRitopa Das, Thinh T Le, Benjamin Schiff, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 1, 2023
Novel approaches to determine the functional role of cardiomyocyte specific E3 ligase, Pellino-1 following myocardial infarctionSeetur R Pradeep, Mahesh Thirunavukkarasu, Diego Accorsi, et al.Pageof 1