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Investigative Ophthalmology & Visual Science|June 4, 2016
Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal RetinoschisisAjoy Vincent, Judith Ng, Christina Gerth-Kahlert, et al.
The Lancet. Rheumatology|May 24, 2025
Maternal autoantibodies to the sodium potassium pump α1 subunit AT1A1 and fetal autoimmune congenital heart block: a case-control studyStephanie Benjamin, Lisa Vi, Diptendu Chatterjee, et al.
Plos One|September 9, 2020
Cancer proteome and metabolite changes linked to SHMT2Jiefei Tong, Jonathan R Krieger, Paul Taylor, et al.
European Heart Journal|September 22, 2018
An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesisDiptendu Chatterjee, Meena Fatah, Deniz Akdis, et al.
Elife|September 29, 2023
The chemorepellent, SLIT2, bolsters innate immunity against Staphylococcus aureusVikrant K Bhosle, Chunxiang Sun, Sajedabanu Patel, et al.
JCI Insight|October 22, 2024
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplicationRabiat Adele, Rowaida Hussein, Erika Tavares, et al.
Investigative Ophthalmology & Visual Science|December 23, 2021
Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10Monika K Grudzinska Pechhacker, Samuel G Jacobson, Arlene V Drack, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2020
DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degenerationAnjali Vig, James A Poulter, Daniele Ottaviani, et al.
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