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Ophthalmology Science|June 8, 2026
A Primary Open-Angle Glaucoma Locus Near Transcription Factor PRRX1 Identified in the Million Veteran ProgramTyler G Kinzy, Osahon J Asowata, Lauren A Cruz, et al.JAMA Oncology|September 28, 2023
Radiotherapy Plus Cisplatin With or Without Lapatinib for Non-Human Papillomavirus Head and Neck Carcinoma: A Phase 2 Randomized Clinical TrialStuart J Wong, Pedro A Torres-Saavedra, Nabil F Saba, et al.Journal of Medicinal Chemistry|December 22, 2025
Discovery of Bis-Acyl Hydrazides as Potent and Bioavailable MTA-Cooperative PRMT5 Inhibitors: A Case Study of Leveraging the Deuterium Kinetic Isotope EffectLaurent Debien, Megan K Armstrong, Joshua D Farr, et al.Clinical Endocrinology|September 24, 2021
SDHC phaeochromocytoma and paraganglioma: A UK-wide case seriesSophie T Williams, Prodromos Chatzikyriakou, Paul V Carroll, et al.Molecular Psychiatry|June 2, 2026
Genetics of major depressive disorder in a homogeneous population with uniform phenotypingFloris Huider, Yuri Milaneschi, René Pool, et al.The Lancet. Infectious Diseases|June 15, 2019
The burden of Legionnaires' disease in New Zealand (LegiNZ): a national surveillance studyPatricia C Priest, Sandy Slow, Stephen T Chambers, et al.American Journal of Human Genetics|October 18, 2016
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of ComplementInes Kapferer-Seebacher, Melanie Pepin, Roland Werner, et al.Nature Medicine|June 25, 2024
Adaptive selection at G6PD and disparities in diabetes complicationsJoseph H Breeyear, Jacklyn N Hellwege, Philip H Schroeder, et al.Plos One|March 12, 2014
Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohortsAnna L Mitchell, Katie D R Macarthur, Earn H Gan, et al.Research Square|November 24, 2025
Genetics of Major Depressive Disorder in a Homogeneous Population with Uniform PhenotypingFloris Huider, Yuri Milaneschi, René Pool, et al.Pageof 201