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American Journal of Human Genetics|July 6, 2026
Bi-allelic variants in CDK20 cause a severe ciliopathy with midline brain and facial anomaliesGabrielle Lemire, Aren E Marshall, Tejan S Patel, et al.
Cell|February 19, 2025
Reprogrammable RNA-targeting CRISPR systems evolved from RNA toxin-antitoxinsShai Zilberzwige-Tal, Han Altae-Tran, Soumya Kannan, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
Plos Pathogens|January 22, 2020
CFTR dysregulation drives active selection of the gut microbiomeStacey M Meeker, Kevin S Mears, Naseer Sangwan, et al.
Molecular Cancer|May 28, 2026
AcTor, a novel mTOR stimulator, potentiates ixazomib for the treatment of acute myeloid leukemiaShakti P Pattanayak, Odai Darawshi, Omid Hajihassani, et al.
Research Square|May 4, 2026
AcTor, a novel mTOR stimulator, potentiates ixazomib for the treatment of acute myeloid leukemiaShakti P Pattanayak, Odai Darawshi, Omid Hajihassani, et al.
Elife|April 11, 2015
Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide bindingPaul Chappell, El Kahina Meziane, Michael Harrison, et al.
Journal of Cell Science|February 10, 2023
DRP1 mutations associated with EMPF1 encephalopathy alter mitochondrial membrane potential and metabolic programsGabriella L Robertson, Stellan Riffle, Mira Patel, et al.
Journal of Clinical Nursing|August 1, 2025
Co-Designing a Model of Brilliant Care for Older PeopleAnn Dadich, Rachael Kearns, Ben Harris-Roxas, et al.
The Journal of Physiology|December 19, 2022
Adaptive exhaustion during prolonged intermittent hypoxia causes dysregulated skeletal muscle protein homeostasisAmy H Attaway, Annette Bellar, Saurabh Mishra, et al.
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