Showing results (1031-1040 of 1,067) with videos related to

Sort By:
Pageof 107
Science Translational Medicine|June 15, 2022
Granzyme K+ CD8 T cells form a core population in inflamed human tissueA Helena Jonsson, Fan Zhang, Garrett Dunlap, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
American Journal of Medical Genetics. Part A|November 10, 2023
Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approachLeanne de Kock, Alexanne Cuillerier, Meredith Gillespie, et al.
Journal of Neurosurgery|June 17, 2023
Safety and feasibility clinical trial of nucleus accumbens deep brain stimulation for treatment-refractory opioid use disorderAli R Rezai, James J Mahoney, Manish Ranjan, et al.
American Heart Journal|October 16, 2020
Rationale and design of ApoA-I Event Reducing in Ischemic Syndromes II (AEGIS-II): A phase 3, multicenter, double-blind, randomized, placebo-controlled, parallel-group study to investigate the efficacy and safety of CSL112 in subjects after acute myocardial infarctionC Michael Gibson, John J P Kastelein, Adam T Phillips, et al.
Molecular Psychiatry|February 11, 2026
Neonatal gut Bifidobacterium associates with indole-3-lactic acid levels in blood and risk of ADHD at age 10Michael Widdowson, Shiraz Shah, Jonathan Thorsen, et al.
Neurology. Genetics|October 27, 2021
Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1Alison M R Castle, Smrithi Salian, Haim Bassan, et al.
Journal of the National Cancer Institute|June 19, 2014
Impact of patient navigation on timely cancer care: the Patient Navigation Research ProgramKaren M Freund, Tracy A Battaglia, Elizabeth Calhoun, et al.
Nature Medicine|May 25, 2024
IL-6 inhibition with clazakizumab in patients receiving maintenance dialysis: a randomized phase 2b trialGlenn M Chertow, Anna Marie Chang, G Michael Felker, et al.
American Journal of Human Genetics|September 29, 2021
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomaliesGabrielle Lemire, Yoko A Ito, Aren E Marshall, et al.
Pageof 107