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JCI Insight|January 24, 2023
Delayed boosting improves human antigen-specific Ig and B cell responses to the RH5.1/AS01B malaria vaccineCarolyn M Nielsen, Jordan R Barrett, Christine Davis, et al.Contemporary Clinical Trials Communications|April 25, 2019
A randomized pilot study comparing graft-first to fistula-first strategies in older patients with incident end-stage kidney disease: Clinical rationale and study designMariana Murea, Randolph L Geary, Matthew S Edwards, et al.Communications Biology|February 23, 2023
MacroH2A histone variants modulate enhancer activity to repress oncogenic programs and cellular reprogrammingWazim Mohammed Ismail, Amelia Mazzone, Flavia G Ghiraldini, et al.American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.Pediatric Blood & Cancer|July 22, 2025
High Prevalence of Abnormal Baseline Lung Function in Pediatric and Young Adult Hematopoietic Stem Cell Transplant Recipients: A Report from the TRANSPIRE StudyJane Koo, Richard Cooper, Stephanie L Edwards, et al.Journal of the American Society of Nephrology : JASN|April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.Nature|June 21, 2019
Noncoding deletions reveal a gene that is critical for intestinal functionDanit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, et al.Journal of the American Society of Nephrology : JASN|February 12, 2022
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and DeafnessNaomi Issler, Sara Afonso, Irith Weissman, et al.Journal of the American Society of Nephrology : JASN|April 15, 2018
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney FailureMarkus Reichold, Enriko D Klootwijk, Joerg Reinders, et al.Medrxiv : the Preprint Server for Health Sciences|March 18, 2026
Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiationDonato Iacovazzo, Federica Begalli, Oniz Suleyman, et al.Pageof 46