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Human Genetics|September 5, 2015
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor geneMinaka Ishibashi, Elizabeth Manning, Cheryl Shoubridge, et al.Iscience|May 11, 2026
Ambient temperature regulates CD4+ T cell tonic T cell receptor signaling and responsivenessKeisuke Sawada, John Eom, Bree A Mahoney-Sutherland, et al.Clinical Nuclear Medicine|May 4, 2026
Outcomes of Radiotherapy With or Without Dose Escalation to Lymph Node Metastases Detected by PET PSMA or Conventional Imaging in Node-Positive Prostate Cancer: A Real-World Multicenter Propensity Score-Matched (PRIMENOD) AnalysisMateusz Bilski, Federico Mastroleo, Artur J Chyrek, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2020
Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditionsTomasz Gambin, Qian Liu, Justyna A Karolak, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2012
Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1AIan M Campbell, Svetlana A Yatsenko, Patricia Hixson, et al.Cell Reports|February 2, 2023
Spatial compartmentalization of signaling imparts source-specific functions on secreted factorsElena Groppa, Paolo Martini, Nima Derakhshan, et al.Pediatric Neurology|July 4, 2025
Cyclical Vomiting Syndrome in Individuals With BPTF HaploinsufficiencyAlessandro Ferretti, Margherita Furlan, Kevin E Glinton, et al.American Journal of Medical Genetics. Part A|February 27, 2010
22q13.3 deletion syndrome: clinical and molecular analysis using array CGHS U Dhar, D del Gaudio, J R German, et al.Journal of Contemporary Brachytherapy|June 3, 2026
Polish Brachytherapy Society clinical recommendations and expert consensus on radical high-dose-rate brachytherapy for prostate cancerArtur J Chyrek, Marcin Hetnał, Andrzej Kukiełka, et al.Genome Medicine|April 25, 2019
Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndromeClaudia M B Carvalho, Zeynep Coban-Akdemir, Hadia Hijazi, et al.Pageof 185