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Nature Communications|October 22, 2020
Early-onset autoimmunity associated with SOCS1 haploinsufficiencyJérôme Hadjadj, Carla Noemi Castro, Maud Tusseau, et al.The Journal of Clinical Investigation|September 25, 2019
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, et al.Stroke|May 21, 2025
SUMMIT MAX: A randomized trial of the super large bore HiPoint Reperfusion System versus Vecta System for aspiration thrombectomyThanh N Nguyen, Guilherme Dabus, Ben McGuinness, et al.Biological Psychiatry|August 25, 2019
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β SignalingBrett V Johnson, Raman Kumar, Sabrina Oishi, et al.Pageof 5