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FEBS Open Bio|December 20, 2025
Long-term culture of skin biopsies: maintenance of fibroblast production and competency of reprogrammingSudiksha Rathan-Kumar, Michael A Ripperger, Grant M Westlake, et al.Neurobiology of Disease|September 13, 2011
Neuronal and glia abnormalities in Tsc1-deficient forebrain and partial rescue by rapamycinRobert P Carson, Dominic L Van Nielen, Peggy A Winzenburger, et al.Cerebral Cortex (New York, N.Y. : 1991)|October 25, 2011
GABAergic interneuron development and function is modulated by the Tsc1 geneCary Fu, Bryan Cawthon, William Clinkscales, et al.Disease Models & Mechanisms|April 13, 2013
Heterozygous inactivation of tsc2 enhances tumorigenesis in p53 mutant zebrafishSeok-Hyung Kim, Marie L Kowalski, Robert P Carson, et al.Stem Cell Research|December 23, 2017
Reproducible and efficient generation of functionally active neurons from human hiPSCs for preclinical disease modelingYunyao Xie, Ryan J Schutte, Nathan N Ng, et al.Neuroimage|September 25, 2015
Evaluation of diffusion kurtosis imaging in ex vivo hypomyelinated mouse brainsNathaniel D Kelm, Kathryn L West, Robert P Carson, et al.Neuroimage|December 28, 2016
Myelin volume fraction imaging with MRIKathryn L West, Nathaniel D Kelm, Robert P Carson, et al.Human Molecular Genetics|October 4, 2017
Heterozygous loss of TSC2 alters p53 signaling and human stem cell reprogrammingLaura C Armstrong, Grant Westlake, John P Snow, et al.Clinical Case Reports|November 29, 2023
A rare cause of posterior reversible encephalopathy syndrome: Acute lymphoblastic leukemiaJessica Hayes, Anne Byrd Mahoney, Claci Ayers, et al.Journal of Pediatric Neuropsychology|August 28, 2025
Virtual Reality Water Maze Navigation in Children with Neurofibromatosis Type 1 and Reading Disability: an Exploratory StudyMicah A D'Archangel, Stephanie N Del Tufo, Laurie E Cutting, et al.Pageof 7