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Plos Genetics|June 21, 2013
Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiencySeok-Hyung Kim, Sarah A Scott, Michael J Bennett, et al.
Plos One|October 4, 2023
Non-canonical functions of a mutant TSC2 protein in mitotic divisionMary-Bronwen L Chalkley, Rachel B Mersfelder, Maria Sundberg, et al.
Neurotoxicology|October 27, 2012
Genetic risk for Parkinson's disease correlates with alterations in neuronal manganese sensitivity between two human subjectsAsad A Aboud, Andrew M Tidball, Kevin K Kumar, et al.
Neurobiology of Disease|April 30, 2020
Neuronal modeling of alternating hemiplegia of childhood reveals transcriptional compensation and replicates a trigger-induced phenotypeJohn P Snow, Grant Westlake, Lindsay K Klofas, et al.
Peerj|January 7, 2014
Gammaretroviral vector encoding a fluorescent marker to facilitate detection of reprogrammed human fibroblasts during iPSC generationNarasimhachar Srinivasakumar, Michail Zaboikin, Andrew M Tidball, et al.
Neurobiology of Disease|March 24, 2018
Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhoodChristine Q Simmons, Christopher H Thompson, Bryan E Cawthon, et al.
Human Molecular Genetics|January 29, 2025
Human TSC2 mutant cells exhibit aberrations in early neurodevelopment accompanied by changes in the DNA MethylomeMary-Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Human TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA MethylomeMary-Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, et al.
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