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Frontiers in Genetics|November 9, 2013
Channelopathy pathogenesis in autism spectrum disordersGalina Schmunk, J Jay GargusScientific Reports|February 2, 2017
High-throughput screen detects calcium signaling dysfunction in typical sporadic autism spectrum disorderGalina Schmunk, Rachel L Nguyen, David L Ferguson, et al.Annals of the New York Academy of Sciences|January 22, 2009
Genetic calcium signaling abnormalities in the central nervous system: seizures, migraine, and autismJ Jay GargusBiological Psychiatry|February 25, 2006
Ion channel functional candidate genes in multigenic neuropsychiatric diseaseJ Jay GargusAmerican Journal of Human Genetics|March 12, 2003
Unraveling monogenic channelopathies and their implications for complex polygenic diseaseJ Jay GargusPediatric Neurology|November 21, 2007
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3J Jay Gargus, Anne TournayJournal of Human Genetics|August 26, 2003
Identification of a novel candidate gene in the iron-sulfur pathway implicated in ataxia-susceptibility: human gene encoding HscB, a J-type co-chaperoneGuifeng Sun, J Jay Gargus, Dennis T Ta, et al.European Journal of Pediatrics|July 12, 2002
Progressive neurologic disability in methylmalonic acidemia despite transplantation of the liverWilliam L Nyhan, J Jay Gargus, Karen Boyle, et al.Cell Metabolism|December 5, 2006
Serotonin targets the DAF-16/FOXO signaling pathway to modulate stress responsesBin Liang, Mustapha Moussaif, Chih-Jen Kuan, et al.Proceedings of the National Academy of Sciences of the United States of America|July 23, 2005
Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2Laura Segall, Alessandra Mezzetti, Rosemarie Scanzano, et al.Pageof 3