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G Sweeney

Showing results (191-200 of 220) with videos related to

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Plos One|January 7, 2016
A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial DiseaseSanjeev Rajakulendran, Robert D S Pitceathly, Jan-Willem Taanman, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Neurology|December 24, 2013
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesDavina J Hensman Moss, Mark Poulter, Jon Beck, et al.
European Radiology|May 22, 2015
Extra-ocular muscle MRI in genetically-defined mitochondrial diseaseRobert D S Pitceathly, Jasper M Morrow, Christopher D J Sinclair, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 6, 2019
Conditional, inducible gene silencing in dopamine neurons reveals a sex-specific role for Rit2 GTPase in acute cocaine response and striatal functionCarolyn G Sweeney, Patrick J Kearney, Rita R Fagan, et al.
Oncogene|July 11, 2012
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutationsZ Yao, A W E Jones, E Fassone, et al.
Neurobiology of Aging|October 14, 2014
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismLucia V Schottlaender, James M Polke, Helen Ling, et al.
Neurobiology of Aging|August 28, 2017
Erratum to "The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism" [Neurobiol. Aging 36 (2015) 1221.e1-1221.e6]Lucia V Schottlaender, James M Polke, Helen Ling, et al.
Human Mutation|May 15, 2012
Toward a mtDNA locus-specific mutation database using the LOVD platformJoanna L Elson, Mary G Sweeney, Vincent Procaccio, et al.
Circulation. Cardiovascular Genetics|October 13, 2010
Endothelial, sympathetic, and cardiac function in inherited (6R)-L-erythro-5,6,7,8-tetrahydro-L-biopterin deficiencyLila Mayahi, Lydia Mason, Katherine Bleasdale-Barr, et al.
Pageof 22

Showing results (191-200 of 220) with videos related to

Sort By:
Pageof 22
Plos One|January 7, 2016
A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial DiseaseSanjeev Rajakulendran, Robert D S Pitceathly, Jan-Willem Taanman, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Neurology|December 24, 2013
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesDavina J Hensman Moss, Mark Poulter, Jon Beck, et al.
European Radiology|May 22, 2015
Extra-ocular muscle MRI in genetically-defined mitochondrial diseaseRobert D S Pitceathly, Jasper M Morrow, Christopher D J Sinclair, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 6, 2019
Conditional, inducible gene silencing in dopamine neurons reveals a sex-specific role for Rit2 GTPase in acute cocaine response and striatal functionCarolyn G Sweeney, Patrick J Kearney, Rita R Fagan, et al.
Oncogene|July 11, 2012
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutationsZ Yao, A W E Jones, E Fassone, et al.
Neurobiology of Aging|October 14, 2014
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismLucia V Schottlaender, James M Polke, Helen Ling, et al.
Neurobiology of Aging|August 28, 2017
Erratum to "The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism" [Neurobiol. Aging 36 (2015) 1221.e1-1221.e6]Lucia V Schottlaender, James M Polke, Helen Ling, et al.
Human Mutation|May 15, 2012
Toward a mtDNA locus-specific mutation database using the LOVD platformJoanna L Elson, Mary G Sweeney, Vincent Procaccio, et al.
Circulation. Cardiovascular Genetics|October 13, 2010
Endothelial, sympathetic, and cardiac function in inherited (6R)-L-erythro-5,6,7,8-tetrahydro-L-biopterin deficiencyLila Mayahi, Lydia Mason, Katherine Bleasdale-Barr, et al.
Pageof 22