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Neurogenetics

Showing results (581-590 of 1,081) with videos related to

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Neurogenetics|September 13, 2021
Correction to: Increased unfolded protein responses caused by MED17 mutationsTakeshi Terabayashi, Satoru Hashimoto
Neurogenetics|August 3, 2005
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizuresC L Bennett, H M Huynh, P F Chance, et al.
Neurogenetics|June 21, 2005
Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinosesSara E Mole, Ruth E Williams, Hans H Goebel
Neurogenetics|March 30, 2006
Identification of Alu elements mediating a partial PMP22 deletionVerena Matejas, Kathrin Huehne, Christian Thiel, et al.
Neurogenetics|August 11, 2006
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndromeJeffrey M Long, Patricia LaPorte, Sandra Merscher, et al.
Neurogenetics|June 14, 2006
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysisPing-I Lin, Eden R Martin, Carrie A Browning-Large, et al.
Neurogenetics|April 14, 2005
LGI1: a gene involved in epileptogenesis and glioma progression?W Gu, E Brodtkorb, T Piepoli, et al.
Neurogenetics|June 11, 2005
Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease familyK W Chung, I N Sunwoo, S M Kim, et al.
Neurogenetics|June 5, 2021
Revisiting the pathogenic mechanism of the GJB1 5' UTR c.-103C > T mutation causing CMTX1Bianca R Grosz, John Svaren, Gonzalo Perez-Siles, et al.
Neurogenetics|January 18, 2023
INPP4A-related genetic and phenotypic spectrum and functional relevance of subcellular targeting of INPP4A isoformsLaura Hecher, Frederike L Harms, Jasmin Lisfeld, et al.
Pageof 109

Showing results (581-590 of 1,081) with videos related to

Sort By:
Pageof 109
Neurogenetics|September 13, 2021
Correction to: Increased unfolded protein responses caused by MED17 mutationsTakeshi Terabayashi, Satoru Hashimoto
Neurogenetics|August 3, 2005
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizuresC L Bennett, H M Huynh, P F Chance, et al.
Neurogenetics|June 21, 2005
Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinosesSara E Mole, Ruth E Williams, Hans H Goebel
Neurogenetics|March 30, 2006
Identification of Alu elements mediating a partial PMP22 deletionVerena Matejas, Kathrin Huehne, Christian Thiel, et al.
Neurogenetics|August 11, 2006
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndromeJeffrey M Long, Patricia LaPorte, Sandra Merscher, et al.
Neurogenetics|June 14, 2006
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysisPing-I Lin, Eden R Martin, Carrie A Browning-Large, et al.
Neurogenetics|April 14, 2005
LGI1: a gene involved in epileptogenesis and glioma progression?W Gu, E Brodtkorb, T Piepoli, et al.
Neurogenetics|June 11, 2005
Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease familyK W Chung, I N Sunwoo, S M Kim, et al.
Neurogenetics|June 5, 2021
Revisiting the pathogenic mechanism of the GJB1 5' UTR c.-103C > T mutation causing CMTX1Bianca R Grosz, John Svaren, Gonzalo Perez-Siles, et al.
Neurogenetics|January 18, 2023
INPP4A-related genetic and phenotypic spectrum and functional relevance of subcellular targeting of INPP4A isoformsLaura Hecher, Frederike L Harms, Jasmin Lisfeld, et al.
Pageof 109