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Neurogenetics

Showing results (331-340 of 1,080) with videos related to

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Neurogenetics|September 2, 2008
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22Bouchra Ouled Amar Ben Cheikh, Stéphanie Baulac, Fatiha Lahjouji, et al.
Neurogenetics|December 18, 2008
Familial risks for amyotrophic lateral sclerosis and autoimmune diseasesKari Hemminki, Xinjun Li, Jan Sundquist, et al.
Neurogenetics|May 22, 2009
Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystoniaKang Wang, Yuji Takahashi, Zong-Liang Gao, et al.
Neurogenetics|May 28, 2009
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorderAyelet Erez, Amina J Patel, Xueqing Wang, et al.
Neurogenetics|May 29, 2009
U1 snRNA mis-binding: a new cause of CMT1BHervé Crehalet, Philippe Latour, Véronique Bonnet, et al.
Neurogenetics|June 11, 2009
A novel variation in the Twinkle linker region causing late-onset dementiaAndoni Echaniz-Laguna, Jean-Baptiste Chanson, Jean-Marie Wilhelm, et al.
Neurogenetics|December 11, 2008
Gene expression in blood of subjects with Duchenne muscular dystrophyBrenda Wong, Donald L Gilbert, Wynn L Walker, et al.
Neurogenetics|November 26, 2008
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing lossAlessandra Terracciano, Carlo Casali, Gaetano S Grieco, et al.
Neurogenetics|July 1, 2009
A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in miceAlexis Tapanes-Castillo, Eli J Weaver, Robin P Smith, et al.
Neurogenetics|June 24, 2009
COL25A1 triggers and promotes Alzheimer's disease-like pathology in vivoYing Tong, Ying Xu, Kimberly Scearce-Levie, et al.
Pageof 108

Showing results (331-340 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|September 2, 2008
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22Bouchra Ouled Amar Ben Cheikh, Stéphanie Baulac, Fatiha Lahjouji, et al.
Neurogenetics|December 18, 2008
Familial risks for amyotrophic lateral sclerosis and autoimmune diseasesKari Hemminki, Xinjun Li, Jan Sundquist, et al.
Neurogenetics|May 22, 2009
Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystoniaKang Wang, Yuji Takahashi, Zong-Liang Gao, et al.
Neurogenetics|May 28, 2009
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorderAyelet Erez, Amina J Patel, Xueqing Wang, et al.
Neurogenetics|May 29, 2009
U1 snRNA mis-binding: a new cause of CMT1BHervé Crehalet, Philippe Latour, Véronique Bonnet, et al.
Neurogenetics|June 11, 2009
A novel variation in the Twinkle linker region causing late-onset dementiaAndoni Echaniz-Laguna, Jean-Baptiste Chanson, Jean-Marie Wilhelm, et al.
Neurogenetics|December 11, 2008
Gene expression in blood of subjects with Duchenne muscular dystrophyBrenda Wong, Donald L Gilbert, Wynn L Walker, et al.
Neurogenetics|November 26, 2008
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing lossAlessandra Terracciano, Carlo Casali, Gaetano S Grieco, et al.
Neurogenetics|July 1, 2009
A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in miceAlexis Tapanes-Castillo, Eli J Weaver, Robin P Smith, et al.
Neurogenetics|June 24, 2009
COL25A1 triggers and promotes Alzheimer's disease-like pathology in vivoYing Tong, Ying Xu, Kimberly Scearce-Levie, et al.
Pageof 108