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Neurogenetics

Showing results (611-620 of 949) with videos related to

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Neurogenetics|February 26, 2009
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypesS Russo, M Marchi, F Cogliati, et al.
Neurogenetics|January 22, 2009
Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson's diseaseA González-Pérez, J Gayán, J Marín, et al.
Neurogenetics|September 25, 2008
Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid betaJohn S K Kauwe, Jun Wang, Kevin Mayo, et al.
Neurogenetics|July 28, 2009
Identification of CACNA1A large deletions in four patients with episodic ataxiaFlorence Riant, Christelle Lescoat, Katayoun Vahedi, et al.
Neurogenetics|February 18, 2009
The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromasMeena Upadhyaya, Gill Spurlock, Lan Kluwe, et al.
Neurogenetics|February 14, 2009
A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson's diseaseCécile Cazeneuve, Channkanira Sân, Salah A Ibrahim, et al.
Neurogenetics|October 2, 2007
Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain diseaseUte Hehr, Goekhan Uyanik, Claudia Gross, et al.
Neurogenetics|September 18, 2009
Intratumoral patterns of clonal evolution in gliomasAna Luísa Vital, Maria Dolores Tabernero, Inês Crespo, et al.
Neurogenetics|September 18, 2009
Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in miceSilke Nuber, Thomas Franck, Hartwig Wolburg, et al.
Neurogenetics|September 20, 2005
Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla diseaseR Biancheri, A Rossi, H A Verbeek, et al.
Pageof 95

Showing results (611-620 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|February 26, 2009
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypesS Russo, M Marchi, F Cogliati, et al.
Neurogenetics|January 22, 2009
Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson's diseaseA González-Pérez, J Gayán, J Marín, et al.
Neurogenetics|September 25, 2008
Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid betaJohn S K Kauwe, Jun Wang, Kevin Mayo, et al.
Neurogenetics|July 28, 2009
Identification of CACNA1A large deletions in four patients with episodic ataxiaFlorence Riant, Christelle Lescoat, Katayoun Vahedi, et al.
Neurogenetics|February 18, 2009
The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromasMeena Upadhyaya, Gill Spurlock, Lan Kluwe, et al.
Neurogenetics|February 14, 2009
A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson's diseaseCécile Cazeneuve, Channkanira Sân, Salah A Ibrahim, et al.
Neurogenetics|October 2, 2007
Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain diseaseUte Hehr, Goekhan Uyanik, Claudia Gross, et al.
Neurogenetics|September 18, 2009
Intratumoral patterns of clonal evolution in gliomasAna Luísa Vital, Maria Dolores Tabernero, Inês Crespo, et al.
Neurogenetics|September 18, 2009
Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in miceSilke Nuber, Thomas Franck, Hartwig Wolburg, et al.
Neurogenetics|September 20, 2005
Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla diseaseR Biancheri, A Rossi, H A Verbeek, et al.
Pageof 95