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Neurogenetics

Showing results (391-400 of 1,080) with videos related to

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Neurogenetics|August 29, 2001
Analysis of p53 mutation and expression in pleomorphic xanthoastrocytomaC Giannini, D Hebrink, B W Scheithauer, et al.
Neurogenetics|August 29, 2001
Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continentsS Kösel, E M Grasbon-Frodl, K Arima, et al.
Neurogenetics|November 21, 2001
Similar target, different effects: late-onset ataxia and spatial learning in prion protein-deficient mouse linesP Valenti, A Cozzio, N Nishida, et al.
Neurogenetics|November 21, 2000
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34I P Blair, C L Bennett, A Abel, et al.
Neurogenetics|November 21, 2000
The survival motor neuron (SMN) protein: effect of exon loss and mutation on protein localizationT T Le, D D Coovert, U R Monani, et al.
Neurogenetics|November 14, 2019
A novel cysteine-sparing G73A mutation of NOTCH3 in a Chinese CADASIL familyLiyan Huang, Wei Li, Yi Li, et al.
Neurogenetics|January 5, 2019
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndromeNurun Nahar Borna, Yoshihito Kishita, Masakazu Kohda, et al.
Neurogenetics|April 22, 2006
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican familiesPetra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, et al.
Neurogenetics|March 31, 2006
Gene expression analyses reveal molecular relationships among 20 regions of the human CNSRichard B Roth, Peter Hevezi, Jerry Lee, et al.
Neurogenetics|March 28, 2006
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12Stephan Züchner, Melanie E Kail, Martha A Nance, et al.
Pageof 108

Showing results (391-400 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|August 29, 2001
Analysis of p53 mutation and expression in pleomorphic xanthoastrocytomaC Giannini, D Hebrink, B W Scheithauer, et al.
Neurogenetics|August 29, 2001
Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continentsS Kösel, E M Grasbon-Frodl, K Arima, et al.
Neurogenetics|November 21, 2001
Similar target, different effects: late-onset ataxia and spatial learning in prion protein-deficient mouse linesP Valenti, A Cozzio, N Nishida, et al.
Neurogenetics|November 21, 2000
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34I P Blair, C L Bennett, A Abel, et al.
Neurogenetics|November 21, 2000
The survival motor neuron (SMN) protein: effect of exon loss and mutation on protein localizationT T Le, D D Coovert, U R Monani, et al.
Neurogenetics|November 14, 2019
A novel cysteine-sparing G73A mutation of NOTCH3 in a Chinese CADASIL familyLiyan Huang, Wei Li, Yi Li, et al.
Neurogenetics|January 5, 2019
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndromeNurun Nahar Borna, Yoshihito Kishita, Masakazu Kohda, et al.
Neurogenetics|April 22, 2006
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican familiesPetra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, et al.
Neurogenetics|March 31, 2006
Gene expression analyses reveal molecular relationships among 20 regions of the human CNSRichard B Roth, Peter Hevezi, Jerry Lee, et al.
Neurogenetics|March 28, 2006
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12Stephan Züchner, Melanie E Kail, Martha A Nance, et al.
Pageof 108