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Neurogenetics

Showing results (381-390 of 1,080) with videos related to

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Neurogenetics|May 1, 1997
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)D J Duggan, D Manchester, K P Stears, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Neurogenetics|September 13, 2000
The murine Bis1 seizure gene and the Kcnab2 gene encoding the beta2-subunit of the K+ channel are differentP Zerr, B Martin, J P Adelman
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
Neurogenetics|March 25, 2000
Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological diseaseD D Einum, J Zhang, P J Arneson, et al.
Neurogenetics|March 25, 2000
A novel mutation in the predicted TM2 domain of the presenilin 2 gene in a Spanish patient with late-onset Alzheimer's diseaseJ I Lao, K Beyer, L Fernández-Novoa, et al.
Neurogenetics|May 17, 2001
Hereditary demyelinating neuropathies: from gene to diseaseC O Hanemann
Neurogenetics|May 17, 2001
Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stressC A Evans, M S Harbuz, T Ostenfeld, et al.
Neurogenetics|August 29, 2001
Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonismJ C Leung, C Klein, J Friedman, et al.
Neurogenetics|August 29, 2001
Genetic susceptibility to MS: a second stage analysis in Canadian MS familiesD A Dyment, C J Willer, B Scott, et al.
Pageof 108

Showing results (381-390 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|May 1, 1997
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)D J Duggan, D Manchester, K P Stears, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Neurogenetics|September 13, 2000
The murine Bis1 seizure gene and the Kcnab2 gene encoding the beta2-subunit of the K+ channel are differentP Zerr, B Martin, J P Adelman
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
Neurogenetics|March 25, 2000
Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological diseaseD D Einum, J Zhang, P J Arneson, et al.
Neurogenetics|March 25, 2000
A novel mutation in the predicted TM2 domain of the presenilin 2 gene in a Spanish patient with late-onset Alzheimer's diseaseJ I Lao, K Beyer, L Fernández-Novoa, et al.
Neurogenetics|May 17, 2001
Hereditary demyelinating neuropathies: from gene to diseaseC O Hanemann
Neurogenetics|May 17, 2001
Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stressC A Evans, M S Harbuz, T Ostenfeld, et al.
Neurogenetics|August 29, 2001
Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonismJ C Leung, C Klein, J Friedman, et al.
Neurogenetics|August 29, 2001
Genetic susceptibility to MS: a second stage analysis in Canadian MS familiesD A Dyment, C J Willer, B Scott, et al.
Pageof 108