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Neurogenetics

Showing results (711-720 of 949) with videos related to

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Neurogenetics|January 7, 2012
Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalusMariola Marx, Simone Diestel, Muriel Bozon, et al.
Neurogenetics|March 29, 2012
Forkhead family transcription factor FoxO and neural differentiationQiang Wen, Haitao Wang, Peter J Little, et al.
Neurogenetics|March 22, 2012
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosisMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
Neurogenetics|April 3, 2012
Axonal transport deficit in a KIF5A( -/- ) mouse modelKathrin N Karle, Diana Möckel, Evan Reid, et al.
Neurogenetics|August 13, 2011
Homozygosity for the MTX1 c.184T>A (p.S63T) alteration modifies the age of onset in GBA-associated Parkinson's diseaseZiv Gan-Or, Anat Bar-Shira, Tanya Gurevich, et al.
Neurogenetics|July 30, 2011
Up-regulation of metallothionein gene expression in parkinsonian astrocytesGregory J Michael, Sharmin Esmailzadeh, Linda B Moran, et al.
Neurogenetics|July 30, 2011
Genetic variability in SNCA and Parkinson's diseaseLasse Pihlstrøm, Mathias Toft
Neurogenetics|July 29, 2011
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)Anas M Alazami, Nouran Adly, Hisham Al Dhalaan, et al.
Neurogenetics|April 13, 2011
FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletionGinevra Zanni, Sabina Barresi, Lorena Travaglini, et al.
Neurogenetics|November 19, 2011
Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sampleChristina M Lill, Brit-Maren M Schjeide, Denis A Akkad, et al.
Pageof 95

Showing results (711-720 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|January 7, 2012
Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalusMariola Marx, Simone Diestel, Muriel Bozon, et al.
Neurogenetics|March 29, 2012
Forkhead family transcription factor FoxO and neural differentiationQiang Wen, Haitao Wang, Peter J Little, et al.
Neurogenetics|March 22, 2012
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosisMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
Neurogenetics|April 3, 2012
Axonal transport deficit in a KIF5A( -/- ) mouse modelKathrin N Karle, Diana Möckel, Evan Reid, et al.
Neurogenetics|August 13, 2011
Homozygosity for the MTX1 c.184T>A (p.S63T) alteration modifies the age of onset in GBA-associated Parkinson's diseaseZiv Gan-Or, Anat Bar-Shira, Tanya Gurevich, et al.
Neurogenetics|July 30, 2011
Up-regulation of metallothionein gene expression in parkinsonian astrocytesGregory J Michael, Sharmin Esmailzadeh, Linda B Moran, et al.
Neurogenetics|July 30, 2011
Genetic variability in SNCA and Parkinson's diseaseLasse Pihlstrøm, Mathias Toft
Neurogenetics|July 29, 2011
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)Anas M Alazami, Nouran Adly, Hisham Al Dhalaan, et al.
Neurogenetics|April 13, 2011
FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletionGinevra Zanni, Sabina Barresi, Lorena Travaglini, et al.
Neurogenetics|November 19, 2011
Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sampleChristina M Lill, Brit-Maren M Schjeide, Denis A Akkad, et al.
Pageof 95