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Neurogenetics

Showing results (431-440 of 1,081) with videos related to

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Neurogenetics|August 18, 2014
DPP6 gene disruption in a family with Gilles de la Tourette syndromePaolo Prontera, Valerio Napolioni, Valentina Ottaviani, et al.
Neurogenetics|August 19, 2014
miR-338-3p is over-expressed in blood, CFS, serum and spinal cord from sporadic amyotrophic lateral sclerosis patientsBruna De Felice, Anna Annunziata, Giuseppe Fiorentino, et al.
Neurogenetics|April 30, 2013
Peripheral blood gene expression signature differentiates children with autism from unaffected siblingsS W Kong, Y Shimizu-Motohashi, M G Campbell, et al.
Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.
Neurogenetics|November 8, 2013
Evidence of a role for SNCA in impulse control in humansCasey R Guillot, Jennifer R Fanning, Tiebing Liang, et al.
Neurogenetics|November 13, 2013
Mutations in MAPT give rise to aneuploidy in animal models of tauopathyGiacomina Rossi, Donatella Conconi, Elena Panzeri, et al.
Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
Neurogenetics|August 6, 2013
Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous womanI Borgulová, R Mazanec, I Sakmaryová, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
Neurogenetics|July 24, 2013
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndromeRanad Shaheen, Eissa Faqeih, Shinu Ansari, et al.
Pageof 109

Showing results (431-440 of 1,081) with videos related to

Sort By:
Pageof 109
Neurogenetics|August 18, 2014
DPP6 gene disruption in a family with Gilles de la Tourette syndromePaolo Prontera, Valerio Napolioni, Valentina Ottaviani, et al.
Neurogenetics|August 19, 2014
miR-338-3p is over-expressed in blood, CFS, serum and spinal cord from sporadic amyotrophic lateral sclerosis patientsBruna De Felice, Anna Annunziata, Giuseppe Fiorentino, et al.
Neurogenetics|April 30, 2013
Peripheral blood gene expression signature differentiates children with autism from unaffected siblingsS W Kong, Y Shimizu-Motohashi, M G Campbell, et al.
Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.
Neurogenetics|November 8, 2013
Evidence of a role for SNCA in impulse control in humansCasey R Guillot, Jennifer R Fanning, Tiebing Liang, et al.
Neurogenetics|November 13, 2013
Mutations in MAPT give rise to aneuploidy in animal models of tauopathyGiacomina Rossi, Donatella Conconi, Elena Panzeri, et al.
Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
Neurogenetics|August 6, 2013
Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous womanI Borgulová, R Mazanec, I Sakmaryová, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
Neurogenetics|July 24, 2013
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndromeRanad Shaheen, Eissa Faqeih, Shinu Ansari, et al.
Pageof 109