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Neurogenetics

Showing results (761-770 of 949) with videos related to

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Neurogenetics|May 1, 1997
ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3K Ueki, S Ramaswamy, S J Billings, et al.
Neurogenetics|May 28, 2002
Molecular cell biology of Charcot-Marie-Tooth diseasePhilipp Berger, Peter Young, Ueli Suter
Neurogenetics|May 28, 2002
A typical migraine susceptibility region localizes to chromosome 1q31Rod A Lea, A Graeme Shepherd, Robert P Curtain, et al.
Neurogenetics|May 28, 2002
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze FamilyValérie Delague, Corinne Bareil, Patrice Bouvagnet, et al.
Neurogenetics|May 28, 2002
Expression of the survival of motor neuron (SMN) gene in primary neurons and increase in SMN levels by activation of the N-methyl-D-aspartate glutamate receptorCatia Andreassi, Anna Letizia Patrizi, Umrao R Monani, et al.
Neurogenetics|May 28, 2002
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathiesKoen Venken, Emilio Di Maria, Emilia Bellone, et al.
Neurogenetics|December 17, 2002
Frontotemporal lobar degeneration--tau as a pied piper?Markus Tolnay, Alphonse Probst
Neurogenetics|December 17, 2002
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432Marcy C Speer, Felicia Lennon Graham, Erin Bonner, et al.
Neurogenetics|November 10, 2016
DRD2 C957T polymorphism is associated with improved 6-month verbal learning following traumatic brain injuryJohn K Yue, Ethan A Winkler, Jonathan W Rick, et al.
Neurogenetics|January 16, 2008
Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated alleleFrancesca Orzan, Michela Stroppi, Marco Venturin, et al.
Pageof 95

Showing results (761-770 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|May 1, 1997
ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3K Ueki, S Ramaswamy, S J Billings, et al.
Neurogenetics|May 28, 2002
Molecular cell biology of Charcot-Marie-Tooth diseasePhilipp Berger, Peter Young, Ueli Suter
Neurogenetics|May 28, 2002
A typical migraine susceptibility region localizes to chromosome 1q31Rod A Lea, A Graeme Shepherd, Robert P Curtain, et al.
Neurogenetics|May 28, 2002
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze FamilyValérie Delague, Corinne Bareil, Patrice Bouvagnet, et al.
Neurogenetics|May 28, 2002
Expression of the survival of motor neuron (SMN) gene in primary neurons and increase in SMN levels by activation of the N-methyl-D-aspartate glutamate receptorCatia Andreassi, Anna Letizia Patrizi, Umrao R Monani, et al.
Neurogenetics|May 28, 2002
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathiesKoen Venken, Emilio Di Maria, Emilia Bellone, et al.
Neurogenetics|December 17, 2002
Frontotemporal lobar degeneration--tau as a pied piper?Markus Tolnay, Alphonse Probst
Neurogenetics|December 17, 2002
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432Marcy C Speer, Felicia Lennon Graham, Erin Bonner, et al.
Neurogenetics|November 10, 2016
DRD2 C957T polymorphism is associated with improved 6-month verbal learning following traumatic brain injuryJohn K Yue, Ethan A Winkler, Jonathan W Rick, et al.
Neurogenetics|January 16, 2008
Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated alleleFrancesca Orzan, Michela Stroppi, Marco Venturin, et al.
Pageof 95