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E N Burright

Showing results (11-20 of 15) with videos related to

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Human Molecular Genetics|September 1, 1996
Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenaseB Koshy, T Matilla, E N Burright, et al.
Human Gene Therapy|June 14, 2008
Identification and allele-specific silencing of the mutant huntingtin allele in Huntington's disease patient-derived fibroblastsP H J van Bilsen, L Jaspers, M S Lombardi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 20, 1997
Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterationsH B Clark, E N Burright, W S Yunis, et al.
Cell|September 22, 1995
SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeatE N Burright, H B Clark, A Servadio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 3, 1998
Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitationA Matilla, E D Roberson, S Banfi, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Human Molecular Genetics|September 1, 1996
Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenaseB Koshy, T Matilla, E N Burright, et al.
Human Gene Therapy|June 14, 2008
Identification and allele-specific silencing of the mutant huntingtin allele in Huntington's disease patient-derived fibroblastsP H J van Bilsen, L Jaspers, M S Lombardi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 20, 1997
Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterationsH B Clark, E N Burright, W S Yunis, et al.
Cell|September 22, 1995
SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeatE N Burright, H B Clark, A Servadio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 3, 1998
Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitationA Matilla, E D Roberson, S Banfi, et al.
Pageof 2