It remains a matter of speculation as to whether the sense CUG-containing RNA and/or the antisense CAG-encoding polyglutamine peptide serves as the pathogenic moiety in Huntington's disease like-2 (HDL2). In this issue of Neuron, Wilburn et al. show that in a HDL2 mouse model, the polyglutamine peptide drives disease progression
Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is character...
Expansion of CAG trinucleotide repeats coding for polyglutamine in unrelated proteins causes at leas...
Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is character...
SummaryHuntington's disease-like-2 (HDL2) is a phenocopy of Huntington's disease caused by CTG/CAG r...
AbstractThe mechanisms of neurodegeneration in the CAG repeat polyglutamine diseases, including Spin...
Thesis: Ph. D. in Neuroscience, Massachusetts Institute of Technology, Department of Brain and Cogni...
Background. Huntington's disease (HD) is a fatal neurodegenerative disorder with an autosomal domina...
Huntington disease is an inherited neurodegeneration, for which the associated mutation was isolated...
The coordinated regulation of gene expression and protein interactions determines how mammalian nerv...
International audienceEight neurodegenerative diseases have been shown to be caused by the expansion...
BACKGROUND:Huntington's disease (HD) is an inherited progressive neurodegenerative disorder caused b...
Huntington disease (HD) is a hereditary neurodegenerative disorder that causes a progressively debil...
Huntington’s disease (HD) is one of a class of inherited progressive neurodegenerative disorders tha...
Polyglutamine (polyQ) expansion mutation causes conformational, neurodegenerative diseases, such as ...
Polyglutamine diseases are a collection of nine CAG trinucleotide expansion disorders, presenting wi...
Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is character...
Expansion of CAG trinucleotide repeats coding for polyglutamine in unrelated proteins causes at leas...
Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is character...
SummaryHuntington's disease-like-2 (HDL2) is a phenocopy of Huntington's disease caused by CTG/CAG r...
AbstractThe mechanisms of neurodegeneration in the CAG repeat polyglutamine diseases, including Spin...
Thesis: Ph. D. in Neuroscience, Massachusetts Institute of Technology, Department of Brain and Cogni...
Background. Huntington's disease (HD) is a fatal neurodegenerative disorder with an autosomal domina...
Huntington disease is an inherited neurodegeneration, for which the associated mutation was isolated...
The coordinated regulation of gene expression and protein interactions determines how mammalian nerv...
International audienceEight neurodegenerative diseases have been shown to be caused by the expansion...
BACKGROUND:Huntington's disease (HD) is an inherited progressive neurodegenerative disorder caused b...
Huntington disease (HD) is a hereditary neurodegenerative disorder that causes a progressively debil...
Huntington’s disease (HD) is one of a class of inherited progressive neurodegenerative disorders tha...
Polyglutamine (polyQ) expansion mutation causes conformational, neurodegenerative diseases, such as ...
Polyglutamine diseases are a collection of nine CAG trinucleotide expansion disorders, presenting wi...
Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is character...
Expansion of CAG trinucleotide repeats coding for polyglutamine in unrelated proteins causes at leas...
Huntington's disease is an autosomal dominant genetic neurodegenerative disorder, which is character...