Association of ataxin-7 with the proteasome subunit S4 of the 19S regulatory complex
A Matilla, C Gorbea, DD Einum… - Human Molecular …, 2001 - academic.oup.com
Abstract Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disorder
characterized by ataxia and selective neuronal cell loss caused by the expansion of a …
characterized by ataxia and selective neuronal cell loss caused by the expansion of a …
[HTML][HTML] dAtaxin-2 Mediates Expanded Ataxin-1-Induced Neurodegeneration in a Drosophila Model of SCA1
I Al-Ramahi, AM Pérez, J Lim, M Zhang… - PLoS …, 2007 - journals.plos.org
Spinocerebellar ataxias (SCAs) are a genetically heterogeneous group of
neurodegenerative disorders sharing atrophy of the cerebellum as a common feature. SCA1 …
neurodegenerative disorders sharing atrophy of the cerebellum as a common feature. SCA1 …
Impaired oligodendrocyte maturation is an early feature in SCA3 disease pathogenesis
Spinocerebellar ataxia Type 3 (SCA3), the most common dominantly inherited ataxia, is a
polyglutamine neurodegenerative disease for which there is no disease-modifying therapy …
polyglutamine neurodegenerative disease for which there is no disease-modifying therapy …
ATXN2‐AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis
Objective Spinocerebellar ataxia type 2 (SCA2) is a neurodegenerative disease caused by a
CAG repeat expansion in the gene ataxin‐2 (ATXN2). ATXN2 intermediate‐length CAG …
CAG repeat expansion in the gene ataxin‐2 (ATXN2). ATXN2 intermediate‐length CAG …
Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model
KM Gehrking, JM Andresen, L Duvick… - Human molecular …, 2011 - academic.oup.com
Abstract Spinocerebellar ataxia type 1 (SCA1) is one of nine dominantly inherited
neurodegenerative diseases caused by polyglutamine tract expansion. In SCA1, the …
neurodegenerative diseases caused by polyglutamine tract expansion. In SCA1, the …
Structural and functional analysis of ataxin‐2 and ataxin‐3
M Albrecht, M Golatta, U Wüllner… - European journal of …, 2004 - Wiley Online Library
Spinocerebellar ataxia types 2 (SCA2) and 3 (SCA3) are autosomal‐dominantly inherited,
neurodegenerative diseases caused by CAG repeat expansions in the coding regions of the …
neurodegenerative diseases caused by CAG repeat expansions in the coding regions of the …
An integrative approach to gain insights into the cellular function of human ataxin-2
M Ralser, M Albrecht, U Nonhoff, T Lengauer… - Journal of molecular …, 2005 - Elsevier
Spinocerebellar ataxia type 2 (SCA2) is a hereditary neurodegenerative disorder caused by
a trinucleotide expansion in the SCA2 gene, encoding a polyglutamine stretch in the gene …
a trinucleotide expansion in the SCA2 gene, encoding a polyglutamine stretch in the gene …
[HTML][HTML] Nucleocytoplasmic shuttling activity of ataxin-3
Spinocerebellar ataxia type-3, also known as Machado-Joseph Disease (MJD), is one of
many inherited neurodegenerative disorders caused by polyglutamine-encoding CAG …
many inherited neurodegenerative disorders caused by polyglutamine-encoding CAG …
A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes
M Latouche, C Lasbleiz, E Martin… - Journal of …, 2007 - Soc Neuroscience
Spinocerebellar ataxia 7 (SCA7) is a neurodegenerative disease caused by a polyglutamine
(polyQ) expansion in the ataxin 7 (ATXN7) protein, a member of a multiprotein complex …
(polyQ) expansion in the ataxin 7 (ATXN7) protein, a member of a multiprotein complex …
Ataxin-3 phosphorylation decreases neuronal defects in spinocerebellar ataxia type 3 models
Different neurodegenerative diseases are caused by aberrant elongation of repeated
glutamine sequences normally found in particular human proteins. Although the proteins …
glutamine sequences normally found in particular human proteins. Although the proteins …