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ATXN2 protein, human
Known as:
ataxin-2 protein, human
, Spinocerebellar Ataxia Type 2 Protein
, ATX2 protein, human
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Ataxin-2 (1313 aa, ~140 kDa) is encoded by the human ATXN2 gene. This protein plays a role in the modulation of epidermal growth factor receptor…
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National Institutes of Health
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Related topics
Related topics
9 relations
ATXN2 gene
Cellular Membrane
Cytoplasm
Ligand Binding
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Broader (1)
Ataxin-2
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis
Hai-Peng Lu
,
Shi-Rui Gan
,
+5 authors
Zhi-Ying Wu
Neurobiology of Aging
2015
Corpus ID: 24573997
2014
2014
Neuropathological Staging of Spinocerebellar Ataxia Type 2 by Semiquantitative 1C2‐Positive Neuron Typing. Nuclear Translocation of Cytoplasmic 1C2 Underlies Disease Progression of Spinocerebellar…
S. Koyano
,
S. Yagishita
,
Y. Kuroiwa
,
F. Tanaka
,
T. Uchihara
Brain Pathology
2014
Corpus ID: 24545131
Spinocerebellar ataxia type 2 (SCA2) is a hereditary neurodegenerative disorder caused by the expansion of the trinucleotide CAG…
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2007
2007
Gene expression in opening and senescing petals of morning glory (Ipomoea nil) flowers
Tetsuya Yamada
,
K. Ichimura
,
M. Kanekatsu
,
W. Doorn
Plant Cell Reports
2007
Corpus ID: 8629149
We isolated several senescence-associated genes (SAGs) from the petals of morning glory (Ipomoea nil) flowers, with the aim of…
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2007
2007
INCLUSION FORMATION BY ATAXINS -1, -2, -3, AND -7
V. Tarlac
,
V. Turnbull
,
D. Stefani
,
L. Kelly
,
Renae Walsh
,
E. Storey
International Journal of Neuroscience
2007
Corpus ID: 30193537
The authors studied inclusion formation in vitro using transiently transfected PC12 cells, with epitope-tagged and untagged full…
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2005
2005
Relative Atrophy of the Flocculus and Ocular Motor Dysfunction in SCA2 and SCA6
S. Ying
,
S. Choi
,
+4 authors
D. Zee
Annals of the New York Academy of Sciences
2005
Corpus ID: 45047026
Abstract: Two hereditary ataxia syndromes show distinct profiles of region‐specific atrophy and ocular motor deficits. Selective…
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2004
2004
Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?
P. Bauer
,
P. Bauer
,
A. Zumrová
,
V. Maťoška
,
K. Mitsui
,
P. Goetz
Medical Hypotheses
2004
Corpus ID: 22699625
Highly Cited
2003
Highly Cited
2003
The gene for HMSN2C maps to 12q23-24
Christopher J. Klein
,
Julie M. Cunningham
,
+8 authors
P. Dyck
Neurology
2003
Corpus ID: 31204789
Background: Hereditary motor and sensory neuropathy type 2C (HMSN2C, Charcot–Marie–Tooth 2C [CMT2C]) is an autosomal dominant…
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2002
2002
Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats.
J. Hussey
,
P. Lockhart
,
+5 authors
M. Farrer
Genetic Testing
2002
Corpus ID: 33502353
Spinocerebellar ataxia, type 2 (SCA2), results from an expansion of a stretch of polyglutamine repeats within the coding sequence…
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Highly Cited
2001
Highly Cited
2001
Amino acid sequences flanking polyglutamine stretches influence their potential for aggregate formation
K. Nozaki
,
O. Onodera
,
H. Takano
,
Shoji Tsuji
NeuroReport
2001
Corpus ID: 23935655
Expanded polyglutamine stretches have been shown to form aggregates and to be toxic to cells. In this study, we hypothesized that…
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2001
2001
Localization of ataxin-2 within the cerebellar cortex of the rat
F. Fusco
,
M. T. Viscomi
,
G. Bernardi
,
M. Molinari
Brain Research Bulletin
2001
Corpus ID: 24054957
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