Related references
Note: Only part of the references are listed.SCA1-like Disease in Mice Expressing Wild-Type Ataxin-1 with a Serine to Aspartic Acid Replacement at Residue 776
Lisa Duvick et al.
NEURON (2010)
Serines 13 and 16 Are Critical Determinants of Full-Length Human Mutant Huntingtin Induced Disease Pathogenesis in HD Mice
Xiaofeng Gu et al.
NEURON (2009)
Amyloid beta-Protein Assembly as a Therapeutic Target of Alzheimer's Disease
Ghiam Yamin et al.
CURRENT PHARMACEUTICAL DESIGN (2008)
Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1
Janghoo Lim et al.
NATURE (2008)
Intranuclear immunolocalization of 14-3-3 protein isoforms in brains with spinocerebellar ataxia type 1
Takahiko Umahara et al.
NEUROSCIENCE LETTERS (2007)
Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes
Aaron B. Bowman et al.
NATURE GENETICS (2007)
ATAXIN-1 interacts with the repressor capicua in its native complex to cause SCA1 neuropathology
Yung C. Lam et al.
CELL (2006)
Swallowing in degenerative ataxias
Lluis Ramio-Torrenta et al.
JOURNAL OF NEUROLOGY (2006)
Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin
Rona K. Graham et al.
CELL (2006)
Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins
Corinne M. Spencer et al.
HUMAN MOLECULAR GENETICS (2006)
Polyglutamine is not all: The functional role of the AXH domain in the ataxin-1 protein
C de Chiara et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
The AXH domain of Ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/senseless proteins
H Tsuda et al.
CELL (2005)
Connecting the dots in Huntington's disease with protein interaction networks
F Giorgini et al.
GENOME BIOLOGY (2005)
The 14-3-3 proteins: Gene, gene expression, and function
Y Takahashi
NEUROCHEMICAL RESEARCH (2003)
14-3-3ε is important for neuronal migration by binding to NUDEL:: a molecular explanation for Miller-Dieker syndrome
K Toyo-oka et al.
NATURE GENETICS (2003)
Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1
HK Chen et al.
CELL (2003)
Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice
ES Emamian et al.
NEURON (2003)
Mammalian and yeast 14-3-3 isoforms form distinct patterns of dimers in vivo
M Chaudhri et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2003)
Functional specificity in 14-3-3 isoform interactions through dimer formation and phosphorylation. Chromosome location of mammalian isoforms and variants.
A Aitken
PLANT MOLECULAR BIOLOGY (2002)
The UCH-L1 gene encodes two opposing enzymatic activities that affect α-synuclein degradation and Parkinson's disease susceptibility
YC Liu et al.
CELL (2002)
A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration
K Watase et al.
NEURON (2002)
14-3-3 proteins: Active cofactors in cellular regulation by serine/threonine phosphorylation
G Tzivion et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Immunolocalisation of 14-3-3 isoforms in normal and scrapie-infected murine brain
HC Baxter et al.
NEUROSCIENCE (2002)
Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus
D Lorenzetti et al.
HUMAN MOLECULAR GENETICS (2000)