相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Polyglutamine expansion reduces the association of TATA-binding protein with DNA and induces DNA binding-independent neurotoxicity
Meyer J. Friedman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Sex-dependent effect of BAG1 in ameliorating motor deficits of Huntington disease transgenic mice
Adam L. Orr et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Hsp27 Protects against Ischemic Brain Injury via Attenuation of a Novel Stress-Response Cascade Upstream of Mitochondrial Cell Death Signaling
R. Anne Stetler et al.
JOURNAL OF NEUROSCIENCE (2008)
Optimisation of region-specific reference gene selection and relative gene expression analysis methods for pre-clinical trials of Huntington's disease
Caroline L. Benn et al.
MOLECULAR NEURODEGENERATION (2008)
Expression of the small heat shock protein family in the mouse CNS: differential anatomical and biochemical compartmentalization
S. Quraishe et al.
NEUROSCIENCE (2008)
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration
Meyer J. Friedman et al.
NATURE NEUROSCIENCE (2007)
Regulation of stress-induced intracellular sorting and chaperone function of Hsp27 (HspB1) in mammalian cells
Anton L. Bryantsev et al.
BIOCHEMICAL JOURNAL (2007)
Cooperative interactions between androgen receptor (AR) and heat-shock protein 27 facilitate AR transcriptional activity
Arnina Zoubeidi et al.
CANCER RESEARCH (2007)
Insights into function and regulation of small heat shock protein 25 (HSPB1) in a mouse model with targeted gene disruption
Lei Huang et al.
GENESIS (2007)
Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation
Alexandra Zourlidou et al.
HUMAN MOLECULAR GENETICS (2007)
Neuroprotection by Hsp104 and Hsp27 in lentiviral-based rat models of Huntington's disease
Valerie Perrin et al.
MOLECULAR THERAPY (2007)
Abnormal small heat shock protein interactions involving neuropathy-associated HSP22 (HSPB8) mutants
Jean-Marc Fontaine et al.
FASEB JOURNAL (2006)
Heat shock protein 27 is involved in neurite extension and branching of dorsal root ganglion neurons in vitro
Kristy L. Williams et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2006)
Heat shock protein 25 or inducible heat shock protein 70 activates heat shock factor 1 - Dephosphorylation on serine 307 through inhibition of ERK1/2 phosphorylation
Haeng Ran Seo et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Decreased expression of Hsp27 and Hsp70 in transformed lymphoblastoid cells from patients with spinocerebellar ataxia type 7
HF Tsai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
HSP27 and cell survival in neurones
DS Latchman
INTERNATIONAL JOURNAL OF HYPERTHERMIA (2005)
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells
S Carra et al.
HUMAN MOLECULAR GENETICS (2005)
Hsp27 and axonal growth in adult sensory neurons in vitro -: art. no. 24
KL Williams et al.
BMC NEUROSCIENCE (2005)
Small heat shock proteins in inherited peripheral neuropathies
I Dierick et al.
ANNALS OF MEDICINE (2005)
Heat stress-induced localization of small heat shock proteins in mouse myoblasts:: intranuclear lamin A/C speckles as target for αB-crystallin and Hsp25
AS Adhikari et al.
EXPERIMENTAL CELL RESEARCH (2004)
Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approach
DG Hay et al.
HUMAN MOLECULAR GENETICS (2004)
Gene expression profiling in ataxin-3 expressing cell lines reveals distinct effects of normal and mutant ataxin-3
BO Evert et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2003)
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)
A Rolfs et al.
ANNALS OF NEUROLOGY (2003)
Polyglutamine expansion induces a protein-damaging stress connecting heat shock protein 70 to the JNK pathway
K Merienne et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Progressive retinal degeneration and dysfunction in R6 Huntington's disease mice
D Helmlinger et al.
HUMAN MOLECULAR GENETICS (2002)
Molecular chaperones as modulators of polyglutamine protein aggregation and toxicity
H Sakahira et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Mechanism of antiandrogen action:: Key role of Hsp90 in conformational change and transcriptional activity of the androgen receptor
V Georget et al.
BIOCHEMISTRY (2002)
Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease
AW Dunah et al.
SCIENCE (2002)
Disassembly of transcriptional regulatory complexes by molecular chaperones
BC Freeman et al.
SCIENCE (2002)
Phosphorylation-dependent cellular localization and thermoprotective role of heat shock protein 25 in hippocampal progenitor cells
D Geum et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtin
A Wyttenbach et al.
HUMAN MOLECULAR GENETICS (2002)
Interaction of Huntington disease protein with transcriptional activator Sp1
SH Li et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
Chaperone suppression of cellular toxicity of Huntingtin is independent of polyglutamine aggregation
H Zhou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
H Fujigasaki et al.
BRAIN (2001)
SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
K Nakamura et al.
HUMAN MOLECULAR GENETICS (2001)
Constitutive expression of heat shock protein HSP25 in the central nervous system of the developing and adult mouse
CL Armstrong et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2001)
分享论文
