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。Association studies indicate that protein disulfide isomerase is a risk factor in amyotrophic lateral sclerosis
Chun Tak Kwok et al.
FREE RADICAL BIOLOGY AND MEDICINE (2013)
Ataxin-2 interacts with FUS and intermediate-length polyglutamine expansions enhance FUS-related pathology in amyotrophic lateral sclerosis
Manal A. Farg et al.
HUMAN MOLECULAR GENETICS (2013)
Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo
Alexandra Vaccaro et al.
NEUROBIOLOGY OF DISEASE (2013)
Reticulon1-C modulates protein disulphide isomerase function
P. Bernardoni et al.
CELL DEATH & DISEASE (2013)
TDP-43 aggregation in neurodegeneration: Are stress granules the key?
Colleen M. Dewey et al.
BRAIN RESEARCH (2012)
Redox signalling directly regulates TDP-43 via cysteine oxidation and disulphide cross-linking
Todd J. Cohen et al.
EMBO JOURNAL (2012)
XBP1 depletion precedes ubiquitin aggregation and Golgi fragmentation in TDP-43 transgenic rats
Jianbin Tong et al.
JOURNAL OF NEUROCHEMISTRY (2012)
TDP-43 toxicity is mediated by the unfolded protein response-unrelated induction of C/EBP homologous protein expression
Hiroaki Suzuki et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2012)
Mutant FUS induces endoplasmic reticulum stress in amyotrophic lateral sclerosis and interacts with protein disulfide-isomerase
Manal A. Farg et al.
NEUROBIOLOGY OF AGING (2012)
Endogenous TDP-43 localized to stress granules can subsequently form protein aggregates
Sarah J. Parker et al.
NEUROCHEMISTRY INTERNATIONAL (2012)
Bim Links ER Stress and Apoptosis in Cells Expressing Mutant SOD1 Associated with Amyotrophic Lateral Sclerosis
Kai Y. Soo et al.
PLOS ONE (2012)
Cell stress induces TDP-43 pathological changes associated with ERK1/2 dysfunction: implications in ALS
Victoria Ayala et al.
ACTA NEUROPATHOLOGICA (2011)
Protein disulfide isomerase-immunopositive inclusions in patients with amyotrophic lateral sclerosis
Yasuyuki Honjo et al.
AMYOTROPHIC LATERAL SCLEROSIS (2011)
The unfolded protein response in familial amyotrophic lateral sclerosis
Lijun Wang et al.
HUMAN MOLECULAR GENETICS (2011)
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
Karli K. McDonald et al.
HUMAN MOLECULAR GENETICS (2011)
Mutant HFE H63D Protein Is Associated with Prolonged Endoplasmic Reticulum Stress and Increased Neuronal Vulnerability
Yiting Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
TDP-43-induced Death Is Associated with Altered Regulation of BIM and Bcl-xL and Attenuated by Caspase-mediated TDP-43 Cleavage
Hiroaki Suzuki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
TDP-43 Is Directed to Stress Granules by Sorbitol, a Novel Physiological Osmotic and Oxidative Stressor
Colleen M. Dewey et al.
MOLECULAR AND CELLULAR BIOLOGY (2011)
C-Jun N-terminal kinase controls TDP-43 accumulation in stress granules induced by oxidative stress
Jodi Meyerowitz et al.
MOLECULAR NEURODEGENERATION (2011)
Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis
Adam K. Walker et al.
BRAIN (2010)
Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6
Fabienne C. Fiesel et al.
EMBO JOURNAL (2010)
TDP-43 M337V Mutation in Familial Amyotrophic Lateral Sclerosis in Japan
Akira Tamaoka et al.
INTERNAL MEDICINE (2010)
OGFOD1, a Novel Modulator of Eukaryotic Translation Initiation Factor 2α Phosphorylation and the Cellular Response to Stress
Karen A. Wehner et al.
MOLECULAR AND CELLULAR BIOLOGY (2010)
Tar DNA Binding Protein-43 (TDP-43) Associates with Stress Granules: Analysis of Cultured Cells and Pathological Brain Tissue
Liqun Liu-Yesucevitz et al.
PLOS ONE (2010)
Activation of the Endoplasmic Reticulum Stress-Associated Transcription Factor X Box-Binding Protein-1 Occurs in a Subset of Normal Germinal-Center B Cells and in Aggressive B-Cell Lymphomas with Prognostic Implications
Olga Balague et al.
AMERICAN JOURNAL OF PATHOLOGY (2009)
Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells
Takashi Nonaka et al.
FEBS LETTERS (2009)
XBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagy
Claudio Hetz et al.
GENES & DEVELOPMENT (2009)
High Frequency of TARDBP Gene Mutations in Italian Patients With Amyotrophic Lateral Sclerosis
Lucia Corrado et al.
HUMAN MUTATION (2009)
VCP Mutations Causing Frontotemporal Lobar Degeneration Disrupt Localization of TDP-43 and Induce Cell Death
Michael A. Gitcho et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Protein disulphide isomerase family members show distinct substrate specificity: P5 is targeted to BiP client proteins
Catherine E. Jessop et al.
JOURNAL OF CELL SCIENCE (2009)
ALS-linked P56S-VAPB, an aggregated loss-of-function mutant of VAPB, predisposes motor neurons to ER stress-related death by inducing aggregation of co-expressed wild-type VAPB
Hiroaki Suzuki et al.
JOURNAL OF NEUROCHEMISTRY (2009)
Reticulon-4A (Nogo-A) Redistributes Protein Disulfide Isomerase to Protect Mice from SOD1-Dependent Amyotrophic Lateral Sclerosis
Yvonne S. Yang et al.
JOURNAL OF NEUROSCIENCE (2009)
A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice
Smita Saxena et al.
NATURE NEUROSCIENCE (2009)
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
Iga Wegorzewska et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity
Yong-Jie Zhang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
TDP-43 A315T mutation in familial motor neuron disease
Michael A. Gitcho et al.
ANNALS OF NEUROLOGY (2008)
The Amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors
Hiroshi Tsuda et al.
CELL (2008)
Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation
Matthew J. Winton et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Structural determinants of the cellular localization and shuttling of TDP-43
Youhna M. Ayala et al.
JOURNAL OF CELL SCIENCE (2008)
Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells
Yeo Kyoung Oh et al.
JOURNAL OF NEUROCHEMISTRY (2008)
Formation of stress granules inhibits apoptosis by suppressing stress-responsive MAPK pathways
Kyoko Arimoto et al.
NATURE CELL BIOLOGY (2008)
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi et al.
NATURE GENETICS (2008)
Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis
Julie D. Atkin et al.
NEUROBIOLOGY OF DISEASE (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Novel Mutations in TARDBP(TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
Nicola J. Rutherford et al.
PLOS GENETICS (2008)
Endoplasmic reticulum stress responses
M. Schroeder
CELLULAR AND MOLECULAR LIFE SCIENCES (2008)
Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis
Ekaterina V. Ilieva et al.
BRAIN (2007)
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
Yong-Jie Zhang et al.
JOURNAL OF NEUROSCIENCE (2007)
Vaticanol B, a resveratrol tetramer, regulates endoplasmic reticulum stress and inflammation
Yoshiyuki Tabata et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Tetsuaki Arai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
被撤回的出版物: Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1 (Retracted article. See vol. 292, pg. 12007, 2017)
Julie D. Atkin et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice
Y Furukawa et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Mapping superoxide dismutase 1 domains of non-native interaction: roles of intra- and intermolecular disulfide bonding in aggregation
J Wang et al.
JOURNAL OF NEUROCHEMISTRY (2006)
A selective inhibitor-of eIF2α dephosphorylation protects cells from ER stress
M Boyce et al.
SCIENCE (2005)
Proteins of the PDI family: Unpredicted non-ER locations and functions
C Turano et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2002)
Higher order arrangement of the eukaryotic nuclear bodies
IF Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Two distinct stress signaling pathways converge upon the CHOP promoter during the mammalian unfolded protein response
YJ Ma et al.
JOURNAL OF MOLECULAR BIOLOGY (2002)
The luminal domain of ATF6 senses endoplasmic reticulum (ER) stress and causes translocation of ATF6 from the ER to the Golgi
X Chen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
E Buratti et al.
EMBO JOURNAL (2001)
Coupling of stress in the ER to activation of JNK protein kinases by transmembrane protein kinase IRE1
F Urano et al.
SCIENCE (2000)