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。Genetics of Amyotrophic Lateral Sclerosis
Mehdi Ghasemi et al.
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE (2018)
Biological Spectrum of Amyotrophic Lateral Sclerosis Prions
Magdalini Polymenidou et al.
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE (2017)
Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model
Leslie Bargsted et al.
SCIENTIFIC REPORTS (2017)
Protein folding alterations in amyotrophic lateral sclerosis
Sonam Parakh et al.
BRAIN RESEARCH (2016)
ALS-linked protein disulfide isomerase variants cause motor dysfunction
Ute Woehlbier et al.
EMBO JOURNAL (2016)
Mitochondria and endoplasmic reticulum crosstalk in amyotrophic lateral sclerosis
Giovanni Manfredi et al.
NEUROBIOLOGY OF DISEASE (2016)
Rab1-dependent ER-Golgi transport dysfunction is a common pathogenic mechanism in SOD1, TDP-43 and FUS-associated ALS
Kai Y. Soo et al.
ACTA NEUROPATHOLOGICA (2015)
Endoplasmic reticulum stress and proteasomal system in amyotrophic lateral sclerosis
Betul Karademir et al.
FREE RADICAL BIOLOGY AND MEDICINE (2015)
Protein disulfide-isomerase, a folding catalyst and a redox-regulated chaperone
Lei Wang et al.
FREE RADICAL BIOLOGY AND MEDICINE (2015)
Structures and functions of protein disulfide isomerase family members involved in proteostasis in the endoplasmic reticulum
Masaki Okumura et al.
FREE RADICAL BIOLOGY AND MEDICINE (2015)
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients
Paloma Gonzalez-Perez et al.
GENE (2015)
The Protein-disulfide Isomerase ERp57 Regulates the Steady-state Levels of the Prion Protein
Mauricio Torres et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
The expanding syndrome of amyotrophic lateral sclerosis: a clinical and molecular odyssey
Martin R. Turner et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2015)
Amyotrophic lateral sclerosis: mechanisms and therapeutics in the epigenomic era
Ximena Paez-Colasante et al.
NATURE REVIEWS NEUROLOGY (2015)
TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets
Emma L. Scotter et al.
NEUROTHERAPEUTICS (2015)
Distinct partitioning of ALS associated TDP-43, FUS and SOD1 mutants into cellular inclusions
Natalie E. Farrawell et al.
SCIENTIFIC REPORTS (2015)
Functional Role of the Disulfide Isomerase ERp57 in Axonal Regeneration
Valentina Castillo et al.
PLOS ONE (2015)
Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress
Yong-Jie Zhang et al.
ACTA NEUROPATHOLOGICA (2014)
Partial inhibition of Cdk1 in G2 phase overrides the SAC and decouples mitotic events
Rachael A. McCloy et al.
CELL CYCLE (2014)
Mutant SOD1 inhibits ER-Golgi transport in amyotrophic lateral sclerosis
Julie D. Atkin et al.
JOURNAL OF NEUROCHEMISTRY (2014)
Potential Effect of S-Nitrosylated Protein Disulfide Isomerase on Mutant SOD1 Aggregation and Neuronal Cell Death in Amyotrophic Lateral Sclerosis
Gye Sun Jeon et al.
MOLECULAR NEUROBIOLOGY (2014)
Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases
Claudio Hetz et al.
NATURE REVIEWS NEUROSCIENCE (2014)
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)
Ero1-α and PDIs constitute a hierarchical electron transfer network of endoplasmic reticulum oxidoreductases
Kazutaka Araki et al.
JOURNAL OF CELL BIOLOGY (2013)
Genetics of amyotrophic lateral sclerosis: an update
Sheng Chen et al.
MOLECULAR NEURODEGENERATION (2013)
ALS-Associated TDP-43 Induces Endoplasmic Reticulum Stress, Which Drives Cytoplasmic TDP-43 Accumulation and Stress Granule Formation
Adam K. Walker et al.
PLOS ONE (2013)
Chronic excitotoxin-induced axon degeneration in a compartmented neuronal culture model
Katherine A. Hosie et al.
ASN NEURO (2012)
Redox signalling directly regulates TDP-43 via cysteine oxidation and disulphide cross-linking
Todd J. Cohen et al.
EMBO JOURNAL (2012)
The unfolded protein response in models of human mutant G93A amyotrophic lateral sclerosis
T. Prell et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2012)
The unfolded protein response: controlling cell fate decisions under ER stress and beyond
Claudio Hetz
NATURE REVIEWS MOLECULAR CELL BIOLOGY (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)
Bim Links ER Stress and Apoptosis in Cells Expressing Mutant SOD1 Associated with Amyotrophic Lateral Sclerosis
Kai Y. Soo et al.
PLOS ONE (2012)
Protein disulfide isomerase-immunopositive inclusions in patients with amyotrophic lateral sclerosis
Yasuyuki Honjo et al.
AMYOTROPHIC LATERAL SCLEROSIS (2011)
A PDI Family Network Acts Distinctly and Coordinately with ERp29 To Facilitate Polyomavirus Infection
Christopher P. Walczak et al.
JOURNAL OF VIROLOGY (2011)
Amyotrophic Lateral Sclerosis Multiprotein Biomarkers in Peripheral Blood Mononuclear Cells
Giovanni Nardo et al.
PLOS ONE (2011)
ER Stress and Its Functional Link to Mitochondria: Role in Cell Survival and Death
Jyoti D. Malhotra et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2011)
Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis
Adam K. Walker et al.
BRAIN (2010)
A structural overview of the PDI family of proteins
Guennadi Kozlov et al.
FEBS JOURNAL (2010)
Functional Relationship between Protein Disulfide Isomerase Family Members during the Oxidative Folding of Human Secretory Proteins
Lori A. Rutkevich et al.
MOLECULAR BIOLOGY OF THE CELL (2010)
TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity
Brian S. Johnson 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)
Recruitment of mitochondria into apoptotic signaling correlates with the presence of inclusions formed by amyotrophic lateral sclerosis-associated SOD1 mutations
Kai Y. Soo et al.
JOURNAL OF NEUROCHEMISTRY (2009)
A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice
Smita Saxena et al.
NATURE NEUROSCIENCE (2009)
TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations
Satomi Maekawa et al.
NEUROPATHOLOGY (2009)
The Ubiquitin-Proteasome Reporter GFPu Does Not Accumulate in Neurons of the R6/2 Transgenic Mouse Model of Huntington's Disease
John S. Bett et al.
PLOS ONE (2009)
The Amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors
Hiroshi Tsuda et al.
CELL (2008)
The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS
Makoto Urushitani et al.
FASEB JOURNAL (2008)
ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1
Hideki Nishitoh et al.
GENES & DEVELOPMENT (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)
Endoplasmic reticulum stress responses
M. Schroeder
CELLULAR AND MOLECULAR LIFE SCIENCES (2008)
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
Ian R. A. Mackenzie et al.
ANNALS OF NEUROLOGY (2007)
ERp57 is essential for efficient folding of glycoproteins sharing common structural domains
Catherine E. Jessop et al.
EMBO JOURNAL (2007)
A guided tour into subcellular colocalization analysis in light microscopy
S. Bolte et al.
JOURNAL OF MICROSCOPY (2006)
ERp57 and PDI: multifunctional protein disulfide isomerases with similar domain architectures but differing substrate-partner associations
P. Maattanen et al.
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Cooperative activity of Ref-1/APE and Erp57 in reductive activation of transcription factors
Caterina Grillo et al.
FREE RADICAL BIOLOGY AND MEDICINE (2006)
Localization of glutamate receptors in developing cortical neurons in culture and relationship to susceptibility to excitotoxicity
A. E. King et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2006)
Consequences of ERp57 deletion on oxidative folding of obligate and facultative clients of the calnexin cycle
T Soldà et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (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)
In cerebrospinal fluid ER chaperones ERp57 and calreticulin bind β-amyloid
RR Erickson et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis
BJ Turner et al.
JOURNAL OF NEUROSCIENCE (2005)
Roles of CHOP/GADD153 in endoplasmic reticulum stress
S Oyadomari et al.
CELL DEATH AND DIFFERENTIATION (2004)
Parkinsonian mimetics induce aspects of unfolded protein response in death of dopaminergic neurons
WA Holtz et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis
M Urushitani et al.
JOURNAL OF NEUROCHEMISTRY (2002)
Proteins of the PDI family: Unpredicted non-ER locations and functions
C Turano et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2002)
Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues
M Watanabe et al.
NEUROBIOLOGY OF DISEASE (2001)
分享论文
