Reference health
Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases
2 of 207 checkable references need attention · checked 2026-09-05
At the dated check, the references listed below either did not resolve in Crossref or DataCite, or carried a retraction notice. Each one is shown with the registry record that put it there.
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References needing attention
marked retracted — notice via Crossref, record curated by Retraction Watch10.1016/j.nbd.2008.02.009
RETRACTED: Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis
marked retracted — notice via Crossref, record curated by Retraction Watch10.1074/jbc.M603393200
Induction of the Unfolded Protein Response in Familial Amyotrophic Lateral Sclerosis and Association of Protein-disulfide Isomerase with Superoxide Dismutase 1
The 205 checked references that resolve
resolves10.1146/annurev-biochem-062209-093836
Protein Folding and Modification in the Mammalian Endoplasmic Reticulum
resolves10.1038/nrm3270
The unfolded protein response: controlling cell fate decisions under ER stress and beyond
resolves10.1126/science.1209038
The Unfolded Protein Response: From Stress Pathway to Homeostatic Regulation
resolves10.1152/physrev.00001.2011
The Unfolded Protein Response: Integrating Stress Signals Through the Stress Sensor IRE1α
resolves10.1016/j.celrep.2013.03.024
Stress-Independent Activation of XBP1s and/or ATF6 Reveals Three Functionally Diverse ER Proteostasis Environments
resolves10.1126/science.1081208
BAX and BAK Regulation of Endoplasmic Reticulum Ca
<sup>2+</sup>
: A Control Point for Apoptosis
resolves10.1038/ncb0311-184
Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress
resolves10.1016/j.ceb.2010.11.003
Signaling cell death from the endoplasmic reticulum stress response
resolves10.1038/ncb2738
ER-stress-induced transcriptional regulation increases protein synthesis leading to cell death
resolves10.1016/S1097-2765(00)80330-5
Perk Is Essential for Translational Regulation and Cell Survival during the Unfolded Protein Response
resolves10.1126/science.287.5453.664
Coupling of Stress in the ER to Activation of JNK Protein Kinases by Transmembrane Protein Kinase IRE1
resolves10.1038/nrm2101
Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid β-peptide
resolves10.1111/j.1471-4159.2007.04764.x
Neuropathology, biochemistry, and biophysics of α‐synuclein aggregation
resolves10.1038/nrneurol.2011.150
Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
resolves10.1101/cshperspect.a004507
Chemical and Biological Approaches for Adapting Proteostasis to Ameliorate Protein Misfolding and Aggregation Diseases-Progress and Prognosis
resolves10.2174/156652411794474419
Converging Pathways in the Occurrence of Endoplasmic Reticulum (ER) Stress in Huntingtons Disease
resolves10.1371/journal.pone.0025545
Amyotrophic Lateral Sclerosis Multiprotein Biomarkers in Peripheral Blood Mononuclear Cells
resolves10.1126/science.1245296
Identification and Rescue of α-Synuclein Toxicity in Parkinson Patient–Derived Neurons
resolves10.1371/journal.pone.0047950
ATF6alpha Promotes Astroglial Activation and Neuronal Survival in a Chronic Mouse Model of Parkinson’s Disease
resolves10.1074/jbc.M110.156430
The Endoplasmic Reticulum Stress Sensor, ATF6α, Protects against Neurotoxin-induced Dopaminergic Neuronal Death
resolves10.1038/mt.2012.28
Glucose Regulated Protein 78 Diminishes α-Synuclein Neurotoxicity in a Rat Model of Parkinson Disease
resolves10.1523/JNEUROSCI.5367-11.2012
Endoplasmic Reticulum Stress Is Important for the Manifestations of α-Synucleinopathy
<i>In Vivo</i>
resolves10.1126/science.1101902
A Selective Inhibitor of eIF2α Dephosphorylation Protects Cells from ER Stress
resolves10.1111/j.1471-4159.2005.03428.x
CHOP/GADD153 is a mediator of apoptotic death in substantia nigra dopamine neurons in an <i>in vivo</i> neurotoxin model of parkinsonism
resolves10.1038/nn.2297
A role for motoneuron subtype–selective ER stress in disease manifestations of FALS mice
resolves10.1371/journal.pone.0066672
Functional Contribution of the Transcription Factor ATF4 to the Pathogenesis of Amyotrophic Lateral Sclerosis
resolves10.1038/sj.cdd.4402166
The proapoptotic BCL-2 family member BIM mediates motoneuron loss in a model of amyotrophic lateral sclerosis
resolves10.1073/pnas.0707906105
Deletion of the BH3-only protein
<i>puma</i>
protects motoneurons from ER stress-induced apoptosis and delays motoneuron loss in ALS mice
resolves10.1101/gad.1640108
ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1
resolves10.1016/j.nbd.2013.03.015
Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo
resolves10.1101/gad.1830709
XBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagy
resolves10.1093/hmg/dds040
Targeting the UPR transcription factor XBP1 protects against Huntington's disease through the regulation of FoxO1 and autophagy
resolves10.1038/cr.2013.2
XBP-1u suppresses autophagy by promoting the degradation of FoxO1 in cancer cells
resolves10.1016/j.tins.2010.04.003
The propagation of prion-like protein inclusions in neurodegenerative diseases
resolves10.1523/JNEUROSCI.4090-04.2005
The Disulfide Isomerase Grp58 Is a Protective Factor against Prion Neurotoxicity
resolves10.1093/emboj/cdg537
Caspase‐12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein
resolves10.1073/pnas.0711094105
Unfolded protein response transcription factor XBP-1 does not influence prion replication or pathogenesis
resolves10.1038/nature11058
Sustained translational repression by eIF2α-P mediates prion neurodegeneration
resolves10.1126/scitranslmed.3006767
Oral Treatment Targeting the Unfolded Protein Response Prevents Neurodegeneration and Clinical Disease in Prion-Infected Mice
resolves10.1242/jcs.123000
The
<i>ire-1</i>
ER Stress-Response Pathway is Required for Normal Secretory- Protein Metabolism in
<i>C. elegans</i>
resolves10.1038/nn.3486
Suppression of eIF2α kinases alleviates Alzheimer's disease–related plasticity and memory deficits
resolves10.1016/j.cmet.2013.11.002
TNF-α Mediates PKR-Dependent Memory Impairment and Brain IRS-1 Inhibition Induced by Alzheimer’s β-Amyloid Oligomers in Mice and Monkeys
resolves10.1038/sj.emboj.7601477
Unfolded protein response in a Drosophila model for retinal degeneration
resolves10.1073/pnas.0911991107
Restoration of visual function in P23H rhodopsin transgenic rats by gene delivery of BiP/Grp78
resolves10.1038/cddis.2012.8
Activation of the unfolded protein response enhances motor recovery after spinal cord injury
resolves10.1016/j.nbd.2013.04.021
Restoring endoplasmic reticulum homeostasis improves functional recovery after spinal cord injury
resolves10.3892/etm.2012.745
C/EBP homologous protein (CHOP) mediates neuronal apoptosis in rats with spinal cord injury
resolves10.1002/glia.21191
Attenuating the endoplasmic reticulum stress response improves functional recovery after spinal cord injury
resolves10.1089/neu.2011.1940
Deletion of the Pro-Apoptotic Endoplasmic Reticulum Stress Response Effector CHOP Does Not Result in Improved Locomotor Function after Severe Contusive Spinal Cord Injury
resolves10.1016/j.neuron.2011.11.026
Differential Effects of Unfolded Protein Response Pathways on Axon Injury-Induced Death of Retinal Ganglion Cells
resolves10.1523/JNEUROSCI.4289-06.2007
Endoplasmic Reticulum Stress Inhibition Protects against Excitotoxic Neuronal Injury in the Rat Brain
resolves10.1016/j.jvs.2010.06.172
Sodium 4-phenylbutyrate protects against spinal cord ischemia by inhibition of endoplasmic reticulum stress
resolves10.1093/brain/awl044
Interferon-γ inhibits central nervous system remyelination through a process modulated by endoplasmic reticulum stress
resolves10.2353/ajpath.2008.080449
Enhanced Integrated Stress Response Promotes Myelinating Oligodendrocyte Survival in Response to Interferon-γ
resolves10.1172/JCI29571
The integrated stress response prevents demyelination by protecting oligodendrocytes against immune-mediated damage
resolves10.1523/JNEUROSCI.1636-12.2013
Oligodendrocyte-Specific Activation of PERK Signaling Protects Mice against Experimental Autoimmune Encephalomyelitis
resolves10.1016/S0896-6273(02)01045-0
The Unfolded Protein Response Modulates Disease Severity in Pelizaeus-Merzbacher Disease
resolves10.1084/jem.20122005
Resetting translational homeostasis restores myelination in Charcot-Marie-Tooth disease type 1B mice
resolves10.1016/j.neuron.2007.12.021
Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice
resolves10.1016/j.cmet.2012.03.007
The Role of Endoplasmic Reticulum in Hepatic Lipid Homeostasis and Stress Signaling
resolves10.1083/jcb.201208152
Lysosomal storage disorders: The cellular impact of lysosomal dysfunction
resolves10.1093/hmg/ddm324
ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones
resolves10.1093/hmg/ddi451
Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL
resolves10.1016/j.molcel.2004.08.029
GM1-Ganglioside-Mediated Activation of the Unfolded Protein Response Causes Neuronal Death in a Neurodegenerative Gangliosidosis
resolves10.1016/j.molcel.2009.10.021
GM1-Ganglioside Accumulation at the Mitochondria-Associated ER Membranes Links ER Stress to Ca2+-Dependent Mitochondrial Apoptosis
resolves10.1038/70265
Presenilin-1 mutations downregulate the signalling pathway of the unfolded-protein response
resolves10.1101/gad.992302
ASK1 is essential for endoplasmic reticulum stress-induced neuronal cell death triggered by expanded polyglutamine repeats
resolves10.1038/47513
Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-β
resolves10.1093/hmg/ddr274
Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death
resolves10.1016/j.molmed.2011.04.002
ER stress in retinal degeneration: a target for rational therapy?
resolves10.1523/JNEUROSCI.5368-11.2012
Accumulation of Toxic α-Synuclein Oligomer within Endoplasmic Reticulum Occurs in α-Synucleinopathy<i>In Vivo</i>
resolves10.1111/j.1471-4159.2010.07143.x
Induction of the unfolded protein response by α-synuclein in experimental models of Parkinson’s disease
resolves10.1073/pnas.0509227103
Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model
resolves10.1096/fj.07-092783
The endoplasmic reticulum‐Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS
resolves10.1038/nn1603
Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis
resolves10.1523/JNEUROSCI.4253-04.2005
Impaired Extracellular Secretion of Mutant Superoxide Dismutase 1 Associates with Neurotoxicity in Familial Amyotrophic Lateral Sclerosis
resolves10.1016/j.neurobiolaging.2012.02.009
Mutant FUS induces endoplasmic reticulum stress in amyotrophic lateral sclerosis and interacts with protein disulfide-isomerase
resolves10.1371/journal.pone.0081170
ALS-Associated TDP-43 Induces Endoplasmic Reticulum Stress, Which Drives Cytoplasmic TDP-43 Accumulation and Stress Granule Formation
resolves10.1371/journal.ppat.1000608
Interactome Analyses Identify Ties of PrPC and Its Mammalian Paralogs to Oligomannosidic N-Glycans and Endoplasmic Reticulum-Derived Chaperones
resolves10.1093/brain/awp267
Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis
resolves10.1038/nature04782
S-Nitrosylated protein-disulphide isomerase links protein misfolding to neurodegeneration
resolves10.1038/nchembio.467
Inhibitors of protein disulfide isomerase suppress apoptosis induced by misfolded proteins
resolves10.1101/gad.1673408
Impaired ERAD and ER stress are early and specific events in polyglutamine toxicity
resolves10.1371/journal.pone.0008905
Huntingtin Interacts with the Cue Domain of gp78 and Inhibits gp78 Binding to Ubiquitin and p97/VCP
resolves10.1523/JNEUROSCI.5397-12.2013
Tau Accumulation Activates the Unfolded Protein Response by Impairing Endoplasmic Reticulum-Associated Degradation
resolves10.1073/pnas.0710685105
The Parkinson's disease protein α-synuclein disrupts cellular Rab homeostasis
resolves10.1126/science.1129462
α-Synuclein Blocks ER-Golgi Traffic and Rab1 Rescues Neuron Loss in Parkinson's Models
resolves10.1091/mbc.e09-09-0801
α-Synuclein Delays Endoplasmic Reticulum (ER)-to-Golgi Transport in Mammalian Cells by Antagonizing ER/Golgi SNAREs
resolves10.1093/hmg/dds206
Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity
resolves10.1038/emboj.2013.131
The ALS8 protein VAPB interacts with the ER–Golgi recycling protein YIF1A and regulates membrane delivery into dendrites
resolves10.1093/hmg/ddt594
The amyotrophic lateral sclerosis 8 protein, VAP, is required for ER protein quality control
resolves10.1523/JNEUROSCI.3873-06.2006
Mutant huntingtin Impairs the Post-Golgi Trafficking of Brain-Derived Neurotrophic Factor But Not Its Val66Met Polymorphism
resolves10.1096/fj.09-147850
A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum
resolves10.1016/j.bbrc.2005.10.061
siRNA-mediated inhibition of endogenous Huntington disease gene expression induces an aberrant configuration of the ER network in vitro
resolves10.1111/cns.12064
Polymorphism −116<scp>C</scp>/<scp>G</scp>of Human<scp>X</scp>‐box‐Binding Protein 1 Promoter is Associated with Risk of<scp>A</scp>lzheimer's Disease
resolves10.1038/ng1235
Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder
resolves10.1016/j.freeradbiomed.2013.01.001
Association studies indicate that protein disulfide isomerase is a risk factor in amyotrophic lateral sclerosis
resolves10.1038/nature10353
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
resolves10.1007/s00401-013-1090-0
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology
resolves10.1016/j.nbd.2010.08.014
Impaired ATF6α processing, decreased Rheb and neuronal cell cycle re-entry in Huntington's disease
resolves10.1074/jbc.M605049200
Characterization of Amyotrophic Lateral Sclerosis-linked P56S Mutation of Vesicle-associated Membrane Protein-associated Protein B (VAPB/ALS8)
resolves10.1111/j.1471-4159.2008.05857.x
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
resolves10.1371/journal.pone.0022354
Dysregulated LRRK2 Signaling in Response to Endoplasmic Reticulum Stress Leads to Dopaminergic Neuron Degeneration in C. elegans
resolves10.1074/jbc.M808255200
Caenorhabditits elegans LRK-1 and PINK-1 Act Antagonistically in Stress Response and Neurite Outgrowth
resolves10.1016/S0092-8674(00)81667-0
A Role for Presenilin-1 in Nuclear Accumulation of Ire1 Fragments and Induction of the Mammalian Unfolded Protein Response
resolves10.1016/S0896-6273(03)00366-0
Huntingtin and Huntingtin-Associated Protein 1 Influence Neuronal Calcium Signaling Mediated by Inositol-(1,4,5) Triphosphate Receptor Type 1
resolves10.1186/1750-1326-6-81
Dantrolene is neuroprotective in Huntington's disease transgenic mouse model
resolves10.1093/hmg/ddr502
The homocysteine-inducible endoplasmic reticulum (ER) stress protein Herp counteracts mutant α-synuclein-induced ER stress via the homeostatic regulation of ER-resident calcium release channel proteins
resolves10.1172/JCI61332
Neurotoxin-induced ER stress in mouse dopaminergic neurons involves downregulation of TRPC1 and inhibition of AKT/mTOR signaling
resolves10.1038/nchembio.368
Endoplasmic reticulum Ca2+ increases enhance mutant glucocerebrosidase proteostasis
resolves10.1371/journal.pone.0015658
Prion Protein Misfolding Affects Calcium Homeostasis and Sensitizes Cells to Endoplasmic Reticulum Stress
resolves10.1016/j.molcel.2007.06.011
XBP1 Controls Diverse Cell Type- and Condition-Specific Transcriptional Regulatory Networks
resolves10.1196/annals.1397.085
Altered Subcellular Distribution of the Alzheimer's Amyloid Precursor Protein Under Stress Conditions
resolves10.1074/jbc.273.40.25552
The Chaperone BiP/GRP78 Binds to Amyloid Precursor Protein and Decreases Aβ40 and Aβ42 Secretion
resolves10.1016/j.neuron.2008.10.047
Phosphorylation of the Translation Initiation Factor eIF2α Increases BACE1 Levels and Promotes Amyloidogenesis
resolves10.1038/cdd.2010.142
Parkin is transcriptionally regulated by ATF4: evidence for an interconnection between mitochondrial stress and ER stress
resolves10.1242/jcs.127340
ER-stress-associated functional link between Parkin and DJ-1 via a transcriptional cascade involving the tumor suppressor p53 and the spliced X-box binding protein XBP-1
resolves10.1128/MCB.00315-13
Establishing Links between Endoplasmic Reticulum-Mediated Hormesis and Cancer
resolves10.1128/MCB.23.20.7198-7209.2003
Nrf2 Is a Direct PERK Substrate and Effector of PERK-Dependent Cell Survival
resolves10.1371/journal.pgen.1001075
Inactivation of VCP/ter94 Suppresses Retinal Pathology Caused by Misfolded Rhodopsin in Drosophila
resolves10.1128/MCB.00922-10
Protein Misfolding Induces Hypoxic Preconditioning via a Subset of the Unfolded Protein Response Machinery
resolves10.4161/auto.5.8.10247
XBP-1 deficiency in the nervous system reveals a homeostatic switch to activate autophagy
resolves10.1016/j.neuron.2008.10.055
Translational Control of Long-Lasting Synaptic Plasticity and Memory
resolves10.1016/j.cell.2007.01.050
eIF2α Phosphorylation Bidirectionally Regulates the Switch from Short- to Long-Term Synaptic Plasticity and Memory
resolves10.1038/nature03897
Translational control of hippocampal synaptic plasticity and memory by the eIF2α kinase GCN2
resolves10.1016/j.cell.2011.11.029
Suppression of PKR Promotes Network Excitability and Enhanced Cognition by Interferon-γ-Mediated Disinhibition
resolves10.1523/JNEUROSCI.2322-12.2013
Blocking the eIF2α Kinase (PKR) Enhances Positive and Negative Forms of Cortex-Dependent Taste Memory
resolves10.7554/eLife.00498
Pharmacological brake-release of mRNA translation enhances cognitive memory
resolves10.1016/j.celrep.2012.04.010
Brain-Specific Disruption of the eIF2α Kinase PERK Decreases ATF4 Expression and Impairs Behavioral Flexibility
resolves10.1016/j.physbeh.2012.01.024
Cage food location alters energy balance and endoplasmic reticulum stress in the brain of mice
resolves10.1016/j.brainres.2009.12.062
Three weeks voluntary running wheel exercise increases endoplasmic reticulum stress in the brain of mice
resolves10.1016/j.brainres.2006.07.008
Behavioral stress and activated serotonergic neurotransmission induce XBP-1 splicing in the rat brain
resolves10.1074/jbc.M704300200
The Role of Brain-derived Neurotrophic Factor (BDNF)-induced XBP1 Splicing during Brain Development
resolves10.1016/j.bbrc.2008.09.059
Attenuated BDNF-induced upregulation of GABAergic markers in neurons lacking Xbp1
resolves10.1091/mbc.e04-02-0108
The Unfolded Protein Response Regulates Glutamate Receptor Export from the Endoplasmic Reticulum
resolves10.1016/j.celrep.2013.09.046
Xbp1-Independent Ire1 Signaling Is Required for Photoreceptor Differentiation and Rhabdomere Morphogenesis in Drosophila
resolves10.1016/j.neures.2010.07.2042
Behavioral and gene expression analyses in heterozygous XBP1 knockout mice: Possible contribution of chromosome 11qA1 locus to prepulse inhibition
resolves10.1371/journal.pgen.1002833
Drosophila Fatty Acid Transport Protein Regulates Rhodopsin-1 Metabolism and Is Required for Photoreceptor Neuron Survival
resolves10.1016/j.cell.2010.02.034
Endoplasmic Reticulum Stress and the Inflammatory Basis of Metabolic Disease
resolves10.1016/j.cmet.2008.12.004
Endoplasmic Reticulum Stress Plays a Central Role in Development of Leptin Resistance
resolves10.1016/j.cell.2013.09.003
Mitofusin 2 in POMC Neurons Connects ER Stress with Leptin Resistance and Energy Imbalance
resolves10.1073/pnas.1015959108
Light-dependent and circadian clock-regulated activation of sterol regulatory element-binding protein, X-box-binding protein 1, and heat shock factor pathways
resolves10.1016/j.neuroscience.2012.02.016
Salubrinal, an endoplasmic reticulum stress blocker, modulates sleep homeostasis and activation of sleep- and wake-regulatory neurons
resolves10.1073/pnas.0902882106
Collapse of proteostasis represents an early molecular event in
<i>Caenorhabditis elegans</i>
aging
resolves10.1038/embor.2012.100
Organismal regulation of XBP‐1‐mediated unfolded protein response during development and immune activation
resolves10.1016/j.cell.2013.05.042
XBP-1 Is a Cell-Nonautonomous Regulator of Stress Resistance and Longevity
resolves10.1073/pnas.1002575107
Insulin/IGF-1 signaling mutants reprogram ER stress response regulators to promote longevity
resolves10.1016/j.cell.2013.05.015
Regulation of Organismal Proteostasis by Transcellular Chaperone Signaling
resolves10.1083/jcb.201003138
Regulation of basal cellular physiology by the homeostatic unfolded protein response
resolves10.1002/iub.1224
Role of the unfolded protein response in organ physiology: Lessons from mouse models
resolves10.1016/j.coi.2010.10.016
Regulation of innate immunity by signaling pathways emerging from the endoplasmic reticulum
resolves10.1016/j.biocel.2012.04.023
Endoplasmic reticulum: The unfolded protein response is tangled in neurodegeneration
resolves10.1016/j.brainres.2010.06.016
Protein disulfide isomerase-immunopositive inclusions in patients with Alzheimer disease
resolves10.1096/fj.13-234864
Unfolded protein response signaling by transcription factor XBP‐1 regulates ADAM10 and is affected in Alzheimer's disease
resolves10.1002/path.3969
The unfolded protein response is associated with early tau pathology in the hippocampus of tauopathies
resolves10.1016/j.brainres.2004.07.026
Identification of the protein disulfide isomerase family member PDIp in experimental Parkinson's disease and Lewy body pathology
resolves10.1016/j.bbrc.2007.01.043
Activation of the unfolded protein response in Parkinson’s disease
resolves10.1093/brain/awm190
Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis
resolves10.1016/j.nbd.2009.08.013
Involvement of CHOP, an ER-stress apoptotic mediator, in both human sporadic ALS and ALS model mice
resolves10.1097/NEN.0b013e3181d44992
Endoplasmic Reticulum Stress in Motor Neurons of the Spinal Cord in Sporadic Amyotrophic Lateral Sclerosis
resolves10.1016/S0304-3940(02)01071-6
Overexpressed protein disulfide isomerase in brains of patients with sporadic Creutzfeldt–Jakob disease
resolves10.1097/01.jnen.0000218445.30535.6f
Endoplasmic Reticulum Stress Features Are Prominent in Alzheimer Disease but Not in Prion Diseases In Vivo
resolves10.1016/j.brainres.2008.11.104
Protective effect against Parkinson's disease-related insults through the activation of XBP1
resolves10.1016/j.bbrc.2012.03.033
AAV-mediated delivery of the transcription factor XBP1s into the striatum reduces mutant Huntingtin aggregation in a mouse model of Huntington’s disease
resolves10.1371/journal.pone.0063205
Ablation of C/EBP Homologous Protein Does Not Protect T17M RHO Mice from Retinal Degeneration
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