Pages that link to "Q38921570"
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The following pages link to Nucleolar stress and impaired stress granule formation contribute to C9orf72 RAN translation-induced cytotoxicity (Q38921570):
Displaying 50 items.
- Inside out: the role of nucleocytoplasmic transport in ALS and FTLD (Q26748482) (← links)
- An amyloid-like cascade hypothesis for C9orf72 ALS/FTD (Q26778174) (← links)
- Impaired neurodevelopment by the low complexity domain of CPEB4 reveals a convergent pathway with neurodegeneration (Q27331630) (← links)
- Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death (Q28854599) (← links)
- A C9ORF72/SMCR8-containing complex regulates ULK1 and plays a dual role in autophagy (Q29465530) (← links)
- Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration (Q33577239) (← links)
- Cytoplasmic poly-GA aggregates impair nuclear import of TDP-43 in C9orf72 ALS/FTLD. (Q33614771) (← links)
- C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten (Q33614811) (← links)
- Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their degeneration. (Q35776562) (← links)
- Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers (Q36073660) (← links)
- Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing (Q36073675) (← links)
- Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS. (Q36108576) (← links)
- Distinct C9orf72-Associated Dipeptide Repeat Structures Correlate with Neuronal Toxicity. (Q36173153) (← links)
- C9orf72 BAC Transgenic Mice Display Typical Pathologic Features of ALS/FTD (Q36353773) (← links)
- ALS biomarkers for therapy development: State of the field and future directions (Q36479616) (← links)
- Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice (Q36788842) (← links)
- Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS. (Q36795394) (← links)
- C9orf72 Hexanucleotide Expansions Are Associated with Altered Endoplasmic Reticulum Calcium Homeostasis and Stress Granule Formation in Induced Pluripotent Stem Cell-Derived Neurons from Patients with Amyotrophic Lateral Sclerosis and Frontotemporal (Q37164667) (← links)
- ALS mutant SOD1 interacts with G3BP1 and affects stress granule dynamics (Q37256571) (← links)
- C9ORF72 poly(GA) aggregates sequester and impair HR23 and nucleocytoplasmic transport proteins (Q37476206) (← links)
- Dysfunction of autophagy as the pathological mechanism of motor neuron disease based on a patient-specific disease model (Q38556198) (← links)
- Iron and Neurodegeneration: Is Ferritinophagy the Link? (Q38607505) (← links)
- Old versus New Mechanisms in the Pathogenesis of ALS. (Q38700722) (← links)
- C9ORF72 Regulates Stress Granule Formation and Its Deficiency Impairs Stress Granule Assembly, Hypersensitizing Cells to Stress (Q38781435) (← links)
- Insights into the pathogenic mechanisms of Chromosome 9 open reading frame 72 (C9orf72) repeat expansions (Q38789426) (← links)
- RAN translation-What makes it run? (Q38802827) (← links)
- Genetics of Frontotemporal Lobar Degeneration: From the Bench to the Clinic (Q38814847) (← links)
- The expanding biology of the C9orf72 nucleotide repeat expansion in neurodegenerative disease (Q38826893) (← links)
- A critical role of Hrd1 in the regulation of optineurin degradation and aggresome formation (Q38882232) (← links)
- Pathogenic determinants and mechanisms of ALS/FTD linked to hexanucleotide repeat expansions in the C9orf72 gene (Q38952327) (← links)
- Disease Mechanisms of C9ORF72 Repeat Expansions (Q39107075) (← links)
- The Role of Dipeptide Repeats in C9ORF72-Related ALS-FTD. (Q39153670) (← links)
- Control of mRNA Translation in ALS Proteinopathy (Q39225382) (← links)
- RNA Misprocessing in C9orf72-Linked Neurodegeneration (Q39458329) (← links)
- C9ORF72 is a GDP/GTP exchange factor for Rab8 and Rab39 and regulates autophagy (Q39520699) (← links)
- Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics (Q40287573) (← links)
- Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers (Q40535548) (← links)
- RNA biology of disease-associated microsatellite repeat expansions (Q41542861) (← links)
- Regulation of mRNA Translation in Neurons-A Matter of Life and Death (Q46818543) (← links)
- Repeat-associated non-AUG translation from antisense CCG repeats in fragile X tremor/ataxia syndrome (Q46839217) (← links)
- A recurrent de novo missense mutation in UBTF causes developmental neuroregression (Q47209697) (← links)
- A peptidylic inhibitor for neutralizing expanded CAG RNA-induced nucleolar stress in polyglutamine diseases (Q47236927) (← links)
- The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration (Q47693846) (← links)
- C9orf72 poly GA RAN-translated protein plays a key role in amyotrophic lateral sclerosis via aggregation and toxicity (Q47707045) (← links)
- Unraveling the Role of RNA Mediated Toxicity of C9orf72 Repeats in C9-FTD/ALS. (Q49314473) (← links)
- C-terminal short arginine/serine repeat sequence-dependent regulation of Y14 (RBM8A) localization (Q49445321) (← links)
- Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome. (Q49905433) (← links)
- Assay to Measure Nucleocytoplasmic Transport in Real Time within Motor Neuron-like NSC-34 Cells (Q50200695) (← links)
- Biology and Pathobiology of TDP-43 and Emergent Therapeutic Strategies. (Q50350613) (← links)
- Folliculin, a tumor suppressor associated with Birt-Hogg-Dubé (BHD) syndrome, is a novel modifier of TDP-43 cytoplasmic translocation and aggregation. (Q52147386) (← links)