Pages that link to "Q37992334"
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The following pages link to RNA-binding proteins in microsatellite expansion disorders: Mediators of RNA toxicity (Q37992334):
Displaying 50 items.
- RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention (Q24562489) (← links)
- There has been an awakening: Emerging mechanisms of C9orf72 mutations in FTD/ALS (Q26750577) (← links)
- Structural studies of CNG repeats (Q26851232) (← links)
- Fragile X-associated tremor/ataxia syndrome (Q26852667) (← links)
- Evolutionary conservation and expression of human RNA-binding proteins and their role in human genetic disease (Q26991754) (← links)
- Intrabodies as neuroprotective therapeutics (Q27003896) (← links)
- The unstable repeats--three evolving faces of neurological disease (Q27025923) (← links)
- Defective control of pre-messenger RNA splicing in human disease (Q28077564) (← links)
- TWEAK Regulates Muscle Functions in a Mouse Model of RNA Toxicity (Q30277293) (← links)
- TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy (Q30301119) (← links)
- Single-molecule study of the CUG repeat-MBNL1 interaction and its inhibition by small molecules. (Q30541488) (← links)
- Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion (Q33878156) (← links)
- RNA-protein interactions in unstable microsatellite diseases. (Q34243144) (← links)
- Developing bivalent ligands to target CUG triplet repeats, the causative agent of myotonic dystrophy type 1. (Q35031314) (← links)
- Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat (Q35667019) (← links)
- RNA-binding protein misregulation in microsatellite expansion disorders (Q35789502) (← links)
- RNA Structures as Mediators of Neurological Diseases and as Drug Targets (Q35868044) (← links)
- MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain (Q35984230) (← links)
- A flow cytometry-based screen identifies MBNL1 modulators that rescue splicing defects in myotonic dystrophy type I. (Q36378612) (← links)
- Actinomycin D Specifically Reduces Expanded CUG Repeat RNA in Myotonic Dystrophy Models. (Q36405529) (← links)
- RNA toxicity in polyglutamine disorders: concepts, models, and progress of research (Q36859984) (← links)
- Repeat-associated non-ATG (RAN) translation in neurological disease (Q37195032) (← links)
- RNA-mediated toxicity in neurodegenerative disease (Q37216891) (← links)
- Clinical neurogenetics: amyotrophic lateral sclerosis (Q37274526) (← links)
- Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms (Q37524454) (← links)
- A brief history of triplet repeat diseases (Q37553564) (← links)
- Therapy and clinical trials in frontotemporal dementia: past, present, and future (Q37566888) (← links)
- Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome (Q37580522) (← links)
- Molecular determinants of the axonal mRNA transcriptome (Q37600828) (← links)
- Aberrant splicing in neurological diseases. (Q38118935) (← links)
- Antisense oligonucleotide therapy for the treatment of C9ORF72 ALS/FTD diseases. (Q38210259) (← links)
- Mechanisms of transcriptional dysregulation in repeat expansion disorders (Q38238667) (← links)
- Modeling simple repeat expansion diseases with iPSC technology. (Q38853911) (← links)
- Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management (Q38875623) (← links)
- Structures of RNA repeats associated with neurological diseases (Q38994216) (← links)
- DNA repair in the trinucleotide repeat disorders (Q39039735) (← links)
- RNA toxicity and foci formation in microsatellite expansion diseases (Q39139063) (← links)
- Alternative splicing as a regulator of development and tissue identity. (Q39295240) (← links)
- TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases. (Q41498579) (← links)
- A novel CUG(exp)·MBNL1 inhibitor with therapeutic potential for myotonic dystrophy type 1. (Q41825220) (← links)
- Functional Mechanisms of Microsatellite DNA in Eukaryotic Genomes. (Q42096577) (← links)
- Purα Repaired Expanded Hexanucleotide GGGGCC Repeat Noncoding RNA-Caused Neuronal Toxicity in Neuro-2a Cells (Q47702534) (← links)
- C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2α phosphorylation. (Q47882860) (← links)
- Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31. (Q48244919) (← links)
- Structure and Dynamics of DNA and RNA Double Helices Obtained from the CCG and GGC Trinucleotide Repeats. (Q52607744) (← links)
- Trinucleotide Repeat Expansion Diseases, RNAi, and Cancer (Q57190619) (← links)
- A census of human RNA-binding proteins (Q58283908) (← links)
- Neurodegenerative diseases: G-quadruplex poses quadruple threat (Q58623071) (← links)
- RNA Degradation in Neurodegenerative Disease (Q89146094) (← links)
- Deregulation of RNA Metabolism in Microsatellite Expansion Diseases (Q89146104) (← links)