(Q38079170)

28 August 2017

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title

RNA quality control and protein aggregates in amyotrophic lateral sclerosis: a review (English)

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amyotrophic lateral sclerosis

28 August 2017

main subject

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quality control

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author name string

Ashok Verma

series ordinal

1

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28 August 2017

Rup Tandan

series ordinal

2

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28 August 2017

publication date

4 February 2013

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28 August 2017

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28 August 2017

volume

47

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28 August 2017

issue

3

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28 August 2017

page(s)

330-338

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

28 August 2017

cites work

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DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

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ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

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Mutations of optineurin in amyotrophic lateral sclerosis

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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

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Exome sequencing reveals VCP mutations as a cause of familial ALS

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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

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A yeast functional screen predicts new candidate ALS disease genes

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SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis

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Onset and progression in inherited ALS determined by motor neurons and microglia

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Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis

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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

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Understanding the role of TDP-43 and FUS/TLS in ALS and beyond.

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1 reference

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

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TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

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Identification and characterization of a spinal muscular atrophy-determining gene

21 January 2018

1 reference

Repeat expansion affects both transcription initiation and elongation in friedreich ataxia cells

21 January 2018

1 reference

Pathogenic mechanisms of myotonic dystrophy

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1 reference

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

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Fine structural analysis of the neuronal inclusions of frontotemporal lobar degeneration with TDP-43 proteinopathy.

21 January 2018

1 reference

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

21 January 2018

1 reference

TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis.

21 January 2018

1 reference

Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions

21 January 2018

1 reference

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

RNA processing pathways in amyotrophic lateral sclerosis

21 January 2018

1 reference

Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation.

21 January 2018

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Structural determinants of the cellular localization and shuttling of TDP-43.

21 January 2018

1 reference

Genomic structure of the human RBP56/hTAFII68 and FUS/TLS genes

21 January 2018

1 reference

TLS, EWS and TAF15: a model for transcriptional integration of gene expression

21 January 2018

1 reference

TLS (Translocated-in-Liposarcoma) Is a High-Affinity Interactor for Steroid, Thyroid Hormone, and Retinoid Receptors

21 January 2018

1 reference

Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

21 January 2018

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Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo

21 January 2018

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TDP-43 overexpression enhances exon 7 inclusion during the survival of motor neuron pre-mRNA splicing

21 January 2018

1 reference

The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology.

21 January 2018

1 reference

Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior

21 January 2018

1 reference

TDP-43 promotes microRNA biogenesis as a component of the Drosha and Dicer complexes

21 January 2018

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Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.

21 January 2018

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Characterizing the RNA targets and position-dependent splicing regulation by TDP-43.

21 January 2018

1 reference

Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes

21 January 2018

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RNA targets of TDP-43 identified by UV-CLIP are deregulated in ALS.

21 January 2018

1 reference

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

21 January 2018

1 reference

Amyotrophic lateral sclerosis-associated proteins TDP-43 and FUS/TLS function in a common biochemical complex to co-regulate HDAC6 mRNA.

21 January 2018

1 reference

TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein

21 January 2018

1 reference

TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines

21 January 2018

1 reference

RNA targets of wild-type and mutant FET family proteins

21 January 2018

1 reference

Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

21 January 2018

1 reference

The seeds of neurodegeneration: prion-like spreading in ALS

21 January 2018

1 reference

UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

21 January 2018

1 reference

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis

21 January 2018

1 reference

Astrocytes from familial and sporadic ALS patients are toxic to motor neurons

21 January 2018

1 reference

Interaction with polyglutamine aggregates reveals a Q/N-rich domain in TDP-43.

21 January 2018

1 reference

Prion-like disorders: blurring the divide between transmissibility and infectivity

21 January 2018

1 reference

A seeding reaction recapitulates intracellular formation of Sarkosyl-insoluble transactivation response element (TAR) DNA-binding protein-43 inclusions

21 January 2018

1 reference

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

21 January 2018

1 reference

A systematic survey identifies prions and illuminates sequence features of prionogenic proteins

21 January 2018

1 reference

FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration

21 January 2018

1 reference

Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6

21 January 2018

1 reference

A Drosophila model for TDP-43 proteinopathy

21 January 2018

1 reference

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

21 January 2018

1 reference

Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis

21 January 2018

1 reference

Neurotoxic effects of TDP-43 overexpression in C. elegans

21 January 2018

1 reference

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

21 January 2018

1 reference

Progressive motor weakness in transgenic mice expressing human TDP-43.

21 January 2018

1 reference

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration

21 January 2018

1 reference

Transgenic rat model of neurodegeneration caused by mutation in the TDP gene.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.23673

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28 August 2017

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