RNA-binding proteins in neurological diseases. (Q38198537)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

title

RNA-binding proteins in neurological diseases (English)

1 reference

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11 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

HuaLin Zhou

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

JiangHong Liu

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

Li Zhu

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

Jane Y Wu

series ordinal

1 reference

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11 March 2020

publication date

1 April 2014

1 reference

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Science in China. Series C: Life Sciences

11 March 2020

published in

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11 March 2020

volume

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11 March 2020

issue

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11 March 2020

page(s)

432-444

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

RNA regulons: coordination of post-transcriptional events

11 March 2020

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The neuronal RNA-binding protein Nova-2 is implicated as the autoantigen targeted in POMA patients with dementia

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21 January 2018

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21 January 2018

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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

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Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

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Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

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Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments

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Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis

21 January 2018

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

21 January 2018

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Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

21 January 2018

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Structural insights into TDP-43 in nucleic-acid binding and domain interactions

21 January 2018

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Identification of an RNA binding specificity for the potential splicing factor TLS

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 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

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

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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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Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.

21 January 2018

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

21 January 2018

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Tar DNA binding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS).

21 January 2018

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HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS

21 January 2018

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TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells.

21 January 2018

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Identification of RNA bound to the TDP-43 ribonucleoprotein complex in the adult mouse brain.

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https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

TDP-43 is a developmentally regulated protein essential for early embryonic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

A Drosophila model for TDP-43 proteinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Domain architectures and characterization of an RNA-binding protein, TLS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

A yeast functional screen predicts new candidate ALS disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Glutamate receptor RNA editing in vitro by enzymatic conversion of adenosine to inosine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

RNA editing of brain glutamate receptor channels: mechanism and physiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

Spinocerebellar ataxia 2 (SCA2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-014-4647-9

10.1007/S11427-014-4647-9

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 March 2020

1027896624

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24658850%20AND%20SRC:MED&resulttype=core&format=json