Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation
about
Heterogeneous nuclear ribonucleoprotein P2 is an autoantibody target in mice deficient for Mer, Axl, and Tyro3 receptor tyrosine kinasesHuman 100-kDa homologous DNA-pairing protein is the splicing factor PSF and promotes DNA strand invasionAbundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion diseaseInduced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcriptionA new subtype of frontotemporal lobar degeneration with FUS pathologyTLS inhibits RNA polymerase III transcriptionMechanisms of FUS mutations in familial amyotrophic lateral sclerosisRoles of RNA-Binding Proteins in DNA Damage ResponseFUS-mediated regulation of alternative RNA processing in neurons: insights from global transcriptome analysisThe potential of pathological protein fragmentation in blood-based biomarker development for dementia - with emphasis on Alzheimer's diseaseIdentification of an RNA binding specificity for the potential splicing factor TLSThe splicing factor U1C represses EWS/FLI-mediated transactivationCharacterization of two evolutionarily conserved, alternatively spliced nuclear phosphoproteins, NFAR-1 and -2, that function in mRNA processing and interact with the double-stranded RNA-dependent protein kinase, PKRMutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisThe RING finger protein SNURF is a bifunctional protein possessing DNA binding activityEWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functionsNucleic acid-binding specificity of human FUS protein.A reliable and simple method for two-dimensional electrophoresis and identification of HeLa nuclear alkaline nucleic acid-binding proteins using immobilized pH gradient.CRISPR/Cas9-mediated targeted gene correction in amyotrophic lateral sclerosis patient iPSCs.FUS immunogold labeling TEM analysis of the neuronal cytoplasmic inclusions of neuronal intermediate filament inclusion disease: a frontotemporal lobar degeneration with FUS proteinopathy.The TET family of proteins: functions and roles in disease.De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis.Functions of FUS/TLS from DNA repair to stress response: implications for ALS.Nuclear localization sequence of FUS and induction of stress granules by ALS mutants.The effect of PRMT1-mediated arginine methylation on the subcellular localization, stress granules, and detergent-insoluble aggregates of FUS/TLS.Male sterility and enhanced radiation sensitivity in TLS(-/-) mice.The RNA-binding protein fused in sarcoma (FUS) functions downstream of poly(ADP-ribose) polymerase (PARP) in response to DNA damageALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation.A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathiesA fruitful endeavor: modeling ALS in the fruit flyEwing sarcoma gene EWS is essential for meiosis and B lymphocyte developmentFUS/TLS contributes to replication-dependent histone gene expression by interaction with U7 snRNPs and histone-specific transcription factorsTLS/FUS (translocated in liposarcoma/fused in sarcoma) regulates target gene transcription via single-stranded DNA response elementsEntorhinal cortical neurons are the primary targets of FUS mislocalization and ubiquitin aggregation in FUS transgenic rats.Structural delineation of stem-loop RNA binding by human TAF15 protein.The RRM domain of human fused in sarcoma protein reveals a non-canonical nucleic acid binding site.Expression of human FUS protein in Drosophila leads to progressive neurodegenerationRad51 and Rad54 promote noncrossover recombination between centromere repeats on the same chromatid to prevent isochromosome formation.FUsed in sarcoma is a novel regulator of manganese superoxide dismutase gene transcription.
P2860
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P2860
Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@ast
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@en
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@nl
type
label
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@ast
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@en
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@nl
prefLabel
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@ast
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@en
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@nl
P2093
P2860
P921
P3181
P356
P1476
Human 75-kDa DNA-pairing prote ...... le to promote D-loop formation
@en
P2093
P2860
P304
P3181
P356
10.1074/JBC.274.48.34337
P407
P50
P577
1999-11-26T00:00:00Z