Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy
about
Genome analysis reveals interplay between 5'UTR introns and nuclear mRNA export for secretory and mitochondrial genesA family of human RNA-binding proteins related to the Drosophila Bruno translational regulatorRecruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophyThe CELF family of RNA binding proteins is implicated in cell-specific and developmentally regulated alternative splicingInteraction of muscleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicingCompetition of CUGBP1 and calreticulin for the regulation of p21 translation determines cell fate.CELF6, a member of the CELF family of RNA-binding proteins, regulates muscle-specific splicing enhancer-dependent alternative splicingCalreticulin interacts with C/EBPalpha and C/EBPbeta mRNAs and represses translation of C/EBP proteinsRNPC1, an RNA-binding protein and a target of the p53 family, is required for maintaining the stability of the basal and stress-induced p21 transcriptEpidermal growth factor receptor stimulation activates the RNA binding protein CUG-BP1 and increases expression of C/EBPbeta-LIP in mammary epithelial cellsFailure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophyEDEN and EDEN-BP, a cis element and an associated factor that mediate sequence-specific mRNA deadenylation in Xenopus embryos.CUG-BP binds to RNA substrates and recruits PARN deadenylaseMolecular basis for impaired muscle differentiation in myotonic dystrophyCytoplasmic polyadenylation in development and beyondIn vivo co-localisation of MBNL protein with DMPK expanded-repeat transcriptsDifferentiation-induced colocalization of the KH-type splicing regulatory protein with polypyrimidine tract binding protein and the c-src pre-mRNAExpanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSThe perinucleolar compartmentConserved GU-rich elements mediate mRNA decay by binding to CUG-binding protein 1Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout miceElevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophyCUG-BP1/CELF1 requires UGU-rich sequences for high-affinity bindingDefining early steps in mRNA transport: mutant mRNA in myotonic dystrophy type I is blocked at entry into SC-35 domains.HnRNP H inhibits nuclear export of mRNA containing expanded CUG repeats and a distal branch point sequence.The importance of CELF control: molecular and biological roles of the CUG-BP, Elav-like family of RNA-binding proteinsMyotonic dystrophy: is a narrow focus obscuring the rest of the field?Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasisRNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndromeThe unstable repeats--three evolving faces of neurological diseaseTriplet repeat-derived siRNAs enhance RNA-mediated toxicity in a Drosophila model for myotonic dystrophyStructural basis for the sequence-specific RNA-recognition mechanism of human CUG-BP1 RRM3Structural Insights into RNA Recognition by the Alternate-Splicing Regulator CUG-Binding Protein 1Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotypeRNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1c-Jun ARE targets mRNA deadenylation by an EDEN-BP (embryo deadenylation element-binding protein)-dependent pathwayAlternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1MBNL1 is the primary determinant of focus formation and aberrant insulin receptor splicing in DM1The CUGBP2 splicing factor regulates an ensemble of branchpoints from perimeter binding sites with implications for autoregulationCoordinate repression of a trio of neuron-specific splicing events by the splicing regulator PTB
P2860
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P2860
Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy
description
1996 nî lūn-bûn
@nan
1996 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@ast
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en-gb
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@nl
type
label
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@ast
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en-gb
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@nl
prefLabel
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@ast
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en-gb
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@nl
P2093
P2860
P3181
P356
P1476
Identification of a (CUG)n tri ...... pression in myotonic dystrophy
@en
P2093
C T Caskey
D R DeVore
J W Miller
L T Timchenko
N A Timchenko
P2860
P304
P3181
P356
10.1093/NAR/24.22.4407
P407
P577
1996-11-01T00:00:00Z