Maintenance of an open reading frame as an additional level of scrutiny during splice site selection.
about
Mammalian orthologues of a yeast regulator of nonsense transcript stabilityStructure of the GM2A gene: identification of an exon 2 nonsense mutation and a naturally occurring transcript with an in-frame deletion of exon 2The molecular genetics of Marfan syndrome and related disordersThe molecular genetics of Marfan syndrome and related microfibrillopathiesMutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathiesCloning and characterization of the promoter for the liver isoform of the rat carnitine palmitoyltransferase I (L-CPT I) genemRNA stability in mammalian cellsWhere do introns come from?Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patients.Frame-disrupting mutations elicit pre-mRNA accumulation independently of frame disruptionEvidence that translation reinitiation abrogates nonsense-mediated mRNA decay in mammalian cellsA premature termination codon interferes with the nuclear function of an exon splicing enhancer in an open reading frame-dependent mannerMultiple splicing defects in an intronic false exon.Nonsense-mediated decay of human HEXA mRNA.Stop codons affect 5' splice site selection by surveillance of splicing.Optimizing exon skipping therapies for DMD.Unspliced precursors of NMD-sensitive β-globin transcripts exhibit decreased steady-state levels in erythroid cellsMultifunctional regulatory proteins that control gene expression in both the nucleus and the cytoplasm.Evidence that the decay of nucleus-associated nonsense mRNA for human triosephosphate isomerase involves nonsense codon recognition after splicing.Intron function in the nonsense-mediated decay of beta-globin mRNA: indications that pre-mRNA splicing in the nucleus can influence mRNA translation in the cytoplasm.Nonsense mutations in the alcohol dehydrogenase gene of Drosophila melanogaster correlate with an abnormal 3' end processing of the corresponding pre-mRNA.Premature termination codons do not affect the rate of splicing of neighboring introns.Alternative splicing induced by nonsense mutations in the immunoglobulin mu VDJ exon is independent of truncation of the open reading frameNonsense-associated alternative splicing of T-cell receptor beta genes: no evidence for frame dependencePotential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy.The exon sequence TAGG can inhibit splicingWhen cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.Unusual patterns of exon skipping in Bruton tyrosine kinase are associated with mutations involving the intron 17 3' splice site.Cotranscriptional effect of a premature termination codon revealed by live-cell imaging.A nonsense mutation in the fibrillin-1 gene of a Marfan syndrome patient induces NMD and disrupts an exonic splicing enhancer.A splicing-dependent regulatory mechanism that detects translation signals.T cell receptor (TCR) mini-gene mRNA expression regulated by nonsense codons: a nuclear-associated translation-like mechanismEffects of nonsense mutations on nuclear and cytoplasmic adenine phosphoribosyltransferase RNA.Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selection.Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.Infrequent translation of a nonsense codon is sufficient to decrease mRNA levelScanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product.Exon skipping in IVD RNA processing in isovaleric acidemia caused by point mutations in the coding region of the IVD gene.Nonsense-mediated decay of glutathione peroxidase 1 mRNA in the cytoplasm depends on intron position.Missense, nonsense, and neutral mutations define juxtaposed regulatory elements of splicing in cystic fibrosis transmembrane regulator exon 9.
P2860
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P2860
Maintenance of an open reading frame as an additional level of scrutiny during splice site selection.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Maintenance of an open reading ...... during splice site selection.
@en
Maintenance of an open reading ...... during splice site selection.
@nl
type
label
Maintenance of an open reading ...... during splice site selection.
@en
Maintenance of an open reading ...... during splice site selection.
@nl
prefLabel
Maintenance of an open reading ...... during splice site selection.
@en
Maintenance of an open reading ...... during splice site selection.
@nl
P2860
P356
P1433
P1476
Maintenance of an open reading ...... during splice site selection.
@en
P2093
R J Kendzior
P2860
P2888
P304
P356
10.1038/NG1094-183
P407
P577
1994-10-01T00:00:00Z
P5875
P6179
1022232503