Maintenance of an open reading frame as an additional level of scrutiny during splice site selection (Q42689167)

4 November 2017

title

Maintenance of an open reading frame as an additional level of scrutiny during splice site selection (English)

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4 November 2017

H C Dietz

1

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4 November 2017

R J Kendzior

series ordinal

2

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4 November 2017

language of work or name

English

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publication date

1 October 1994

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4 November 2017

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4 November 2017

volume

8

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4 November 2017

issue

2

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4 November 2017

page(s)

183-188

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Splicing of messenger RNA precursors

4 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

The role of small nuclear ribonucleoprotein particles in pre-mRNA splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Exon definition may facilitate splice site selection in RNAs with multiple exons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Exon as well as intron sequences are cis-regulating elements for the mutually exclusive alternative splicing of the beta tropomyosin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Identification of a specific exon sequence that is a major determinant in the selection between a natural and a cryptic 5' splice site

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Premature translation termination mediates triosephosphate isomerase mRNA degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Nonsense mutations in the dihydrofolate reductase gene affect RNA processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Translation to near the distal end of the penultimate exon is required for normal levels of spliced triosephosphate isomerase mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Nonsense codons can reduce the abundance of nuclear mRNA without affecting the abundance of pre-mRNA or the half-life of cytoplasmic mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Splicing mutants and their second-site suppressors at the dihydrofolate reductase locus in Chinese hamster ovary cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Order of intron removal during splicing of endogenous adenine phosphoribosyltransferase and dihydrofolate reductase pre-mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

Are vertebrate exons scanned during splice-site selection?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

A catalogue of splice junction sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Signals for the selection of a splice site in pre-mRNA. Computer analysis of splice junction sequences and like sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Splicing of messenger RNA precursors

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

A multicomponent complex is involved in the splicing of messenger RNA precursors

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

A role for exon sequences and splice-site proximity in splice-site selection

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

The skipping of constitutive exons in vivo induced by nonsense mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Nonsense mutations inhibit splicing of MVM RNA in cis when they interrupt the reading frame of either exon of the final spliced product.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

A nonsense mutation and exon skipping in the Fanconi anaemia group C gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Does steric interference between splice sites block the splicing of a short c-src neuron-specific exon in non-neuronal cells?

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Beta-globin nonsense mutation: deficient accumulation of mRNA occurs despite normal cytoplasmic stability

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

A survey on intron and exon lengths

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domains

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Site-directed mutagenesis of virtually any plasmid by eliminating a unique site

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-183

7 January 2021

Identifiers

DOI

10.1038/NG1094-183

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Dimensions Publication ID

4 November 2017

1022232503

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1 reference