Loss of exon identity is a common mechanism of human inherited disease (Q35451644)

8 August 2017

title

Loss of exon identity is a common mechanism of human inherited disease (English)

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8 August 2017

4

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8 August 2017

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Matthew Mort

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8 August 2017

author name string

Timothy Sterne-Weiler

series ordinal

1

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8 August 2017

Jonathan Howard

series ordinal

2

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8 August 2017

Jeremy R Sanford

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5

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8 August 2017

publication date

12 July 2011

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8 August 2017

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8 August 2017

volume

21

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8 August 2017

issue

10

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8 August 2017

page(s)

1563-1571

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Using positional distribution to identify splicing elements and predict pre-mRNA processing defects in human genes

8 August 2017

cites work

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27 July 2018

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27 July 2018

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27 July 2018

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Dynamic regulation of alternative splicing by silencers that modulate 5' splice site competition

27 July 2018

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Alternative splicing resulting in nonsense-mediated mRNA decay: what is the meaning of nonsense?

27 July 2018

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27 July 2018

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27 July 2018

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Splicing in disease: disruption of the splicing code and the decoding machinery

27 July 2018

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Ultraconserved elements are associated with homeostatic control of splicing regulators by alternative splicing and nonsense-mediated decay

27 July 2018

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General and specific functions of exonic splicing silencers in splicing control

27 July 2018

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Comparative analysis identifies exonic splicing regulatory sequences--The complex definition of enhancers and silencers

27 July 2018

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Hearing silence: non-neutral evolution at synonymous sites in mammals

27 July 2018

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Cell motility is controlled by SF2/ASF through alternative splicing of the Ron protooncogene

27 July 2018

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Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

27 July 2018

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Systematic identification and analysis of exonic splicing silencers.

27 July 2018

1 reference

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Variation in alternative splicing across human tissues

27 July 2018

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Stop codon-mediated suppression of splicing is a novel nuclear scanning mechanism not affected by elements of protein synthesis and NMD.

27 July 2018

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Single nucleotide polymorphism-based validation of exonic splicing enhancers

27 July 2018

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Genomic variants in exons and introns: identifying the splicing spoilers

27 July 2018

1 reference

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Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics

27 July 2018

1 reference

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Identification and characterization of multi-species conserved sequences

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

A conserved signal-responsive sequence mediates activation-induced alternative splicing of CD45.

27 July 2018

1 reference

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ESEfinder: A web resource to identify exonic splicing enhancers

27 July 2018

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27 July 2018

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Predictive identification of exonic splicing enhancers in human genes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Stop codons affect 5' splice site selection by surveillance of splicing

27 July 2018

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Exon Identity Established through Differential Antagonism between Exonic Splicing Silencer-Bound hnRNP A1 and Enhancer-Bound SR Proteins

27 July 2018

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Determination of the RNA binding specificity of the heterogeneous nuclear ribonucleoprotein (hnRNP) H/H'/F/2H9 family

27 July 2018

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The role of U2AF35 and U2AF65 in enhancer-dependent splicing

27 July 2018

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A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes

27 July 2018

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Selection of alternative 5' splice sites: role of U1 snRNP and models for the antagonistic effects of SF2/ASF and hnRNP A1.

27 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Arginine/serine-rich domains of SR proteins can function as activators of pre-mRNA splicing

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

The association of nonsense mutation with exon-skipping in hprt mRNA of Chinese hamster ovary cells results from an artifact of RT-PCR.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Protein-protein interactions and 5'-splice-site recognition in mammalian mRNA precursors

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

The human splicing factors ASF/SF2 and SC35 possess distinct, functionally significant RNA binding specificities

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Deciphering the splicing code

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

NeatMap--non-clustering heat map alternatives in R.

26 September 2018

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Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Splicing regulation: from a parts list of regulatory elements to an integrated splicing code

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Unproductive splicing of SR genes associated with highly conserved and ultraconserved DNA elements

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing

26 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Preferential humoral immune response in prostate cancer to cellular proteins p90 and p62 in a panel of tumor-associated antigens.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Disruption of exonic splicing enhancer elements is the principal cause of exon skipping associated with seven nonsense or missense alleles of NF1.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Missense, nonsense, and neutral mutations define juxtaposed regulatory elements of splicing in cystic fibrosis transmembrane regulator exon 9.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Phylogenetic shadowing of primate sequences to find functional regions of the human genome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Distribution and characterization of regulatory elements in the human genome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Listening to silence and understanding nonsense: exonic mutations that affect splicing

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

A strategy for disease gene identification through nonsense-mediated mRNA decay inhibition

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Probability-based protein identification by searching sequence databases using mass spectrometry data

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

The role of exon sequences in splice site selection.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

Human Gene Mutation Database: towards a comprehensive central mutation database

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202274

The skipping of constitutive exons in vivo induced by nonsense mutations

15 November 2018

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12 December 2020

A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease

1 reference

12 December 2020

Evidence for Purifying Selection Against Synonymous Mutations in Mammalian Exonic Splicing Enhancers

1 reference

12 December 2020

Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the OPA1 gene

1 reference

12 December 2020

SR proteins: a foot on the exon before the transition from intron to exon definition

1 reference

12 December 2020

Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codons

1 reference

12 December 2020

Expression of the muscle glycogen phosphorylase gene in patients with McArdle disease: the role of nonsense-mediated mRNA decay

1 reference

12 December 2020

New TFR2 mutations in young Italian patients with hemochromatosis

1 reference

12 December 2020

Nonsense-associated altered splicing: a frame-dependent response distinct from nonsense-mediated decay

1 reference

12 December 2020

Identifiers

DOI

10.1101/GR.118638.110

1 reference

8 August 2017

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8 August 2017

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