Binding of DAZAP1 and hnRNPA1/A2 to an exonic splicing silencer in a natural BRCA1 exon 18 mutant (Q39026940)

8 September 2017

Binding of DAZAP1 and hnRNPA1/A2 to an exonic splicing silencer in a natural BRCA1 exon 18 mutant (English)

1 reference

8 September 2017

Elisa Goina

1

1 reference

8 September 2017

Natasa Skoko

series ordinal

2

1 reference

8 September 2017

Franco Pagani

series ordinal

3

1 reference

8 September 2017

language of work or name

English

0 references

publication date

7 April 2008

1 reference

Molecular and Cellular Biology

8 September 2017

1 reference

8 September 2017

28

1 reference

8 September 2017

11

1 reference

8 September 2017

3850-3860

1 reference

describes a project that uses

8 September 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2423284/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Phosphorylation of the ARE-binding protein DAZAP1 by ERK2 induces its dissociation from DAZ

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An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers

9 September 2017

1 reference

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A novel nucleocytoplasmic shuttling sequence of DAZAP1, a testis-abundant RNA-binding protein

9 September 2017

1 reference

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Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2.

9 September 2017

1 reference

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Silencers regulate both constitutive and alternative splicing events in mammals

9 September 2017

1 reference

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The RNA ligands for mouse proline-rich RNA-binding protein (mouse Prrp) contain two consensus sequences in separate loop structure

9 September 2017

1 reference

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RESCUE-ESE identifies candidate exonic splicing enhancers in vertebrate exons

9 September 2017

1 reference

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Broad specificity of SR (serine/arginine) proteins in the regulation of alternative splicing of pre-messenger RNA.

9 September 2017

1 reference

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Genomic variants in exons and introns: identifying the splicing spoilers

9 September 2017

1 reference

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Computational definition of sequence motifs governing constitutive exon splicing.

9 September 2017

1 reference

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The spliceosome: the most complex macromolecular machine in the cell?

9 September 2017

1 reference

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Pre-mRNA splicing: awash in a sea of proteins

9 September 2017

1 reference

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ESEfinder: A web resource to identify exonic splicing enhancers

9 September 2017

1 reference

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Mechanisms of alternative pre-messenger RNA splicing

9 September 2017

1 reference

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Pre-mRNA splicing and human disease

9 September 2017

1 reference

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Heterogeneous nuclear ribonucleoprotein particle A/B proteins and the control of alternative splicing of the mammalian heterogeneous nuclear ribonucleoprotein particle A1 pre-mRNA.

9 September 2017

1 reference

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Predictive identification of exonic splicing enhancers in human genes

9 September 2017

1 reference

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Messenger-RNA-binding proteins and the messages they carry

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Alternative splicing: multiple control mechanisms and involvement in human disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

A computational analysis of sequence features involved in recognition of short introns

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Sorting out the complexity of SR protein functions

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Multiple splicing defects in an intronic false exon

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

hnRNP complexes: composition, structure, and function

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

RNA binding specificity of hnRNP A1: significance of hnRNP A1 high-affinity binding sites in pre-mRNA splicing

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Regulation of fibronectin EDA exon alternative splicing: possible role of RNA secondary structure for enhancer display.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Exon inclusion is dependent on predictable exonic splicing enhancers

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

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

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

A BRCA1 nonsense mutation causes exon skipping

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

A pathway of sequential arginine-serine-rich domain-splicing signal interactions during mammalian spliceosome assembly

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12.

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2423284

hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing

21 August 2018

1 reference

12 December 2020

An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN

1 reference

12 December 2020

Splicing Factors Induce Cystic Fibrosis Transmembrane Regulator Exon 9 Skipping through a Nonevolutionary Conserved Intronic Element

1 reference

12 December 2020

A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy

1 reference

12 December 2020

An extended inhibitory context causes skipping of exon 7 of SMN2 in spinal muscular atrophy

1 reference

12 December 2020

Identifiers

DOI

10.1128/MCB.02253-07

1 reference

8 September 2017

1 reference

8 September 2017

1 reference