(Q51276789)

2 April 2018

title

TDP43 depletion rescues aberrant CFTR exon 9 skipping. (English)

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2 April 2018

author

Franco Pagani

series ordinal

2

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2 April 2018

author name string

Youhna M Ayala

series ordinal

1

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2 April 2018

Francisco E Baralle

series ordinal

3

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2 April 2018

language of work or name

English

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publication date

26 January 2006

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2 April 2018

published in

FEBS Letters

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2 April 2018

volume

580

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2 April 2018

issue

5

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2 April 2018

page(s)

1339-1344

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2 April 2018

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

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Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

An intronic polypyrimidine-rich element downstream of the donor site modulates cystic fibrosis transmembrane conductance regulator exon 9 alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Structural diversity and functional implications of the eukaryotic TDP gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: a functional link with disease penetrance

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

Functional analysis of cis-acting elements regulating the alternative splicing of human CFTR exon 9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

A variable dinucleotide repeat in the CFTR gene contributes to phenotype diversity by forming RNA secondary structures that alter splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.01.052

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

21 January 2018

1 reference

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10.1016/J.FEBSLET.2006.01.052

21 January 2018

Identifiers

DOI

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2 April 2018

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2 April 2018