(Q72081738)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7684646%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7684646%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference

Chu CS

1

1 reference

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23 October 2019

Trapnell BC

2

1 reference

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23 October 2019

Curristin S

3

1 reference

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23 October 2019

Cutting GR

4

1 reference

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23 October 2019

Crystal RG

5

1 reference

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23 October 2019

publication date

1 February 1993

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23 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7684646%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

volume

3

1 reference

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23 October 2019

page(s)

151-156

1 reference

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23 October 2019

issue

2

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng0293-151

23 October 2019

exact match

0 references

cites work

Identification of the cystic fibrosis gene: chromosome walking and jumping

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7 January 2021

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

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7 January 2021

Identification of the cystic fibrosis gene: genetic analysis

1 reference

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7 January 2021

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

1 reference

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7 January 2021

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

1 reference

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7 January 2021

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

1 reference

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7 January 2021

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

1 reference

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7 January 2021

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

1 reference

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7 January 2021

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7 January 2021

Cystic fibrosis: a disease in electrolyte transport.

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7 January 2021

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

1 reference

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7 January 2021

Novel function discovered for the cystic fibrosis gene

1 reference

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7 January 2021

Expression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Down-regulation of cystic fibrosis transmembrane conductance regulator gene expression by agents that modulate intracellular divalent cations

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manif

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephew

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Splicing of messenger RNA precursors

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Messenger RNA Splicing in Yeast: Clues to Why the Spliceosome Is a Ribonucleoprotein

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Pre-mRNA splicing in yeast

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Scanning from an independently specified branch point defines the 3' splice site of mammalian introns

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

The organization of 3' splice-site sequences in mammalian introns

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Intron sequences involved in lariat formation during pre-mRNA splicing.

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Role of the 3' splice site consensus sequence in mammalian pre-mRNA splicing.

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Ribonucleoprotein complex formation during pre-mRNA splicing in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

A U-rich tract enhances usage of an alternative 3′ splice site in yeast

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Identification, purification, and biochemical characterization of U2 small nuclear ribonucleoprotein auxiliary factor

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Identification and purification of a 62,000-dalton protein that binds specifically to the polypyrimidine tract of introns

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

A 62,000 molecular weight spliceosome protein crosslinks to the intron polypyrimidine tract

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Patterns of polymorphism and linkage disequilibrium for cystic fibrosis

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingover.

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2FNG0293-151

7 January 2021

Identifiers

DOI

10.1038/NG0293-151

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7684646%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference