(Q48080544)

English

Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type Cftr gene expression.

scientific article published in August 1994

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scholarly article

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type Cftr gene expression. (English)

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

cystic fibrosis

0 references

author name string

J R Dorin

1

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

B J Stevenson

2

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

S Fleming

3

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

E W Alton

4

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

P Dickinson

5

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

D J Porteous

6

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

publication date

1 August 1994

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

number of pages

8

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

5

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

465-472

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

8

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

https://scigraph.springernature.com/pub.10.1007/bf00369314

0 references

Premature translation termination mediates triosephosphate isomerase mRNA degradation

1 reference

https://api.crossref.org/works/10.1007%2FBF00369314

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Nonsense codons in human beta-globin mRNA result in the production of mRNA degradation products

1 reference

https://api.crossref.org/works/10.1007%2FBF00369314

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF00369314

21 January 2018

Ion transport characteristics of the murine trachea and caecum

1 reference

https://api.crossref.org/works/10.1007%2FBF00369314

21 January 2018

Nonsense mutations in the dihydrofolate reductase gene affect RNA processing

1 reference

https://api.crossref.org/works/10.1007%2FBF00369314

21 January 2018

Correlation between genotype and phenotype in patients with cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

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A reappraisal of non-consensus mRNA splice sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and sequence analysis of the murine cDNA for the cystic fibrosis transmembrane conductance regulator

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable deletion of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis mouse with intestinal obstruction

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

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Cystic fibrosis in the mouse by targeted insertional mutagenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsense mutations and diminished mRNA levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and structural analysis of mouse gene and pseudogenes for proliferating cell nuclear antigen

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turbo cloning: a fast, efficient method for cloning PCR products and other blunt-ended DNA fragments into plasmids

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Production of a severe cystic fibrosis mutation in mice by gene targeting

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A targeted mutation reveals a role for N-myc in branching morphogenesis in the embryonic mouse lung

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An animal model for cystic fibrosis made by gene targeting

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The new mouse genetics: altering the genome by gene targeting

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal regulation of ion channels in cystic fibrosis epithelia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7949729

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00369314

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/7949729

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