(Q52231074)

27 April 2018

title

Disruption of the cystic fibrosis transmembrane conductance regulator gene in embryonic stem cells by gene targeting. (English)

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27 April 2018

main subject

cystic fibrosis

0 references

transmembrane protein

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author

William H. Colledge

6

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27 April 2018

author name string

R Ratcliff

1

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27 April 2018

M J Evans

2

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27 April 2018

J Doran

3

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27 April 2018

B J Wainwright

4

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27 April 2018

R Williamson

5

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27 April 2018

publication date

1 July 1992

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27 April 2018

published in

Transgenic Research

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27 April 2018

volume

1

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27 April 2018

issue

4

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27 April 2018

page(s)

177-181

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27 April 2018

Testing an "in-out" targeting procedure for making subtle genomic modifications in mouse embryonic stem cells

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF02522536

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

1 reference

12 December 2020

An efficient salt-chloroform extraction of DNA from blood and tissues

1 reference

12 December 2020

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

1 reference

12 December 2020

Altering the genome by homologous recombination

1 reference

12 December 2020

Targeted homologous recombination at the endogenous adenine phosphoribosyltransferase locus in Chinese hamster cells

1 reference

12 December 2020

Phosphorylation fails to activate chloride channels from cystic fibrosis airway cells

1 reference

12 December 2020

Effect of Deleting the R Domain on CFTR-Generated Chloride Channels

1 reference

12 December 2020

A frame-shift mutation in the cystic fibrosis gene.

1 reference

12 December 2020

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

1 reference

12 December 2020

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

1 reference

12 December 2020

Introduction of a subtle mutation into the Hox-2.6 locus in embryonic stem cells

1 reference

12 December 2020

Chloride and potassium channels in cystic fibrosis airway epithelia

1 reference

12 December 2020

Recombinant fragment assay for gene targetting based on the polymerase chain reaction

1 reference

12 December 2020

Potential for genetic manipulation of mammals

1 reference

12 December 2020

Identification of the cystic fibrosis gene: genetic analysis

1 reference

12 December 2020

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

1 reference

12 December 2020

Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells

1 reference

12 December 2020

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

1 reference

12 December 2020

Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes

1 reference

12 December 2020

Regulatory elements in the introns of the human HPRT gene are necessary for its expression in embryonic stem cells

1 reference

12 December 2020

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02522536

1 reference

27 April 2018

1 reference

27 April 2018