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Literature DB >> 7515441

Cystic fibrosis gene update.

A Cuthbert¹.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 1994 PMID： 7515441 PMCID： PMC1294257

Source DB: PubMed Journal: J R Soc Med ISSN： 0141-0768 Impact factor: 5.344

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21 in total

1. CFTR protein expression in primary and cultured epithelia.

Authors: P L Zeitlin; I Crawford; L Lu; S Woel; M E Cohen; M Donowitz; M H Montrose; A Hamosh; G R Cutting; D Gruenert
Journal: Proc Natl Acad Sci U S A Date: 1992-01-01 Impact factor: 11.205

2. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis.

Authors: S H Cheng; R J Gregory; J Marshall; S Paul; D W Souza; G A White; C R O'Riordan; A E Smith
Journal: Cell Date: 1990-11-16 Impact factor: 41.582

3. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.

Authors: W Dalemans; P Barbry; G Champigny; S Jallat; K Dott; D Dreyer; R G Crystal; A Pavirani; J P Lecocq; M Lazdunski
Journal: Nature Date: 1991 Dec 19-26 Impact factor: 49.962

4. Identification of the cystic fibrosis gene: genetic analysis.

Authors: B Kerem; J M Rommens; J A Buchanan; D Markiewicz; T K Cox; A Chakravarti; M Buchwald; L C Tsui
Journal: Science Date: 1989-09-08 Impact factor: 47.728

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

Authors: D P Rich; M P Anderson; R J Gregory; S H Cheng; S Paul; D M Jefferson; J D McCann; K W Klinger; A E Smith; M J Welsh
Journal: Nature Date: 1990-09-27 Impact factor: 49.962

1. Faster activation of polymorphonuclear neutrophils in resistant mice during early innate response to Pseudomonas aeruginosa lung infection.

Authors: P Ø Jensen; C Moser; O Kobayashi; H P Hougen; A Kharazmi; N Høiby
Journal: Clin Exp Immunol Date: 2004-09 Impact factor: 4.330

1 in total

Cystic fibrosis gene update.

1. CFTR protein expression in primary and cultured epithelia.

2. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis.

3. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.

4. Identification of the cystic fibrosis gene: genetic analysis.

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

6. Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

7. Demonstration that CFTR is a chloride channel by alteration of its anion selectivity.

8. Effect of deleting the R domain on CFTR-generated chloride channels.

9. Cystic fibrosis in the mouse by targeted insertional mutagenesis.

10. Identification of the cystic fibrosis gene: chromosome walking and jumping.

1. Faster activation of polymorphonuclear neutrophils in resistant mice during early innate response to Pseudomonas aeruginosa lung infection.