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Literature DB >> 7682047

The cystic fibrosis transmembrane conductance regulator.

J R Riordan¹.

Abstract

Entities: Gene

Mesh：

Substances：

Year: 1993 PMID： 7682047 DOI： 10.1146/annurev.ph.55.030193.003141

Source DB: PubMed Journal: Annu Rev Physiol ISSN： 0066-4278 Impact factor: 19.318

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76 in total

1. Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions.

Authors: J R Davies; N Svitacheva; L Lannefors; R Kornfält; I Carlstedt
Journal: Biochem J Date: 1999-12-01 Impact factor: 3.857

2. The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.

Authors: R Schreiber; A Hopf; M Mall; R Greger; K Kunzelmann
Journal: Proc Natl Acad Sci U S A Date: 1999-04-27 Impact factor: 11.205

Review 3. Tubular fluid secretion in the seminiferous epithelium: ion transporters and aquaporins in Sertoli cells.

Authors: Luís Rato; Sílvia Socorro; José E B Cavaco; Pedro F Oliveira
Journal: J Membr Biol Date: 2010-08-10 Impact factor: 1.843

4. The H-loop in the second nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator is required for efficient chloride channel closing.

Authors: Monika Kloch; Michał Milewski; Ewa Nurowska; Beata Dworakowska; Garry R Cutting; Krzysztof Dołowy
Journal: Cell Physiol Biochem Date: 2010-01-12

5. CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity.

Authors: Stefania Monterisi; Maria Favia; Lorenzo Guerra; Rosa A Cardone; Domenico Marzulli; Stephan J Reshkin; Valeria Casavola; Manuela Zaccolo
Journal: J Cell Sci Date: 2012-02-02 Impact factor: 5.285

6. Activation mechanisms for the cystic fibrosis transmembrane conductance regulator protein involve direct binding of cAMP.

Authors: Malcolm M C Pereira; Jody Parker; Fiona L L Stratford; Margaret McPherson; Robert L Dormer
Journal: Biochem J Date: 2007-07-01 Impact factor: 3.857

The cystic fibrosis transmembrane conductance regulator.

1. Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions.

2. The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.

Review 3. Tubular fluid secretion in the seminiferous epithelium: ion transporters and aquaporins in Sertoli cells.

4. The H-loop in the second nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator is required for efficient chloride channel closing.

5. CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity.

6. Activation mechanisms for the cystic fibrosis transmembrane conductance regulator protein involve direct binding of cAMP.

7. The nature of amino acid 482 of human ABCG2 affects substrate transport and ATP hydrolysis but not substrate binding.

Review 8. CFTR and TNR-CFTR expression and function in the kidney.

Review 9. CFTR structure and function: is there a role in the kidney?

10. CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes.