Literature DB >> 8869207

Sodium/glucose cotransporter activity in cystic fibrosis.

P T Hardcastle, C J Taylor.   

Abstract

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Year:  1996        PMID： 8869207      PMCID： PMC1511621          DOI： 10.1136/adc.75.2.170

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  3 in total

1.  Preparation and properties of brush-border membrane vesicles from human small intestine.

Authors:  S P Shirazi-Beechey; A G Davies; K Tebbutt; J Dyer; A Ellis; C J Taylor; P Fairclough; R B Beechey
Journal:  Gastroenterology       Date:  1990-03       Impact factor: 22.682

2.  Glucose intolerance in cystic fibrosis.

Authors:  C J Taylor; P S Baxter; J Hardcastle; P T Hardcastle; J Goldhill
Journal:  Arch Dis Child       Date:  1989-05       Impact factor: 3.791

3.  CFTR as a cAMP-dependent regulator of sodium channels.

Authors:  M J Stutts; C M Canessa; J C Olsen; M Hamrick; J A Cohn; B C Rossier; R C Boucher
Journal:  Science       Date:  1995-08-11       Impact factor: 47.728
  3 in total
  1 in total

1.  Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect.

Authors:  Michael A Russo; Christoph Hogenauer; Stephen W Coates; Carol A Santa Ana; Jack L Porter; Randall L Rosenblatt; Michael Emmett; John S Fordtran
Journal:  J Clin Invest       Date:  2003-07       Impact factor: 14.808
  1 in total

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