Molecular Biology of Cystic Fibrosis-Reference-Cited by-同舟云学术

Molecular Biology of Cystic Fibrosis

Published:1993 Issue: Volume: Page:33-68
ISSN:
Container-title:Molecular Genetic Medicine
language:
Short-container-title:

Author:

Drumm Mitchell L.,Collins Francis S.

Publisher

Elsevier

Reference73 articles.

1. Recombinant human DNase inhalation in normal subjects and patients with cystic fibrosis.);Aitken;Am. Med. Assoc.,1992

2. Bacterial periplasmic permeases belong to a family of transport proteins operating from Escherichia coli to human traffic ATPases;Ames;FEMS Microbiol. Rev.,1990

3. Cystic fibrosis of the pancreas and its relation to celiac disease: A clinical and pathological study;Anderson;Am. J. Dis. Child.,1938

4. Nucleoside triphosphates are required to open the CFTR chloride channel;Anderson;Cell (Cambridge, Mass.),1991

5. Congenital absence of the vas deferens: A primarily genital form of cystic fibrosis;Anguiano;J. Am. Med. Assoc.,1992

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