Literature DB >> 8869353

A mild variant of cystic fibrosis.

E W Alton1.   

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Year:  1996        PMID： 8869353      PMCID： PMC1090707          DOI： 10.1136/thx.51.suppl_2.s51

Source DB:  PubMed          Journal:  Thorax        ISSN： 0040-6376            Impact factor:   9.139


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  15 in total

1.  Enhanced intestinal glucose and alanine transport in cystic fibrosis.

Authors:  P Baxter; J Goldhill; J Hardcastle; P T Hardcastle; C J Taylor
Journal:  Gut       Date:  1990-07       Impact factor: 23.059

Review 2.  Electrolyte transport by airway epithelia.

Authors:  M J Welsh
Journal:  Physiol Rev       Date:  1987-10       Impact factor: 37.312

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

Authors:  J R Riordan; J M Rommens; B Kerem; N Alon; R Rozmahel; Z Grzelczak; J Zielenski; S Lok; N Plavsic; J L Chou
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

4.  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

5.  The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment.

Authors:  Y Yang; S Janich; J A Cohn; J M Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

6.  Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

Authors:  G B Pier; M Grout; T S Zaidi; J C Olsen; L G Johnson; J R Yankaskas; J B Goldberg
Journal:  Science       Date:  1996-01-05       Impact factor: 47.728

Review 7.  Delayed diagnosis of cystic fibrosis in children with a rare genotype (delta F508/R117H).

Authors:  D Fitzgerald; P Van Asperen; R Henry; D Waters; M Freelander; M Wilson; B Wilcken; K Gaskin
Journal:  J Paediatr Child Health       Date:  1995-06       Impact factor: 1.954

8.  Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.

Authors:  M Knowles; J Gatzy; R Boucher
Journal:  N Engl J Med       Date:  1981-12-17       Impact factor: 91.245

9.  Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype.

Authors:  H J Veeze; D J Halley; J Bijman; J C de Jongste; H R de Jonge; M Sinaasappel
Journal:  J Clin Invest       Date:  1994-02       Impact factor: 14.808

10.  Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

Authors:  J J Smith; S M Travis; E P Greenberg; M J Welsh
Journal:  Cell       Date:  1996-04-19       Impact factor: 41.582
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