about
Defective beta adrenergic response of cystic fibrosis sweat glands in vivo and in vitroRole of adherence in the pathogenesis of Pseudomonas aeruginosa lung infection in cystic fibrosis patients.Role of an alginate lyase for alginate transport in mucoid Pseudomonas aeruginosaPartial purification and characterization of a polymannuronic acid depolymerase produced by a mucoid strain of Pseudomonas aeruginosa isolated from a patient with cystic fibrosisThe immunoglobulin G subclass composition of immune complexes in cystic fibrosis. Implications for the pathogenesis of the Pseudomonas lung lesionEnvironmental factors and diseases of the pancreas.Needs for animal models of human diseases of the respiratory systemCloning and expression in Pseudomonas aeruginosa of a gene involved in the production of alginate.Locus of the Pseudomonas aeruginosa toxin A gene.Selection of nonmucoid derivatives of mucoid Pseudomonas aeruginosa is strongly influenced by the level of iron in the culture medium.Induction of phagocytic inhibitory activity in cats with chronic Pseudomonas aeruginosa pulmonary infectionGenetic mapping of chromosomal determinants for the production of the exopolysaccharide alginate in a Pseudomonas aeruginosa cystic fibrosis isolate.Serum bactericidal effect on Pseudomonas aeruginosa isolates from cystic fibrosis patients.Alginate synthesis by Pseudomonas aeruginosa: a key pathogenic factor in chronic pulmonary infections of cystic fibrosis patients.Impaired beta adrenergic receptor binding and function in cystic fibrosis neutrophilsAvirulence and altered physiological properties of cystic fibrosis strains of Pseudomonas aeruginosa.In vitro evidence that human airway lysozyme is cleaved and inactivated by Pseudomonas aeruginosa elastase and not by human leukocyte elastaseMitrochondrial NADH dehydrogenase in cystic fibrosis.Epidemiology of Burkholderia cepacia infection in patients with cystic fibrosis: analysis by randomly amplified polymorphic DNA fingerprinting.Hypochlorite scavenging by Pseudomonas aeruginosa alginate.Flagella and motility alterations in Pseudomonas aeruginosa strains from patients with cystic fibrosis: relationship to patient clinical condition.Detection by enzyme-linked immunosorbent assays of antibody specific for Pseudomonas proteases and exotoxin A in sera from cystic fibrosis patients.Protease phenotypes of Pseudomonas aeruginosa isolated from patients with cystic fibrosis.Immunohistopathologic localization of Pseudomonas aeruginosa in lungs from patients with cystic fibrosis. Implications for the pathogenesis of progressive lung deterioration.
P2860
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P2860
description
1976 nî lūn-bûn
@nan
1976年の論文
@ja
1976年学术文章
@wuu
1976年学术文章
@zh-cn
1976年学术文章
@zh-hans
1976年学术文章
@zh-my
1976年学术文章
@zh-sg
1976年學術文章
@yue
1976年學術文章
@zh
1976年學術文章
@zh-hant
name
Research in cystic fibrosis (third of three parts).
@en
Research in cystic fibrosis
@nl
type
label
Research in cystic fibrosis (third of three parts).
@en
Research in cystic fibrosis
@nl
prefLabel
Research in cystic fibrosis (third of three parts).
@en
Research in cystic fibrosis
@nl
P1476
Research in cystic fibrosis (third of three parts).
@en
P2093
di Sant'Agnese PA
P304
P356
10.1056/NEJM197609092951105
P407
P577
1976-09-01T00:00:00Z