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Volumn 1, Issue 7, 1995, Pages 703-705

Protection against bronchial asthma by CFTR Δf508 mutation: A heterozygote advantage in cystic fibrosis

Author keywords

[No Author keywords available]

Indexed keywords

ANTIINFLAMMATORY AGENT; BRONCHODILATING AGENT; CHLORIDE; CYCLIC AMP; DNA; PHENYLALANINE; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0029016718     PISSN: 10788956     EISSN: 1546170X     Source Type: Journal    
DOI: 10.1038/nm0795-703     Document Type: Article
Times cited : (115)

References (15)
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  • 3
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  • 4
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    • Pulmonary abnormalities in obligate heterozygotes for cystic fibrosis
    • Davis, P.B. and Vargo, K. Pulmonary abnormalities in obligate heterozygotes for cystic fibrosis. Thorax 42, 120-125 (1987).
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    • Davis, P.B.1    Vargo, K.2
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    • Heterozygotes for cystic fibrosis: Models for study of airway and autonomic reactivity
    • Davis, P.B. and Byard, P.J. Heterozygotes for cystic fibrosis: Models for study of airway and autonomic reactivity. J. appl. Physiol. 66, 2124-2128 (1989).
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    • American Thoracic Society
    • American Thoracic Society. Standards for the diagnosis and care of patients with chronic obstructive pulmonary disease (COPD) and asthma. Am. Rev. resp. Dis. 136, 225-244 (1977).
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    • Guidelines for the diagnosis and management of asthma, National Institutes of Health, Bethesda, MD
    • National Asthma Education Program. Guidelines for the diagnosis and management of asthma. (National Institutes of Health, Bethesda, MD, 1991. DHMS publication no. NIH 91-3042).
    • (1991) DHMS Publication No. NIH 91-3042
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    • Friedman, K.J.1    Highsmith, W.E.2    Silverman, L.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.