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Volumn 181, Issue 10, 2010, Pages 1017-1019

Bronchiectasis: A continuum of ion transport dysfunction or multiple hits?

Author keywords

[No Author keywords available]

Indexed keywords

EPITHELIAL SODIUM CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR PROTEIN, HUMAN;

EID: 77953280986     PISSN: 1073449X     EISSN: 15354970     Source Type: Journal    
DOI: 10.1164/rccm.201002-0284ED     Document Type: Editorial
Times cited : (17)

References (17)
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    • Boucher, R.C.1
  • 5
    • 55149107169 scopus 로고    scopus 로고
    • Update on gene modifiers in cystic fibrosis
    • Collaco JM, Cutting GR. Update on gene modifiers in cystic fibrosis. Curr Opin Pulm Med 2008;14:559-566.
    • (2008) Curr Opin Pulm Med , vol.14 , pp. 559-566
    • Collaco, J.M.1    Cutting, G.R.2
  • 9
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    • + absorption and absence of pulmonary disease in the airways of patients with Liddle's syndrome: Potential role of CFTR
    • abstract
    • + absorption and absence of pulmonary disease in the airways of patients with Liddle's syndrome: potential role of CFTR [abstract]. Pediatr Pulmonol 1998;Suppl. 17:217.
    • (1998) Pediatr Pulmonol , Issue.SUPPL. 17 , pp. 217
    • Stutts, M.J.1    Homolya, V.2    Robinson, J.3    Zhou, J.4    Boucher, R.C.5    Knowles, M.R.6
  • 11
    • 78049393958 scopus 로고    scopus 로고
    • Genetic deletion of MYD88-mediated signaling in ΔENaC over-expressing mice reduces airway neutrophilia but promotes spontaneous, mucus-associated bacterial infection
    • abstract
    • Livraghi A, Klem ER, Hudson EJ, Wilkinson KJ, Wolfgang MC, Boucher RC, Randell SH. Genetic deletion of MYD88-mediated signaling in ΔENaC over-expressing mice reduces airway neutrophilia but promotes spontaneous, mucus-associated bacterial infection [abstract]. Pediatr Pulmonol 2008;Suppl. 31:262.
    • (2008) Pediatr Pulmonol , Issue.SUPPL. 31 , pp. 262
    • Livraghi, A.1    Klem, E.R.2    Hudson, E.J.3    Wilkinson, K.J.4    Wolfgang, M.C.5    Boucher, R.C.6    Randell, S.H.7
  • 14
    • 0028309683 scopus 로고
    • Human airway ion transport. Part 1
    • Boucher RC. Human airway ion transport. Part 1. Am J Respir Crit Care Med 1994;150:271-281.
    • (1994) Am J Respir Crit Care Med , vol.150 , pp. 271-281
    • Boucher, R.C.1
  • 15
    • 33746255217 scopus 로고    scopus 로고
    • Use of 16S rRNA gene profiling by terminal restriction fragment length polymorphism analysis to compare bacterial communities in sputum and mouthwash samples from patients with cystic fibrosis
    • DOI 10.1128/JCM.02282-05
    • Rogers GB, Carroll MP, Serisier DJ, Hockey PM, Jones G, Kehagia V, Connett GJ, Bruce KD. Use of 16S rRNA gene profiling by terminal restriction fragment length polymorphism analysis to compare bacterial communities in sputum and mouthwash samples from patients with cystic fibrosis. J Clin Microbiol 2006;44:2601-2604. (Pubitemid 44092439)
    • (2006) Journal of Clinical Microbiology , vol.44 , Issue.7 , pp. 2601-2604
    • Rogers, G.B.1    Carroll, M.P.2    Serisier, D.J.3    Hockey, P.M.4    Jones, G.5    Kehagia, V.6    Connett, G.J.7    Bruce, K.D.8
  • 16
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    • A controlled trial of longterm inhaled hypertonic saline in patients with cystic fibrosis
    • National Hypertonic Saline in Cystic Fibrosis (NHSCF) Study Group
    • Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, Belousova EG, XuanW, Bye PTP; National Hypertonic Saline in Cystic Fibrosis (NHSCF) Study Group. A controlled trial of longterm inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006;354:229-240.
    • (2006) N Engl J Med , vol.354 , pp. 229-240
    • Elkins, M.R.1    Robinson, M.2    Rose, B.R.3    Harbour, C.4    Moriarty, C.P.5    Marks, G.B.6    Belousova, E.G.7    Xuan, W.8    Bye, P.T.P.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.