메뉴 건너뛰기




Volumn 188, Issue 11, 2013, Pages 1376-1378

Basic research funding by philanthropic organizations: A case in point

Author keywords

[No Author keywords available]

Indexed keywords

4 PHENYLBUTYRIC ACID; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; IVACAFTOR; KALYEDO; LUMACAFTOR; MUTANT PROTEIN; UNCLASSIFIED DRUG;

EID: 84890012305     PISSN: 1073449X     EISSN: 15354970     Source Type: Journal    
DOI: 10.1164/rccm.201307-1275LE     Document Type: Letter
Times cited : (3)

References (10)
  • 6
    • 0015503810 scopus 로고
    • Nucleotide sequence of the gene coding for the bacteriophage MS2 coat protein
    • Min Jou W, Haegeman G, Ysebaert M, Fiers W. Nucleotide sequence of the gene coding for the bacteriophage MS2 coat protein. Nature 1972; 237:82-88.
    • (1972) Nature , vol.237 , pp. 82-88
    • Min Jou, W.1    Haegeman, G.2    Ysebaert, M.3    Fiers, W.4
  • 7
    • 0025310336 scopus 로고
    • A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein
    • Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui LC, Antonarakis SE, Kazazian HH Jr. A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. Nature 1990;346:366-369.
    • (1990) Nature , vol.346 , pp. 366-369
    • Cutting, G.R.1    Kasch, L.M.2    Rosenstein, B.J.3    Zielenski, J.4    Tsui, L.C.5    Antonarakis, S.E.6    Kazazian Jr., H.H.7
  • 8
    • 0026725724 scopus 로고
    • Cystic fibrosis patients bearing both the common missense mutation GlyAsp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus
    • Hamosh A, King TM, Rosenstein BJ, Corey M, Levison H, Durie P, Tsui LC, McIntosh I, Keston M, Brock DJ, et al. Cystic fibrosis patients bearing both the common missense mutation GlyAsp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus. Am J Hum Genet 1992;51:245-250.
    • (1992) Am J Hum Genet , vol.51 , pp. 245-250
    • Hamosh, A.1    King, T.M.2    Rosenstein, B.J.3    Corey, M.4    Levison, H.5    Durie, P.6    Tsui, L.C.7    McIntosh, I.8    Keston, M.9    Brock, D.J.10
  • 9
    • 0030809817 scopus 로고    scopus 로고
    • In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR
    • Rubenstein RC, Egan ME, Zeitlin PL. In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR. J Clin Invest 1997;100:2457-2465.
    • (1997) J Clin Invest , vol.100 , pp. 2457-2465
    • Rubenstein, R.C.1    Egan, M.E.2    Zeitlin, P.L.3
  • 10
    • 44649197130 scopus 로고    scopus 로고
    • Front-runners for pharmacotherapeutic correction of the airway ion transport defect in cystic fibrosis
    • Clunes MT, Boucher RC. Front-runners for pharmacotherapeutic correction of the airway ion transport defect in cystic fibrosis. Curr Opin Pharmacol 2008;8:292-299.
    • (2008) Curr Opin Pharmacol , vol.8 , pp. 292-299
    • Clunes, M.T.1    Boucher, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.