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Volumn 3, Issue SUPPL. 2, 2004, Pages 159-163

Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers

Author keywords

CFTR; Classification of cystic fibrosis; Epithelial chloride secretion; Intestinal epithelium; Ussing chamber

Indexed keywords

ANION CHANNEL; BICARBONATE; CHLORIDE ION; POTASSIUM ION; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 11044232030     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2004.05.034     Document Type: Article
Times cited : (72)

References (11)
  • 1
    • 0025772974 scopus 로고
    • Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis
    • Veeze H.J. Sinaasappel M. Bijman J. Bouquet J. De Jonge H.R. Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis Gastroenterology 101 1991 398-401
    • (1991) Gastroenterology , vol.101 , pp. 398-401
    • Veeze, H.J.1    Sinaasappel, M.2    Bijman, J.3    Bouquet, J.4    De Jonge, H.R.5
  • 3
    • 0034234755 scopus 로고    scopus 로고
    • Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis
    • Bronsveld I. Mekus F. Bijman J. Ballmann M. Greipel J. Hundrieser J. et al. Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis Gastroenterology 119 2000 32-40
    • (2000) Gastroenterology , vol.119 , pp. 32-40
    • Bronsveld, I.1    Mekus, F.2    Bijman, J.3    Ballmann, M.4    Greipel, J.5    Hundrieser, J.6
  • 4
    • 0035213684 scopus 로고    scopus 로고
    • Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings
    • Bronsveld I. Mekus F. Bijman J. Ballmann M. De Jonge H.R. Laabs U. et al. Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings J. Clin. Invest. 108 2001 1705-1715
    • (2001) J. Clin. Invest. , vol.108 , pp. 1705-1715
    • Bronsveld, I.1    Mekus, F.2    Bijman, J.3    Ballmann, M.4    De Jonge, H.R.5    Laabs, U.6
  • 5
    • 11044226517 scopus 로고    scopus 로고
    • Transepithelial measurements using the Ussing chamber
    • Hug M. Transepithelial measurements using the Ussing chamber Eur. Work. Group CFTR Expr. Newsl. 2 2 2001 1-6
    • (2001) Eur. Work. Group CFTR Expr. Newsl. , vol.2 , Issue.2 , pp. 1-6
    • Hug, M.1
  • 9
    • 0036471320 scopus 로고    scopus 로고
    • The severe G480C cystic fibrosis mutation when replicated in the mouse demonstrates mistrafficking, normal survival and organ specific bioelectrics
    • Dickinson P. Smith S.N. Porteous D.J. Willemsen R. De Jonge H.R. Alton E.W.F.W. et al. The severe G480C cystic fibrosis mutation when replicated in the mouse demonstrates mistrafficking, normal survival and organ specific bioelectrics Hum. Mol. Genet. 11 2002 243-251
    • (2002) Hum. Mol. Genet. , vol.11 , pp. 243-251
    • Dickinson, P.1    Smith, S.N.2    Porteous, D.J.3    Willemsen, R.4    De Jonge, H.R.5    Alton, E.W.F.W.6
  • 10
    • 0033646566 scopus 로고    scopus 로고
    • Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: An evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion
    • Högenauer C. Santa Ana C.A. Porter J.L. Millard M. Gelfand A. Rosenblatt R.L. Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: An evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion Am. J. Hum. Genet. 67 2000 1422-1427
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 1422-1427
    • Högenauer, C.1    Santa Ana, C.A.2    Porter, J.L.3    Millard, M.4    Gelfand, A.5    Rosenblatt, R.L.6
  • 11
    • 11044231602 scopus 로고    scopus 로고
    • Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis
    • Mall M. Hirtz S. Gonska T. Kunzelmann K. Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis J. Cystic Fibrosis 3 2004 165-169
    • (2004) J. Cystic Fibrosis , vol.3 , pp. 165-169
    • Mall, M.1    Hirtz, S.2    Gonska, T.3    Kunzelmann, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.