메뉴 건너뛰기




Volumn 95, Issue 8, 2000, Pages 2061-2067

Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0033899522     PISSN: 00029270     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9270(00)01020-0     Document Type: Article
Times cited : (106)

References (37)
  • 3
    • 0029929154 scopus 로고    scopus 로고
    • Role of the necrosis-fibrosis sequence in the pathogenesis of alcoholic chronic pancreatitis
    • (1996) Gastroenterology , vol.111 , pp. 258-259
    • Longnecker, D.S.1
  • 14
    • 84897363199 scopus 로고    scopus 로고
    • Entzuendliche Pankreaserkrankungen
    • Gebel M, ed. Gastroenterologische und hepatologische Sonographie. Berlin, Wien: Blackwell
    • (1999) , pp. 132-139
    • Ockenga, J.1
  • 18
    • 84897364434 scopus 로고    scopus 로고
    • Longitudinal long term study on the epidemiology and the humoral immune response in the pseudomonas aeruginosa infection in cystic fibrosis. Proceedings of the 17th European Cystic Fibrosis Conference 1991, Copenhagen 51
    • Kubesch, P.1    Jahnke, B.2    Roemling, U.3
  • 23
    • 2442727497 scopus 로고    scopus 로고
    • Screening for mutations of the cationic trypsinogen gene: Are they of relevance in chronic alcoholic pancreatitis?
    • (1999) Gut , vol.44 , pp. 413-416
    • Teich, N.1    Moessner, J.2    Keim, V.3
  • 24
    • 0028218460 scopus 로고
    • Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype
    • (1994) J Clin Invest , vol.93 , pp. 461-466
    • Veeze, H.J.1    Halley, D.J.2    Bijman, J.3
  • 36
    • 0030067573 scopus 로고    scopus 로고
    • Pancreatic dysfunction in cystic fibrosis occurs as a result of impairments in luminal pH, apical trafficking of zymogen granule membranes, and solubilization of secretory enzymes
    • (1996) Pancreas , vol.12 , pp. 1-9
    • Scheele, G.A.1    Fukuoka, S.I.2    Kern, H.F.3
  • 37
    • 0027730638 scopus 로고
    • Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR gene
    • (1993) Genomics , vol.18 , pp. 693-697
    • Cuppens, H.1    Marynen, P.2    De Boeck, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.