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Journal Abstract Search

578 related items for PubMed ID: 1381723

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  • 2. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA.
    Chu CS, Trapnell BC, Curristin S, Cutting GR, Crystal RG.
    Nat Genet; 1993 Feb; 3(2):151-6. PubMed ID: 7684646
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  • 4. A 32-bp deletion (2991del32) in the cystic fibrosis gene associated with CFTR mRNA reduction.
    Dörk T, Will K, Grade K, Krawczak M, Tümmler B.
    Hum Mutat; 1994 Feb; 4(1):65-70. PubMed ID: 7524915
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  • 10. Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Strong TV, Smit LS, Nasr S, Wood DL, Cole JL, Iannuzzi MC, Stern RC, Collins FS.
    Hum Mutat; 1992 Feb; 1(5):380-7. PubMed ID: 1284540
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  • 11. A cystic fibrosis allele encoding missense mutations in both nucleotide binding folds of the cystic fibrosis transmembrane conductance regulator.
    Kälin N, Dörk T, Tümmler B.
    Hum Mutat; 1992 Feb; 1(3):204-10. PubMed ID: 1284535
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  • 13. [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].
    Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.
    Srp Arh Celok Lek; 2001 Feb; 129 Suppl 1():6-9. PubMed ID: 15637983
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  • 17. A frame-shift mutation in the cystic fibrosis gene.
    White MB, Amos J, Hsu JM, Gerrard B, Finn P, Dean M.
    Nature; 1990 Apr 12; 344(6267):665-7. PubMed ID: 1691449
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  • 19. CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium.
    Dupuit F, Kälin N, Brézillon S, Hinnrasky J, Tümmler B, Puchelle E.
    J Clin Invest; 1995 Sep 12; 96(3):1601-11. PubMed ID: 7544810
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  • 20. Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.
    Trapnell BC, Chu CS, Paakko PK, Banks TC, Yoshimura K, Ferrans VJ, Chernick MS, Crystal RG.
    Proc Natl Acad Sci U S A; 1991 Aug 01; 88(15):6565-9. PubMed ID: 1713683
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