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Journal Abstract Search

89 related items for PubMed ID: 130092

  • 21. Specificity of an isolated salivary factor material to cystic fibrosis.
    Impero JE, Harrison GM, Nelson TE.
    Pediatr Res; 1981 Jun; 15(6):940-4. PubMed ID: 6165957
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  • 22. Evaluation of laboratory tests proposed as aids for the diagnosis of cystic fibrosis.
    Rennert OM.
    Ann Clin Lab Sci (1971); 1973 Jun; 3(1):1-12. PubMed ID: 4570835
    [No Abstract] [Full Text] [Related]

  • 23. [Are there mucoviscidosis specific humoral factors? 1: Properties, prevalence, preparation, formation].
    Hein J.
    Z Erkr Atmungsorgane; 1985 Jun; 164(1):19-24. PubMed ID: 2580397
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  • 24. Gene delivery to human sweat glands: a model for cystic fibrosis gene therapy.
    Lee H, Koehler DR, Pang CY, Levine RH, Ng P, Palmer DJ, Quinton PM, Hu J.
    Gene Ther; 2005 Dec; 12(24):1752-60. PubMed ID: 16034452
    [Abstract] [Full Text] [Related]

  • 25. Altered sialyl- and fucosyl-linkage on mucins in cystic fibrosis patients promotes formation of the sialyl-Lewis X determinant on salivary MUC-5B and MUC-7.
    Shori DK, Genter T, Hansen J, Koch C, Wyatt H, Kariyawasam HH, Knight RA, Hodson ME, Kalogeridis A, Tsanakas I.
    Pflugers Arch; 2001 Dec; 443 Suppl 1():S55-61. PubMed ID: 11845304
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  • 26. Electron microscopy and microchemical analysis of cystic fibrosis diploid fibroblasts in vitro.
    Baur PS, Bolton WE, Barranco SC.
    Tex Rep Biol Med; 1976 Dec; 34(1):114-34. PubMed ID: 996784
    [Abstract] [Full Text] [Related]

  • 27. Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis.
    Farrell PM, Koscik RE.
    Pediatrics; 1996 Apr; 97(4):524-8. PubMed ID: 8632940
    [Abstract] [Full Text] [Related]

  • 28. Proteomic analysis of nasal cells from cystic fibrosis patients and non-cystic fibrosis control individuals: search for novel biomarkers of cystic fibrosis lung disease.
    Roxo-Rosa M, da Costa G, Luider TM, Scholte BJ, Coelho AV, Amaral MD, Penque D.
    Proteomics; 2006 Apr; 6(7):2314-25. PubMed ID: 16518875
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  • 31. Iontophoretic beta-adrenergic stimulation of human sweat glands: possible assay for cystic fibrosis transmembrane conductance regulator activity in vivo.
    Shamsuddin AK, Reddy MM, Quinton PM.
    Exp Physiol; 2008 Aug; 93(8):969-81. PubMed ID: 18441335
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  • 35. A cystic fibrosis phenotype in cells cultured from sweat gland secretory coil. Altered kinetics of 36Cl efflux.
    Wood LC, Neufeld EF.
    J Biol Chem; 1990 Aug 05; 265(22):12796-800. PubMed ID: 2376576
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  • 36. Cystic fibrosis: isolation and physical properties of a salivary cystic fibrosis factor.
    Impero JE, Harrison GM, Nelson TE.
    Pediatr Res; 1978 Feb 05; 12(2):108-14. PubMed ID: 25407
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  • 39. Use of salivary levels to predict clearance of caffeine in patients with cystic fibrosis.
    Bianchetti MG, Kraemer R, Passweg J, Jost J, Preisig R.
    J Pediatr Gastroenterol Nutr; 1988 Feb 05; 7(5):688-93. PubMed ID: 3183872
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  • 40. Genetic effects on the longevity of cultured human fibroblasts. IV. Enhanced growth potential of cystic fibrosis cells.
    Thompson KV, Holliday R.
    Gerontology; 1983 Feb 05; 29(2):97-101. PubMed ID: 6840565
    [Abstract] [Full Text] [Related]

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