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Journal Abstract Search
89 related items for PubMed ID: 130092
1. Cystic fibrosis. A dilemma in the metabolic pathogenesis of genetic disease. Changus JE, Pitot HC. Arch Pathol Lab Med; 1976 Jan; 100(1):7-11. PubMed ID: 130092 [Abstract] [Full Text] [Related]
2. Cystic fibrosis. Carbohydrate metabolism in CF and in animal models for CF. Bardoń A. Acta Paediatr Scand Suppl; 1987 Jan; 332():1-30. PubMed ID: 3474861 [Abstract] [Full Text] [Related]
3. Expression of the cystic fibrosis genotype in cultured somatic cells. Danes BS. Tex Rep Biol Med; 1976 Jan; 34(1):135-50. PubMed ID: 63153 [Abstract] [Full Text] [Related]
4. Cystic fibrosis - ultrastructural and microanalytical studies. Roomans GM, von Euler AM, Müller RM. Scan Electron Microsc; 1983 Jan; (Pt 2):697-712. PubMed ID: 6356334 [Abstract] [Full Text] [Related]
5. Cystic fibrosis. In vitro and in vivo studies on the biochemical background to the pathogenesis. Ceder O. Acta Paediatr Scand Suppl; 1983 Jan; 309():1-47. PubMed ID: 6581681 [Abstract] [Full Text] [Related]
6. Dynamics of protein and fluid secretion from the major salivary glands of rat: relevance of research findings to clinically observed defective secretion in cystic fibrosis. Shori DK, Asking B. Pflugers Arch; 2001 Jan; 443 Suppl 1():S11-6. PubMed ID: 11845296 [Abstract] [Full Text] [Related]
8. Research in cystic fibrosis (second of three parts). di Sant'Agnese PA, Davis PB. N Engl J Med; 1976 Sep 02; 295(10):534-41. PubMed ID: 781536 [No Abstract] [Full Text] [Related]
10. Differentiation of immortalized epithelial cells derived from cystic fibrosis airway submucosal glands. Chopra DP, Reddy L, Gupta SK, Wan L, Mathieu PA, Shoemaker RL, Rhim JS. In Vitro Cell Dev Biol Anim; 1994 Aug 02; 30A(8):539-46. PubMed ID: 7527286 [Abstract] [Full Text] [Related]
11. Studies on the synthesis of plasma membrane proteins of fibroblasts from patients with cystic fibrosis. Changus JE, Quissell DO, Sukup MR, Pitot HC. Am J Pathol; 1975 Aug 02; 80(2):317-28. PubMed ID: 1163632 [Abstract] [Full Text] [Related]
12. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients. Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C. Hepatology; 1999 Jun 02; 29(6):1624-34. PubMed ID: 10347100 [Abstract] [Full Text] [Related]
13. Studies on ciliary dyskinesia factor in cystic fibrosis. 3. Skin fibroblasts and cultured amniotic fluid cells. Beratis NG, Conover JH, Conod EJ, Bonforte RJ, Hirschhorn K. Pediatr Res; 1973 Dec 02; 7(12):958-64. PubMed ID: 4753049 [No Abstract] [Full Text] [Related]
14. [Current views on the etiopathogenesis of mucoviscidosis and on the characterization of the defect]. Mengoli C. Recenti Prog Med; 1971 Mar 02; 50(3):215-33. PubMed ID: 4255261 [No Abstract] [Full Text] [Related]
15. Acid mucins in human intestinal goblet cells. Morrissey SM, Tymvios MC. J Pathol; 1978 Dec 02; 126(4):197-208. PubMed ID: 748514 [Abstract] [Full Text] [Related]
17. Sulphation of the salivary mucin MG1 (MUC-5B) is not correlated to the degree of its sialylation and is unaffected by cystic fibrosis. Shori DK, Kariyawasam HH, Knight RA, Hodson ME, Genter T, Hansen J, Koch C, Kalogeridis A. Pflugers Arch; 2001 Dec 02; 443 Suppl 1():S50-4. PubMed ID: 11845303 [Abstract] [Full Text] [Related]
18. Salivary secretion assay for drug efficacy for cystic fibrosis in mice. Best JA, Quinton PM. Exp Physiol; 2005 Mar 02; 90(2):189-93. PubMed ID: 15572461 [Abstract] [Full Text] [Related]
19. Dysfunction of the non-neuronal cholinergic system in the airways and blood cells of patients with cystic fibrosis. Wessler I, Bittinger F, Kamin W, Zepp F, Meyer E, Schad A, Kirkpatrick CJ. Life Sci; 2007 May 30; 80(24-25):2253-8. PubMed ID: 17346753 [Abstract] [Full Text] [Related]