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56 related items for PubMed ID: 946902
1. The chronically reserpinized rat as a possible animal model for cystic fibrosis. IV. The protein composition of pulmonary lavage fluid. Thompson FE, Quissell DO, Williams CH, Martinez JR. Pediatr Res; 1976 Jun; 10(6):632-5. PubMed ID: 946902 [Abstract] [Full Text] [Related]
2. The chronically reserpinized rat as an animal model for cystic fibrosis: I. Acute effect of isoproterenol and pilocarpine upon pulmonary lavage fluid. Mawhinney TP, Feather MS, Martinez JR, Barbero GJ. Pediatr Res; 1979 Jun; 13(6):760-3. PubMed ID: 481944 [No Abstract] [Full Text] [Related]
3. The chronically reserpinized rat as a possible model for cystic fibrosis. VI. Synergistic effects of isoproterenol on Ca++ and protein in the submaxillary gland. Wood DL, Martinez R. Pediatr Res; 1977 Jul; 11(7):827-32. PubMed ID: 876704 [Abstract] [Full Text] [Related]
4. Alterations of pancreatic growth and of GP-2 content in the reserpinized rat model of cystic fibrosis. Leblond FA, Morisset J, LeBel D. Pediatr Res; 1989 May; 25(5):478-81. PubMed ID: 2717264 [Abstract] [Full Text] [Related]
6. Chronically reserpinized rat as a model for cystic fibrosis: Na+ transport inhibitory effect in submaxillary saliva. Martinez JR, Martinez AM, Garrett L, Korman P. Pediatr Res; 1979 Oct; 13(10):1156-9. PubMed ID: 503644 [Abstract] [Full Text] [Related]
8. The chronically reserpinized rat as a possible model for cystic fibrosis. II. Comparison and cilioinhibitory effects of submaxillary saliva. Martinez JR, Adshead PC, Quissell DO, Barbero GJ. Pediatr Res; 1975 May; 9(5):470-5. PubMed ID: 1134845 [Abstract] [Full Text] [Related]
9. Reduced proteolysis of surfactant protein A and changes of the bronchoalveolar lavage fluid proteome by inhaled alpha 1-protease inhibitor in cystic fibrosis. Griese M, von Bredow C, Birrer P. Electrophoresis; 2001 Jan; 22(1):165-71. PubMed ID: 11197168 [Abstract] [Full Text] [Related]
10. The chronically reserpinized rat as a model for cystic fibrosis: abnormal Cl- transport as the basis for reduced salivary fluid secretion. Martinez JR, Cassity N. Pediatr Res; 1985 Jul; 19(7):711-6. PubMed ID: 4022678 [Abstract] [Full Text] [Related]
12. Cystic fibrosis. Carbohydrate metabolism in CF and in animal models for CF. Bardoń A. Acta Paediatr Scand Suppl; 1987 Jul; 332():1-30. PubMed ID: 3474861 [Abstract] [Full Text] [Related]
13. Essential fatty acid deficient rats in the study of cystic fibrosis: an X-ray microanalytical and ultrastructural study in chronically reserpinized rats. Hjelte L, Strandvik B, Müller RM, Sagström S, Roomans GM. J Submicrosc Cytol Pathol; 1990 Jul; 22(3):409-14. PubMed ID: 2390763 [Abstract] [Full Text] [Related]
14. Plasma immunoreactive cationic trypsin(ogen) pattern in reserpinized rat model of cystic fibrosis. Resemblance to humans. Weizman Z. Dig Dis Sci; 1996 May; 41(5):853-8. PubMed ID: 8625754 [Abstract] [Full Text] [Related]
15. The chronically reserpinized rat as a possible model for cystic fibrosis. VII. Alterations in the secretory response to cholecystokinin and to secretin from the pancreas in vivo. Perlmutter J, Martinez JR. Pediatr Res; 1978 Mar; 12(3):188-94. PubMed ID: 643388 [No Abstract] [Full Text] [Related]