These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
131 related articles for article (PubMed ID: 905823)
1. Bovine protoporphyria: the first nonhuman model of this hereditary photosensitizing disease. RUTH GR; Schwartz S; Stephenson B Science; 1977 Oct; 198(4313):199-201. PubMed ID: 905823 [TBL] [Abstract][Full Text] [Related]
2. Protoporphyria in Limousin cattle. Healy PJ; Camilleri L; Poulos V; Hart KG; Kemp BJ; Moore RE; Dooley J; Warner M Aust Vet J; 1992 Jun; 69(6):144-5. PubMed ID: 1642600 [No Abstract] [Full Text] [Related]
3. Bovine protoporphyria: documentation of autosomal recessive inheritance and comparison with the human disease through measurement of heme synthase activity. Bloomer JR; Morton KO; Reuter RJ; Ruth GR Am J Hum Genet; 1982 Mar; 34(2):322-30. PubMed ID: 7072720 [TBL] [Abstract][Full Text] [Related]
4. Observation on bovine congenital erythrocytic protoporphyria in the blonde d'Aquitaine breed. Schelcher F; Delverdier M; Bezille P; Cabanie P; Espinasse J Vet Rec; 1991 Nov; 129(18):403-7. PubMed ID: 1767483 [TBL] [Abstract][Full Text] [Related]
5. Fatal liver failure in protoporphyria. Synergism between ethanol excess and the genetic defect. Bonkovsky HL; Schned AR Gastroenterology; 1986 Jan; 90(1):191-201. PubMed ID: 3940245 [TBL] [Abstract][Full Text] [Related]
9. Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts. Bonkowsky HL; Bloomer JR; Ebert PS; Mahoney MJ J Clin Invest; 1975 Nov; 56(5):1139-48. PubMed ID: 1184741 [TBL] [Abstract][Full Text] [Related]
10. Studies in porphyria: functional evidence for a partial deficiency of ferrochelatase activity in mitogen-stimulated lymphocytes from patients with erythropoietic protoporphyria. Sassa S; Zalar GL; Poh-Fitzpatrick MB; Anderson KE; Kappas A J Clin Invest; 1982 Apr; 69(4):809-15. PubMed ID: 6804493 [TBL] [Abstract][Full Text] [Related]
11. Zinc chelatase in human lymphocytes: detection of the enzymatic defect in erythropoietic protoporphyria. Nunn AV; Norris P; Hawk JL; Cox TM Anal Biochem; 1988 Oct; 174(1):146-50. PubMed ID: 3218729 [TBL] [Abstract][Full Text] [Related]
12. Comparison of human and bovine protoporphyria. Brenner DA; Bloomer JR Yale J Biol Med; 1979; 52(5):449-54. PubMed ID: 392959 [TBL] [Abstract][Full Text] [Related]
13. Pathogenesis and therapy of liver disease in protoporphyria. Bloomer JR Yale J Biol Med; 1979; 52(1):39-48. PubMed ID: 452621 [TBL] [Abstract][Full Text] [Related]
14. Carboxyhemoglobin and fecal urobilinogen in bovine erythropoietic porphyria. Engel RR; Bracho M; Schwartz S; Rodkey FL Am J Vet Res; 1973 Jun; 34(6):743-6. PubMed ID: 4707558 [No Abstract] [Full Text] [Related]
15. Erythropoietic protoporphyria and lead intoxication: the molecular basis for difference in cutaneous photosensitivity. I. Different rates of disappearance of protoporphyrin from the erythrocytes, both in vivo and in vitro. Piomelli S; Lamola AA; Poh-Fitzpatrick MF; Seaman C; Harber LC J Clin Invest; 1975 Dec; 56(6):1519-27. PubMed ID: 1202082 [TBL] [Abstract][Full Text] [Related]
16. Comparison of bile porphyrin concentrations in cattle and human beings with protoporphyria. Bloomer JR; Straka JG; Hill H; Weimer MK; Ruth GR Am J Vet Res; 1990 Jul; 51(7):1144-6. PubMed ID: 2389893 [TBL] [Abstract][Full Text] [Related]
17. Accumulation of protoporphyrin IX from delta-aminolevulinic acid in bovine skin fibroblasts with hereditary erythropoietic protoporphyria. A gene-dosage effect. Sassa S; Schwartz S; Ruth G J Exp Med; 1981 May; 153(5):1094-101. PubMed ID: 6788885 [TBL] [Abstract][Full Text] [Related]
18. Immunochemical studies of ferrochelatase protein: characterization of the normal and mutant protein in bovine and human protoporphyria. Straka JG; Hill HD; Krikava JM; Kools AM; Bloomer JR Am J Hum Genet; 1991 Jan; 48(1):72-8. PubMed ID: 1985464 [TBL] [Abstract][Full Text] [Related]
19. The enzyme defect in bovine protoporphyria. Studies with purified ferrochelatase. Bloomer JR; Hill HD; Morton KO; Anderson-Burnham LA; Straka JG J Biol Chem; 1987 Jan; 262(2):667-71. PubMed ID: 3805002 [TBL] [Abstract][Full Text] [Related]
20. Enzyme defects in hereditary porphyria. Civin WH; Epstein E Ann Clin Lab Sci; 1980; 10(5):395-401. PubMed ID: 6999973 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]