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5. Studies in porphyria. V. Drug oxidation rates in hereditary hepatic porphyria. Anderson KE; Alvares AP; Sassa S; Kappas A Clin Pharmacol Ther; 1976 Jan; 19(1):47-54. PubMed ID: 1245093 [TBL] [Abstract][Full Text] [Related]
6. Effect of lead on hepatic delta-aminolaevulinic acid synthetase activity in the rat: a model for drug sensitivity in intermittent acute porphyria. Maxwell JD; Meyer UA Eur J Clin Invest; 1976 Sep; 6(5):373-9. PubMed ID: 976299 [TBL] [Abstract][Full Text] [Related]
7. Studies in porphyria. IV. Expression of the gene defect of acute intermittent porphyria in cultured human skin fibroblasts and amniotic cells: prenatal diagnosis of the porphyric trait. Sassa S; Solish G; Levere RD; Kappas A J Exp Med; 1975 Sep; 142(3):722-31. PubMed ID: 1165472 [TBL] [Abstract][Full Text] [Related]
8. Gas chromatography-mass spectrometry profiling of steroids in urine of patients with acute intermittent porphyria. Casals G; Marcos J; Pozo ÓJ; Aguilera P; Herrero C; To-Figueras J Clin Biochem; 2013 Jun; 46(9):819-24. PubMed ID: 23499585 [TBL] [Abstract][Full Text] [Related]
9. Endocrine-gene interaction in the pathogenesis of acute intermittent porphyria. Kappas A; Sassa S; Granick S; Bradlow HL Res Publ Assoc Res Nerv Ment Dis; 1974; 53():225-37. PubMed ID: 4612660 [No Abstract] [Full Text] [Related]
10. Studies in porphyria. VII. Induction of uroporphyrinogen-I synthase and expression of the gene defect of acute intermittent porphyria in mitogen-stimulated human lymphocytes. Sassa S; Zalar GL; Kappas A J Clin Invest; 1978 Feb; 61(2):499-508. PubMed ID: 621286 [TBL] [Abstract][Full Text] [Related]
11. Hepatic porphyrias: new findings on the nature of metabolic defects. Meyer UA Prog Liver Dis; 1976; 5():280-93. PubMed ID: 775544 [No Abstract] [Full Text] [Related]
12. Enhancement of RNA synthesis in avian liver cell cultures by a 5beta-steroid metabolite during induction of delta-aminolevulinate synthase. Incefy GS; Kappas A Proc Natl Acad Sci U S A; 1974 Jun; 71(6):2290-4. PubMed ID: 4526207 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Porphyrin synthesis and mitochondrial respiration in acute intermittent porphyria: studies using cultured human fibroblasts. Bonkowsky HL; Tschudy DP; Weinbach EC; Ebert PS; Doherty JM J Lab Clin Med; 1975 Jan; 85(1):93-102. PubMed ID: 1141734 [TBL] [Abstract][Full Text] [Related]
16. Hepatic siderosis and porphyria cutanea tarda: relation of iron excess to the metabolic defect. Felsher BF; Kushner JP Semin Hematol; 1977 Apr; 14(2):243-51. PubMed ID: 323986 [No Abstract] [Full Text] [Related]
17. Hepatic porphyrias. Current concepts. Walsh JR Postgrad Med; 1977 Aug; 62(2):71-81. PubMed ID: 329249 [TBL] [Abstract][Full Text] [Related]
18. Porphyrin biosynthesis. Enhancement of the fractional catabolic rate of microsomal haem in chemically induced porphyria. Meyer UA; Marver HS S Afr Med J; 1971 Sep; ():175-7. PubMed ID: 5150273 [No Abstract] [Full Text] [Related]
19. Studies in porphyria. VIII. Relationship of the 5 alpha-reductive metabolism of steroid hormones to clinical expression of the genetic defect in acute intermittent porphyria. Anderson KE; Bradlow HL; Sassa S; Kappas A Am J Med; 1979 Apr; 66(4):644-50. PubMed ID: 433969 [No Abstract] [Full Text] [Related]
20. Cytoplasmic receptor protein for etiochalanolone in chick embryo liver. Lane SE; Gidari AS; Levere RD J Biol Chem; 1975 Oct; 250(20):8209-13. PubMed ID: 170283 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]