Literature DB >> 4791052

Intermittent acute porphyria. Clinical and biochemical studies of disordered heme biosynthesis.

U A Meyer.   

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Year:  1973        PMID： 4791052

Source DB:  PubMed          Journal:  Enzyme        ISSN： 0013-9432


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  7 in total

1.  Perspectives in acute intermittent porphyria.

Authors:  I C Verma; S Singh
Journal:  Indian J Pediatr       Date:  1976-07       Impact factor: 1.967

2.  Study of factors causing excess protoporphyrin accumulation in cultured skin fibroblasts from patients with protoporphyria.

Authors:  J R Bloomer; D A Brenner; M J Mahoney
Journal:  J Clin Invest       Date:  1977-12       Impact factor: 14.808

3.  Studies in porphyria. VII. Induction of uroporphyrinogen-I synthase and expression of the gene defect of acute intermittent porphyria in mitogen-stimulated human lymphocytes.

Authors:  S Sassa; G L Zalar; A Kappas
Journal:  J Clin Invest       Date:  1978-02       Impact factor: 14.808

Review 4.  Enzymatic defects of hereditary porphyrias: an explanation of dominance at the molecular level.

Authors:  G Romeo
Journal:  Hum Genet       Date:  1977-12-23       Impact factor: 4.132

5.  Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.

Authors:  H L Bonkowsky; J R Bloomer; P S Ebert; M J Mahoney
Journal:  J Clin Invest       Date:  1975-11       Impact factor: 14.808

6.  Heme content of normal and porphyric cultured skin fibroblasts.

Authors:  D A Brenner; J R Bloomer
Journal:  Biochem Genet       Date:  1977-12       Impact factor: 1.890

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.

Authors:  S Sassa; G Solish; R D Levere; A Kappas
Journal:  J Exp Med       Date:  1975-09-01       Impact factor: 14.307
  7 in total

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