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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 1376018)

  • 21. Photosensitivity of a protoporphyrin-accumulating, light-sensitive mutant (visA) of Escherichia coli K-12.
    Nakahigashi K; Nishimura K; Miyamoto K; Inokuchi H
    Proc Natl Acad Sci U S A; 1991 Dec; 88(23):10520-4. PubMed ID: 1835790
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Structure and function of ferrochelatase.
    Ferreira GC; Franco R; Lloyd SG; Moura I; Moura JJ; Huynh BH
    J Bioenerg Biomembr; 1995 Apr; 27(2):221-9. PubMed ID: 7592569
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation.
    Bloomer J; Bruzzone C; Zhu L; Scarlett Y; Magness S; Brenner D
    J Clin Invest; 1998 Jul; 102(1):107-14. PubMed ID: 9649563
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular defect in human erythropoietic protoporphyria with fatal liver failure.
    Nakahashi Y; Miyazaki H; Kadota Y; Naitoh Y; Inoue K; Yamamoto M; Hayashi N; Taketani S
    Hum Genet; 1993 May; 91(4):303-6. PubMed ID: 8500787
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Molecular analysis of functional and nonfunctional genes for human ferrochelatase: isolation and characterization of a FECH pseudogene and its sublocalization on chromosome 3.
    Whitcombe DM; Albertson DG; Cox TM
    Genomics; 1994 Apr; 20(3):482-6. PubMed ID: 8034322
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Protoporphyrin accumulation by mitogen stimulated lymphocytes and protoporphyrinogen oxidase activity in patients with porphyria variegata and erythropoietic protoporphyria: evidence for deficiency of protoporphyrinogen oxidase and ferrochelatase in both diseases.
    Siepker LJ; Kramer S
    Br J Haematol; 1985 May; 60(1):65-74. PubMed ID: 3924091
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase allele.
    Gouya L; Deybach JC; Lamoril J; Da Silva V; Beaumont C; Grandchamp B; Nordmann Y
    Am J Hum Genet; 1996 Feb; 58(2):292-9. PubMed ID: 8571955
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel stop codon mutation (X417L) of the ferrochelatase gene in bovine protoporphyria, a natural animal model of the human disease.
    Jenkins MM; LeBoeuf RD; Ruth GR; Bloomer JR
    Biochim Biophys Acta; 1998 Oct; 1408(1):18-24. PubMed ID: 9784594
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital erythropoietic porphyria and erythropoietic protoporphyria: Identification of 7 uroporphyrinogen III synthase and 20 ferrochelatase novel mutations.
    Weiss Y; Balwani M; Chen B; Yasuda M; Nazarenko I; Desnick RJ
    Mol Genet Metab; 2019 Nov; 128(3):358-362. PubMed ID: 30454868
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Phototaxis away from blue light by an Escherichia coli mutant accumulating protoporphyrin IX.
    Yang H; Inokuchi H; Adler J
    Proc Natl Acad Sci U S A; 1995 Aug; 92(16):7332-6. PubMed ID: 7638191
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Autosomal recessive erythropoietic protoporphyria: a syndrome of severe photosensitivity and liver failure.
    Sarkany RP; Cox TM
    QJM; 1995 Aug; 88(8):541-9. PubMed ID: 7648240
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular characterization of a ferrochelatase gene defect causing anomalous RNA splicing in erythropoietic protoporphyria.
    Sarkany RP; Whitcombe DM; Cox TM
    J Invest Dermatol; 1994 Apr; 102(4):481-4. PubMed ID: 8151124
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Reduced ferrochelatase activity: a defect common to porphyria variegata and protoporphyria.
    Becker DM; Viljoen JD; Katz J; Kramer S
    Br J Haematol; 1977 Jun; 36(2):171-9. PubMed ID: 871431
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel splicing mutation in the ferrochelatase gene responsible for erythropoietic protoporphyria.
    Wang X; Poh-Fitzpatrick M; Piomelli S
    Biochim Biophys Acta; 1994 Oct; 1227(1-2):25-7. PubMed ID: 7918679
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Crystal structure of ferrochelatase: the terminal enzyme in heme biosynthesis.
    Al-Karadaghi S; Hansson M; Nikonov S; Jönsson B; Hederstedt L
    Structure; 1997 Nov; 5(11):1501-10. PubMed ID: 9384565
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Systematic analysis of molecular defects in the ferrochelatase gene from patients with erythropoietic protoporphyria.
    Rüfenacht UB; Gouya L; Schneider-Yin X; Puy H; Schäfer BW; Aquaron R; Nordmann Y; Minder EI; Deybach JC
    Am J Hum Genet; 1998 Jun; 62(6):1341-52. PubMed ID: 9585598
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Four novel mutations in the ferrochelatase gene among erythropoietic protoporphyria patients.
    Henriksson M; Timonen K; Mustajoki P; Pihlaja H; Tenhunen R; Peltonen L; Kauppinen R
    J Invest Dermatol; 1996 Feb; 106(2):346-50. PubMed ID: 8601739
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Acquired erythropoietic protoporphyria: A systematic review of the literature.
    Snast I; Kaftory R; Sherman S; Edel Y; Hodak E; Levi A; Lapidoth M
    Photodermatol Photoimmunol Photomed; 2020 Jan; 36(1):29-33. PubMed ID: 31374130
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies.
    Frank J; Nelson J; Wang X; Yang L; Ahmad W; Lam H; Jugert FK; Kalka K; Poh-Fitzpatrick MB; Goerz G; Merk HF; Christiano AM
    J Investig Med; 1999 Jul; 47(6):278-84. PubMed ID: 10431482
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.