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 *

161 related articles for article (PubMed ID: 2222353)

  • 21. A mouse model for South African (R59W) variegate porphyria: construction and initial characterization.
    Medlock AE; Meissner PN; Davidson BP; Corrigall AV; Dailey HA
    Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):71-8. PubMed ID: 11929050
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Variegate porphyria.
    Kirsch RE; Meissner PN; Hift RJ
    Semin Liver Dis; 1998; 18(1):33-41. PubMed ID: 9516676
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A review of the enzymic errors in the various porphyrias.
    Rimington C
    Scand J Clin Lab Invest; 1985 Jun; 45(4):291-301. PubMed ID: 3892647
    [No Abstract]   [Full Text] [Related]  

  • 24. Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria.
    de Villiers JN; Kotze MJ; van Heerden CJ; Sadie A; Gardner HF; Liebenberg J; van Zyl R; du Plessis L; Kimberg M; Frank J; Warnich L
    Exp Dermatol; 2005 Jan; 14(1):50-5. PubMed ID: 15660919
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The genetic basis of "Scarsdale Gourmet Diet" variegate porphyria: a missense mutation in the protoporphyrinogen oxidase gene.
    Frank J; Poh-Fitzpatrick MB; King LE; Christiano AM
    Arch Dermatol Res; 1998 Aug; 290(8):441-5. PubMed ID: 9763307
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyria.
    Deybach JC; Puy H; Robréau AM; Lamoril J; Da Silva V; Grandchamp B; Nordmann Y
    Hum Mol Genet; 1996 Mar; 5(3):407-10. PubMed ID: 8852667
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Review: molecular pathogenesis of hepatic acute porphyrias.
    Grandchamp B; Puy H; Lamoril J; Deybach JC; Nordmann Y
    J Gastroenterol Hepatol; 1996 Nov; 11(11):1046-52. PubMed ID: 8985829
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel mutation (1320InsT) identified in two Argentine families with variegate porphyria.
    Siervi AD; Parera VE; Varela LS; Batlle AM; Rossetti MV
    Hum Mutat; 2000 Jul; 16(1):96. PubMed ID: 10874330
    [No Abstract]   [Full Text] [Related]  

  • 29. Variegate porphyria: diagnostic value of fluorometric scanning of plasma porphyrins.
    Da Silva V; Simonin S; Deybach JC; Puy H; Nordmann Y
    Clin Chim Acta; 1995 Jul; 238(2):163-8. PubMed ID: 7586575
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification and characterisation of a deletion (537delAT) in the protoporphyrinogen oxidase gene in a South African variegate porphyria family.
    Corrigall AV; Hift RJ; Hancock V; Meissner D; Davids L; Kirsch RE; Meissner PN
    Hum Mutat; 1998; 12(6):403-7. PubMed ID: 9829909
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New aspects of porphyrias.
    Mascaro JM; Lecha M; Herrero C; Muniesa AM
    Curr Probl Dermatol; 1985; 13():11-32. PubMed ID: 3882335
    [No Abstract]   [Full Text] [Related]  

  • 32. [Neurological, dermatological and biological manifestations of porphyria variegata. A study of 3 families of Italian origin in Marseilles area].
    Aquaron R; Lacombe D; Topi GC; Lamoril J
    Rev Neurol (Paris); 1992; 148(8-9):532-40. PubMed ID: 1494724
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The inherited enzymatic defect in porphyria variegata.
    Deybach JC; de Verneuil H; Nordmann Y
    Hum Genet; 1981; 58(4):425-8. PubMed ID: 7327566
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Homozygous variegate porphyria: a compound heterozygote with novel mutations in the protoporphyrinogen oxidase gene.
    Palmer RA; Elder GH; Barrett DF; Keohane SG
    Br J Dermatol; 2001 Apr; 144(4):866-9. PubMed ID: 11298551
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria.
    De Siervi A; Parera VE; del C Batlle AM; Rossetti MV
    Hum Mutat; 2000 Dec; 16(6):532. PubMed ID: 11102990
    [No Abstract]   [Full Text] [Related]  

  • 36. Porphyrin metabolism and haem biosynthesis in Gilbert's syndrome.
    McColl KE; Thompson GG; el Omar E; Moore MR; Goldberg A
    Gut; 1987 Feb; 28(2):125-30. PubMed ID: 3557184
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Gne symbol: PPOX. Disease: variegate porphyria.
    Patti E; Di Pierro E; Cappellini MD
    Hum Genet; 2004 Jul; 115(2):170. PubMed ID: 15300965
    [No Abstract]   [Full Text] [Related]  

  • 38. Identification of the first variegate porphyria mutation in an indigenous black South African and further evidence for heterogeneity in variegate porphyria.
    Corrigall AV; Hift RJ; Davids LM; Hancock V; Meissner D; Kirsch RE; Meissner PN
    Mol Genet Metab; 2001 May; 73(1):91-6. PubMed ID: 11350188
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner families.
    Kotze MJ; De Villiers JN; Groenewald JZ; Rooney RN; Loubser O; Thiart R; Oosthuizen CJ; van Niekerk MM; Groenewald IM; Retief AE; Warnich L
    Mol Cell Probes; 1998 Oct; 12(5):293-300. PubMed ID: 9778454
    [TBL] [Abstract][Full Text] [Related]  

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