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Items: 13

1.

Oxidative stress, Nrf2 and keratin up-regulation associate with Mallory-Denk body formation in mouse erythropoietic protoporphyria.

Singla A, Moons DS, Snider NT, Wagenmaker ER, Jayasundera VB, Omary MB.

Hepatology. 2012 Jul;56(1):322-31. doi: 10.1002/hep.25664. Epub 2012 Apr 25.

2.

CarF mediates signaling by singlet oxygen, generated via photoexcited protoporphyrin IX, in Myxococcus xanthus light-induced carotenogenesis.

Galbis-Martínez M, Padmanabhan S, Murillo FJ, Elías-Arnanz M.

J Bacteriol. 2012 Mar;194(6):1427-36. doi: 10.1128/JB.06662-11. Epub 2012 Jan 20.

3.

The diagnosis and management of erythropoietic protoporphyria.

Thapar M, Bonkovsky HL.

Gastroenterol Hepatol (N Y). 2008 Aug;4(8):561-6.

4.

Abnormal mitoferrin-1 expression in patients with erythropoietic protoporphyria.

Wang Y, Langer NB, Shaw GC, Yang G, Li L, Kaplan J, Paw BH, Bloomer JR.

Exp Hematol. 2011 Jul;39(7):784-94. doi: 10.1016/j.exphem.2011.05.003. Epub 2011 May 11.

5.

Ferrochelatase forms an oligomeric complex with mitoferrin-1 and Abcb10 for erythroid heme biosynthesis.

Chen W, Dailey HA, Paw BH.

Blood. 2010 Jul 29;116(4):628-30. doi: 10.1182/blood-2009-12-259614. Epub 2010 Apr 28.

7.

Erythropoietic protoporphyria.

Lecha M, Puy H, Deybach JC.

Orphanet J Rare Dis. 2009 Sep 10;4:19. doi: 10.1186/1750-1172-4-19. Review.

8.

Novel null-allele mutations and genotype-phenotype correlation in Argentinean patients with erythropoietic protoporphyria.

Parera VE, Koole RH, Minderman G, Edixhoven A, Rossetti MV, Batlle A, de Rooij FW.

Mol Med. 2009 Nov-Dec;15(11-12):425-31. doi: 10.2119/molmed.2009.00006. Epub 2009 Aug 12.

9.

Liver disease in erythropoietic protoporphyria: insights and implications for management.

Anstey AV, Hift RJ.

Postgrad Med J. 2007 Dec;83(986):739-48. Review. No abstract available.

10.

Liver disease in erythropoietic protoporphyria: insights and implications for management.

Anstey AV, Hift RJ.

Gut. 2007 Jul;56(7):1009-18. Epub 2007 Mar 14. Review. No abstract available.

11.

Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria.

Gouya L, Martin-Schmitt C, Robreau AM, Austerlitz F, Da Silva V, Brun P, Simonin S, Lyoumi S, Grandchamp B, Beaumont C, Puy H, Deybach JC.

Am J Hum Genet. 2006 Jan;78(1):2-14. Epub 2005 Nov 15.

12.

Production and characterization of erythropoietic protoporphyric heterodimeric ferrochelatases.

Najahi-Missaoui W, Dailey HA.

Blood. 2005 Aug 1;106(3):1098-104. Epub 2005 Apr 14.

13.

Theodore Woodward Award. Pathogenesis of biochemical abnormalities in protoporphyria.

Bloomer JR, Poh-Fitzpatrick MB.

Trans Am Clin Climatol Assoc. 2000;111:245-56; discussion 256-7. Review.

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