105 related articles for article (PubMed ID: 17598218)
21. Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.
Grandchamp B; Lamoril J; Puy H
J Bioenerg Biomembr; 1995 Apr; 27(2):215-9. PubMed ID: 7592568
[TBL] [Abstract][Full Text] [Related]
22. Comment on: "A cascade analysis of the interaction of mercury and coproporphyrinogen oxidase (CPOX) polymorphism on the heme biosynthetic pathway and porphyrin production" by Heyer et al. [Toxicol. Lett. 161 (2006) 159-166].
Björkman L; Vahter M
Toxicol Lett; 2007 Feb; 169(1):91-2; author reply 93-4. PubMed ID: 17215094
[No Abstract] [Full Text] [Related]
23. Three novel mutations in the coproporphyrinogen oxidase gene.
Lamoril J; Deybach JC; Puy H; Grandchamp B; Nordmann Y
Hum Mutat; 1997; 9(1):78-80. PubMed ID: 8990017
[No Abstract] [Full Text] [Related]
24. [Polymorphism of TNF gene and CPOX gene in chemical industry workers].
Med Tr Prom Ekol; 2011; (11):29-32. PubMed ID: 22288185
[TBL] [Abstract][Full Text] [Related]
25. Hereditary cataract of the Nakano mouse: Involvement of a hypomorphic mutation in the coproporphyrinogen oxidase gene.
Mori M; Gotoh S; Taketani S; Hiai H; Higuchi K
Exp Eye Res; 2013 Jul; 112():45-50. PubMed ID: 23631845
[TBL] [Abstract][Full Text] [Related]
26. The association between genetic polymorphisms of coproporphyrinogen oxidase and an atypical porphyrinogenic response to mercury exposure in humans.
Woods JS; Echeverria D; Heyer NJ; Simmonds PL; Wilkerson J; Farin FM
Toxicol Appl Pharmacol; 2005 Aug; 206(2):113-20. PubMed ID: 15967199
[TBL] [Abstract][Full Text] [Related]
27. A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.
Lamoril J; Martasek P; Deybach JC; Da Silva V; Grandchamp B; Nordmann Y
Hum Mol Genet; 1995 Feb; 4(2):275-8. PubMed ID: 7757079
[TBL] [Abstract][Full Text] [Related]
28. Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria.
Hasegawa K; Tanaka H; Yamashita M; Higuchi Y; Miyai T; Yoshimoto J; Okada A; Suzuki N; Iwatsuki K; Tsukahara H
JIMD Rep; 2017; 37():99-106. PubMed ID: 28349448
[TBL] [Abstract][Full Text] [Related]
29. Compound heterozygous hereditary coproporphyria with fluorescing teeth.
Doss MO; Gross U; Lamoril J; Kranl C; Jacob K; Doss M; da Silva V; Freesemann AG; Deybach JC; Sepp N; Nordmann Y
Ann Clin Biochem; 1999 Sep; 36 ( Pt 5)():680-2. PubMed ID: 10505225
[No Abstract] [Full Text] [Related]
30. BALB.NCT-
Kang X; Shimada S; Miyahara H; Higuchi K; Mori M
Mol Genet Metab Rep; 2023 Jun; 35():100964. PubMed ID: 36967721
[TBL] [Abstract][Full Text] [Related]
31. A case report of hereditary coproporphyria with neurological, haematological and renal involvement.
Martín-Lagos Maldonado A; Borrego García E; Ruiz Sancho A
Gastroenterol Hepatol; 2019; 42(7):438-439. PubMed ID: 30948142
[No Abstract] [Full Text] [Related]
32. A comparative density-functional study of the reaction mechanism of the O2-dependent coproporphyrinogen III oxidase.
Silva PJ; Ramos MJ
Bioorg Med Chem; 2008 Mar; 16(6):2726-33. PubMed ID: 18226911
[TBL] [Abstract][Full Text] [Related]
33. Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia.
Jiménez-Jiménez FJ; Agúndez JA; Martínez C; Navacerrada F; Plaza-Nieto JF; Pilo-de-la-Fuente B; Alonso-Navarro H; García-Martín E
Tremor Other Hyperkinet Mov (N Y); 2013; 3():. PubMed ID: 24156084
[TBL] [Abstract][Full Text] [Related]
34. Analysis of lolB gene sequence and its use in the development of a PCR assay for the detection of Vibrio cholerae.
Lalitha P; Siti Suraiya MN; Lim KL; Lee SY; Nur Haslindawaty AR; Chan YY; Ismail A; Zainuddin ZF; Ravichandran M
J Microbiol Methods; 2008 Sep; 75(1):142-4. PubMed ID: 18579241
[TBL] [Abstract][Full Text] [Related]
35. Use of di- and tripropionate substrate analogs to probe the active site of human recombinant coproporphyrinogen oxidase.
Morgenthaler JB; Barto RL; Lash TD; Jones MA
Med Sci Monit; 2008 Jan; 14(1):BR1-7. PubMed ID: 18160932
[TBL] [Abstract][Full Text] [Related]
36. Hereditary coproporphyria: case report of an acute crisis.
McDonnell C; O'Donovan F
Ir Med J; 2005 May; 98(5):150-1. PubMed ID: 16010787
[No Abstract] [Full Text] [Related]
37. Hexachlorobenzene treatment on hepatic mitochondrial function parameters and intracellular coproporphyrinogen oxidase location.
Sopena YE; Ferramola de Sancovich AM; Sancovich HA
Int J Toxicol; 2008 Nov; 27(6):455-65. PubMed ID: 19482825
[TBL] [Abstract][Full Text] [Related]
38. Coproporphyrinuria as an index of lead absorption.
JOHNSON WS; WHITMAN NE
Arch Ind Hyg Occup Med; 1950 Aug; 2(2):170-4. PubMed ID: 15433525
[No Abstract] [Full Text] [Related]
39. [Primary carcinoma of the duodenum with type I coproporphyrinuria].
ROF CARBALLO J; CASTRO MENDOZA H
Rev Clin Esp; 1953 Jan; 48(2):76-81. PubMed ID: 13074831
[No Abstract] [Full Text] [Related]
40. Coproporphyrinuria (Type III) in acute poliomyelitis.
WATSON CJ; SCHULZE W
Proc Soc Exp Biol Med; 1947 Jan; 64(1):73-8. PubMed ID: 20285467
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
