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.
118 related articles for article (PubMed ID: 1783383)
1. Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22. Whitcombe DM; Carter NP; Albertson DG; Smith SJ; Rhodes DA; Cox TM Genomics; 1991 Dec; 11(4):1152-4. PubMed ID: 1783383 [TBL] [Abstract][Full Text] [Related]
2. Deletion of the ferrochelatase gene in a patient with protoporphyria. Magness ST; Tugores A; Christensen SR; Wagner-Mcpherson C; Evans GA; Naylor EW; Brenner DA Hum Mol Genet; 1994 Sep; 3(9):1695-7. PubMed ID: 7833934 [No Abstract] [Full Text] [Related]
3. 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]
4. A molecular defect in human protoporphyria. Brenner DA; Didier JM; Frasier F; Christensen SR; Evans GA; Dailey HA Am J Hum Genet; 1992 Jun; 50(6):1203-10. PubMed ID: 1376018 [TBL] [Abstract][Full Text] [Related]
5. Human erythropoietic protoporphyria: two point mutations in the ferrochelatase gene. Lamoril J; Boulechfar S; de Verneuil H; Grandchamp B; Nordmann Y; Deybach JC Biochem Biophys Res Commun; 1991 Dec; 181(2):594-9. PubMed ID: 1755842 [TBL] [Abstract][Full Text] [Related]
6. The ferrochelatase gene structure and molecular defects associated with erythropoietic protoporphyria. Taketani S; Fujita H J Bioenerg Biomembr; 1995 Apr; 27(2):231-8. PubMed ID: 7592570 [TBL] [Abstract][Full Text] [Related]
7. Immunochemical studies of ferrochelatase protein: characterization of the normal and mutant protein in bovine and human protoporphyria. Straka JG; Hill HD; Krikava JM; Kools AM; Bloomer JR Am J Hum Genet; 1991 Jan; 48(1):72-8. PubMed ID: 1985464 [TBL] [Abstract][Full Text] [Related]
8. Targeted disruption of the mouse ferrochelatase gene producing an exon 10 deletion. Magness ST; Brenner DA Biochim Biophys Acta; 1999 Jan; 1453(1):161-74. PubMed ID: 9989256 [TBL] [Abstract][Full Text] [Related]
9. The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria. Nakahashi Y; Fujita H; Taketani S; Ishida N; Kappas A; Sassa S Proc Natl Acad Sci U S A; 1992 Jan; 89(1):281-5. PubMed ID: 1729699 [TBL] [Abstract][Full Text] [Related]
10. Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease. Tutois S; Montagutelli X; Da Silva V; Jouault H; Rouyer-Fessard P; Leroy-Viard K; Guénet JL; Nordmann Y; Beuzard Y; Deybach JC J Clin Invest; 1991 Nov; 88(5):1730-6. PubMed ID: 1939658 [TBL] [Abstract][Full Text] [Related]
11. Acquired erythropoietic protoporphyria as a result of myelodysplasia causing loss of chromosome 18. Sarkany RP; Ross G; Willis F Br J Dermatol; 2006 Aug; 155(2):464-6. PubMed ID: 16882191 [TBL] [Abstract][Full Text] [Related]
13. Gene dosage analysis identifies large deletions of the FECH gene in 10% of families with erythropoietic protoporphyria. Whatley SD; Mason NG; Holme SA; Anstey AV; Elder GH; Badminton MN J Invest Dermatol; 2007 Dec; 127(12):2790-4. PubMed ID: 17597821 [TBL] [Abstract][Full Text] [Related]
14. Dinucleotide repeat polymorphism at the locus for human ferrochelatase (FECH). Whitcombe DM; Cox TM Hum Mol Genet; 1993 Jun; 2(6):826. PubMed ID: 8353511 [No Abstract] [Full Text] [Related]
15. Structure of the human ferrochelatase gene. Exon/intron gene organization and location of the gene to chromosome 18. Taketani S; Inazawa J; Nakahashi Y; Abe T; Tokunaga R Eur J Biochem; 1992 Apr; 205(1):217-22. PubMed ID: 1555582 [TBL] [Abstract][Full Text] [Related]
16. CRISPR/Cas9-Mediated Wijerathna HMSM; Shanaka KASN; Raguvaran SS; Jayamali BPMV; Kim SH; Kim MJ; Jung S; Lee J Int J Mol Sci; 2024 Oct; 25(19):. PubMed ID: 39409147 [TBL] [Abstract][Full Text] [Related]
17. Generation of a human chromosome 18-specific YAC clone collection and mapping of 55 unique YACs by FISH and fingerprinting. Chang E; Welch S; Luna J; Giacalone J; Francke U Genomics; 1993 Aug; 17(2):393-402. PubMed ID: 7691716 [TBL] [Abstract][Full Text] [Related]
18. Ferrochelatase structural mutant (Fechm1Pas) in the house mouse. Boulechfar S; Lamoril J; Montagutelli X; Guenet JL; Deybach JC; Nordmann Y; Dailey H; Grandchamp B; de Verneuil H Genomics; 1993 Jun; 16(3):645-8. PubMed ID: 8325637 [TBL] [Abstract][Full Text] [Related]
19. Porphyrin production and liver involvement in a patient with erythropoietic protoporphyria. Romslo I; Høvding G; Hamre E; Laerum OD Scand J Clin Lab Invest; 1978 Oct; 38(6):529-35. PubMed ID: 705235 [TBL] [Abstract][Full Text] [Related]
20. Biochemical abnormality in erythropoietic protoporphyria: cause and consequences. Bloomer JR; Wang Y; Singhal A; Risheg H J Pediatr Gastroenterol Nutr; 2006 Jul; 43 Suppl 1():S36-40. PubMed ID: 16819399 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]