896 related articles for article (PubMed ID: 8696333)
1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.
Feder JN; Gnirke A; Thomas W; Tsuchihashi Z; Ruddy DA; Basava A; Dormishian F; Domingo R; Ellis MC; Fullan A; Hinton LM; Jones NL; Kimmel BE; Kronmal GS; Lauer P; Lee VK; Loeb DB; Mapa FA; McClelland E; Meyer NC; Mintier GA; Moeller N; Moore T; Morikang E; Prass CE; Quintana L; Starnes SM; Schatzman RC; Brunke KJ; Drayna DT; Risch NJ; Bacon BR; Wolff RK
Nat Genet; 1996 Aug; 13(4):399-408. PubMed ID: 8696333
[TBL] [Abstract][Full Text] [Related]
2. Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor.
Lebrón JA; Bennett MJ; Vaughn DE; Chirino AJ; Snow PM; Mintier GA; Feder JN; Bjorkman PJ
Cell; 1998 Apr; 93(1):111-23. PubMed ID: 9546397
[TBL] [Abstract][Full Text] [Related]
3. The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression.
Feder JN; Tsuchihashi Z; Irrinki A; Lee VK; Mapa FA; Morikang E; Prass CE; Starnes SM; Wolff RK; Parkkila S; Sly WS; Schatzman RC
J Biol Chem; 1997 May; 272(22):14025-8. PubMed ID: 9162021
[TBL] [Abstract][Full Text] [Related]
4. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding.
Feder JN; Penny DM; Irrinki A; Lee VK; Lebrón JA; Watson N; Tsuchihashi Z; Sigal E; Bjorkman PJ; Schatzman RC
Proc Natl Acad Sci U S A; 1998 Feb; 95(4):1472-7. PubMed ID: 9465039
[TBL] [Abstract][Full Text] [Related]
5. Global prevalence of putative haemochromatosis mutations.
Merryweather-Clarke AT; Pointon JJ; Shearman JD; Robson KJ
J Med Genet; 1997 Apr; 34(4):275-8. PubMed ID: 9138148
[TBL] [Abstract][Full Text] [Related]
6. Haemochromatosis and HLA-H.
Jouanolle AM; Gandon G; Jézéquel P; Blayau M; Campion ML; Yaouanq J; Mosser J; Fergelot P; Chauvel B; Bouric P; Carn G; Andrieux N; Gicquel I; Le Gall JY; David V
Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
[No Abstract] [Full Text] [Related]
7. Haemochromatosis and HLA-H.
Jazwinska EC; Cullen LM; Busfield F; Pyper WR; Webb SI; Powell LW; Morris CP; Walsh TP
Nat Genet; 1996 Nov; 14(3):249-51. PubMed ID: 8896549
[No Abstract] [Full Text] [Related]
8. HFE gene knockout produces mouse model of hereditary hemochromatosis.
Zhou XY; Tomatsu S; Fleming RE; Parkkila S; Waheed A; Jiang J; Fei Y; Brunt EM; Ruddy DA; Prass CE; Schatzman RC; O'Neill R; Britton RS; Bacon BR; Sly WS
Proc Natl Acad Sci U S A; 1998 Mar; 95(5):2492-7. PubMed ID: 9482913
[TBL] [Abstract][Full Text] [Related]
9. Cloning and characterization of a mammalian proton-coupled metal-ion transporter.
Gunshin H; Mackenzie B; Berger UV; Gunshin Y; Romero MF; Boron WF; Nussberger S; Gollan JL; Hediger MA
Nature; 1997 Jul; 388(6641):482-8. PubMed ID: 9242408
[TBL] [Abstract][Full Text] [Related]
10. Hereditary hemochromatosis: gene discovery and its implications for population-based screening.
Burke W; Thomson E; Khoury MJ; McDonnell SM; Press N; Adams PC; Barton JC; Beutler E; Brittenham G; Buchanan A; Clayton EW; Cogswell ME; Meslin EM; Motulsky AG; Powell LW; Sigal E; Wilfond BS; Collins FS
JAMA; 1998 Jul; 280(2):172-8. PubMed ID: 9669792
[TBL] [Abstract][Full Text] [Related]
11. Molecular medicine and hemochromatosis: at the crossroads.
Bacon BR; Powell LW; Adams PC; Kresina TF; Hoofnagle JH
Gastroenterology; 1999 Jan; 116(1):193-207. PubMed ID: 9869618
[No Abstract] [Full Text] [Related]
12. Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.
Fleming MD; Romano MA; Su MA; Garrick LM; Garrick MD; Andrews NC
Proc Natl Acad Sci U S A; 1998 Feb; 95(3):1148-53. PubMed ID: 9448300
[TBL] [Abstract][Full Text] [Related]
13. Real time quantitative PCR.
Heid CA; Stevens J; Livak KJ; Williams PM
Genome Res; 1996 Oct; 6(10):986-94. PubMed ID: 8908518
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis in hereditary hemochromatosis.
Beutler E; Gelbart T; West C; Lee P; Adams M; Blackstone R; Pockros P; Kosty M; Venditti CP; Phatak PD; Seese NK; Chorney KA; Ten Elshof AE; Gerhard GS; Chorney M
Blood Cells Mol Dis; 1996; 22(2):187-94; discussion 194a-194b. PubMed ID: 8931958
[TBL] [Abstract][Full Text] [Related]
15. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells.
Waheed A; Parkkila S; Zhou XY; Tomatsu S; Tsuchihashi Z; Feder JN; Schatzman RC; Britton RS; Bacon BR; Sly WS
Proc Natl Acad Sci U S A; 1997 Nov; 94(23):12384-9. PubMed ID: 9356458
[TBL] [Abstract][Full Text] [Related]
16. Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis.
Guyader D; Jacquelinet C; Moirand R; Turlin B; Mendler MH; Chaperon J; David V; Brissot P; Adams P; Deugnier Y
Gastroenterology; 1998 Oct; 115(4):929-36. PubMed ID: 9753496
[TBL] [Abstract][Full Text] [Related]
17. Hemochromatosis in Ireland and HFE.
Ryan E; O'keane C; Crowe J
Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
[TBL] [Abstract][Full Text] [Related]
18. Hemochromatosis and "HLA-H": definite!
Jazwinska EC; Powell LW
Hepatology; 1997 Feb; 25(2):495-6. PubMed ID: 9021970
[TBL] [Abstract][Full Text] [Related]
19. Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency?
Datz C; Haas T; Rinner H; Sandhofer F; Patsch W; Paulweber B
Clin Chem; 1998 Dec; 44(12):2429-32. PubMed ID: 9836708
[TBL] [Abstract][Full Text] [Related]
20. Phenotype-genotype correlation in haemochromatosis subjects.
Mura C; Nousbaum JB; Verger P; Moalic MT; Raguenes O; Mercier AY; Ferec C
Hum Genet; 1997 Dec; 101(3):271-6. PubMed ID: 9439654
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
