63 related articles for article (PubMed ID: 15020277)
1. Homozygosity for transferrin receptor-2 Y250X mutation induces early iron overload.
Piperno A; Roetto A; Mariani R; Pelucchi S; Corengia C; Daraio F; Piga A; Garozzo G; Camaschella C
Haematologica; 2004 Mar; 89(3):359-60. PubMed ID: 15020277
[TBL] [Abstract][Full Text] [Related]
2. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
Majore S; Milano F; Binni F; Stuppia L; Cerrone A; Tafuri A; De Bernardo C; Palka G; Grammatico P
Haematologica; 2006 Aug; 91(8 Suppl):ECR33. PubMed ID: 16923517
[TBL] [Abstract][Full Text] [Related]
3. Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload.
Wallace DF; Summerville L; Subramaniam VN
Gastroenterology; 2007 Jan; 132(1):301-10. PubMed ID: 17241880
[TBL] [Abstract][Full Text] [Related]
4. Analyses for binding of the transferrin family of proteins to the transferrin receptor 2.
Kawabata H; Tong X; Kawanami T; Wano Y; Hirose Y; Sugai S; Koeffler HP
Br J Haematol; 2004 Nov; 127(4):464-73. PubMed ID: 15521925
[TBL] [Abstract][Full Text] [Related]
5. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.
Le Gac G; Mons F; Jacolot S; Scotet V; Férec C; Frébourg T
Br J Haematol; 2004 Jun; 125(5):674-8. PubMed ID: 15147384
[TBL] [Abstract][Full Text] [Related]
6. New TFR2 mutations in young Italian patients with hemochromatosis.
Biasiotto G; Camaschella C; Forni GL; Polotti A; Zecchina G; Arosio P
Haematologica; 2008 Feb; 93(2):309-10. PubMed ID: 18245657
[TBL] [Abstract][Full Text] [Related]
7. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
de Diego C; Opazo S; Murga MJ; Martínez-Castro P
Eur J Haematol; 2007 Jan; 78(1):66-71. PubMed ID: 17042772
[TBL] [Abstract][Full Text] [Related]
8. Commentary: mutations of transferrin receptor 2 (Trf-2) and iron storage disease.
Beutler E
Blood Cells Mol Dis; 2001; 27(1):294-5. PubMed ID: 11358391
[No Abstract] [Full Text] [Related]
9. Iron absorption and hepatic iron uptake are increased in a transferrin receptor 2 (Y245X) mutant mouse model of hemochromatosis type 3.
Drake SF; Morgan EH; Herbison CE; Delima R; Graham RM; Chua AC; Leedman PJ; Fleming RE; Bacon BR; Olynyk JK; Trinder D
Am J Physiol Gastrointest Liver Physiol; 2007 Jan; 292(1):G323-8. PubMed ID: 16935854
[TBL] [Abstract][Full Text] [Related]
10. Increased serum transferrin receptor concentrations in Friedreich ataxia.
Wilson RB; Lynch DR; Farmer JM; Brooks DG; Fischbeck KH
Ann Neurol; 2000 May; 47(5):659-61. PubMed ID: 10805340
[TBL] [Abstract][Full Text] [Related]
11. Screening for hemochromatosis in asymptomatic subjects with or without a family history.
Powell LW; Dixon JL; Ramm GA; Purdie DM; Lincoln DJ; Anderson GJ; Subramaniam VN; Hewett DG; Searle JW; Fletcher LM; Crawford DH; Rodgers H; Allen KJ; Cavanaugh JA; Bassett ML
Arch Intern Med; 2006 Feb; 166(3):294-301. PubMed ID: 16476869
[TBL] [Abstract][Full Text] [Related]
12. No evidence of Y250X transferrin receptor type 2 mutation in patients with porphyria cutanea tarda. A study of 38 cases.
Dereure O; Esculier C; Aguilar-Martinez P; Dessis D; Guillot B; Guilhou JJ
Dermatology; 2002; 204(2):158-9. PubMed ID: 11937750
[No Abstract] [Full Text] [Related]
13. Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
Koyama C; Wakusawa S; Hayashi H; Suzuki R; Yano M; Yoshioka K; Kozuru M; Takayamam Y; Okada T; Mabuchi H
Haematologica; 2005 Mar; 90(3):302-7. PubMed ID: 15749661
[TBL] [Abstract][Full Text] [Related]
14. Evaluation of the Association of Transferrin Receptor Type 2 Gene Mutation (Y250X) with Iron Overload in Major β- Thalassemia.
Abdulmalek Jaafar J; Al-Rashedi NAM
Arch Razi Inst; 2021 Nov; 76(5):1551-1554. PubMed ID: 35355750
[TBL] [Abstract][Full Text] [Related]
15. Transferrin receptor 2 is frequently expressed in human cancer cell lines.
Calzolari A; Oliviero I; Deaglio S; Mariani G; Biffoni M; Sposi NM; Malavasi F; Peschle C; Testa U
Blood Cells Mol Dis; 2007; 39(1):82-91. PubMed ID: 17428703
[TBL] [Abstract][Full Text] [Related]
16. Soluble transferrin receptor and mutations in hemochromatosis and transferrin genes in a general Catalan population.
Bérez V; Camps J; Arija V; Aranda N; Fernández-Ballart J; Vilella E; Figuera L; Ferré N; Joven J
Clin Chim Acta; 2005 Mar; 353(1-2):205-8. PubMed ID: 15698609
[TBL] [Abstract][Full Text] [Related]
17. Transferrin receptor-2 polymorphisms and iron overload in transfusion independent b-thalassemia intermedia.
Ma ES; Lam KK; Chan AY; Ha SY; Au WY; Chan LC
Haematologica; 2003 Mar; 88(3):345-6. PubMed ID: 12651274
[No Abstract] [Full Text] [Related]
18. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects.
Cruz E; Melo G; Lacerda R; Almeida S; Porto G
Blood Cells Mol Dis; 2006; 37(1):33-9. PubMed ID: 16762569
[TBL] [Abstract][Full Text] [Related]
19. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry.
Kowdley KV; Brandhagen DJ; Gish RG; Bass NM; Weinstein J; Schilsky ML; Fontana RJ; McCashland T; Cotler SJ; Bacon BR; Keeffe EB; Gordon F; Polissar N;
Gastroenterology; 2005 Aug; 129(2):494-503. PubMed ID: 16083706
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.
Wallace DF; Clark RM; Harley HA; Subramaniam VN
J Hepatol; 2004 Apr; 40(4):710-3. PubMed ID: 15030991
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]