122 related articles for article (PubMed ID: 15749661)
1. 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]
2. Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis.
Bergamaschi G
Haematologica; 2005 Mar; 90(3):289A. PubMed ID: 15749651
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy.
Radio FC; Majore S; Binni F; Valiante M; Ricerca BM; De Bernardo C; Morrone A; Grammatico P
Blood Cells Mol Dis; 2014; 52(2-3):83-7. PubMed ID: 24055163
[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. Type 3 hemochromatosis and beta-thalassemia trait.
Riva A; Mariani R; Bovo G; Pelucchi S; Arosio C; Salvioni A; Vergani A; Piperno A
Eur J Haematol; 2004 May; 72(5):370-4. PubMed ID: 15059075
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis.
Hattori A; Wakusawa S; Hayashi H; Harashima A; Sanae F; Kawanaka M; Yamada G; Yano M; Yoshioka K
Hepatol Res; 2003 Jun; 26(2):154-156. PubMed ID: 12809944
[TBL] [Abstract][Full Text] [Related]
10. Hemochromatosis due to mutations in transferrin receptor 2.
Roetto A; Daraio F; Alberti F; Porporato P; Calì A; De Gobbi M; Camaschella C
Blood Cells Mol Dis; 2002; 29(3):465-70. PubMed ID: 12547237
[TBL] [Abstract][Full Text] [Related]
11. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis.
Sherrington CA; Knuiman MW; Divitini ML; Bartholomew HC; Cullen DJ; Olynyk JK
J Gastroenterol Hepatol; 2006 Mar; 21(3):595-8. PubMed ID: 16638105
[TBL] [Abstract][Full Text] [Related]
12. Investigation of genetic variants of genes of the hemochromatosis pathway and their role in breast cancer.
Abraham BK; Justenhoven C; Pesch B; Harth V; Weirich G; Baisch C; Rabstein S; Ko YD; Brüning T; Fischer HP; Haas S; Brod S; Oberkanins C; Hamann U; Brauch H;
Cancer Epidemiol Biomarkers Prev; 2005 May; 14(5):1102-7. PubMed ID: 15894659
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Inactivation of the murine Transferrin Receptor 2 gene using the Cre recombinase: loxP system.
Wallace DF; Tonks ID; Zournazi A; Kay GF; Subramaniam VN
Genesis; 2004 May; 39(1):38-41. PubMed ID: 15124225
[TBL] [Abstract][Full Text] [Related]
15. 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]
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. Searching for hereditary hemochromatosis.
Laudicina RJ
Clin Lab Sci; 2006; 19(3):174-83. PubMed ID: 16910235
[TBL] [Abstract][Full Text] [Related]
18. Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis.
Fleming RE; Ahmann JR; Migas MC; Waheed A; Koeffler HP; Kawabata H; Britton RS; Bacon BR; Sly WS
Proc Natl Acad Sci U S A; 2002 Aug; 99(16):10653-8. PubMed ID: 12134060
[TBL] [Abstract][Full Text] [Related]
19. Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent.
Gérolami V; Le Gac G; Mercier L; Nezri M; Bergé-Lefranc JL; Férec C
Haematologica; 2008 May; 93(5):e45-6. PubMed ID: 18450729
[No Abstract] [Full Text] [Related]
20. Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification.
Robinson G; Narasimhan S; Weatherall M; Beasley R
J Gastroenterol Hepatol; 2007 Jun; 22(6):852-4. PubMed ID: 17565641
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
