161 related articles for article (PubMed ID: 21039223)
1. Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload.
de Lima Santos PC; Pereira AC; Cançado RD; Schettert IT; Hirata RD; Hirata MH; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
Genet Test Mol Biomarkers; 2010 Dec; 14(6):803-6. PubMed ID: 21039223
[TBL] [Abstract][Full Text] [Related]
2. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
[TBL] [Abstract][Full Text] [Related]
3. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene.
Altès A; Bach V; Ruiz A; Esteve A; Felez J; Remacha AF; Sardà MP; Baiget M
Ann Hematol; 2009 Oct; 88(10):951-5. PubMed ID: 19214511
[TBL] [Abstract][Full Text] [Related]
4. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
Merryweather-Clarke AT; Cadet E; Bomford A; Capron D; Viprakasit V; Miller A; McHugh PJ; Chapman RW; Pointon JJ; Wimhurst VL; Livesey KJ; Tanphaichitr V; Rochette J; Robson KJ
Hum Mol Genet; 2003 Sep; 12(17):2241-7. PubMed ID: 12915468
[TBL] [Abstract][Full Text] [Related]
5. Non-
Lv T; Zhang W; Xu A; Li Y; Zhou D; Zhang B; Li X; Zhao X; Wang Y; Wang X; Duan W; Wang Q; Xu H; Zheng J; Zhao R; Zhu L; Dong Y; Lu L; Chen Y; Long J; Zheng S; Wang W; You H; Jia J; Ou X; Huang J
J Med Genet; 2018 Oct; 55(10):650-660. PubMed ID: 30166352
[TBL] [Abstract][Full Text] [Related]
6. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?
Santos PC; Pereira AC; Cançado RD; Schettert IT; Sobreira TJ; Oliveira PS; Hirata RD; Hirata MH; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
Blood Cells Mol Dis; 2010 Dec; 45(4):302-7. PubMed ID: 20843714
[TBL] [Abstract][Full Text] [Related]
7. Iron stores modulate hepatic hepcidin expression by an HFE-independent pathway.
Gehrke SG; Herrmann T; Kulaksiz H; Merle U; Bents K; Kaiser I; Riedel HD; Stremmel W
Digestion; 2005; 72(1):25-32. PubMed ID: 16103673
[TBL] [Abstract][Full Text] [Related]
8. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
Barton JC; Lafreniere SA; Leiendecker-Foster C; Li H; Acton RT; Press RD; Eckfeldt JH
Am J Hematol; 2009 Nov; 84(11):710-4. PubMed ID: 19787796
[TBL] [Abstract][Full Text] [Related]
9. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians.
Dhillon BK; Chopra G; Jamwal M; Chandak GR; Duseja A; Malhotra P; Chawla YK; Garewal G; Das R
Blood Cells Mol Dis; 2018 Nov; 73():14-21. PubMed ID: 30195625
[TBL] [Abstract][Full Text] [Related]
10. HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype.
Jacolot S; Le Gac G; Scotet V; Quere I; Mura C; Ferec C
Blood; 2004 Apr; 103(7):2835-40. PubMed ID: 14670915
[TBL] [Abstract][Full Text] [Related]
11. Down-regulation of hepcidin in porphyria cutanea tarda.
Ajioka RS; Phillips JD; Weiss RB; Dunn DM; Smit MW; Proll SC; Katze MG; Kushner JP
Blood; 2008 Dec; 112(12):4723-8. PubMed ID: 18809758
[TBL] [Abstract][Full Text] [Related]
12. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload.
Biasiotto G; Belloli S; Ruggeri G; Zanella I; Gerardi G; Corrado M; Gobbi E; Albertini A; Arosio P
Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868
[TBL] [Abstract][Full Text] [Related]
13. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
Barton JC; Acton RT; Leiendecker-Foster C; Lovato L; Adams PC; McLaren GD; Eckfeldt JH; McLaren CE; Reboussin DM; Gordeuk VR; Speechley MR; Reiss JA; Press RD; Dawkins FW;
Genet Test; 2007; 11(3):269-75. PubMed ID: 17949288
[TBL] [Abstract][Full Text] [Related]
14. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.
Mendes AI; Ferro A; Martins R; Picanço I; Gomes S; Cerqueira R; Correia M; Nunes AR; Esteves J; Fleming R; Faustino P
Ann Hematol; 2009 Mar; 88(3):229-34. PubMed ID: 18762941
[TBL] [Abstract][Full Text] [Related]
15. Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele.
Biasiotto G; Roetto A; Daraio F; Polotti A; Gerardi GM; Girelli D; Cremonesi L; Arosio P; Camaschella C
Blood Cells Mol Dis; 2004; 33(3):338-43. PubMed ID: 15528154
[TBL] [Abstract][Full Text] [Related]
16. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype.
Le Gac G; Scotet V; Ka C; Gourlaouen I; Bryckaert L; Jacolot S; Mura C; Férec C
Hum Mol Genet; 2004 Sep; 13(17):1913-8. PubMed ID: 15254010
[TBL] [Abstract][Full Text] [Related]
17. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
Loréal O; Ropert M; Mosser A; Déhais V; Deugnier Y; David V; Brissot P; Jouanolle AM
Presse Med; 2007 Sep; 36(9 Pt 2):1271-7. PubMed ID: 17521857
[TBL] [Abstract][Full Text] [Related]
18. Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis.
Nicolas G; Viatte L; Lou DQ; Bennoun M; Beaumont C; Kahn A; Andrews NC; Vaulont S
Nat Genet; 2003 May; 34(1):97-101. PubMed ID: 12704388
[TBL] [Abstract][Full Text] [Related]
19. HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis.
Shukla P; Julka S; Bhatia E; Shah S; Nagral A; Aggarwal R
Natl Med J India; 2006; 19(1):20-3. PubMed ID: 16570681
[TBL] [Abstract][Full Text] [Related]
20. Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three families.
Wallace DF; Dixon JL; Ramm GA; Anderson GJ; Powell LW; Subramaniam N
Haematologica; 2005 Feb; 90(2):254-5. PubMed ID: 15710580
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
