118 related articles for article (PubMed ID: 22735619)
1. Sample-to-SNP kit: a reliable, easy and fast tool for the detection of HFE p.H63D and p.C282Y variations associated to hereditary hemochromatosis.
Nielsen PB; Petersen MS; Ystaas V; Andersen RV; Hansen KM; Blaabjerg V; Refstrup M
Gene; 2012 Oct; 507(1):79-84. PubMed ID: 22735619
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
[TBL] [Abstract][Full Text] [Related]
3. Detection of the C282Y and H63D polymorphisms associated with hereditary hemochromatosis using the ABI 7500 fast real time PCR platform.
Tafe LJ; Belloni DR; Tsongalis GJ
Diagn Mol Pathol; 2007 Jun; 16(2):112-5. PubMed ID: 17525682
[TBL] [Abstract][Full Text] [Related]
4. Validation of the Hemochromatosis (2SNP+) Direct EUROArray Assay for the Molecular Diagnosis of
Poon KS; Lee CD; Kok NT; Tan KM
Genet Test Mol Biomarkers; 2020 Sep; 24(9):608-611. PubMed ID: 32762549
[No Abstract] [Full Text] [Related]
5. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
[TBL] [Abstract][Full Text] [Related]
6. Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay.
Cardoso SP; Patel R; Brown C; Navarrete C
Tissue Antigens; 2011 Sep; 78(3):171-7. PubMed ID: 21736562
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
Spínola C; Brehm A; Spínola H
Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF
Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390
[TBL] [Abstract][Full Text] [Related]
10. Evaluation of a high throughput method for the detection of mutations associated with thrombosis and hereditary hemochromatosis in Brazilian blood donors.
Dionisio Tavares Niewiadonski V; Dos Santos Bianchi JV; de Almeida-Neto C; Gaburo N; Sabino EC
PLoS One; 2015; 10(5):e0125460. PubMed ID: 25955572
[TBL] [Abstract][Full Text] [Related]
11. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
Silva B; Pita L; Gomes S; Gonçalves J; Faustino P
Ann Hematol; 2014 Dec; 93(12):2063-6. PubMed ID: 25015054
[TBL] [Abstract][Full Text] [Related]
12. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M
Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433
[TBL] [Abstract][Full Text] [Related]
13. Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000® instrument.
Santos PC; Soares RA; Krieger JE; Guerra-Shinohara EM; Pereira AC
Clin Chem Lab Med; 2011 Oct; 49(10):1633-6. PubMed ID: 21679129
[TBL] [Abstract][Full Text] [Related]
14. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S
Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia.
Rodríguez-López R; Donoso M; Fernández-Cavada M; González LM; Margallo A; Corral C; Gallego M; García de Cáceres MT; Herrera T; González C; Vagace JM; Gervasini G
Gene; 2013 Feb; 514(1):31-5. PubMed ID: 23178241
[TBL] [Abstract][Full Text] [Related]
16. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
Byrnes V; Ryan E; O'Keane C; Crowe J
Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
de Tayrac M; Roth MP; Jouanolle AM; Coppin H; le Gac G; Piperno A; Férec C; Pelucchi S; Scotet V; Bardou-Jacquet E; Ropert M; Bouvet R; Génin E; Mosser J; Deugnier Y
J Hepatol; 2015 Mar; 62(3):664-72. PubMed ID: 25457201
[TBL] [Abstract][Full Text] [Related]
18. Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR.
Moysés CB; Moreira ES; Asprino PF; Guimarães GS; Alberto FL
Braz J Med Biol Res; 2008 Oct; 41(10):833-8. PubMed ID: 19030706
[TBL] [Abstract][Full Text] [Related]
19. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
Leone PE; Giménez P; Collantes JC; Paz-y-Miño C
Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
[TBL] [Abstract][Full Text] [Related]
20. Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.
Shi Z; Johnstone D; Talseth-Palmer BA; Evans TJ; Spigelman AD; Groombridge C; Milward EA; Olynyk JK; Suchy J; Kurzawski G; Lubinski J; Scott RJ
Int J Cancer; 2009 Jul; 125(1):78-83. PubMed ID: 19291797
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
