159 related articles for article (PubMed ID: 32652459)
1. Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels.
Secondes ES; Wallace DF; Rishi G; McLaren GD; McLaren CE; Chen WP; Ramm LE; Powell LW; Ramm GA; Barton JC; Subramaniam VN
Blood Cells Mol Dis; 2020 Nov; 85():102463. PubMed ID: 32652459
[TBL] [Abstract][Full Text] [Related]
2. GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis.
Levstik A; Stuart A; Adams PC
Ann Hepatol; 2016 Nov-Dec 2016; 15(6):907-910. PubMed ID: 27740525
[TBL] [Abstract][Full Text] [Related]
3. Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload.
McLaren CE; Emond MJ; Subramaniam VN; Phatak PD; Barton JC; Adams PC; Goh JB; McDonald CJ; Powell LW; Gurrin LC; Allen KJ; Nickerson DA; Louie T; Ramm GA; Anderson GJ; McLaren GD
Hepatology; 2015 Aug; 62(2):429-39. PubMed ID: 25605615
[TBL] [Abstract][Full Text] [Related]
4. GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors.
Greni F; Valenti L; Mariani R; Pelloni I; Rametta R; Busti F; Ravasi G; Girelli D; Fargion S; Galimberti S; Piperno A; Pelucchi S
Ann Hepatol; 2017; 16(3):451-456. PubMed ID: 28425416
[TBL] [Abstract][Full Text] [Related]
5. GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.
Barton JC; Chen WP; Emond MJ; Phatak PD; Subramaniam VN; Adams PC; Gurrin LC; Anderson GJ; Ramm GA; Powell LW; Allen KJ; Phillips JD; Parker CJ; McLaren GD; McLaren CE
Blood Cells Mol Dis; 2017 Mar; 63():15-20. PubMed ID: 27936396
[TBL] [Abstract][Full Text] [Related]
6. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
Warne CD; Zaloumis SG; Bertalli NA; Delatycki MB; Nicoll AJ; McLaren CE; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ; Gurrin LC;
J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
[TBL] [Abstract][Full Text] [Related]
7. HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.
Gurrin LC; Bertalli NA; Dalton GW; Osborne NJ; Constantine CC; McLaren CE; English DR; Gertig DM; Delatycki MB; Nicoll AJ; Southey MC; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ;
Hepatology; 2009 Jul; 50(1):94-101. PubMed ID: 19554541
[TBL] [Abstract][Full Text] [Related]
8. The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda.
Farrell CP; Overbey JR; Naik H; Nance D; McLaren GD; McLaren CE; Zhou L; Desnick RJ; Parker CJ; Phillips JD
PLoS One; 2016; 11(9):e0163322. PubMed ID: 27661980
[TBL] [Abstract][Full Text] [Related]
9. HFE mutations, iron deficiency and overload in 10,500 blood donors.
Jackson HA; Carter K; Darke C; Guttridge MG; Ravine D; Hutton RD; Napier JA; Worwood M
Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
[TBL] [Abstract][Full Text] [Related]
10. Dysregulated hepcidin response to dietary iron in male mice with reduced Gnpat expression.
Rishi G; Secondes ES; Asplett K; Wallace DF; Ostini L; Berger J; Subramaniam VN
Biosci Rep; 2020 Aug; 40(8):. PubMed ID: 32766721
[TBL] [Abstract][Full Text] [Related]
11. Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes.
Barton JC; McLaren CE; Chen WP; Ramm GA; Anderson GJ; Powell LW; Subramaniam VN; Adams PC; Phatak PD; Gurrin LC; Phillips JD; Parker CJ; Emond MJ; McLaren GD
Ann Hepatol; 2018 Aug; 17(5):871-879. PubMed ID: 30145563
[TBL] [Abstract][Full Text] [Related]
12. HFE genotype in patients with hemochromatosis and other liver diseases.
Bacon BR; Olynyk JK; Brunt EM; Britton RS; Wolff RK
Ann Intern Med; 1999 Jun; 130(12):953-62. PubMed ID: 10383365
[TBL] [Abstract][Full Text] [Related]
13. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
Lawless MW; White M; Mankan AK; O'Dwyer MJ; Norris S
Tissue Antigens; 2007 Oct; 70(4):294-300. PubMed ID: 17767550
[TBL] [Abstract][Full Text] [Related]
14. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
Raddatz D; Legler T; Lynen R; Addicks N; Ramadori G
Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375
[TBL] [Abstract][Full Text] [Related]
15. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
Koefoed P; Dalhoff K; Dissing J; Kramer I; Milman N; Pedersen P; Simonsen K; Tygstrup N; Nielsen FC
Scand J Clin Lab Invest; 2002; 62(7):527-35. PubMed ID: 12512743
[TBL] [Abstract][Full Text] [Related]
16. Differential HFE allele expression in hemochromatosis heterozygotes.
Rosmorduc O; Poupon R; Nion I; Wendum D; Feder J; Béréziat G; Hermelin B
Gastroenterology; 2000 Oct; 119(4):1075-86. PubMed ID: 11040194
[TBL] [Abstract][Full Text] [Related]
17. Gnpat does not play an essential role in systemic iron homeostasis in murine model.
An P; Wang J; Wang H; Jiang L; Wang J; Min J; Wang F
J Cell Mol Med; 2020 Apr; 24(7):4118-4126. PubMed ID: 32108988
[TBL] [Abstract][Full Text] [Related]
18. Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y.
Barton JC; Barton JC; Acton RT
PLoS One; 2022; 17(7):e0271973. PubMed ID: 35895739
[TBL] [Abstract][Full Text] [Related]
19. Prevalence and characteristics of anti-HCV positivity and chronic hepatitis C virus infection in HFE p.C282Y homozygotes.
Barton JC; Barton JC; Adams PC
Ann Hepatol; 2019; 18(2):354-359. PubMed ID: 31056361
[TBL] [Abstract][Full Text] [Related]
20. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
Pedersen P; Milman N
Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
