168 related articles for article (PubMed ID: 26868056)
1. Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis.
Pelucchi S; Galimberti S; Greni F; Rametta R; Mariani R; Pelloni I; Girelli D; Busti F; Ravasi G; Valsecchi MG; Valenti L; Piperno A
J Gastroenterol Hepatol; 2016 Jul; 31(7):1342-8. PubMed ID: 26868056
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis.
Stickel F; Buch S; Zoller H; Hultcrantz R; Gallati S; Österreicher C; Finkenstedt A; Stadlmayr A; Aigner E; Sahinbegovic E; Sarrazin C; Schafmayer C; Braun F; Erhart W; Nothnagel M; Lerch MM; Mayerle J; Völzke H; Schaller A; Kratzer W; Boehm BO; Sipos B; D'Amato M; Torkvist L; Stal P; Arlt A; Franke A; Becker T; Krawczak M; Zwerina J; Berg T; Hinrichsen H; Krones E; Dejaco C; Strasser M; Datz C; Hampe J
Hum Mol Genet; 2014 Jul; 23(14):3883-90. PubMed ID: 24556216
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. HFE genotype, parenchymal iron accumulation, and liver fibrosis in patients with nonalcoholic fatty liver disease.
Valenti L; Fracanzani AL; Bugianesi E; Dongiovanni P; Galmozzi E; Vanni E; Canavesi E; Lattuada E; Roviaro G; Marchesini G; Fargion S
Gastroenterology; 2010 Mar; 138(3):905-12. PubMed ID: 19931264
[TBL] [Abstract][Full Text] [Related]
5. Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis.
Buch S; Sharma A; Ryan E; Datz C; Griffiths WJH; Way M; Buckley TWM; Ryan JD; Stewart S; Wright C; Dongiovanni P; Fracanzani A; Zwerina J; Merle U; Weiss KH; Aigner E; Krones E; Dejaco C; Fischer J; Berg T; Valenti L; Zoller H; McQuillin A; Hampe J; Stickel F; Morgan MY
Aliment Pharmacol Ther; 2021 Apr; 53(7):830-843. PubMed ID: 33565643
[TBL] [Abstract][Full Text] [Related]
6. Common heterozygous hemochromatosis gene mutations are risk factors for inflammation and fibrosis in chronic hepatitis C.
Geier A; Reugels M; Weiskirchen R; Wasmuth HE; Dietrich CG; Siewert E; Gartung C; Lorenzen J; Bosserhoff AK; Brügmann M; Gressner AM; Matern S; Lammert F
Liver Int; 2004 Aug; 24(4):285-94. PubMed ID: 15287851
[TBL] [Abstract][Full Text] [Related]
7. PNPLA3 and RNF7 Gene Variants are Associated with the Risk of Developing Liver Fibrosis and Cirrhosis in an Eastern European Population.
Kupcinskas J; Valantiene I; Varkalaitė G; Steponaitiene R; Skieceviciene J; Sumskiene J; Petrenkiene V; Kondrackiene J; Kiudelis G; Lammert F; Kupcinskas L
J Gastrointestin Liver Dis; 2017 Mar; 26(1):37-43. PubMed ID: 28338112
[TBL] [Abstract][Full Text] [Related]
8. Genetic disruption of NRF2 promotes the development of necroinflammation and liver fibrosis in a mouse model of HFE-hereditary hemochromatosis.
Duarte TL; Caldas C; Santos AG; Silva-Gomes S; Santos-Gonçalves A; Martins MJ; Porto G; Lopes JM
Redox Biol; 2017 Apr; 11():157-169. PubMed ID: 27936457
[TBL] [Abstract][Full Text] [Related]
9. Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany.
Meier P; Schuff-Werner P; Steiner M
Clin Lab; 2005; 51(9-10):539-43. PubMed ID: 16285477
[TBL] [Abstract][Full Text] [Related]
10. A Simple RFLP-Based Method for
Ogouma-Aworet L; Rabes JP; de Mazancourt P
Biomed Res Int; 2020; 2020():9396318. PubMed ID: 33457423
[TBL] [Abstract][Full Text] [Related]
11. Iron-overload-related disease in HFE hereditary hemochromatosis.
Allen KJ; Gurrin LC; Constantine CC; Osborne NJ; Delatycki MB; Nicoll AJ; McLaren CE; Bahlo M; Nisselle AE; Vulpe CD; Anderson GJ; Southey MC; Giles GG; English DR; Hopper JL; Olynyk JK; Powell LW; Gertig DM
N Engl J Med; 2008 Jan; 358(3):221-30. PubMed ID: 18199861
[TBL] [Abstract][Full Text] [Related]
12. PNPLA3 rs738409C/G polymorphism in cirrhosis: relationship with the aetiology of liver disease and hepatocellular carcinoma occurrence.
Falleti E; Fabris C; Cmet S; Cussigh A; Bitetto D; Fontanini E; Fornasiere E; Bignulin S; Fumolo E; Bignulin E; Pirisi M; Toniutto P
Liver Int; 2011 Sep; 31(8):1137-43. PubMed ID: 21745286
[TBL] [Abstract][Full Text] [Related]
13. Reduced phenotypic expression in genetic hemochromatosis with time: Role of exposure to non-genetic modifiers.
Deugnier Y; Morcet J; Lainé F; Hamdi-Roze H; Bollard AS; Guyader D; Moirand R; Bardou-Jacquet E
J Hepatol; 2019 Jan; 70(1):118-125. PubMed ID: 30244162
[TBL] [Abstract][Full Text] [Related]
14. Penetrance of the C28Y/C282Y genotype of the HFE gene.
Asberg A; Hveem K; Kannelønning K; Irgens WØ
Scand J Gastroenterol; 2007 Sep; 42(9):1073-7. PubMed ID: 17710673
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. The rs508487, rs236911, and rs236918 Genetic Variants of the Proprotein Convertase Subtilisin-Kexin Type 7 (
Vargas-Alarcón G; Pérez-Méndez O; González-Pacheco H; Ramírez-Bello J; Posadas-Sánchez R; Escobedo G; Fragoso JM
Cells; 2021 Jun; 10(6):. PubMed ID: 34207761
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. The ancestral haplotype markers HLA -A3 and B7 do not influence the likelihood of advanced hepatic fibrosis or cirrhosis in HFE hemochromatosis.
Olynyk JK; Grainger R; Currie H; Ramm LE; Ramm GA
Sci Rep; 2023 May; 13(1):7775. PubMed ID: 37179448
[TBL] [Abstract][Full Text] [Related]
19. Mutations in the HFE gene and their interaction with exogenous risk factors in hepatocellular carcinoma.
Fargion S; Stazi MA; Fracanzani AL; Mattioli M; Sampietro M; Tavazzi D; Bertelli C; Patriarca V; Mariani C; Fiorelli G
Blood Cells Mol Dis; 2001; 27(2):505-11. PubMed ID: 11500061
[TBL] [Abstract][Full Text] [Related]
20. Population-based analysis of the frequency of HFE gene polymorphisms: Correlation with the susceptibility to develop hereditary hemochromatosis.
Katsarou MS; Latsi R; Papasavva M; Demertzis N; Kalogridis T; Tsatsakis AM; Spandidos DA; Drakoulis N
Mol Med Rep; 2016 Jul; 14(1):630-6. PubMed ID: 27221532
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]