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Items: 1 to 20 of 101

1.

Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene.

Jahanshad N, Kohannim O, Hibar DP, Stein JL, McMahon KL, de Zubicaray GI, Medland SE, Montgomery GW, Whitfield JB, Martin NG, Wright MJ, Toga AW, Thompson PM.

Proc Natl Acad Sci U S A. 2012 Apr 3;109(14):E851-9. doi: 10.1073/pnas.1105543109. Epub 2012 Jan 9.

2.

Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.

Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.

Eur J Immunogenet. 2000 Jun;27(3):129-34.

PMID:
10940080
3.

Variants in iron metabolism genes predict higher blood lead levels in young children.

Hopkins MR, Ettinger AS, Hernández-Avila M, Schwartz J, Téllez-Rojo MM, Lamadrid-Figueroa H, Bellinger D, Hu H, Wright RO.

Environ Health Perspect. 2008 Sep;116(9):1261-6. doi: 10.1289/ehp.11233.

4.

Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins.

Whitfield JB, Cullen LM, Jazwinska EC, Powell LW, Heath AC, Zhu G, Duffy DL, Martin NG.

Am J Hum Genet. 2000 Apr;66(4):1246-58. Epub 2000 Mar 15.

5.

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

Benyamin B, McRae AF, Zhu G, Gordon S, Henders AK, Palotie A, Peltonen L, Martin NG, Montgomery GW, Whitfield JB, Visscher PM.

Am J Hum Genet. 2009 Jan;84(1):60-5. doi: 10.1016/j.ajhg.2008.11.011. Epub 2008 Dec 11.

6.

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. doi: 10.1016/j.jhep.2014.10.017. Epub 2014 Oct 18.

PMID:
25457201
7.

Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.

Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.

Immunogenetics. 1998 Apr;47(5):404-10.

PMID:
9510559
8.

Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.

Aranda N, Viteri FE, Montserrat C, Arija V.

Ann Hematol. 2010 Aug;89(8):767-73. doi: 10.1007/s00277-010-0901-9. Epub 2010 Jan 28.

9.

HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France.

Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou JJ.

Br J Dermatol. 2001 Mar;144(3):533-9.

PMID:
11260010
10.

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in southern Italy.

Greco V, De Marco EV, Rocca FE, Annesi F, Civitelli D, Provenzano G, Tarantino P, Scornaienchi V, Pucci F, Salsone M, Novellino F, Morelli M, Paglionico S, Gambardella A, Quattrone A, Annesi G.

Neurol Sci. 2011 Jun;32(3):525-7. doi: 10.1007/s10072-011-0504-9. Epub 2011 Mar 8.

PMID:
21384276
11.

Iron genes, iron load and risk of Alzheimer's disease.

Lehmann DJ, Worwood M, Ellis R, Wimhurst VL, Merryweather-Clarke AT, Warden DR, Smith AD, Robson KJ.

J Med Genet. 2006 Oct;43(10):e52.

12.

Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease.

Giambattistelli F, Bucossi S, Salustri C, Panetta V, Mariani S, Siotto M, Ventriglia M, Vernieri F, Dell'acqua ML, Cassetta E, Rossini PM, Squitti R.

Neurobiol Aging. 2012 Aug;33(8):1633-41. doi: 10.1016/j.neurobiolaging.2011.03.005. Epub 2011 Apr 21.

PMID:
21514009
13.

HFE gene variants affect iron in the brain.

Nandar W, Connor JR.

J Nutr. 2011 Apr 1;141(4):729S-739S. doi: 10.3945/jn.110.130351. Epub 2011 Feb 23. Review.

14.
15.

Iron overload and HFE gene mutations in Czech patients with chronic liver diseases.

Dostalikova-Cimburova M, Kratka K, Stransky J, Putova I, Cieslarova B, Horak J.

Dis Markers. 2012;32(1):65-72. doi: 10.3233/DMA-2012-0861.

16.

Gender and iron genes may modify associations between brain iron and memory in healthy aging.

Bartzokis G, Lu PH, Tingus K, Peters DG, Amar CP, Tishler TA, Finn JP, Villablanca P, Altshuler LL, Mintz J, Neely E, Connor JR.

Neuropsychopharmacology. 2011 Jun;36(7):1375-84. doi: 10.1038/npp.2011.22. Epub 2011 Mar 9.

17.

HFE genotype and iron metabolism in Chinese patients with myelodysplastic syndromes and aplastic anemia.

Nie L, Li L, Yang L, Zhang Y, Xiao Z.

Ann Hematol. 2010 Dec;89(12):1249-53. doi: 10.1007/s00277-010-1016-z. Epub 2010 Jun 19.

PMID:
20563578
18.

Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.

Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.

Hematol J. 2003;4(6):436-40.

PMID:
14671617
19.

Hemochromatosis and iron-overload screening in a racially diverse population.

Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators..

N Engl J Med. 2005 Apr 28;352(17):1769-78.

20.

A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.

Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK.

Gastroenterology. 2002 Mar;122(3):646-51. Erratum in: Gastroenterology 2002 Apr;122(4):1191.

PMID:
11874997

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