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Results: 1 to 20 of 86

Similar articles for PubMed (Select 21978626)

1.

Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.

Blanco-Rojo R, Baeza-Richer C, López-Parra AM, Pérez-Granados AM, Brichs A, Bertoncini S, Buil A, Arroyo-Pardo E, Soria JM, Vaquero MP.

Nutr Metab (Lond). 2011 Oct 6;8:69. doi: 10.1186/1743-7075-8-69.

2.

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.

3.

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
4.

Hemochromatosis gene mutations, body iron stores, dietary iron, and risk of colorectal adenoma in women.

Chan AT, Ma J, Tranah GJ, Giovannucci EL, Rifai N, Hunter DJ, Fuchs CS.

J Natl Cancer Inst. 2005 Jun 15;97(12):917-26.

5.

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. doi: 10.1007/s00277-008-0679-1. Epub 2009 Jan 22.

PMID:
19159930
6.

Influence of diet, menstruation and genetic factors on iron status: a cross-sectional study in Spanish women of childbearing age.

Blanco-Rojo R, Toxqui L, López-Parra AM, Baeza-Richer C, Pérez-Granados AM, Arroyo-Pardo E, Vaquero MP.

Int J Mol Sci. 2014 Mar 6;15(3):4077-87. doi: 10.3390/ijms15034077.

7.

A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.

Njajou OT, Houwing-Duistermaat JJ, Osborne RH, Vaessen N, Vergeer J, Heeringa J, Pols HA, Hofman A, van Duijn CM.

Eur J Hum Genet. 2003 Mar;11(3):225-31.

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, 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.

PMID:
11529872
10.

[Role of the hemochromatosis gene in prophyria cutanea tarda. Prospective study of 56 cases].

Skowron F, Bérard F, Grézard P, Wolf F, Morel Y, Perrot H.

Ann Dermatol Venereol. 2001 May;128(5):600-4. French.

11.

The G277S transferrin mutation does not affect iron absorption in iron deficient women.

Sarria B, Navas-Carretero S, Lopez-Parra AM, Perez-Granados AM, Arroyo-Pardo E, Roe MA, Teucher B, Vaquero MP, Fairweather-Tait SJ.

Eur J Nutr. 2007 Feb;46(1):57-60. Epub 2007 Jan 5.

PMID:
17206377
12.

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
13.

TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.

An P, Wu Q, Wang H, Guan Y, Mu M, Liao Y, Zhou D, Song P, Wang C, Meng L, Man Q, Li L, Zhang J, Wang F.

Hum Mol Genet. 2012 May 1;21(9):2124-31. doi: 10.1093/hmg/dds028. Epub 2012 Feb 8.

14.

Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.

De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C.

Haematologica. 2003 Apr;88(4):396-401.

15.
16.

Extrinsic factors modifying expressivity of the HFE variant C282Y, H63D, S65C phenotypes in 1,294 Danish men.

Pedersen P, Milman N.

Ann Hematol. 2009 Oct;88(10):957-65. doi: 10.1007/s00277-009-0714-x. Epub 2009 Mar 7.

PMID:
19271219
17.

Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).

Lamoril J, Andant C, Gouya L, Malonova E, Grandchamp B, Martásek P, Deybac JC, Puy H.

Cell Mol Biol (Noisy-le-grand). 2002 Feb;48(1):33-41.

PMID:
11929045
18.
19.

HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.

Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH.

Circ Cardiovasc Genet. 2009 Feb;2(1):34-7. doi: 10.1161/CIRCGENETICS.108.813089. Epub 2009 Jan 23.

20.

HFE genetic variability, body iron stores, and the risk of type 2 diabetes in U.S. women.

Qi L, Meigs J, Manson JE, Ma J, Hunter D, Rifai N, Hu FB.

Diabetes. 2005 Dec;54(12):3567-72.

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