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Results: 1 to 20 of 99

Similar articles for PubMed (Select 19820698)

1.

Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.

Chambers JC, Zhang W, Li Y, Sehmi J, Wass MN, Zabaneh D, Hoggart C, Bayele H, McCarthy MI, Peltonen L, Freimer NB, Srai SK, Maxwell PH, Sternberg MJ, Ruokonen A, Abecasis G, Jarvelin MR, Scott J, Elliott P, Kooner JS.

Nat Genet. 2009 Nov;41(11):1170-2. doi: 10.1038/ng.462. Epub 2009 Oct 11.

2.

Association of TMPRSS6 polymorphisms with ferritin, hemoglobin, and type 2 diabetes risk in a Chinese Han population.

Gan W, Guan Y, Wu Q, An P, Zhu J, Lu L, Jing L, Yu Y, Ruan S, Xie D, Makrides M, Gibson RA, Anderson GJ, Li H, Lin X, Wang F.

Am J Clin Nutr. 2012 Mar;95(3):626-32. doi: 10.3945/ajcn.111.025684. Epub 2012 Feb 1.

3.

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.

4.

Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study.

Galesloot TE, Geurts-Moespot AJ, den Heijer M, Sweep FC, Fleming RE, Kiemeney LA, Vermeulen SH, Swinkels DW.

J Med Genet. 2013 Sep;50(9):593-8. doi: 10.1136/jmedgenet-2013-101673. Epub 2013 Jun 21.

PMID:
23794717
5.

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

Benyamin B, Ferreira MA, Willemsen G, Gordon S, Middelberg RP, McEvoy BP, Hottenga JJ, Henders AK, Campbell MJ, Wallace L, Frazer IH, Heath AC, de Geus EJ, Nyholt DR, Visscher PM, Penninx BW, Boomsma DI, Martin NG, Montgomery GW, Whitfield JB.

Nat Genet. 2009 Nov;41(11):1173-5. doi: 10.1038/ng.456. Epub 2009 Oct 11.

6.

TMPRSS6 rs855791 modulates hepcidin transcription in vitro and serum hepcidin levels in normal individuals.

Nai A, Pagani A, Silvestri L, Campostrini N, Corbella M, Girelli D, Traglia M, Toniolo D, Camaschella C.

Blood. 2011 Oct 20;118(16):4459-62. doi: 10.1182/blood-2011-06-364034. Epub 2011 Aug 26.

7.

A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.

Melis MA, Cau M, Congiu R, Sole G, Barella S, Cao A, Westerman M, Cazzola M, Galanello R.

Haematologica. 2008 Oct;93(10):1473-9. doi: 10.3324/haematol.13342. Epub 2008 Jul 4.

8.

A genome-wide association analysis of serum iron concentrations.

Tanaka T, Roy CN, Yao W, Matteini A, Semba RD, Arking D, Walston JD, Fried LP, Singleton A, Guralnik J, Abecasis GR, Bandinelli S, Longo DL, Ferrucci L.

Blood. 2010 Jan 7;115(1):94-6. doi: 10.1182/blood-2009-07-232496. Epub 2009 Oct 30.

9.

TMPRSS6 rs855791 polymorphism influences the susceptibility to iron deficiency anemia in women at reproductive age.

Pei SN, Ma MC, You HL, Fu HC, Kuo CY, Rau KM, Wang MC, Lee CT.

Int J Med Sci. 2014 Apr 16;11(6):614-9. doi: 10.7150/ijms.8582. eCollection 2014.

10.

The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis.

Pelusi S, Girelli D, Rametta R, Campostrini N, Alfieri C, Traglia M, Dongiovanni P, Como G, Toniolo D, Camaschella C, Messa P, Fargion S, Valenti L.

BMC Nephrol. 2013 Feb 22;14:48. doi: 10.1186/1471-2369-14-48.

11.

A novel TMPRSS6 mutation that prevents protease auto-activation causes IRIDA.

Altamura S, D'Alessio F, Selle B, Muckenthaler MU.

Biochem J. 2010 Nov 1;431(3):363-71. doi: 10.1042/BJ20100668.

12.

The serine protease TMPRSS6 is required to sense iron deficiency.

Du X, She E, Gelbart T, Truksa J, Lee P, Xia Y, Khovananth K, Mudd S, Mann N, Moresco EM, Beutler E, Beutler B.

Science. 2008 May 23;320(5879):1088-92. doi: 10.1126/science.1157121. Epub 2008 May 1.

13.

Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.

Cau M, Melis MA, Congiu R, Galanello R.

Expert Rev Hematol. 2010 Apr;3(2):205-16. doi: 10.1586/ehm.10.2. Review.

PMID:
21083463
14.

Genetic variability of TMPRSS6 and its association with iron deficiency anaemia.

Delbini P, Vaja V, Graziadei G, Duca L, Nava I, Refaldi C, Cappellini MD.

Br J Haematol. 2010 Nov;151(3):281–4. doi: 10.1111/j.1365-2141.2010.08349.x.

PMID:
20738301
15.

Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.

McLaren CE, McLachlan S, Garner CP, Vulpe CD, Gordeuk VR, Eckfeldt JH, Adams PC, Acton RT, Murray JA, Leiendecker-Foster C, Snively BM, Barcellos LF, Cook JD, McLaren GD.

PLoS One. 2012;7(6):e38339. doi: 10.1371/journal.pone.0038339. Epub 2012 Jun 22.

16.

Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia.

Beutler E, Van Geet C, te Loo DM, Gelbart T, Crain K, Truksa J, Lee PL.

Blood Cells Mol Dis. 2010 Jan 15;44(1):16-21. doi: 10.1016/j.bcmd.2009.09.001. Epub 2009 Oct 8.

17.

Retinal expression of the serine protease matriptase-2 (Tmprss6) and its role in retinal iron homeostasis.

Gnana-Prakasam JP, Baldowski RB, Ananth S, Martin PM, Smith SB, Ganapathy V.

Mol Vis. 2014 Apr 26;20:561-74. eCollection 2014.

18.

Inter-ethnic differences in genetic variants within the transmembrane protease, serine 6 (TMPRSS6) gene associated with iron status indicators: a systematic review with meta-analyses.

Gichohi-Wainaina WN, Towers GW, Swinkels DW, Zimmermann MB, Feskens EJ, Melse-Boonstra A.

Genes Nutr. 2015 Jan;10(1):442. doi: 10.1007/s12263-014-0442-2. Epub 2014 Nov 22.

19.

The A736V TMPRSS6 polymorphism influences hepatic iron overload in nonalcoholic fatty liver disease.

Valenti L, Rametta R, Dongiovanni P, Motta BM, Canavesi E, Pelusi S, Pulixi EA, Fracanzani AL, Fargion S.

PLoS One. 2012;7(11):e48804. doi: 10.1371/journal.pone.0048804. Epub 2012 Nov 5.

20.

Cloning and characterization of TMPRSS6, a novel type 2 transmembrane serine protease.

Park TJ, Lee YJ, Kim HJ, Park HG, Park WJ.

Mol Cells. 2005 Apr 30;19(2):223-7.

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