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Results: 16

References for PMC Articles for PubMed (Select 18824595)

1.

Advances in quantitative hepcidin measurements by time-of-flight mass spectrometry.

Swinkels DW, Girelli D, Laarakkers C, Kroot J, Campostrini N, Kemna EH, Tjalsma H.

PLoS One. 2008 Jul 16;3(7):e2706. doi: 10.1371/journal.pone.0002706.

2.

Erythropoietin mediates hepcidin expression in hepatocytes through EPOR signaling and regulation of C/EBPalpha.

Pinto JP, Ribeiro S, Pontes H, Thowfeequ S, Tosh D, Carvalho F, Porto G.

Blood. 2008 Jun 15;111(12):5727-33. doi: 10.1182/blood-2007-08-106195. Epub 2008 Mar 7.

3.

Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1).

Tamary H, Offret H, Dgany O, Foliguet B, Wickramasinghe SN, Krasnov T, Rumilly F, Goujard C, Fénéant-Thibault M, Cynober T, Delaunay J.

Eur J Haematol. 2008 Mar;80(3):271-4. Epub 2007 Dec 7.

PMID:
18081704
4.

Regulation of hepcidin: insights from biochemical analyses on human serum samples.

Kemna EH, Kartikasari AE, van Tits LJ, Pickkers P, Tjalsma H, Swinkels DW.

Blood Cells Mol Dis. 2008 May-Jun;40(3):339-46. Epub 2007 Nov 26.

PMID:
18023212
5.

High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin.

Tanno T, Bhanu NV, Oneal PA, Goh SH, Staker P, Lee YT, Moroney JW, Reed CH, Luban NL, Wang RH, Eling TE, Childs R, Ganz T, Leitman SF, Fucharoen S, Miller JL.

Nat Med. 2007 Sep;13(9):1096-101. Epub 2007 Aug 26.

PMID:
17721544
6.

Liver iron concentrations and urinary hepcidin in beta-thalassemia.

Origa R, Galanello R, Ganz T, Giagu N, Maccioni L, Faa G, Nemeth E.

Haematologica. 2007 May;92(5):583-8.

7.

Hypocholesterolemia in chronic anemias with increased erythropoietic activity.

Shalev H, Kapelushnik J, Moser A, Knobler H, Tamary H.

Am J Hematol. 2007 Mar;82(3):199-202.

PMID:
17039515
8.

Hepcidin and iron-loading anemias.

Nemeth E, Ganz T.

Haematologica. 2006 Jun;91(6):727-32. No abstract available.

9.

Clinical and molecular variability in congenital dyserythropoietic anaemia type I.

Tamary H, Dgany O, Proust A, Krasnov T, Avidan N, Eidelitz-Markus T, Tchernia G, Geneviève D, Cormier-Daire V, Bader-Meunier B, Ferrero-Vacher C, Munzer M, Gruppo R, Fibach E, Konen O, Yaniv I, Delaunay J.

Br J Haematol. 2005 Aug;130(4):628-34.

PMID:
16098079
10.

Hepcidin in iron overload disorders.

Papanikolaou G, Tzilianos M, Christakis JI, Bogdanos D, Tsimirika K, MacFarlane J, Goldberg YP, Sakellaropoulos N, Ganz T, Nemeth E.

Blood. 2005 May 15;105(10):4103-5. Epub 2005 Jan 25.

11.

Hepcidin is decreased in TFR2 hemochromatosis.

Nemeth E, Roetto A, Garozzo G, Ganz T, Camaschella C.

Blood. 2005 Feb 15;105(4):1803-6. Epub 2004 Oct 14.

12.

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.

Am J Hum Genet. 2002 Dec;71(6):1467-74. Epub 2002 Nov 14.

13.

Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis.

Cazzola M, Beguin Y, Bergamaschi G, Guarnone R, Cerani P, Barella S, Cao A, Galanello R.

Br J Haematol. 1999 Sep;106(3):752-5.

PMID:
10468869
14.

Dyserythropoiesis and congenital dyserythropoietic anaemias.

Wickramasinghe SN.

Br J Haematol. 1997 Sep;98(4):785-97. Review. No abstract available.

PMID:
9326170
15.

Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I.

Tamary H, Shalev H, Luria D, Shaft D, Zoldan M, Shalmon L, Gruinspan A, Stark B, Chaison M, Shinar E, Resnitzky P, Zaizov R.

Blood. 1996 Mar 1;87(5):1763-70.

16.

Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts.

Heimpel H, Wendt F.

Helv Med Acta. 1968 Mar;34(2):103-15. No abstract available.

PMID:
5658197
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