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Items: 1 to 20 of 82

1.

Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis.

Percy MJ, Rumi E.

Am J Hematol. 2009 Jan;84(1):46-54. doi: 10.1002/ajh.21313. Review.

2.

[Mutations in hypoxia-inducible factor and its regulatory molecules in familial erythrocytosis].

Komatsu N.

Rinsho Ketsueki. 2009 Oct;50(10):1589-94. Review. Japanese. No abstract available.

PMID:
19915370
3.

The HIF pathway and erythrocytosis.

Lee FS, Percy MJ.

Annu Rev Pathol. 2011;6:165-92. doi: 10.1146/annurev-pathol-011110-130321. Review.

PMID:
20939709
4.

Familial chronic myeloproliferative disorders: the state of the art.

Rumi E.

Hematol Oncol. 2008 Sep;26(3):131-8. doi: 10.1002/hon.863. Review.

PMID:
18484677
5.

[Regulation of erythropoiesis by hypoxia inducible factors (HIFs)].

Kirito K.

Rinsho Ketsueki. 2011 Jun;52(6):368-75. Review. No abstract available.

PMID:
21737989
6.

Advances in understanding the pathogenesis of familial thrombocythaemia.

Teofili L, Larocca LM.

Br J Haematol. 2011 Mar;152(6):701-12. doi: 10.1111/j.1365-2141.2010.08500.x. Review.

PMID:
21303356
7.

Two new mutations in the HIF2A gene associated with erythrocytosis.

Percy MJ, Chung YJ, Harrison C, Mercieca J, Hoffbrand AV, Dinardo CL, Santos PC, Fonseca GH, Gualandro SF, Pereira AC, Lappin TR, McMullin MF, Lee FS.

Am J Hematol. 2012 Apr;87(4):439-42. doi: 10.1002/ajh.23123. No abstract available.

8.

Hereditary erythrocytosis, thrombocytosis and neutrophilia.

Hong WJ, Gotlib J.

Best Pract Res Clin Haematol. 2014 Jun;27(2):95-106. doi: 10.1016/j.beha.2014.07.002. Review.

PMID:
25189721
9.

Narrative review: Thrombocytosis, polycythemia vera, and JAK2 mutations: The phenotypic mimicry of chronic myeloproliferation.

Spivak JL.

Ann Intern Med. 2010 Mar 2;152(5):300-6. doi: 10.7326/0003-4819-152-5-201003020-00008. Review.

PMID:
20194236
10.

Involvement of oxygen-sensing pathways in physiologic and pathologic erythropoiesis.

Semenza GL.

Blood. 2009 Sep 3;114(10):2015-9. doi: 10.1182/blood-2009-05-189985. Review.

11.

Erythrocytosis-associated HIF-2alpha mutations demonstrate a critical role for residues C-terminal to the hydroxylacceptor proline.

Furlow PW, Percy MJ, Sutherland S, Bierl C, McMullin MF, Master SR, Lappin TR, Lee FS.

J Biol Chem. 2009 Apr 3;284(14):9050-8. doi: 10.1074/jbc.M808737200.

12.

Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes.

Stein BL, Williams DM, O'Keefe C, Rogers O, Ingersoll RG, Spivak JL, Verma A, Maciejewski JP, McDevitt MA, Moliterno AR.

Haematologica. 2011 Oct;96(10):1462-9. doi: 10.3324/haematol.2011.045591.

13.

Oxygen sensing: recent insights from idiopathic erythrocytosis.

Lee FS, Percy MJ, McMullin MF.

Cell Cycle. 2006 May;5(9):941-5.

14.

Phenotypic variations and new mutations in JAK2 V617F-negative polycythemia vera, erythrocytosis, and idiopathic myelofibrosis.

Williams DM, Kim AH, Rogers O, Spivak JL, Moliterno AR.

Exp Hematol. 2007 Nov;35(11):1641-6.

15.

A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove.

Percy MJ, Furlow PW, Beer PA, Lappin TR, McMullin MF, Lee FS.

Blood. 2007 Sep 15;110(6):2193-6.

16.

Thrombocytosis.

Skoda RC.

Hematology Am Soc Hematol Educ Program. 2009:159-67. doi: 10.1182/asheducation-2009.1.159. Review.

PMID:
20008195
17.

Regulation of HIF prolyl hydroxylases by hypoxia-inducible factors.

Aprelikova O, Chandramouli GV, Wood M, Vasselli JR, Riss J, Maranchie JK, Linehan WM, Barrett JC.

J Cell Biochem. 2004 Jun 1;92(3):491-501. Erratum in: J Cell Biochem. 2004 Oct 15;93(3):639.

PMID:
15156561
18.

Zebrafish mutants in the von Hippel-Lindau tumor suppressor display a hypoxic response and recapitulate key aspects of Chuvash polycythemia.

van Rooijen E, Voest EE, Logister I, Korving J, Schwerte T, Schulte-Merker S, Giles RH, van Eeden FJ.

Blood. 2009 Jun 18;113(25):6449-60. doi: 10.1182/blood-2008-07-167890.

19.

Regulation of gene expression by the hypoxia-inducible factors.

Fedele AO, Whitelaw ML, Peet DJ.

Mol Interv. 2002 Jul;2(4):229-43. Review.

PMID:
14993394
20.

Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia.

Ladroue C, Hoogewijs D, Gad S, Carcenac R, Storti F, Barrois M, Gimenez-Roqueplo AP, Leporrier M, Casadevall N, Hermine O, Kiladjian JJ, Baruchel A, Fakhoury F, Bressac-de Paillerets B, Feunteun J, Mazure N, Pouysségur J, Wenger RH, Richard S, Gardie B.

Haematologica. 2012 Jan;97(1):9-14. doi: 10.3324/haematol.2011.044644.

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