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Items: 1 to 20 of 101

1.

Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disorders.

Kralovics R, Skoda RC.

Blood Rev. 2005 Jan;19(1):1-13. Review.

PMID:
15572213
2.

Comparison of molecular markers in a cohort of patients with chronic myeloproliferative disorders.

Kralovics R, Buser AS, Teo SS, Coers J, Tichelli A, van der Maas AP, Skoda RC.

Blood. 2003 Sep 1;102(5):1869-71. Epub 2003 May 1.

3.

The chronic myeloproliferative disorders: clonality and clinical heterogeneity.

Spivak JL.

Semin Hematol. 2004 Apr;41(2 Suppl 3):1-5. Review.

PMID:
15190515
4.

Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia.

Puigdecanet E, Espinet B, Villa O, Florensa L, Besses C, Serrano S, Solé F.

Cancer Genet Cytogenet. 2006 May;167(1):39-42.

PMID:
16682284
5.

Molecular detection of c-mpl thrombopoietin receptor gene expression in chronic myeloproliferative disorders.

Duensing S, Duensing A, Meran JG, Kreft A, Büsche G, Ganser A, Georgii A.

Mol Pathol. 1999 Jun;52(3):146-50.

6.

Molecular markers guide diagnosis and treatment in Philadelphia chromosome-negative myeloproliferative disorders (Review).

Vladareanu AM, Müller-Tidow C, Bumbea H, Radesi S.

Oncol Rep. 2010 Mar;23(3):595-604. Review.

PMID:
20126996
7.

[New molecular markers within the chronic myeloproliferative disorders. I: the PRV-1 gene].

Larsen TS, Pallisgaard N, Christensen JH, Gram-Hansen P, Kerndrup GB, Møller MB, Hasselbalch HC.

Ugeskr Laeger. 2006 Sep 25;168(39):3295-9. Review. Danish.

PMID:
17032591
8.

Advances in the molecular characterization of Philadelphia-negative chronic myeloproliferative disorders.

Pikman Y, Levine RL.

Curr Opin Oncol. 2007 Nov;19(6):628-34. Review.

PMID:
17906464
9.

Etiology of the myeloproliferative disorders: the role of thrombopoietin.

Kaushansky K.

Semin Hematol. 2003 Jan;40(1 Suppl 1):6-9. Review.

PMID:
12682875
10.

Expression of the GPI-anchored receptor Prv-1 enhances thrombopoietin and IL-3-induced proliferation in hematopoietic cell lines.

Dillon M, Minear J, Johnson J, Lannutti BJ.

Leuk Res. 2008 May;32(5):811-9. Epub 2007 Nov 5.

PMID:
17980909
11.

Towards a molecular understanding of polycythemia rubra vera.

Pahl HL.

Eur J Biochem. 2000 Jun;267(12):3395-401. Review.

12.

Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis.

Moliterno AR, Williams DM, Gutierrez-Alamillo LI, Salvatori R, Ingersoll RG, Spivak JL.

Proc Natl Acad Sci U S A. 2004 Aug 3;101(31):11444-7. Epub 2004 Jul 21.

13.

Hereditary thrombocytopenia due to reduced platelet production--report on two families and mutational screening of the thrombopoietin receptor gene (c-mpl).

Tonelli R, Strippoli P, Grossi A, Savoia A, Iolascon A, Savino M, Teriaca MS, Servedio V, Morfini M, Zelante L, Borgna-Pignatti C, Rosito P, Pession A, Paolucci G, Bagnara GP.

Thromb Haemost. 2000 Jun;83(6):931-6.

PMID:
10896251
14.

[Dysmegakaryocytopoiesis and dysthrombopoiesis in myeloproliferative syndromes].

Brière J, Kiladjian JJ, Peynaud-Debayle E.

C R Seances Soc Biol Fil. 1996;190(5-6):533-9. French.

PMID:
9074718
15.

MPL W515L mutation in Chinese patients with myeloproliferative diseases.

Xu W, Li JY, Xia J, Zhang SJ, Fan L, Qiao C.

Leuk Lymphoma. 2008 May;49(5):955-8. doi: 10.1080/10428190802035966.

PMID:
18464114
16.
17.

The Jak2V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patients.

Goerttler PS, Steimle C, März E, Johansson PL, Andreasson B, Griesshammer M, Gisslinger H, Heimpel H, Pahl HL.

Blood. 2005 Oct 15;106(8):2862-4. Epub 2005 Jun 28.

18.
19.

Stem cell defects in Philadelphia chromosome negative chronic myeloproliferative disorders: a phenotypic and molecular puzzle?

Bock O, Hussein K, Kreipe H.

Curr Stem Cell Res Ther. 2007 Sep;2(3):253-63. Review.

PMID:
18220909
20.

The genetic basis of myeloproliferative disorders.

Skoda R.

Hematology Am Soc Hematol Educ Program. 2007:1-10.

PMID:
18024602

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