Divoky V - Search Results

1

Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia.

Kapralova K, Horvathova M, Pecquet C, Fialova Kucerova J, Pospisilova D, Leroy E, Kralova B, Milosevic Feenstra JD, Schischlik F, Kralovics R, Constantinescu SN, Divoky V. Kapralova K, et al. Among authors: divoky v. Blood. 2016 Sep 8;128(10):1418-23. doi: 10.1182/blood-2016-02-698951. Epub 2016 Jul 7. Blood. 2016. PMID: 27389715 Free article.

2

Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells.

Priwitzerova M, Pospisilova D, Prchal JT, Indrak K, Hlobilkova A, Mihal V, Ponka P, Divoky V. Priwitzerova M, et al. Among authors: divoky v. Blood. 2004 May 15;103(10):3991-2. doi: 10.1182/blood-2004-01-0225. Blood. 2004. PMID: 15121718 Free article. No abstract available.

3

Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.

Mims MP, Guan Y, Pospisilova D, Priwitzerova M, Indrak K, Ponka P, Divoky V, Prchal JT. Mims MP, et al. Among authors: divoky v. Blood. 2005 Feb 1;105(3):1337-42. doi: 10.1182/blood-2004-07-2966. Epub 2004 Sep 30. Blood. 2005. PMID: 15459009 Free article.

4

Functional consequences of the human DMT1 (SLC11A2) mutation on protein expression and iron uptake.

Priwitzerova M, Nie G, Sheftel AD, Pospisilova D, Divoky V, Ponka P. Priwitzerova M, et al. Among authors: divoky v. Blood. 2005 Dec 1;106(12):3985-7. doi: 10.1182/blood-2005-04-1550. Epub 2005 Aug 9. Blood. 2005. PMID: 16091455 Free article.

5

Most pediatric patients with essential thrombocythemia show hypersensitivity to erythropoietin in vitro, with rare JAK2 V617F-positive erythroid colonies.

Veselovska J, Pospisilova D, Pekova S, Horvathova M, Solna R, Cmejlova J, Cmejla R, Belickova M, Mihal V, Stary J, Divoky V. Veselovska J, et al. Among authors: divoky v. Leuk Res. 2008 Mar;32(3):369-77. doi: 10.1016/j.leukres.2007.07.011. Epub 2007 Aug 23. Leuk Res. 2008. PMID: 17719087

6

Molecular basis of hereditary iron homeostasis defects.

Horvathova M, Ponka P, Divoky V. Horvathova M, et al. Among authors: divoky v. Hematology. 2010 Apr;15(2):96-111. doi: 10.1179/102453310X12583347009810. Hematology. 2010. PMID: 20423570 Free article. Review.

7

Partial glutathione reductase deficiency as a cause of diverse clinical manifestations in a family with unstable hemoglobin (Hemoglobin Haná, β63(E7) His-Asn).

Mojzikova R, Dolezel P, Pavlicek J, Mlejnek P, Pospisilova D, Divoky V. Mojzikova R, et al. Among authors: divoky v. Blood Cells Mol Dis. 2010 Oct 15;45(3):219-22. doi: 10.1016/j.bcmd.2010.07.003. Epub 2010 Aug 9. Blood Cells Mol Dis. 2010. PMID: 20692194

8

New mutation in erythroid-specific delta-aminolevulinate synthase as the cause of X-linked sideroblastic anemia responsive to pyridoxine.

Kucerova J, Horvathova M, Mojzikova R, Belohlavkova P, Cermak J, Divoky V. Kucerova J, et al. Among authors: divoky v. Acta Haematol. 2011;125(4):193-7. doi: 10.1159/000322870. Epub 2011 Jan 20. Acta Haematol. 2011. PMID: 21252495

9

Erythropoietin-driven signaling ameliorates the survival defect of DMT1-mutant erythroid progenitors and erythroblasts.

Horvathova M, Kapralova K, Zidova Z, Dolezal D, Pospisilova D, Divoky V. Horvathova M, et al. Among authors: divoky v. Haematologica. 2012 Oct;97(10):1480-8. doi: 10.3324/haematol.2011.059550. Epub 2012 May 11. Haematologica. 2012. PMID: 22580996 Free PMC article.

10

RUNX1 and NF-E2 upregulation is not specific for MPNs, but is seen in polycythemic disorders with augmented HIF signaling.

Kapralova K, Lanikova L, Lorenzo F, Song J, Horvathova M, Divoky V, Prchal JT. Kapralova K, et al. Among authors: divoky v. Blood. 2014 Jan 16;123(3):391-4. doi: 10.1182/blood-2013-10-534222. Epub 2013 Dec 2. Blood. 2014. PMID: 24297870 Free PMC article.

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