Divoky V - Search Results

1

Coexistence of gain-of-function JAK2 germ line mutations with JAK2V617F in polycythemia vera.

Lanikova L, Babosova O, Swierczek S, Wang L, Wheeler DA, Divoky V, Korinek V, Prchal JT. Lanikova L, et al. Among authors: divoky v. Blood. 2016 Nov 3;128(18):2266-2270. doi: 10.1182/blood-2016-04-711283. Epub 2016 Sep 19. Blood. 2016. PMID: 27647865 Free PMC article. No abstract available.

2

Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene.

Divoky V, Liu Z, Ryan TM, Prchal JF, Townes TM, Prchal JT. Divoky V, et al. Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):986-91. doi: 10.1073/pnas.98.3.986. Proc Natl Acad Sci U S A. 2001. PMID: 11158582 Free PMC article.

3

Non-anemic homozygous beta(o) thalassemia in an African-American family: association of high fetal hemoglobin levels with beta thalassemia alleles.

Divoky V, Mrug M, Thornley-Brown D, Divoka M, Prchal JT. Divoky V, et al. Am J Hematol. 2001 Sep;68(1):43-50. doi: 10.1002/ajh.1147. Am J Hematol. 2001. PMID: 11559936 Free article.

4

Lessons to better understanding of hypoxia sensing. Acquired and congenital mutations resulting in polycythemia.

Prchal JT, Divoky V. Prchal JT, et al. Among authors: divoky v. Adv Exp Med Biol. 2001;502:189-205. Adv Exp Med Biol. 2001. PMID: 11950138 Review.

5

Mouse surviving solely on human erythropoietin receptor (EpoR): model of human EpoR-linked disease.

Divoky V, Prchal JT. Divoky V, et al. Blood. 2002 May 15;99(10):3873-4; author reply 3874-5. doi: 10.1182/blood-2002-01-0301. Blood. 2002. PMID: 12014371 Free article. No abstract available.

6

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.

7

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.

8

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.

9

Hypoxia-inducible factor-1 deficiency results in dysregulated erythropoiesis signaling and iron homeostasis in mouse development.

Yoon D, Pastore YD, Divoky V, Liu E, Mlodnicka AE, Rainey K, Ponka P, Semenza GL, Schumacher A, Prchal JT. Yoon D, et al. Among authors: divoky v. J Biol Chem. 2006 Sep 1;281(35):25703-11. doi: 10.1074/jbc.M602329200. Epub 2006 Jun 19. J Biol Chem. 2006. PMID: 16787915 Free article.

10

Generation of two modified mouse alleles of the Hic1 tumor suppressor gene.

Pospichalova V, Tureckova J, Fafilek B, Vojtechova M, Krausova M, Lukas J, Sloncova E, Takacova S, Divoky V, Leprince D, Plachy J, Korinek V. Pospichalova V, et al. Among authors: divoky v. Genesis. 2011 Mar;49(3):142-51. doi: 10.1002/dvg.20719. Genesis. 2011. PMID: 21309068

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