Prchal JT - Search Results

1

Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women.

Mims MP, Hayes TG, Zheng S, Leal SM, Frolov A, Ittmann MM, Wheeler TM, Prchal JT. Mims MP, et al. Among authors: prchal jt. Cancer Res. 2006 Feb 1;66(3):1880; author reply 1880-1. doi: 10.1158/0008-5472.CAN-05-3774. Cancer Res. 2006. PMID: 16452251 Free PMC article. No abstract available.

2

Divalent metal transporter 1.

Mims MP, Prchal JT. Mims MP, et al. Among authors: prchal jt. Hematology. 2005 Aug;10(4):339-45. doi: 10.1080/10245330500093419. Hematology. 2005. PMID: 16085548 Review.

3

Analysis of the E399D mutation in SLC11A2.

Gunshin H, Jin J, Fujiwara Y, Andrews NC, Mims M, Prchal J. Gunshin H, et al. Blood. 2005 Sep 15;106(6):2221; author reply 2221-2. doi: 10.1182/blood-2005-03-1192. Blood. 2005. PMID: 16140868 Free article. No abstract available.

4

DMT1 mutation: response of anemia to darbepoetin administration and implications for iron homeostasis.

Pospisilova D, Mims MP, Nemeth E, Ganz T, Prchal JT. Pospisilova D, et al. Among authors: prchal jt. Blood. 2006 Jul 1;108(1):404-5. doi: 10.1182/blood-2006-02-003962. Blood. 2006. PMID: 16790587 Free PMC article. No abstract available.

5

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: prchal jt. 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.

6

Chuvash polycythemia VHLR200W mutation is associated with down-regulation of hepcidin expression.

Gordeuk VR, Miasnikova GY, Sergueeva AI, Niu X, Nouraie M, Okhotin DJ, Polyakova LA, Ammosova T, Nekhai S, Ganz T, Prchal JT. Gordeuk VR, et al. Among authors: prchal jt. Blood. 2011 Nov 10;118(19):5278-82. doi: 10.1182/blood-2011-03-345512. Epub 2011 Aug 29. Blood. 2011. PMID: 21876117 Free PMC article.

7

The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia.

Miasnikova GY, Sergueeva AI, Nouraie M, Niu X, Okhotin DJ, Polyakova LA, Ganz T, Prchal JT, Gordeuk VR. Miasnikova GY, et al. Among authors: prchal jt. Haematologica. 2011 Sep;96(9):1371-4. doi: 10.3324/haematol.2011.045609. Epub 2011 May 23. Haematologica. 2011. PMID: 21606165 Free PMC article.

8

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: prchal jt. Blood. 2004 May 15;103(10):3991-2. doi: 10.1182/blood-2004-01-0225. Blood. 2004. PMID: 15121718 Free article. No abstract available.

9

Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietin.

Liu E, Jelinek J, Pastore YD, Guan Y, Prchal JF, Prchal JT. Liu E, et al. Among authors: prchal jf, prchal jt. Blood. 2003 Apr 15;101(8):3294-301. doi: 10.1182/blood-2002-07-2287. Epub 2002 Dec 19. Blood. 2003. PMID: 12515724 Free article.

10

Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancer.

Lanikova L, Lorenzo F, Yang C, Vankayalapati H, Drachtman R, Divoky V, Prchal JT. Lanikova L, et al. Among authors: prchal jt. Blood. 2013 May 9;121(19):3918-24. doi: 10.1182/blood-2012-11-469296. Epub 2013 Mar 28. Blood. 2013. PMID: 23538339 Free PMC article.

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