Prchal JT - Search Results

1

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

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

2

Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias.

Kralovics R, Indrak K, Stopka T, Berman BW, Prchal JF, Prchal JT. Kralovics R, et al. Among authors: prchal jf, prchal jt. Blood. 1997 Sep 1;90(5):2057-61. Blood. 1997. PMID: 9292543 Free article.

3

Molecular basis for polycythemia.

Prchal JF, Prchal JT. Prchal JF, et al. Among authors: prchal jt. Curr Opin Hematol. 1999 Mar;6(2):100-9. doi: 10.1097/00062752-199903000-00008. Curr Opin Hematol. 1999. PMID: 10088640 Review.

4

Congenital and inherited polycythemia.

Kralovics R, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Curr Opin Pediatr. 2000 Feb;12(1):29-34. doi: 10.1097/00008480-200002000-00006. Curr Opin Pediatr. 2000. PMID: 10676771 Review.

5

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. Among authors: prchal jf, prchal jt. 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.

6

Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disorders.

Prchal JT. Prchal JT. Semin Hematol. 2001 Jan;38(1 Suppl 2):10-20. doi: 10.1016/s0037-1963(01)90135-0. Semin Hematol. 2001. PMID: 11242597 Review.

7

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. Among authors: prchal jt. Am J Hematol. 2001 Sep;68(1):43-50. doi: 10.1002/ajh.1147. Am J Hematol. 2001. PMID: 11559936 Free article.

8

Genetic heterogeneity of primary familial and congenital polycythemia.

Kralovics R, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Am J Hematol. 2001 Oct;68(2):115-21. doi: 10.1002/ajh.1162. Am J Hematol. 2001. PMID: 11559951 Free article.

9

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera.

Kralovics R, Guan Y, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Exp Hematol. 2002 Mar;30(3):229-36. doi: 10.1016/s0301-472x(01)00789-5. Exp Hematol. 2002. PMID: 11882360 Free article.

10

Endemic polycythemia in Russia: mutation in the VHL gene.

Ang SO, Chen H, Gordeuk VR, Sergueeva AI, Polyakova LA, Miasnikova GY, Kralovics R, Stockton DW, Prchal JT. Ang SO, et al. Among authors: prchal jt. Blood Cells Mol Dis. 2002 Jan-Feb;28(1):57-62. doi: 10.1006/bcmd.2002.0488. Blood Cells Mol Dis. 2002. PMID: 11987242

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