Prchal JT - Search Results

1

Thrombotic, inflammatory, and HIF-regulated genes and thrombosis risk in polycythemia vera and essential thrombocythemia.

Gangaraju R, Song J, Kim SJ, Tashi T, Reeves BN, Sundar KM, Thiagarajan P, Prchal JT. Gangaraju R, et al. Among authors: prchal jt. Blood Adv. 2020 Mar 24;4(6):1115-1130. doi: 10.1182/bloodadvances.2019001379. Blood Adv. 2020. PMID: 32203583 Free PMC article.

2

Familial and congenital polycythemia in three unrelated families.

Emanuel PD, Eaves CJ, Broudy VC, Papayannopoulou T, Moore MR, D'Andrea AD, Prchal JF, Eaves AC, Prchal JT. Emanuel PD, et al. Among authors: prchal jf, prchal jt. Blood. 1992 Jun 1;79(11):3019-30. Blood. 1992. PMID: 1316790 Free article.

3

Primary familial polycythemia: a frameshift mutation in the erythropoietin receptor gene and increased sensitivity of erythroid progenitors to erythropoietin.

Sokol L, Luhovy M, Guan Y, Prchal JF, Semenza GL, Prchal JT. Sokol L, et al. Among authors: prchal jf, prchal jt. Blood. 1995 Jul 1;86(1):15-22. Blood. 1995. PMID: 7795221 Free article.

4

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.

5

Haematopoietic progenitors and signal transduction in polycythaemia vera and primary thrombocythaemia.

Kralovics R, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Baillieres Clin Haematol. 1998 Dec;11(4):803-18. doi: 10.1016/s0950-3536(98)80040-1. Baillieres Clin Haematol. 1998. PMID: 10640218 Review.

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

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.

8

Mutations in the VHL gene in sporadic apparently congenital polycythemia.

Pastore YD, Jelinek J, Ang S, Guan Y, Liu E, Jedlickova K, Krishnamurti L, Prchal JT. Pastore YD, et al. Among authors: prchal jt. Blood. 2003 Feb 15;101(4):1591-5. doi: 10.1182/blood-2002-06-1843. Epub 2002 Oct 10. Blood. 2003. PMID: 12393546 Free article.

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

Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease.

Kralovics R, Stockton DW, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Blood. 2003 Nov 15;102(10):3793-6. doi: 10.1182/blood-2003-03-0885. Epub 2003 Jun 26. Blood. 2003. PMID: 12829587 Free article.

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