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Josef T. Prchal

Affiliations: 
University of Alabama, Birmingham, Birmingham, AL, United States 
Area:
Biochemistry, Molecular Biology
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"Josef Prchal"
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Salama ME, Swierczek SI, Tashi T, et al. (2014) Calreticulin mutated prefibrotic-stage myelofibrosis and PMF represent an independent clone from coexisting CLL. Blood. 124: 1691-2
Sarangi S, Lanikova L, Kapralova K, et al. (2014) The homozygous VHL(D126N) missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertension. Pediatric Blood & Cancer. 61: 2104-6
Zhang X, Zhang W, Ma SF, et al. (2014) Hypoxic response contributes to altered gene expression and precapillary pulmonary hypertension in patients with sickle cell disease. Circulation. 129: 1650-8
Wang L, Swierczek SI, Lanikova L, et al. (2014) The relationship of JAK2(V617F) and acquired UPD at chromosome 9p in polycythemia vera. Leukemia. 28: 938-41
Wang L, Swierczek SI, Drummond J, et al. (2014) Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytes. Leukemia. 28: 935-8
Dickinson RE, Milne P, Jardine L, et al. (2014) The evolution of cellular deficiency in GATA2 mutation. Blood. 123: 863-74
Ye Z, Liu CF, Lanikova L, et al. (2014) Differential sensitivity to JAK inhibitory drugs by isogenic human erythroblasts and hematopoietic progenitors generated from patient-specific induced pluripotent stem cells. Stem Cells (Dayton, Ohio). 32: 269-78
Zhang X, Zhang W, Ma SF, et al. (2014) Iron deficiency modifies gene expression variation induced by augmented hypoxia sensing. Blood Cells, Molecules & Diseases. 52: 35-45
Boonyawat B, Dhanraj S, Al Abbas F, et al. (2013) Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopenia. Journal of Clinical Immunology. 33: 1150-5
Zhuang Z, Yang C, Lorenzo F, et al. (2012) Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia. The New England Journal of Medicine. 367: 922-30
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