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Josef Prchal

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Lucie Lanikova; Felipe Lorenzo; Vladimir Divoky; Richard Drachtman; Hari Vankayalapati; Chunzhang Yang; Josef T Prchal
Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancer.
Karel Pacak; Josef T Prchal; Tamara Prodanov; Arthur S Tischler; Chunzhang Yang; Tito Fojo; Ivana Jochmanova; Ronald M Lechan; Maria J Merino; Zhengping Zhuang
New syndrome of paraganglioma and somatostatinoma associated with polycythemia.
Josef T Prchal; Victor R Gordeuk
Treatment target in polycythemia vera.

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2013: Lucie Lanikova; Felipe Lorenzo; Vladimir Divoky; Richard Drachtman; Hari Vankayalapati; Chunzhang Yang; Josef T Prchal
Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancer.
Blood 2013;121(19):3918-24.
2013: Karel Pacak; Josef T Prchal; Tamara Prodanov; Arthur S Tischler; Chunzhang Yang; Tito Fojo; Ivana Jochmanova; Ronald M Lechan; Maria J Merino; Zhengping Zhuang
New syndrome of paraganglioma and somatostatinoma associated with polycythemia.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2013;31(13):1690-8.
2013: Josef T Prchal; Victor R Gordeuk
Treatment target in polycythemia vera.
The New England journal of medicine 2013;368(16):1555-6.
2013: Nikica Ljubas Tomasic; Donghoon Yoon; Adelina I Sergueeva; Ernest Bilic; Victor Gordeuk; Chad Huff; Galina Y Miasnikova; Sergei Nekhai; Xiaomei Niu; Lucie Piterkova; Josef T Prchal
The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W).
Haematologica 2013;98(4):560-7.
2013: Maurizio Zangari; Jerry L Spivak; Brady L Stein; Sabina I Swierczek; Giulia Tolomelli; Tamara Berno; Louis Fink; Victor R Gordeuk; Kimberly Hickman; Todd W Kelley; Jasmine C H Lee; Alison R Moliterno; Josef T Prchal
Could hypoxia increase the prevalence of thrombotic complications in polycythemia vera?
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013;24(3):311-6.
2013: Felipe R Lorenzo; Mark Ng Tang Fui; Karel Pacak; Mathis Grossmann; Thanh Huynh; Hariprasad Vankayalapati; Chunzhang Yang; Zhengping Zhuang; Josef T Prchal
A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma.
Journal of molecular medicine (Berlin, Germany) 2013;91(4):507-12.
2013: Chunzhang Yang; Thanh T Huynh; Ronald Lechan; Russell Lonser; Joey Matro; Karel Pacak; Josef T Prchal; Shervin Rahimpour; Michael G Sun; Zhengping Zhuang
Novel HIF2A mutations disrupt oxygen sensing, leading to polycythemia, paragangliomas, and somatostatinomas.
Blood 2013;121(13):2563-6.
2013: Philippe Szankasi; Cecily P Vaughn; David W Bahler; Josef T Prchal; N Scott Reading; Todd W Kelley
A quantitative allele-specific PCR test for the BRAF V600E mutation using a single heterozygous control plasmid for quantitation: a model for qPCR testing without standard curves.
The Journal of molecular diagnostics : JMD 2013;15(2):248-54.
2013: Sabina Swierczek; Helena Urbankova; Karel Indrak; Marie Jarosova; Jaroslav Jelinek; Jana Kucerova; Enli Liu; Jitka Nausova; Josef T Prchal; Paul Roda; Vladimir Divoky
Concomitant JAK2 V617F-positive polycythemia vera and B-cell chronic lymphocytic leukemia in three patients originating from two separate hematopoietic stem cells.
American journal of hematology 2013;88(2):157-8.
2013: Robert D Christensen; Larry D Eggert; Erick Henry; Diane K Lambert; N Scott Reading; Hassan M Yaish; Josef T Prchal
Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system.
Blood cells, molecules & diseases 2013;50(2):105-9.
2013: Donald A McClain; Galina Miasnikova; Xiaomei Niu; Mehdi Nouraie ; David Okhotin; Daniel J Okhotin; Lydia A Polyakova; Josef T Prchal; Juan Salomon-Andonie; Adelina Sergueeva; Judith A Simcox; M Celeste Simon; Jihyun Song; Sabina I Swierczek; Donghoon Yoon; Khadega A Abuelgasim; Rabia Cherqaoui; James E Cox; Jingyu Huang; Victor R Gordeuk
Decreased serum glucose and glycosylated hemoglobin levels in patients with Chuvash polycythemia: a role for HIF in glucose metabolism.
Journal of molecular medicine (Berlin, Germany) 2013;91(1):59-67.
2012: Josef T Prchal
Molecular basis of polycythemic disorders due to aberrant hypoxia sensing and its relevance to acute leukemia.
Best practice & research. Clinical haematology 2012;25(4):493-7.
2012: Roberto H Nussenzveig; Natalie W Ogilvie; Sherrie L Perkins; Lukas Plank; Archana M Agarwal; Tatiana Burjanivova; Juraj Marcinek; Mohamed E Salama; Josef T Prchal
Detection of JAK2 mutations in paraffin marrow biopsies by high resolution melting analysis: identification of L611S alone and in cis with V617F in polycythemia vera.
Leukemia & lymphoma 2012;53(12):2479-86.
2012: Mahmoud Sirdah; Hariprasad Vankayalapati; Lina Aboud; Sherrie L Perkins; N Scott Reading; David Roper; Mohammad E Shubair; Josef T Prchal
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians.
Blood cells, molecules & diseases 2012;49(3-4):152-8.
2012: Zhengping Zhuang; Tito Fojo; Electron Kebebew; Felipe Lorenzo; Maria Merino; Vera Popovic; Josef T Prchal; Constantine A Stratakis; Chunzhang Yang; Karel Pacak
Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia.
The New England journal of medicine 2012;367(10):922-30.
2012: Ri-Li Ge; Chad D Huff; Lynn B Jorde; Josef T Prchal; Ga Qin; Tatum S Simonson; Uran Tanna; David J Witherspoon; Jinchuan Xing; Bai Zhengzhong; Robert C Cooksey; Donald A McClain
Metabolic insight into mechanisms of high-altitude adaptation in Tibetans.
Molecular genetics and metabolism 2012;106(2):244-7.
2012: Mahmoud Sirdah; Lina Aboud; Sherrie L Perkins; N Scott Reading; Mohammad Shubair; Josef T Prchal
Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip.
Blood cells, molecules & diseases 2012;48(4):203-8.
2012: Tatum S Simonson; Lynn B Jorde; Donald A McClain; Josef T Prchal
Genetic determinants of Tibetan high-altitude adaptation.
Human genetics 2012;131(4):527-33.
2012: Sabina I Swierczek; Andrew Wilson; Bradley R Cairns; Neeraj Agarwal; Bradley Cairns; Sue Hammoud; Kimberly Hickman; Jaroslav Jelinek; Charles J Parker; Lucie Piterkova; Josef T Prchal
Methylation of AR locus does not always reflect X chromosome inactivation state.
Blood 2012;119(13):e100-9.
2012: Craig A Sable; Vandana Sachdev; Adelina I Sergueeva; Stanislav Sidenko; Zakari Y Aliyu; Vladimir Bushuev; Oswaldo L Castro; Niti Dham; Mark T Gladwin; Gregory Kato ; Galina Y Miasnikova; Xiaomei Niu; Mehdi Nouraie ; Daniel J Okhotin; Lydia A Polyakova; Josef T Prchal; Alan T Remaley; Victor Roland Gordeuk
Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia).
Haematologica 2012;97(2):193-200.
2011: Victor Roland Gordeuk; Galina Y Miasnikova; Sergei Nekhai; Xiaomei Niu; Mehdi Nouraie ; Daniel J Okhotin; Lydia A Polyakova; Tatyana Ammosova; Tomas Ganz; Adelina I Sergueeva; Josef T Prchal
Chuvash polycythemia VHLR200W mutation is associated with down-regulation of hepcidin expression.
Blood 2011;118(19):5278-82.
2011: Galina Y Miasnikova; Xiaomei Niu; Mehdi Nouraie ; Daniel J Okhotin; Lydia A Polyakova; Josef T Prchal; Adelina I Sergueeva; Tomas Ganz; Victor Roland Gordeuk
The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia.
Haematologica 2011;96(9):1371-4.
2011: Josef T Prchal
Interferon and PV stem cells.
Blood 2011;118(6):1429-30.
2011: Kai Wang; Sabina I Swierczek; Hakon Hakonarson; Kimberly Hickman; Josef T Prchal
Convergent mechanisms of somatic mutations in polycythemia vera.
Discovery medicine 2011;12(62):25-32.
2011: Donghoon Yoon; Prem Ponka; Josef T Prchal
Hypoxia. 5. Hypoxia and hematopoiesis.
American journal of physiology. Cell physiology 2011;300(6):C1215-22.
2011: Sabina I Swierczek; Donghoon Yoon; Christine Bellanné-Chantelot; Soo Jin Kim; Cécile Saint-Martin; Francois Delhommeau; Albert Najman; Josef T Prchal
Extent of hematopoietic involvement by TET2 mutations in JAK2V⁶¹⁷F polycythemia vera.
Haematologica 2011;96(5):775-8.
2011: Felipe R Lorenzo; John D Phillips; Roberto Nussenzveig; Bindu Lingam; Parvaiz Koul; Stanley L Schrier; Josef T Prchal
Molecular basis of two novel mutations found in type I methemoglobinemia.
Blood cells, molecules & diseases 2011;46(4):277-81.
2011: Scott Samuelson; Brenda M Sandmaier; Helen E Heslop; Uday Popat; George Carrum; Richard E Champlin; Rainer Storb; Josef T Prchal; Theodore A Gooley; H Joachim Deeg
Allogeneic haematopoietic cell transplantation for myelofibrosis in 30 patients 60-78 years of age.
British journal of haematology 2011;153(1):76-82.
2011: Hye-Ja Lee; Kyungah Maeng; Hung-The Dang; Gyeoung-jin Kang; Chongsuk Ryou; Jee H Jung; Hee-Kyoung Kang; Josef T Prchal; Eun-Sook Yoo; Donghoon Yoon
Anti-inflammatory effect of methyl dehydrojasmonate (J2) is mediated by the NF-κB pathway.
Journal of molecular medicine (Berlin, Germany) 2011;89(1):83-90.
2011: Kausar Begam Riaz Ahmed; Steven L Warner; Andrew Chen; Eric S Gourley; Xiaohui Liu; Hariprasad Vankayalapati; Roberto Nussenzveig; Josef T Prchal; David J Bearss; Charles J Parker
In vitro and in vivo characterization of SGI-1252, a small molecule inhibitor of JAK2.
Experimental hematology 2011;39(1):14-25.
2011: Victor Roland Gordeuk; Caterina P Minniti; Mehdi Nouraie ; Andrew D Campbell; Sohail R Rana; Lori Luchtman-Jones; Craig A Sable; Niti Dham; Gregory J Ensing; Josef T Prchal; Gregory Kato ; Mark T Gladwin; Oswaldo L Castro
Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia.
Haematologica 2011;96(1):33-40.
2010: Jeffrey J Swensen; Archana M Agarwal; Jose M Esquilin; Sabina I Swierczek; Ajay Perumbeti; Dottie Hussey; Margaret Lee; Clinton H Joiner; Genevieve Pont-Kingdon; Elaine Lyon; Josef T Prchal
Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait.
Blood 2010;116(15):2822-5.
2010: Tatum S Simonson; Yingzhong Yang; Chad D Huff; Haixia Yun; Ga Qin; David J Witherspoon; Zhenzhong Bai; Felipe R Lorenzo; Jinchuan Xing; Lynn B Jorde; Josef T Prchal; RiLi Ge
Genetic evidence for high-altitude adaptation in Tibet.
Science (New York, N.Y.) 2010;329(5987):72-5.
2010: Mehdi Nouraie ; Noel S Reading; Andrew Campbell; Caterina P Minniti; Sohail R Rana; Lori Luchtman-Jones; Gregory Kato ; Mark T Gladwin; Oswaldo L Castro; Josef T Prchal; Victor Roland Gordeuk
Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
British journal of haematology 2010;150(2):218-25.
2010: Carolin J Teman; Andrew Wilson; Sherrie L Perkins; Kimberly Hickman; Josef T Prchal; Mohamed E Salama
Quantification of fibrosis and osteosclerosis in myeloproliferative neoplasms: a computer-assisted image study.
Leukemia research 2010;34(7):871-6.
2010: Donghoon Yoon; David V Okhotin; Bumjun Kim; Yulia Okhotina; Daniel J Okhotin; Galina Y Miasnikova; Adelina I Sergueeva; Lydia A Polyakova; Alexei Maslow; Yonggu Lee; Gregg L Semenza; Josef T Prchal; Victor Roland Gordeuk
Increased size of solid organs in patients with Chuvash polycythemia and in mice with altered expression of HIF-1alpha and HIF-2alpha.
Journal of molecular medicine (Berlin, Germany) 2010;88(5):523-30.
2010: Hana Bruchova-Votavova; Donghoon Yoon; Josef T Prchal
miR-451 enhances erythroid differentiation in K562 cells.
Leukemia & lymphoma 2010;51(4):686-93.
2010: Andrew T Chen; Josef T Prchal
JAK2 kinase inhibitors and myeloproliferative disorders.
Current opinion in hematology 2010;17(2):110-6.
2010: Xiaosong Huang; L Jeanne Pierce; George L Chen; Ko-Tung Chang; Gerald J Spangrude; Josef T Prchal
Erythropoietin receptor signaling regulates both erythropoiesis and megakaryopoiesis in vivo.
Blood cells, molecules & diseases 2010;44(1):1-6.
2010: Silverio Perrotta; Valeria Cucciolla; Marcella Ferraro; Luisa Ronzoni; Annunziata Tramontano; Francesca Rossi; Anna Chiara Scudieri; Adriana Borriello; Domenico Roberti; Bruno Nobili; Maria Domenica Cappellini; Adriana Oliva; Giovanni Amendola; Anna Rita Migliaccio; Patrizia Mancuso; Ines Martin-Padura; Francesco Bertolini; Donghoon Yoon; Josef T Prchal; Fulvio Della Ragione
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors.
PloS one 2010;5(8):e12015.
2009: V Felipe Lorenzo; Yingzhong Yang; Tatum S Simonson; Roberto Nussenzveig; Lynn B Jorde; Josef T Prchal; Ri-Li Ge
Genetic adaptation to extreme hypoxia: study of high-altitude pulmonary edema in a three-generation Han Chinese family.
Blood cells, molecules & diseases 2009;43(3):221-5.
2009: Neeraj Agarwal; Roberto H Nussenzveig; Sabina I Swierczek; Charles J Parker; Josef T Prchal
Does HUMARA assay for assessment of clonal hematopoiesis have shortcomings?
Blood 2009;114(11):2357-8; author reply 2358-9.
2009: Tatiana Usenko; You-Jun Li; Mehran Haeri; Yanmei Li; Laura M Vecchiarelli-Federico; Xiaojun Zhao; Josef T Prchal; Yaacov Ben David
Enrichment of Sca1+ hematopoietic progenitors in polycythemic mice inhibits leukemogenesis.
Blood 2009;114(9):1831-41.
2009: Mohamed E Salama; Sabina I Swierczek; Kimberly Hickman; Andrew Wilson; Josef T Prchal
Plasma quantitation of JAK2 mutation is not suitable as a clinical test: an artifact of storage.
Blood 2009;114(1):223-4; author reply 224.
2009: Roberto H Nussenzveig; Jorge Cortes; Matjaz Sever; Alfonso Quintás-Cardama; Patricia Ault; Taghi Manshouri; Carlos Bueso-Ramos; Josef T Prchal; Andrew Lamb; Srdan Verstovsek
Imatinib mesylate therapy for polycythemia vera: final result of a phase II study initiated in 2001.
International journal of hematology 2009;90(1):58-63.
2009: Hana Bruchova; Donghoon Yoon; Archana M Agarwal; Sabina Swierczek; Josef T Prchal
Erythropoiesis in polycythemia vera is hyper-proliferative and has accelerated maturation.
Blood cells, molecules & diseases 2009;43(1):81-7.
2009: Xiaomei Niu; Mehdi Nouraie ; Andrew Campbell; Sohail Rana; Caterina P Minniti; Craig Sable; Deepika Darbari; Niti Dham; N Scott Reading; Josef T Prchal; Gregory Kato ; Mark T Gladwin; Oswaldo L Castro; Victor Roland Gordeuk
Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease.
PloS one 2009;4(11):e7956.
2009: Neeraj Agarwal; Josef T Prchal
Anemia of chronic disease (anemia of inflammation).
Acta haematologica 2009;122(2-3):103-8.
2009: Eric Lippert; François Girodon; Emma Hammond; Jaroslav Jelinek; N Scott Reading; Boris Fehse; Katy Hanlon; Mirjam Hermans; Céline Richard; Sabina Swierczek; Valérie Ugo; Serge Carillo; Véronique Harrivel; Christophe Marzac; Daniela Pietra; Marta Sobas; Morgane Mounier; Marina Migeon; Sian Ellard; Nicolaus Kröger; Richard Herrmann; Josef T Prchal; Radek C Skoda; Sylvie Hermouet
Concordance of assays designed for the quantification of JAK2V617F: a multicenter study.
Haematologica 2009;94(1):38-45.
2008: Florent M Martin; Josef T Prchal; Jorge Nieva; Alan Saven; Jeffrey Andrey; Kelly Bethel; James C Barton; Gow Aripally; Sylvia S Bottomley; Jeffrey S Friedman
Purification and characterization of sideroblasts from patients with acquired and hereditary sideroblastic anaemia.
British journal of haematology 2008;143(3):446-50.
2008: Sabina I Swierczek; Neeraj Agarwal; Roberto H Nussenzveig; Gerald Rothstein; Andrew Wilson; Andrew Artz; Josef T Prchal
Hematopoiesis is not clonal in healthy elderly women.
Blood 2008;112(8):3186-93.
2008: Neeraj Agarwal; Josef T Prchal
Erythropoietic agents and the elderly.
Seminars in hematology 2008;45(4):267-75.
2008: Hector Sandoval; Perumal Thiagarajan; Swapan K Dasgupta; Armin Schumacher; Josef T Prchal; Min Chen; Jin Wang
Essential role for Nix in autophagic maturation of erythroid cells.
Nature 2008;454(7201):232-5.
2008: Hana Bruchova; Michaela Merkerova; Josef T Prchal
Aberrant expression of microRNA in polycythemia vera.
Haematologica 2008;93(7):1009-16.
2008: Taghi Manshouri; Alfonso Quintás-Cardama; Roberto H Nussenzveig; Amos Gaikwad; Zeev Estrov; Josef T Prchal; Jorge E Cortes; Hagop M Kantarjian; Srdan Verstovsek
The JAK kinase inhibitor CP-690,550 suppresses the growth of human polycythemia vera cells carrying the JAK2V617F mutation.
Cancer science 2008;99(6):1265-73.
2008: Eva Zetterberg; Uday Popat; Hans Hasselbalch; Josef T Prchal; Jan Palmblad
Angiogenesis in pulmonary hypertension with myelofibrosis.
Haematologica 2008;93(6):945-6.
2008: Josef T Prchal; Victor Roland Gordeuk
The HIF2A gene in familial erythrocytosis.
The New England journal of medicine 2008;358(18):1966; author reply 1966-7.
2008: Donghoon Yoon; Bumjun Kim; Josef T Prchal
Cre recombinase expression controlled by the hematopoietic regulatory domain of Gata-1 is erythroid-specific.
Blood cells, molecules & diseases 2008;40(3):381-7.
2008: Donghoon Yoon; Neeraj Agarwal; Josef T Prchal
Does erythropoietin promote tumor growth?
Clinical cancer research : an official journal of the American Association for Cancer Research 2008;14(6):1920; author reply 1920-1.
2008: Scott J Samuelson; Josef T Prchal
Pediatric essential thrombocythemia (ET) from the Czech Republic.
Leukemia research 2008;32(3):367-8.
2008: Adelina I Sergueeva; Galina Y Miasnikova; Daniel J Okhotin; Alla A Levina; Zufan Debebe; Tatiana Ammosova; Xiaomei Niu; Elena A Romanova; Sergei Nekhai; Patricia M DiBello; Donald W Jacobsen; Josef T Prchal; Victor Roland Gordeuk
Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutation.
Haematologica 2008;93(2):279-82.
2008: Scott J Samuelson; Charles J Parker; Josef T Prchal
Revised criteria for the myeloproliferative disorders: too much too soon?
Blood 2008;111(3):1741; author reply 1742.
2008: Josef T Prchal
Philadelphia chromosome-negative myeloproliferative disorders: an historical perspective.
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2008;():68.
2007: Neeraj Agarwal; Ferdane Kutlar; Mariluz P Mojica-Henshaw; Ching N Ou; Amos Gaikwad; N Scott Reading; Lakeia Bailey; Abdullah Kutlar; Josef T Prchal
Missense mutation of the last nucleotide of exon 1 (G->C) of beta globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele.
Haematologica 2007;92(12):1715-6.
2007: Jaroslav Jelinek; Jun Li; Zakar Mnjoyan; Jean-Pierre J Issa; Josef T Prchal; Vahid Afshar-Kharghan
Epigenetic control of PRV-1 expression on neutrophils.
Experimental hematology 2007;35(11):1677-83.
2007: Vesna Najfeld; Amanda Cozza; Windy Berkofsy-Fessler; Josef T Prchal; Angela Scalise
Numerical gain and structural rearrangements of JAK2, identified by FISH, characterize both JAK2617V>F-positive and -negative patients with Ph-negative MPD, myelodysplasia, and B-lymphoid neoplasms.
Experimental hematology 2007;35(11):1668-76.
2007: Hana Bruchova; Donghoon Yoon; Archana M Agarwal; Joshua T Mendell; Josef T Prchal
Regulated expression of microRNAs in normal and polycythemia vera erythropoiesis.
Experimental hematology 2007;35(11):1657-67.
2007: Amos Gaikwad; Josef T Prchal
Study of two tyrosine kinase inhibitors on growth and signal transduction in polycythemia vera.
Experimental hematology 2007;35(11):1647-56.
2007: Melanie J Percy; Mayka Sanchez; Sabina Swierczek; Mary Frances McMullin; Mariluz P Mojica-Henshaw; Martina U Muckenthaler; Josef T Prchal; Matthias W Hentze
Is congenital secondary erythrocytosis/polycythemia caused by activating mutations within the HIF-2 alpha iron-responsive element?
Blood 2007;110(7):2776-7.
2007: George L Chen; Josef T Prchal
X-linked clonality testing: interpretation and limitations.
Blood 2007;110(5):1411-9.
2007: Zhi-Yong Chen; Pundit Asavaritikrai; Josef T Prchal; Constance Tom Noguchi
Endogenous erythropoietin signaling is required for normal neural progenitor cell proliferation.
The Journal of biological chemistry 2007;282(35):25875-83.
2007: Amos Gaikwad; Srdan Verstovsek; Donghoon Yoon; Ko-Tung Chang; Taghi Manshouri; Roberto H Nussenzveig; Jorge Cortes; William Vainchenker; Josef T Prchal
Imatinib effect on growth and signal transduction in polycythemia vera.
Experimental hematology 2007;35(6):931-8.
2007: Neeraj Agarwal; Victor Roland Gordeuk; Josef T Prchal
Are erythropoietin receptors expressed in tumors? Facts and fiction--more careful studies are needed.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2007;25(13):1813-4; author reply 1815.
2007: Zeyu Xiong; Enli Liu; Yan Yan; Richard T Silver; Fan Yang; Irene H Chen; I Hodge; Srdan Verstovsek; F J Segura; Hong Wang; Josef T Prchal; Xiao-Feng Yang
A novel unconventional antigen MPD5 elicits anti-tumor humoral immune responses in a subset of patients with polycythemia vera.
International journal of immunopathology and pharmacology 2007;20(2):373-80.
2007: Scott J Samuelson; Uday Popat; Josef T Prchal
Marrow fibrosis does not account for circulating CD34+ cells in myelofibrosis with myeloid metaplasia.
Haematologica 2007;92(4):e47.
2007: Amos Gaikwad; Roberto H Nussenzveig; Enli Liu; Stephen Gottshalk; KoTung Chang; Josef T Prchal
In vitro expansion of erythroid progenitors from polycythemia vera patients leads to decrease in JAK2 V617F allele.
Experimental hematology 2007;35(4):587-95.
2007: Zeyu Xiong; Yan Yan; Enli Liu; Richard T Silver; Srdan Verstovsek; Fan Yang; Hong Wang; Josef T Prchal; Xiao-Feng Yang
Novel tumor antigens elicit anti-tumor humoral immune reactions in a subset of patients with polycythemia vera.
Clinical immunology (Orlando, Fla.) 2007;122(3):279-87.
2007: Mervin C Yoder; Laura E Mead; Daniel Prater; Theresa R Krier; Karim N Mroueh; Fang Li; Rachel Krasich; Constance J Temm; Josef T Prchal; David A Ingram
Redefining endothelial progenitor cells via clonal analysis and hematopoietic stem/progenitor cell principals.
Blood 2007;109(5):1801-9.
2007: Neeraj Agarwal; Victor Roland Gordeuk; Josef T Prchal
Genetic mechanisms underlying regulation of hemoglobin mass.
Advances in experimental medicine and biology 2007;618():195-210.
2007: Neeraj Agarwal; Mariluz P Mojica-Henshaw; Elizabeth D Simmons; Dottie Hussey; Ching N Ou; Josef T Prchal
Familial polycythemia caused by a novel mutation in the beta globin gene: essential role of P50 in evaluation of familial polycythemia.
International journal of medical sciences 2007;4(4):232-6.
2007: Ronald Hoffman; Josef T Prchal; Scott Samuelson; Stefan O Ciurea; Damiano Rondelli
Philadelphia chromosome-negative myeloproliferative disorders: biology and treatment.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2007;13(1 Suppl 1):64-72.
2007: Roberto H Nussenzveig; Sabina I Swierczek; Jaroslav Jelinek; Amos Gaikwad; Enli Liu; Srdan Verstovsek; Jaroslav F Prchal; Josef T Prchal
Polycythemia vera is not initiated by JAK2V617F mutation.
Experimental hematology 2007;35(1):32-8.
2006: Roberto H Nussenzveig; H Bindu Lingam; Amos Gaikwad; Qiqing Zhu; Naijie Jing; Josef T Prchal
A novel mutation of the cytochrome-b5 reductase gene in an Indian patient: the molecular basis of type I methemoglobinemia.
Haematologica 2006;91(11):1542-5.
2006: Zeyu Xiong; Enli Liu; Yan Yan; Richard T Silver; Fan Yang; Irene H Chen; Yangyang Chen; Srdan Verstovsek; Hong Wang; Josef T Prchal; Xiao-Feng Yang
An unconventional antigen translated by a novel internal ribosome entry site elicits antitumor humoral immune reactions.
Journal of immunology (Baltimore, Md. : 1950) 2006;177(7):4907-16.
2006: Donghoon Yoon; Yves D Pastore; Vladimir Divoky; Enli Liu; Agnieszka E Mlodnicka; Karin Rainey; Prem Ponka; Gregg L Semenza; Armin Schumacher; Josef T Prchal
Hypoxia-inducible factor-1 deficiency results in dysregulated erythropoiesis signaling and iron homeostasis in mouse development.
The Journal of biological chemistry 2006;281(35):25703-11.
2006: Dagmar Pospisilova; Martha P Mims; Elizabeta Nemeth; Tomas Ganz; Josef T Prchal
DMT1 mutation: response of anemia to darbepoetin administration and implications for iron homeostasis.
Blood 2006;108(1):404-5.
2006: George L Chen; Enli Liu; Kubendran Naidoo; Uday Popat; Theresa L Coetzer; Josef T Prchal
Idiopathic myelofibrosis without dacryocytes.
Haematologica 2006;91(6 Suppl):ECR29.
2006: Vladimir I Bushuev; Galina Y Miasnikova; Adelina I Sergueeva; Lydia A Polyakova; Daniel Okhotin; Peter R A Gaskin; Zufan Debebe; Sergei Nekhai; Oswaldo L Castro; Josef T Prchal; Victor Roland Gordeuk
Endothelin-1, vascular endothelial growth factor and systolic pulmonary artery pressure in patients with Chuvash polycythemia.
Haematologica 2006;91(6):744-9.
2006: Uday Popat; Adaani Frost; Enli Liu; Yongli Guan; April Durette; Vishnu Reddy; Josef T Prchal
High levels of circulating CD34 cells, dacrocytes, clonal hematopoiesis, and JAK2 mutation differentiate myelofibrosis with myeloid metaplasia from secondary myelofibrosis associated with pulmonary hypertension.
Blood 2006;107(9):3486-8.
2006: Victor Roland Gordeuk; Josef T Prchal
Vascular complications in Chuvash polycythemia.
Seminars in thrombosis and hemostasis 2006;32(3):289-94.
2006: Martha P Mims; Teresa G Hayes; Shiyan Zheng; Suzanne M Leal; Anna Frolov; Michael Ittmann; Thomas M Wheeler; Josef T Prchal
Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women.
Cancer research 2006;66(3):1880; author reply 1880-1.
2006: Guido Finazzi; Xylina T Gregg; Tiziano Barbui; Josef T Prchal
Idiopathic erythrocytosis and other non-clonal polycythemias.
Best practice & research. Clinical haematology 2006;19(3):471-82.
2006: George Chen; Josef T Prchal
Polycythemia vera and its molecular basis: an update.
Best practice & research. Clinical haematology 2006;19(3):387-97.
2005: Jaroslav Jelinek; Yasuhiro Oki; Vazganush Gharibyan; Carlos E Bueso-Ramos; Josef T Prchal; Srdan Verstovsek; Miloslav Beran; Elihu Estey; Hagop M Kantarjian; Jean-Pierre J Issa
JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia.
Blood 2005;106(10):3370-3.
2005: Radek C Skoda; Josef T Prchal
Lessons from familial myeloproliferative disorders.
Seminars in hematology 2005;42(4):266-73.
2005: Radek C Skoda; Josef T Prchal
Chronic myeloproliferative disorders--introduction.
Seminars in hematology 2005;42(4):181-3.
2005: Uday Popat; Adaani Frost; Enli Liu; Romelia May; Remzi Bag; Vishnu Reddy; Josef T Prchal
New onset of myelofibrosis in association with pulmonary arterial hypertension.
Annals of internal medicine 2005;143(6):466-7.
2005: Hiromi Gunshin; Jie Jin; Yuko Fujiwara; Nancy C Andrews; Martha Mims; Josef T Prchal
Analysis of the E399D mutation in SLC11A2.
Blood 2005;106(6):2221; author reply 2221-2.
2005: Martha P Mims; Josef T Prchal
Divalent metal transporter 1.
Hematology (Amsterdam, Netherlands) 2005;10(4):339-45.
2005: Mingjiang Xu; Edward Bruno; Joseph Chao; Stephen Huang; Guido Finazzi; Steven Fruchtman; Uday Popat; Josef T Prchal; Giovanni Barosi; Ronald Hoffman
Constitutive mobilization of CD34+ cells into the peripheral blood in idiopathic myelofibrosis may be due to the action of a number of proteases.
Blood 2005;105(11):4508-15.
2005: Damiano Rondelli; Giovanni Barosi; Andrea Bacigalupo; Josef T Prchal; Uday Popat; Emilio Paolo Alessandrino; Jerry L Spivak; B Douglas Smith; Hans G Klingemann; Steven Fruchtman; Ronald Hoffman
Allogeneic hematopoietic stem-cell transplantation with reduced-intensity conditioning in intermediate- or high-risk patients with myelofibrosis with myeloid metaplasia.
Blood 2005;105(10):4115-9.
2005: Jey Maran; Yongli Guan; Ching-Nan Ou; Josef T Prchal
Heterogeneity of the molecular biology of methemoglobinemia: a study of eight consecutive patients.
Haematologica 2005;90(5):687-9.
2005: Xylina T Gregg; Josef T Prchal
Recent advances in the molecular biology of congenital polycythemias and polycythemia vera.
Current hematology reports 2005;4(3):238-42.
2005: Josef T Prchal
Polycythemia vera and other primary polycythemias.
Current opinion in hematology 2005;12(2):112-6.
2005: Mingjiang Xu; Edward Bruno; Joseph Chao; Hongyu Ni; Valerie Lindgren; Rafael Nunez; Nadim Mahmud; Guido Finazzi; Steven Fruchtman; Uday Popat; Enli Liu; Josef T Prchal; Damiano Rondelli; Giovanni Barosi; Ronald Hoffman
The constitutive mobilization of bone marrow-repopulating cells into the peripheral blood in idiopathic myelofibrosis.
Blood 2005;105(4):1699-705.
2005: Martha P Mims; Yongli Guan; Dagmar Pospisilova; Monika Priwitzerova; Karel Indrak; Prem Ponka; Vladimir Divoky; Josef T Prchal
Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.
Blood 2005;105(3):1337-42.
2005: Josef T Prchal; Xylina T Gregg
Red cell enzymes.
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2005;():19-23.
2005: Maria Celeste Bento; Ko-Tung Chang; Yongli Guan; Enli Liu; Gabriela Caldas; Richard A Gatti; Josef T Prchal
Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients.
Haematologica 2005;90(1):128-9.
2005: Victor Roland Gordeuk; David Wayne Stockton; Josef T Prchal
Congenital polycythemias/erythrocytoses.
Haematologica 2005;90(1):109-16.
2005: Olga M Mejía; Josef T Prchal; Fabiola León-Velarde; Abdias Hurtado; David Wayne Stockton
Genetic association analysis of chronic mountain sickness in an Andean high-altitude population.
Haematologica 2005;90(1):13-9.
2004: Hoyin Mok; Miriam Mendoza; Josef T Prchal; Péter Balogh; Armin Schumacher
Dysregulation of ferroportin 1 interferes with spleen organogenesis in polycythaemia mice.
Development (Cambridge, England) 2004;131(19):4871-81.
2004: Yunying L Liu; Sonny O Ang; Douglas A Weigent; Josef T Prchal; Joseph R Bloomer
Regulation of ferrochelatase gene expression by hypoxia.
Life sciences 2004;75(17):2035-43.
2004: Jey Maran; Josef T Prchal
Polycythemia and oxygen sensing.
Pathologie-biologie 2004;52(5):280-4.
2004: Jaroslav Jelinek; Katerina Jedlickova; Yongli Guan; Josef T Prchal
Instability of PRV-1 mRNA: a factor to be considered in PRV-1 quantification for the diagnosis of polycythemia vera.
Haematologica 2004;89(6):749-51.
2004: Monika Priwitzerova; Dagmar Pospisilova; Josef T Prchal; Karel Indrak; Alice Hlobilkova; Vladimir Mihal; Prem Ponka; Vladimir Divoky
Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells.
Blood 2004;103(10):3991-2.
2004: Victor Roland Gordeuk; Adelina I Sergueeva; Galina Y Miasnikova; Daniel Okhotin; Yaroslav Voloshin; Peter L Choyke; John A Butman; Katerina Jedlickova; Josef T Prchal; Lydia A Polyakova
Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors.
Blood 2004;103(10):3924-32.
2004: Hoyin Mok; Jaroslav Jelinek; Sonia Pai; Bruce M Cattanach; Josef T Prchal; Hagop Youssoufian; Armin Schumacher
Disruption of ferroportin 1 regulation causes dynamic alterations in iron homeostasis and erythropoiesis in polycythaemia mice.
Development (Cambridge, England) 2004;131(8):1859-68.
2004: Michal Mrug; Bruce A Julian; Josef T Prchal
Angiotensin II receptor type 1 expression in erythroid progenitors: Implications for the pathogenesis of postrenal transplant erythrocytosis.
Seminars in nephrology 2004;24(2):120-30.
2004: Enli Liu; Melanie J Percy; Christopher I Amos; Yongli Guan; Sanjay Shete; David Wayne Stockton; Mary Frances McMullin; Lydia A Polyakova; Sonny O Ang; Yves D Pastore; Katerina Jedlickova; Terence R J Lappin; Victor Roland Gordeuk; Josef T Prchal
The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.
Blood 2004;103(5):1937-40.
2004: Josef T Prchal; Yves D Pastore
Erythropoietin and erythropoiesis: polycythemias due to disruption of oxygen homeostasis.
The hematology journal : the official journal of the European Haematology Association / EHA 2004;5 Suppl 3():S110-3.
2004: Jaroslav Jelinek; Josef T Prchal
Oxygen-dependent regulation of erythropoiesis.
Methods in enzymology 2004;381():201-10.
2003: Robert Kralovics; David Wayne Stockton; Josef T Prchal
Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease.
Blood 2003;102(10):3793-6.
2003: Katerina Jedlickova; David Wayne Stockton; Josef T Prchal
Possible primary familial and congenital polycythemia locus at 7q22.1-7q22.2.
Blood cells, molecules & diseases 2003;31(3):327-31.
2003: Josef T Prchal
Classification and molecular biology of polycythemias (erythrocytoses) and thrombocytosis.
Hematology/oncology clinics of North America 2003;17(5):1151-8, vi.
2003: Katerina Jedlickova; David Wayne Stockton; Hua Chen; James Stray-Gundersen; Sarah Witkowski; Ge Ri-Li; Jaroslav Jelinek; Benjamin D Levine; Josef T Prchal
Search for genetic determinants of individual variability of the erythropoietin response to high altitude.
Blood cells, molecules & diseases 2003;31(2):175-82.
2003: Yves D Pastore; Katerina Jedlickova; Yongli Guan; Enli Liu; James Fahner; Henrik Hasle; Jaroslav F Prchal; Josef T Prchal
Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.
American journal of human genetics 2003;73(2):412-9.
2003: Enli Liu; Jaroslav Jelinek; Yves D Pastore; Yongli Guan; Jaroslav F Prchal; Josef T Prchal
Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietin.
Blood 2003;101(8):3294-301.
2003: Josef T Prchal
Delivery on demand--a new era of gene therapy?
The New England journal of medicine 2003;348(13):1282-3.
2003: Yves D Pastore; Jaroslav Jelinek; Sonny O Ang; Yongli Guan; Enli Liu; Katerina Jedlickova; Lakshmanan Krishnamurti; Josef T Prchal
Mutations in the VHL gene in sporadic apparently congenital polycythemia.
Blood 2003;101(4):1591-5.
2002: Sonny O Ang; Hua Chen; Kiichi Hirota; Victor Roland Gordeuk; Jaroslav Jelinek; Yongli Guan; Enli Liu; Adelina I Sergueeva; Galina Y Miasnikova; David Mole; Patrick H Maxwell; David Wayne Stockton; Gregg L Semenza; Josef T Prchal
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.
Nature genetics 2002;32(4):614-21.
2002: Xylina T Gregg; Vishnu Reddy; Josef T Prchal
Copper deficiency masquerading as myelodysplastic syndrome.
Blood 2002;100(4):1493-5.
2002: Lubomir Sokol; Josef T Prchal
Pure red-cell aplasia and recombinant erythropoietin.
The New England journal of medicine 2002;346(20):1584-6; author reply 1584-6.
2002: Vladimir Divoky; Josef T Prchal
Mouse surviving solely on human erythropoietin receptor (EpoR): model of human EpoR-linked disease.
Blood 2002;99(10):3873-4; author reply 3874-5.
2002: Robert Kralovics; Yongli Guan; Josef T Prchal
Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera.
Experimental hematology 2002;30(3):229-36.
2002: J Ashley Jefferson; Elizabeth Escudero; Maria-Elena Hurtado; Jacqueline Pando; Rosario Tapia; Erik R Swenson; Josef T Prchal; George F Schreiner; Robert B Schoene; Abdias Hurtado; Richard J Johnson
Excessive erythrocytosis, chronic mountain sickness, and serum cobalt levels.
Lancet 2002;359(9304):407-8.
2002: Sonny O Ang; Hua Chen; Victor Roland Gordeuk; Adelina I Sergueeva; Lydia A Polyakova; Galina Y Miasnikova; Robert Kralovics; David Wayne Stockton; Josef T Prchal
Endemic polycythemia in Russia: mutation in the VHL gene.
Blood cells, molecules & diseases 2002;28(1):57-62.
2002: John T Phelan; Josef T Prchal
Clonality studies in cancer based on X chromosome inactivation phenomenon.
Methods in molecular medicine 2002;68():251-70.
2001: Robert Kralovics; Josef T Prchal
Genetic heterogeneity of primary familial and congenital polycythemia.
American journal of hematology 2001;68(2):115-21.
2001: Vladimir Divoky; Michal Mrug; Denyse Thornley-Brown; M Divoka; Josef T Prchal
Non-anemic homozygous beta(o) thalassemia in an African-American family: association of high fetal hemoglobin levels with beta thalassemia alleles.
American journal of hematology 2001;68(1):43-50.
2001: Josef T Prchal
Molecular biology of polycythemias.
Internal medicine (Tokyo, Japan) 2001;40(8):681-7.
2001: B K Adler; Donna E Salzman; Matthew H Carabasi; William P Vaughan; V V Reddy; Josef T Prchal
Fatal sickle cell crisis after granulocyte colony-stimulating factor administration.
Blood 2001;97(10):3313-4.
2001: Vladimir Divoky; Zhongfa Liu; Thomas M Ryan; JF Prchal; Tim M Townes; Josef T Prchal
Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(3):986-91.
2001: Josef T Prchal; Vladimir Divoky
Lessons to better understanding of hypoxia sensing. Acquired and congenital mutations resulting in polycythemia.
Advances in experimental medicine and biology 2001;502():189-205.
2001: Josef T Prchal
Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disorders.
Seminars in hematology 2001;38(1 Suppl 2):10-20.
2000: Xiaoyun Wu; John K Wakefield; H Liu; H Xiao; Robert Kralovics; Josef T Prchal; John C Kappes
Development of a novel trans-lentiviral vector that affords predictable safety.
Molecular therapy : the journal of the American Society of Gene Therapy 2000;2(1):47-55.
2000: Xylina T Gregg; Robert Kralovics; Josef T Prchal
A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assays.
American journal of hematology 2000;63(4):184-91.
2000: J A Thompson; D G Gilliland; Josef T Prchal; J M Bennett; K Larholt; R A Nelson; E H Rose; M H Dugan
Effect of recombinant human erythropoietin combined with granulocyte/ macrophage colony-stimulating factor in the treatment of patients with myelodysplastic syndrome. GM/EPO MDS Study Group.
Blood 2000;95(4):1175-9.
2000: Robert Kralovics; Josef T Prchal
Congenital and inherited polycythemia.
Current opinion in pediatrics 2000;12(1):29-34.
1999: M L Kimberland; V Divoky; Josef T Prchal; U Schwahn; W Berger; Haig Kazazian
Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells.
Human molecular genetics 1999;8(8):1557-60.
1999: JF Prchal; Josef T Prchal
Molecular basis for polycythemia.
Current opinion in hematology 1999;6(2):100-9.
1998: Robert Kralovics; Josef T Prchal
Haematopoietic progenitors and signal transduction in polycythaemia vera and primary thrombocythaemia.
Baillière's clinical haematology 1998;11(4):803-18.
1998: T P Atkinson; C A Smith; Yen-Ming Hsu; Ellen A Garber; L Su; TH Howard; Josef T Prchal; MP Everson; Max D Cooper
Leukocyte transfusion-associated granulocyte responses in a patient with X-linked hyper-IgM syndrome.
Journal of clinical immunology 1998;18(6):430-9.
1998: Tomas Stopka; Jan Zivny; E Goldwasser; JF Prchal; Emanuel Necas; Josef T Prchal
Guinea pig serum erythropoietin (EPO) selectively stimulates guinea pig erythroid progenitors: human or mouse erythroid progenitors do not form erythroid burst-forming unit colonies in response to guinea pig serum EPO.
Experimental hematology 1998;26(9):910-4.
1998: Robert Kralovics; L Sokol; Josef T Prchal
Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia.
The Journal of clinical investigation 1998;102(1):124-9.
1998: Bruce A Julian; R R Brantley; C V Barker; Tomas Stopka; Robert S Gaston; John J Curtis; J Y Lee; Josef T Prchal
Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis.
Journal of the American Society of Nephrology : JASN 1998;9(6):1104-8.
1998: Tomas Stopka; Jan Zivny; P Stopkova; JF Prchal; Josef T Prchal
Human hematopoietic progenitors express erythropoietin.
Blood 1998;91(10):3766-72.
1997: Michal Mrug; Tomas Stopka; Bruce A Julian; JF Prchal; Josef T Prchal
Angiotensin II stimulates proliferation of normal early erythroid progenitors.
The Journal of clinical investigation 1997;100(9):2310-4.
1997: Robert Kralovics; L Sokol; E H Broxson; Josef T Prchal
The erythropoietin receptor gene is not linked with the polycythemia phenotype in a family with autosomal dominant primary polycythemia.
Proceedings of the Association of American Physicians 1997;109(6):580-5.
1997: Robert Kralovics; Karel Indrak; Tomas Stopka; B W Berman; JF Prchal; Josef T Prchal
Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias.
Blood 1997;90(5):2057-61.
1997: J C Hancock; Josef T Prchal; J M Bennett; Catherine M Listinsky
Trilineage extramedullary myeloid cell tumor in myelodysplastic syndrome.
Archives of pathology & laboratory medicine 1997;121(5):520-3.
1997: Yuliang Liu; J Phelan; Rodney C P Go; JF Prchal; Josef T Prchal
Rapid determination of clonality by detection of two closely-linked X chromosome exonic polymorphisms using allele-specific PCR.
The Journal of clinical investigation 1997;99(8):1984-90.
1997: Robert N Haire; Yuko Ota; SJ Strong; Ronda T Litman; Y Liu; Josef T Prchal; Max D Cooper; Gary W Litman
Unusual patterns of exon skipping in Bruton tyrosine kinase are associated with mutations involving the intron 17 3' splice site.
American journal of human genetics 1997;60(4):798-807.
1997: A Sergeyeva; Victor Roland Gordeuk; Y N Tokarev; L Sokol; JF Prchal; Josef T Prchal
Congenital polycythemia in Chuvashia.
Blood 1997;89(6):2148-54.
1997: M M Jenkins; Josef T Prchal
A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-Americans.
Human genetics 1997;99(2):248-50.
1997: Xylina T Gregg; Josef T Prchal
Erythropoietin receptor mutations and human disease.
Seminars in hematology 1997;34(1):70-6.
1996: Petr Jarolim; J L Murray; HL Rubin; W M Taylor; Josef T Prchal; S K Ballas; L M Snyder; L Chrobak; W D Melrose; V Brabec; J Palek
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
Blood 1996;88(11):4366-74.
1996: Josef T Prchal; L Sokol
"Benign erythrocytosis" and other familial and congenital polycythemias.
European journal of haematology 1996;57(4):263-8.
1996: M M Jenkins; Josef T Prchal
A novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemia.
Blood 1996;87(7):2993-9.
1996: E A Lowenthal; A Wells; Peter D Emanuel; R Player; Josef T Prchal
Sickle cell acute chest syndrome associated with parvovirus B19 infection: case series and review.
American journal of hematology 1996;51(3):207-13.
1996: M Lubovy; S McCune; Jian-Yun Dong; JF Prchal; Tim M Townes; Josef T Prchal
Stable transduction of recombinant adeno-associated virus into hematopoietic stem cells from normal and sickle cell patients.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 1996;2(1):24-30.
1996: Josef T Prchal; JF Prchal; M Belickova; S Chen; Y Guan; G Larry Gartland; Max D Cooper
Clonal stability of blood cell lineages indicated by X-chromosomal transcriptional polymorphism.
The Journal of experimental medicine 1996;183(2):561-7.
1995: M Luhovy; Y Liu; M Belickova; JF Prchal; Josef T Prchal
A novel clonality assay based on transcriptional polymorphism of X chromosome gene p55.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 1995;1(2):81-7.
1995: S D Lyman; M Seaberg; R Hanna; J Zappone; K Brasel; J L Abkowitz; Josef T Prchal; J C Schultz; N T Shahidi
Plasma/serum levels of flt3 ligand are low in normal individuals and highly elevated in patients with Fanconi anemia and acquired aplastic anemia.
Blood 1995;86(11):4091-6.
1995: A Schneider; B Westwood; C Yim; Josef T Prchal; R Berkow; Richard J. Labotka; R Warrier; E Beutler
Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families.
American journal of hematology 1995;50(4):263-8.
1995: L Sokol; Josef T Prchal
Human genome--chromosome no. 19.
Casopís lékar̆ů c̆eských 1995;134(19):625-9.
1995: E A Lowenthal; Josef T Prchal
Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosis.
Blood 1995;86(1):411-2.
1995: L Sokol; M Luhovy; Y Guan; JF Prchal; Gregg L Semenza; Josef T Prchal
Primary familial polycythemia: a frameshift mutation in the erythropoietin receptor gene and increased sensitivity of erythroid progenitors to erythropoietin.
Blood 1995;86(1):15-22.
1995: Josef T Prchal; Gregg L Semenza; J Prchal; L Sokol
Familial polycythemia.
Science (New York, N.Y.) 1995;268(5219):1831-2.
1995: Josef T Prchal; B Adler; J B Wilson; E Baysal; W B Qin; TP Molchanova; D D Pobedimskaya; E G Kazanetz; TH Huisman
Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama.
Hemoglobin 1995;19(3-4):151-64.
1995: Josef T Prchal
Primary polycythemias.
Current opinion in hematology 1995;2(2):146-52.
1995: L Beeton; Josef T Prchal; T L Coetzer
A TaqI polymorphism in the human erythroid beta spectrin gene.
Human genetics 1995;95(3):365-6.
1995: Lambert Busque; D Gary Gilliland; Josef T Prchal; C A Sieff; H J Weinstein; J M Sokol; M Belickova; ALAN WAYNE; K S Zuckerman; L Sokol
Clonality in juvenile chronic myelogenous leukemia.
Blood 1995;85(1):21-30.
1994: M Belickova; Harry Schroeder; Y L Guan; J Brierre; Seth Mark Berney; Max D Cooper; Josef T Prchal
Clonal hematopoiesis and acquired thalassemia in common variable immunodeficiency.
Molecular medicine (Cambridge, Mass.) 1994;1(1):56-61.
1994: M J Fisher; JF Prchal; Josef T Prchal; Alan D D'Andrea
Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera.
Blood 1994;84(6):1982-91.
1994: D L Wethers; G M Ramirez; M Koshy; M H Steinberg; G Phillips; R S Siegel; J R Eckman; Josef T Prchal
Accelerated healing of chronic sickle-cell leg ulcers treated with RGD peptide matrix. RGD Study Group.
Blood 1994;84(6):1775-9.
1994: L Sokol; JF Prchal; A D'Andrea; T A Rado; Josef T Prchal
Mutation in the negative regulatory element of the erythropoietin receptor gene in a case of sporadic primary polycythemia.
Experimental hematology 1994;22(5):447-53.
1994: Josef T Prchal; J F Prchal
Evolving understanding of the cellular defect in polycythemia vera: implications for its clinical diagnosis and molecular pathophysiology.
Blood 1994;83(1):1-4.
1994: L Sokol; Josef T Prchal
Two microsatellite repeat polymorphisms in the EPO gene.
Human molecular genetics 1994;3(1):219.
1994: D C Molthrop; R H Wheeler; K M Hall; Josef T Prchal
Evaluation of the methemoglobinemia associated with sulofenur.
Investigational new drugs 1994;12(2):99-102.
1993: L Sokol; J Prchal; Josef T Prchal
Primary familial and congenital polycythaemia.
Lancet 1993;342(8863):115-6.
1993: Josef T Prchal; Abdullah Kutlar; K Hall; C A Robinson; C W Scott
Case report: alpha G-Philadelphia, beta O-Arab, and beta C globins present in a single patient.
The American journal of the medical sciences 1993;305(5):307-11.
1993: Manjit Hanspal; Josef T Prchal; J Palek
Biogenesis of erythrocyte membrane skeleton in health and disease.
Stem cells (Dayton, Ohio) 1993;11 Suppl 1():8-12.
1993: Josef T Prchal; Y L Guan
A novel clonality assay based on transcriptional analysis of the active X chromosome.
Stem cells (Dayton, Ohio) 1993;11 Suppl 1():62-5.
1993: Ferdane Kutlar; Abdullah Kutlar; E Nuguid; Josef T Prchal; TH Huisman
Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia.
Hemoglobin 1993;17(1):55-66.
1993: Josef T Prchal; Y L Guan; J F Prchal; F Barany
Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis.
Blood 1993;81(1):269-71.
1992: Reiko Akagi; Josef T Prchal; C E Eberhart; Shigeru Sassa
An acquired acute hepatic porphyria: a novel type of delta-aminolevulinate dehydratase inhibition.
Clinica chimica acta; international journal of clinical chemistry 1992;212(1-2):79-84.
1992: Petr Jarolim; J Palek; HL Rubin; Josef T Prchal; C Korsgren; C M Cohen
Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2.
Blood 1992;80(2):523-9.
1992: E Beutler; B Westwood; Josef T Prchal; G Vaca; C S Bartsocas; L Baronciani
New glucose-6-phosphate dehydrogenase mutations from various ethnic groups.
Blood 1992;80(1):255-6.
1992: Peter D Emanuel; C J Eaves; V C Broudy; T Papayannopoulou; M R Moore; Alan D D'Andrea; JF Prchal; A C Eaves; Josef T Prchal
Familial and congenital polycythemia in three unrelated families.
Blood 1992;79(11):3019-30.
1992: A C Kay; W Kuhl; Josef T Prchal; E Beutler
The origin of glucose-6-phosphate-dehydrogenase (G6PD) polymorphisms in African-Americans.
American journal of human genetics 1992;50(2):394-8.
1991: T L Coetzer; Kenneth E Sahr; Josef T Prchal; H Blacklock; L Peterson; R Koler; J Doyle; J Manaster; J Palek
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.
The Journal of clinical investigation 1991;88(3):743-9.
1991: S H Yoon; H Yu; S Eber; Josef T Prchal
Molecular defect of truncated beta-spectrin associated with hereditary elliptocytosis. Beta-spectrin Gottingen.
The Journal of biological chemistry 1991;266(13):8490-4.
1991: Manjit Hanspal; S H Yoon; H Yu; J S Hanspal; S Lambert; J Palek; Josef T Prchal
Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.
Blood 1991;77(1):165-73.
1990: Josef T Prchal; N Borgese; M R Moore; H Moreno; E Hegesh; M K Hall
Congenital methemoglobinemia due to methemoglobin reductase deficiency in two unrelated American black families.
The American journal of medicine 1990;89(4):516-22.
1990: Josef T Prchal; T Papayannopoulou; S H Yoon
Patterns of spectrin transcripts in erythroid and non-erythroid cells.
Journal of cellular physiology 1990;144(2):287-94.
1990: S H Yoon; C G Kentros; Josef T Prchal
Identification of an unusual deletion within homologous repeats of human reticulocyte beta-spectrin and probable peptide polymorphism.
Gene 1990;91(2):297-302.
1990: T Coetzer; J Palek; J Lawler; Shih-Chun Liu; Petr Jarolim; M Lahav; Josef T Prchal; W Wang; BLANCHE ALTER; G Schewitz
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
Blood 1990;75(11):2235-44.
1990: J B Wilson; B B Webber; H Hu; Abdullah Kutlar; Ferdane Kutlar; J F Codrington; Josef T Prchal; K M Hall; J M de Pablos; I Rodriguez
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions.
Blood 1990;75(9):1883-7.
1990: Jiri Mestecky; Zina Moldoveanu; B A Julian; Josef T Prchal
J. chain disease: a novel form of plasma cell dyscrasia.
The American journal of medicine 1990;88(4):411-6.
1990: S Lambert; H Yu; Josef T Prchal; J Lawler; P Ruff; D Speicher; M C Cheung; Y W Kan; J Palek
cDNA sequence for human erythrocyte ankyrin.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(5):1730-4.
1989: E Beutler; W Kuhl; J L Vives-Corrons; Josef T Prchal
Molecular heterogeneity of glucose-6-phosphate dehydrogenase A-.
Blood 1989;74(7):2550-5.
1989: S H Yoon; H Skalka; Josef T Prchal
Presence of erythroid and nonerythroid spectrin transcripts in human lens and cerebellum.
Investigative ophthalmology & visual science 1989;30(8):1860-6.
1989: M Csepreghy; M K Hall; Roger L Berkow; S Jackson; Josef T Prchal
Characterization of a new G6PD variant: G6PD Titusville.
The American journal of the medical sciences 1989;297(2):114-7.
1989: A Chabanel; K L Paul Sung; J Rapiejko; Josef T Prchal; J Palek; S C Liu; Shu Chien
Viscoelastic properties of red cell membrane in hereditary elliptocytosis.
Blood 1989;73(2):592-5.
1989: Josef T Prchal; C W Scott; S Rahbar; R L Nagel; Abdullah Kutlar; J H Galla; K Hall
Mild sickle cell anemia associated with alpha globin mutant alpha Montgomery.
The American journal of medicine 1989;86(2):232-6.
1989: A Tarkowski; C Lue; Zina Moldoveanu; Hiroshi Kiyono; J R McGhee; Josef T Prchal; N B Halpern; Jiri Mestecky
Systemic immunization for the induction of IgA responses.
Current topics in microbiology and immunology 1989;146():161-8.
1989: E Beutler; J L Vives-Corrons; A Hirono; Josef T Prchal; W Crader
The molecular biology of variation in glucose-6-phosphate dehydrogenase.
Progress in clinical and biological research 1989;319():39-50; discussion 51-4.
1988: J Lawler; T L Coetzer; Vipul N Mankad; R B Moore; Josef T Prchal; J Palek
Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis.
Blood 1988;72(4):1412-5.
1988: A Yoshida; T Takizawa; Josef T Prchal
RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in blacks.
American journal of human genetics 1988;42(6):872-6.
1988: M Csepreghy; A Yeilding; M Lilly; K Hall; C W Scott; Josef T Prchal
Characterization of a new glucose-6-phosphate dehydrogenase variant: G6PD Central City.
American journal of hematology 1988;28(1):61-2.
1988: K Hall; M T Schreeder; Josef T Prchal
G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemia.
Human genetics 1988;79(1):90-1.
1988: Josef T Prchal; K Hall; M Csepreghy; M Lilly; Roger L Berkow; C W Scott
Two apparent glucose-6-phosphate dehydrogenase variants in normal XY males: G6PD Alabama.
The American journal of medicine 1988;84(3 Pt 1):517-23.
1988: Kevin R Siebenlist; Josef T Prchal; M W Mosesson
Fibrinogen Birmingham: a heterozygous dysfibrinogenemia (A alpha 16 Arg----His) containing heterodimeric molecules.
Blood 1988;71(3):613-8.
1988: T L Coetzer; J Lawler; Shih-Chun Liu; Josef T Prchal; R J Gualtieri; M C Brain; J V Dacie; J Palek
Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
The New England journal of medicine 1988;318(4):230-4.
1988: Man-Chiu Poon; K Hall; C W Scott; Josef T Prchal
G6PD Viangchan: a new glucose 6-phosphate dehydrogenase variant from Laos.
Human genetics 1988;78(1):98-9.
1987: Josef T Prchal; B J Morley; S H Yoon; T L Coetzer; J Palek; J G Conboy; Y W Kan
Isolation and characterization of cDNA clones for human erythrocyte beta-spectrin.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(21):7468-72.
1987: T Coetzer; J Lawler; Josef T Prchal; J Palek
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis.
Blood 1987;70(3):766-72.
1987: Luigi F Bertoli; Hiromi Kubagawa; G V Borzillo; M Mayumi; Josef T Prchal; J F Kearney; J R Durant; Max D Cooper
Analysis with antiidiotype antibody of a patient with chronic lymphocytic leukemia and a large cell lymphoma (Richter's syndrome).
Blood 1987;70(1):45-50.
1987: M N Saleh; B Rodu; Josef T Prchal; E R de Leon
Acute myelofibrosis and multiple chloromas of the mandible and skin.
International journal of oral and maxillofacial surgery 1987;16(1):108-11.
1986: M B Lilly; A J Carroll; Josef T Prchal
Lack of association between glutathione content and development of thermal tolerance in human fibroblasts.
Radiation research 1986;106(1):41-6.
1986: Josef T Prchal; D P Cashman; Y W Kan
Hemoglobin Long Island is caused by a single mutation (adenine to cytosine) resulting in a failure to cleave amino-terminal methionine.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(1):24-7.
1985: A J Carroll; R P Castleberry; Josef T Prchal; W H Finley
Translocation (6;9)(p23;q34) in acute nonlymphocytic leukemia: three new cases.
Cancer genetics and cytogenetics 1985;18(4):303-6.
1985: Josef T Prchal; W M Crist; E Goldwasser; G Perrine; J F Prchal
Autosomal dominant polycythemia.
Blood 1985;66(5):1208-14.
1985: R C Barwick; Richard T Jones; C G Head; M F Shih; Josef T Prchal; D T Shih
Hb Long Island: a hemoglobin variant with a methionyl extension at the NH2 terminus and a prolyl substitution for the normal histidyl residue 2 of the beta chain.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(14):4602-5.
1985: R Hoffman; S Zaknoen; H H Yang; E Bruno; A F LoBuglio; J B Arrowsmith; Josef T Prchal
An antibody cytotoxic to megakaryocyte progenitor cells in a patient with immune thrombocytopenic purpura.
The New England journal of medicine 1985;312(18):1170-4.
1985: Josef T Prchal; S T Huang; W S Court; M C Poon
Immune hemolytic anemia following administration of antithymocyte globulin.
American journal of hematology 1985;19(1):95-8.
1985: E F Prasthofer; Josef T Prchal; W E Grizzle; C E Grossi
Plasmacytoid T-cell lymphoma associated with chronic myeloproliferative disorder.
The American journal of surgical pathology 1985;9(5):380-7.
1985: M T Schreeder; Josef T Prchal; Rick Parmley; A J Carroll; A M Gewirtz; R Hoffman
An acute myeloproliferative disorder characterized by myelofibrosis and blast cells that express phenotypic properties associated with multiple hematopoietic lineages.
American journal of clinical pathology 1985;83(1):114-21.
1985: A Yoshida; V Davé; Josef T Prchal
Uncertainty in identification of blood group A subtypes by agglutination test.
Human heredity 1985;35(1):1-6.
1985: A Velardi; Josef T Prchal; E F Prasthofer; C E Grossi
Expression of NK-lineage markers on peripheral blood lymphocytes with T-helper (Leu3+/T4+) phenotype in B cell chronic lymphocytic leukemia.
Blood 1985;65(1):149-55.
1984: J Lawler; S C Liu; J Palek; Josef T Prchal
A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.
The Journal of clinical investigation 1984;73(6):1688-95.
1984: H Skalka; Josef T Prchal
Presenile cataracts.
Archives of ophthalmology 1984;102(4):507.
1984: D Frei-Lahr; J C Barton; R Hoffman; L L Burkett; Josef T Prchal
Blastic transformation of essential thrombocythemia: dual expression of myelomonoblastic/megakaryoblastic phenotypes.
Blood 1984;63(4):866-72.
1984: M Tomana; Josef T Prchal; L C Garner; H W Skalka; S A Barker
Gas chromatographic analysis of lens monosaccharides.
The Journal of laboratory and clinical medicine 1984;103(1):137-42.
1984: S Gay; R E Gay; Josef T Prchal
Immunohistological studies of bone marrow collagen.
Progress in clinical and biological research 1984;154():291-306.
1983: J Lawler; J Palek; S C Liu; Josef T Prchal; William M Butler
Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit.
Blood 1983;62(6):1182-9.
1983: S A Barker; F P Fish; M Tomana; L C Garner; R L Settine; Josef T Prchal
Gas chromatographic/mass spectrometric evidence for the identification of a heptitol and an octitol in human and Octodon degu eye lenses.
Biochemical and biophysical research communications 1983;116(3):988-93.
1983: Josef T Prchal; W M Crist; M Roper; V P Wellner
Hemolytic anemia, recurrent metabolic acidosis, and incomplete albinism associated with glutathione synthetase deficiency.
Blood 1983;62(4):754-7.
1983: G Lucivero; Josef T Prchal; A R Lawton; S Antonaci; L Bonomo
Abnormal T-cell functions in B-cell chronic lymphocytic leukemia do not imply T-lymphocyte involvement in the leukemic process: report of a case with demonstrated "polyclonality" of T lymphocytes.
Journal of clinical immunology 1983;3(2):111-6.
1983: M T Schreeder; Josef T Prchal
Successful treatment of thrombotic thrombocytopenia purpura by vincristine.
American journal of hematology 1983;14(1):75-8.
1982: H M Hittner; A J Carroll; Josef T Prchal
Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.
American journal of human genetics 1982;34(6):966-71.
1982: J Lawler; S C Liu; J Palek; Josef T Prchal
Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association.
The Journal of clinical investigation 1982;70(5):1019-30.
1982: Josef T Prchal; R P Castleberry; Rick Parmley; W M Crist; A Malluh
Hereditary pyropoikilocytosis and elliptocytosis: clinical, laboratory, and ultrastructural features in infants and children.
Pediatric research 1982;16(6):484-9.
1982: S C Liu; J Palek; Josef T Prchal
Defective spectrin dimer-dimer association with hereditary elliptocytosis.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(6):2072-6.
1982: C C Adolphson; Josef T Prchal; A J Carroll
Colonic villous adenoma. Monoclonal origin.
JAMA : the journal of the American Medical Association 1982;247(6):829-30.
1982: M R Moore; M E Conrad; E L Bradley; Josef T Prchal
Studies of nicotinamide adenine dinucleotide methemoglobin reductase activity in a Jewish population.
American journal of hematology 1982;12(1):13-8.
1981: H M Barnes; Josef T Prchal; C W Scott
Extramedullary blast transformation in the central nervous system in idiopathic myelofibrosis.
American journal of hematology 1981;11(3):305-8.
1981: S C Liu; J Palek; Josef T Prchal; R P Castleberry
Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.
The Journal of clinical investigation 1981;68(3):597-605.
1981: H W Skalka; Josef T Prchal
Cataracts and riboflavin deficiency.
The American journal of clinical nutrition 1981;34(5):861-3.
1981: Josef T Prchal; S S Crago; J Mestecky; A J Okos; Andrew Flint
Immunoblastic lymphoma: an immunologic study.
Cancer 1981;47(9):2312-8.
1981: H W Skalka; Josef T Prchal
The effect of diabetes mellitus and diabetic therapy on cataract formation.
Ophthalmology 1981;88(2):117-25.
1981: J Palek; S C Liu; P Y Liu; Josef T Prchal; R P Castleberry
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis.
Blood 1981;57(1):130-9.
1981: S C Liu; J Palek; Josef T Prchal
Defective membrane skeleton assembly in hereditary elliptocytosis.
Progress in clinical and biological research 1981;56():157-69.
1981: H W Skalka; Josef T Prchal
Riboflavin deficiency and cataract formation.
Metabolic and pediatric ophthalmology 1981;5(1):17-20.
1981: Josef T Prchal; G Stamatoyannopoulos
Two siblings with unusually mild homozygous beta-thalassemia: a didactic example of the effect of a nonallelic modifier gene of the expressivity of a monogenic disorder.
American journal of medical genetics 1981;10(3):291-300.
1980: Josef T Prchal; A J Carroll; J F Prchal; W M Crist; H W Skalka; W J Gealy; J Harley; A Malluh
Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection.
Blood 1980;56(6):1048-54.
1980: H W Skalka; Josef T Prchal
Effect of corticosteroids on cataract formation.
Archives of ophthalmology 1980;98(10):1773-7.
1980: Josef T Prchal; W M Crist; A Malluh; A Vitek; W N Tauxe; A J Carroll
A new glucose-6-phosphate dehydrogenase deficient variant in a patient with Chediak-Higashi syndrome.
Blood 1980;56(3):476-80.
1980: S G Rostand; R M Culpepper; Josef T Prchal
Urinary acidification in a patient with glucose-6-phosphate dehydrogenase deficiency. A reevaluation of the role of the hexose monophosphate shunt in renal acid secretion.
The American journal of medicine 1980;69(1):155-8.
1980: A J Carroll; Josef T Prchal; W M Crist; J F Prchal
Cellular expression of Wiskott-Aldrich allele.
Lancet 1980;1(8168 Pt 1):601-2.
1980: H W Skalka; Josef T Prchal
Presenile cataract formation and decreased activity of galactosemic enzymes.
Archives of ophthalmology 1980;98(2):269-73.
1980: J Mestecky; J L Preud'homme; S S Crago; E Mihaesco; Josef T Prchal; A J Okos
Presence of J chain in human lymphoid cells.
Clinical and experimental immunology 1980;39(2):371-85.
1980: Josef T Prchal; H Skalka; R S Clements; E L Bradley; M E Conrad; C Pittman
Diabetes and risk of cataract development.
Metabolic and pediatric ophthalmology 1980;4(4):185-9.
1979: H L Laws; M W Burlingame; J T Carpenter; Josef T Prchal; M E Conrad
Splenectomy for hematologic disease.
Surgery, gynecology & obstetrics 1979;149(4):509-12.
1979: Josef T Prchal; G Lucivero; A J Carroll; A R Lawton; C W Scott
A study of a patient with chronic lymphocytic leukemia (CLL) which demonstrates that proliferation of the lymphocytic clone in CLL does not include T lymphocytes.
Clinical immunology and immunopathology 1979;13(2):231-6.
1979: M C Poon; Josef T Prchal; T M Murad; J G Galbraith
Multiple myeloma masquerading as chromophobe adenoma.
Cancer 1979;43(4):1513-5.
1979: W Pruzanski; D M Parr; Josef T Prchal; E Y Chan
Gamma 3-heavy-chain disease (gamma 3-HCD) in a young patient with Down syndrome. Study of peripheral blood lymphocytes and of susceptibility to infection.
Clinical immunology and immunopathology 1979;12(3):253-62.
1978: Josef T Prchal; D W Throckmorton; A J Carroll; E W Fuson; Richard Gams; J F Prchal
A common progenitor for human myeloid and lymphoid cells.
Nature 1978;274(5671):590-1.
1978: Josef T Prchal; M E Conrad; H W Skalka
Association of presenile cataracts with heterozygosity for galactosaemic states and with riboflavin deficiency.
Lancet 1978;1(8054):12-3.
1977: J Blakely; Josef T Prchal; M F Glynn; J Bitmanis; E Girouard-Antonopoulos; M Bailey
An in vitro measurement of bleeding time.
The Journal of laboratory and clinical medicine 1977;89(6):1306-13.
1975: Josef T Prchal; S K Srivastava; E Beutler
Active transport of GSSG from reconstituted erythrocyte ghosts.
Blood 1975;46(1):111-7.
1973: Josef T Prchal; J Blakely
Letter: Granulocyte platelet rosettes.
The New England journal of medicine 1973;289(21):1146.
1968: I Manová; Josef T Prchal; B Konopásek; J Wagner
[Glucose-6-phosphate dehydrogenase deficiency in the erythrocytes of foreign students].
Casopís lékar̆ů c̆eských 1968;107(38):1165-7.
1968: Josef T Prchal; J Neuwirt
Synthesis of adult and fetal hemoglobins in the cord blood.
Folia haematologica (Leipzig, Germany : 1928) 1968;90(2):120-4.
1968: P Ponka; J Neuwirt; Josef T Prchal
Heme synthesis in impaired globin synthesis.
Folia haematologica (Leipzig, Germany : 1928) 1968;90(2):117-9.