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Journal Articles

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

P Jarolim, JL Murray, HL Rubin, WM Taylor, JT Prchal, SK Ballas, LM Snyder, L Chrobak, WD Melrose, V Brabec, J Palek

Blood (1996) 88 (11): 4366–4374.

https://doi.org/10.1182/blood.V88.11.4366.4366

Published: 1996

Journal Articles

A novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemia

MM Jenkins, JT Prchal

Blood (1996) 87 (7): 2993–2999.

https://doi.org/10.1182/blood.V87.7.2993.bloodjournal8772993

Published: 1996

Journal Articles

Plasma/serum levels of flt3 ligand are low in normal individuals and highly elevated in patients with Fanconi anemia and acquired aplastic anemia

SD Lyman, M Seaberg, R Hanna, J Zappone, K Brasel, JL Abkowitz, JT Prchal, JC Schultz, NT Shahidi

Blood (1995) 86 (11): 4091–4096.

https://doi.org/10.1182/blood.V86.11.4091.bloodjournal86114091

Published: 1995

Journal Articles

Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosis [letter]

EA Lowenthal, JT Prchal

Blood (1995) 86 (1): 411–412.

https://doi.org/10.1182/blood.V86.1.411.bloodjournal861411

Published: 1995

Journal Articles

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

L Sokol, M Luhovy, Y Guan, JF Prchal, GL Semenza, JT Prchal

Blood (1995) 86 (1): 15–22.

https://doi.org/10.1182/blood.V86.1.15.bloodjournal86115

Published: 1995

Journal Articles

Clonality in juvenile chronic myelogenous leukemia

L Busque, DG Gilliland, JT Prchal, CA Sieff, HJ Weinstein, JM Sokol, M Belickova, AS Wayne, KS Zuckerman, L Sokol

Blood (1995) 85 (1): 21–30.

https://doi.org/10.1182/blood.V85.1.21.bloodjournal85121

Published: 1995

Journal Articles

Accelerated healing of chronic sickle-cell leg ulcers treated with RGD peptide matrix. RGD Study Group

DL Wethers, GM Ramirez, M Koshy, MH Steinberg, G Jr Phillips, RS Siegel, JR Eckman, JT Prchal

Blood (1994) 84 (6): 1775–1779.

https://doi.org/10.1182/blood.V84.6.1775.1775

Published: 1994

Journal Articles

Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera

MJ Fisher, JF Prchal, JT Prchal, AD D'Andrea

Blood (1994) 84 (6): 1982–1991.

https://doi.org/10.1182/blood.V84.6.1982.1982

Published: 1994

Journal Articles

Evolving understanding of the cellular defect in polycythemia vera: implications for its clinical diagnosis and molecular pathophysiology [editorial; comment]

JT Prchal, JF Prchal

Blood (1994) 83 (1): 1–4.

https://doi.org/10.1182/blood.V83.1.1.1

Published: 1994

Journal Articles

Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis [letter]

JT Prchal, YL Guan, JF Prchal, F Barany

Blood (1993) 81 (1): 269–271.

https://doi.org/10.1182/blood.V81.1.269.269

Published: 1993

Journal Articles

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

P Jarolim, J Palek, HL Rubin, JT Prchal, C Korsgren, CM Cohen

Blood (1992) 80 (2): 523–529.

https://doi.org/10.1182/blood.V80.2.523.523

Published: 1992

Journal Articles

New glucose-6-phosphate dehydrogenase mutations from various ethnic groups

E Beutler, B Westwood, JT Prchal, G Vaca, CS Bartsocas, L Baronciani

Blood (1992) 80 (1): 255–256.

https://doi.org/10.1182/blood.V80.1.255.255

Published: 1992

Journal Articles

Familial and congenital polycythemia in three unrelated families

PD Emanuel, CJ Eaves, VC Broudy, T Papayannopoulou, MR Moore, AD D'Andrea, JF Prchal, AC Eaves, JT Prchal

Blood (1992) 79 (11): 3019–3030.

https://doi.org/10.1182/blood.V79.11.3019.3019

Published: 1992

Journal Articles

Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin

M Hanspal, SH Yoon, H Yu, JS Hanspal, S Lambert, J Palek, JT Prchal

Blood (1991) 77 (1): 165–173.

https://doi.org/10.1182/blood.V77.1.165.165

Published: 1991

Journal Articles

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

T Coetzer, J Palek, J Lawler, SC Liu, P Jarolim, M Lahav, JT Prchal, W Wang, BP Alter, G Schewitz

Blood (1990) 75 (11): 2235–2244.

https://doi.org/10.1182/blood.V75.11.2235.2235

Published: 1990

Journal Articles

Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions

JB Wilson, BB Webber, H Hu, A Kutlar, F Kutlar, JF Codrington, JT Prchal, KM Hall, JM de Pablos, I Rodriguez

Blood (1990) 75 (9): 1883–1887.

https://doi.org/10.1182/blood.V75.9.1883.1883

Published: 1990

Journal Articles

Molecular heterogeneity of glucose-6-phosphate dehydrogenase A-

E Beutler, W Kuhl, JL Vives-Corrons, JT Prchal

Blood (1989) 74 (7): 2550–2555.

https://doi.org/10.1182/blood.V74.7.2550.2550

Published: 1989

Journal Articles

Viscoelastic properties of red cell membrane in hereditary elliptocytosis

A Chabanel, KL Sung, J Rapiejko, JT Prchal, J Palek, SC Liu, S Chien

Blood (1989) 73 (2): 592–595.

https://doi.org/10.1182/blood.V73.2.592.592

Published: 1989

Journal Articles

Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis

J Lawler, TL Coetzer, VN Mankad, RB Moore, JT Prchal, J Palek

Blood (1988) 72 (4): 1412–1415.

https://doi.org/10.1182/blood.V72.4.1412.1412

Published: 1988

Journal Articles

Fibrinogen Birmingham: a heterozygous dysfibrinogenemia (A alpha 16 Arg- ---His) containing heterodimeric molecules

KR Siebenlist, JT Prchal, MW Mosesson

Blood (1988) 71 (3): 613–618.

https://doi.org/10.1182/blood.V71.3.613.613

Published: 1988

NARROW

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

A novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemia

Plasma/serum levels of flt3 ligand are low in normal individuals and highly elevated in patients with Fanconi anemia and acquired aplastic anemia

Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosis [letter]

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

Clonality in juvenile chronic myelogenous leukemia

Accelerated healing of chronic sickle-cell leg ulcers treated with RGD peptide matrix. RGD Study Group

Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera

Evolving understanding of the cellular defect in polycythemia vera: implications for its clinical diagnosis and molecular pathophysiology [editorial; comment]

Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis [letter]

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

New glucose-6-phosphate dehydrogenase mutations from various ethnic groups

Familial and congenital polycythemia in three unrelated families

Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin

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

Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions

Molecular heterogeneity of glucose-6-phosphate dehydrogenase A-

Viscoelastic properties of red cell membrane in hereditary elliptocytosis

Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis

Fibrinogen Birmingham: a heterozygous dysfibrinogenemia (A alpha 16 Arg- ---His) containing heterodimeric molecules

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American Society of Hematology

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American Society of Hematology

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