-
1
-
-
0035574894
-
Lessons to better understanding of hypoxia sensing: Acquired and congenital mutations resulting in polycythemia
-
Prchal JT, Divoky V. Lessons to better understanding of hypoxia sensing: acquired and congenital mutations resulting in polycythemia. Adv Exp Med Biol 2001;502:189-205.
-
(2001)
Adv Exp Med Biol
, vol.502
, pp. 189-205
-
-
Prchal, J.T.1
Divoky, V.2
-
2
-
-
0027978142
-
Trends in the incidence of polycythemia vera among Olmsted County, Minnesota residents, 1935-1989
-
Ania BJ, Suman VJ, Sobell JL, Codd MB, Silverstein MN, Melton 3rd LJ. Trends in the incidence of polycythemia vera among Olmsted County, Minnesota residents, 1935-1989. Am J Hematol 1994;47:89-93.
-
(1994)
Am J Hematol
, vol.47
, pp. 89-93
-
-
Ania, B.J.1
Suman, V.J.2
Sobell, J.L.3
Codd, M.B.4
Silverstein, M.N.5
Melton L.J. III6
-
3
-
-
0016793754
-
Diagnosis and classification of polycythemias
-
Berlin NI. Diagnosis and classification of polycythemias. Semin Hematol 1975;12:339-51.
-
(1975)
Semin Hematol
, vol.12
, pp. 339-351
-
-
Berlin, N.I.1
-
5
-
-
0016391236
-
Bone-marrow responses in polycythemia vera
-
Prchal JF, Axelrad AA. Bone-marrow responses in polycythemia vera [letter]. N Engl J Med 1974;290:1382.
-
(1974)
N Engl J Med
, vol.290
, pp. 1382
-
-
Prchal, J.F.1
Axelrad, A.A.2
-
6
-
-
0028146159
-
Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera
-
Fisher MJ, Prchal JF, Prchal JT, D'Andrea AD. Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera. Blood 1994;84:1982-91.
-
(1994)
Blood
, vol.84
, pp. 1982-1991
-
-
Fisher, M.J.1
Prchal, J.F.2
Prchal, J.T.3
D'Andrea, A.D.4
-
7
-
-
2642609475
-
Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera
-
Moliterno AR, Hankins WD, Spivak JL. Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera. N Engl J Med 1998;338:572-80.
-
(1998)
N Engl J Med
, vol.338
, pp. 572-580
-
-
Moliterno, A.R.1
Hankins, W.D.2
Spivak, J.L.3
-
8
-
-
0032568003
-
Expression of Bcl-x in erythroid precursors from patients with polycythemia vera
-
Silva M, Richard C, Benito A, Sanz C, Olalla I, Femandez-Luna JL. Expression of Bcl-x in erythroid precursors from patients with polycythemia vera. N Engl J Med 1998;338:564-71.
-
(1998)
N Engl J Med
, vol.338
, pp. 564-571
-
-
Silva, M.1
Richard, C.2
Benito, A.3
Sanz, C.4
Olalla, I.5
Femandez-Luna, J.L.6
-
9
-
-
0036786364
-
Biochemical characterization of PRV-1, a novel hematopoietic cell surface receptor, which is overexpressed in polycythemia rubra vera
-
Klippel S, Strunck E, Busse CE, Behringer D, Pahl HL. Biochemical characterization of PRV-1, a novel hematopoietic cell surface receptor, which is overexpressed in polycythemia rubra vera. Blood 2002;100:2441-8.
-
(2002)
Blood
, vol.100
, pp. 2441-2448
-
-
Klippel, S.1
Strunck, E.2
Busse, C.E.3
Behringer, D.4
Pahl, H.L.5
-
11
-
-
0035383807
-
Increased expression of INK4a/ARF locus in polycythemia vera
-
Dai C, Krantz B. Increased expression of INK4a/ARF locus in polycythemia vera. Blood 2001;97:3424-32.
-
(2001)
Blood
, vol.97
, pp. 3424-3432
-
-
Dai, C.1
Krantz, B.2
-
12
-
-
0036191941
-
Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect inpolycythemia vera
-
Kralovics R, Guan Y, Prchal JT. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect inpolycythemia vera. Exp Hematol 2002;30:229-36.
-
(2002)
Exp Hematol
, vol.30
, pp. 229-236
-
-
Kralovics, R.1
Guan, Y.2
Prchal, J.T.3
-
13
-
-
0036439588
-
Exploring polycythaemia vera with fluorescence in situ hybridization: Additional cryptic 9p is the most frequent abnormality detected
-
Najfeld V, Montella L, Scalise A, Fruchtman S. Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected. Br J Haematol 2002;119:558-66.
-
(2002)
Br J Haematol
, vol.119
, pp. 558-566
-
-
Najfeld, V.1
Montella, L.2
Scalise, A.3
Fruchtman, S.4
-
14
-
-
0022217637
-
Autosomal dominant polycythemia
-
Prchal JT, Crist WM, Goldwasser E, Perrine G, Prchal JF. Autosomal dominant polycythemia. Blood 1985;66:1208-14.
-
(1985)
Blood
, vol.66
, pp. 1208-1214
-
-
Prchal, J.T.1
Crist, W.M.2
Goldwasser, E.3
Perrine, G.4
Prchal, J.F.5
-
15
-
-
0035970090
-
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. Mouse model of congenital polycythemia: homologous replacement of murine gene by mutant human erythropoietin receptor gene. Proc Natl Acad Sci U S A 2001;98:986-91.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 986-991
-
-
Divoky, V.1
Liu, Z.2
Ryan, T.M.3
Prchal, J.F.4
Townes, T.M.5
Prchal, J.T.6
-
16
-
-
0034839931
-
Genetic heterogeneity of primary familial and congenital polycythemia
-
Kralovics R, Prchal JT. Genetic heterogeneity of primary familial and congenital polycythemia. Am J Hematol 2001;68:115-21.
-
(2001)
Am J Hematol
, vol.68
, pp. 115-121
-
-
Kralovics, R.1
Prchal, J.T.2
-
17
-
-
0003023429
-
Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia
-
Scriver C, Beaudet A, Sly W, Valle D, editors. New York: McGraw-Hill
-
Weatherall DJ, Clegg JB, Higgs DR, Wood WG. Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia. In: Scriver C, Beaudet A, Sly W, Valle D, editors. The metabolic and molecular basis of inherited disease. 8th edition. New York: McGraw-Hill; 2001. p. 4571-636.
-
(2001)
The Metabolic and Molecular Basis of Inherited Disease. 8th Edition
, pp. 4571-4636
-
-
Weatherall, D.J.1
Clegg, J.B.2
Higgs, D.R.3
Wood, W.G.4
-
18
-
-
0017144203
-
Detection of mutant hemoglobins with altered affinity for oxygen: A simplified technique
-
Lichtman MA, Murphy MS, Adamson JW. Detection of mutant hemoglobins with altered affinity for oxygen: a simplified technique. Ann Intern Med 1976;84:517-20.
-
(1976)
Ann Intern Med
, vol.84
, pp. 517-520
-
-
Lichtman, M.A.1
Murphy, M.S.2
Adamson, J.W.3
-
19
-
-
0021344981
-
Diphosphoglyceromutase deficiency: New cases associated with erythrocytosis
-
Galacteros F, Rosa R, Prehu MO, Najean Y, Calvin MC. Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis. Nouv Rev Fr Hematol 1984;26:69-74.
-
(1984)
Nouv Rev Fr Hematol
, vol.26
, pp. 69-74
-
-
Galacteros, F.1
Rosa, R.2
Prehu, M.O.3
Najean, Y.4
Calvin, M.C.5
-
20
-
-
0005746215
-
Red cell enzymopathies
-
Hoffman R, editor. Philadelphia: WB Saunders
-
Prchal JT, Gregg X. Red cell enzymopathies. In: Hoffman R, editor. Hematology. 3rd edition. Philadelphia: WB Saunders; 1999. p. 561-76.
-
(1999)
Hematology. 3rd Edition
, pp. 561-576
-
-
Prchal, J.T.1
Gregg, X.2
-
21
-
-
0034663989
-
HIF-1 and human disease: One highly involved factor
-
Semenza GL. HIF-1 and human disease: one highly involved factor. Genes Dev 2000;14:1983-91.
-
(2000)
Genes Dev
, vol.14
, pp. 1983-1991
-
-
Semenza, G.L.1
-
22
-
-
0033587146
-
The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis
-
Maxwell PH, Wiesener MS, Chang GW, et al. The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. Nature 1999;399:271-5.
-
(1999)
Nature
, vol.399
, pp. 271-275
-
-
Maxwell, P.H.1
Wiesener, M.S.2
Chang, G.W.3
-
23
-
-
0033407456
-
Von Hippel-Lindau syndrome: A pleomorphic condition
-
Friedrich CA. Von Hippel-Lindau syndrome: a pleomorphic condition. Cancer 1999;86:2478-82.
-
(1999)
Cancer
, vol.86
, pp. 2478-2482
-
-
Friedrich, C.A.1
-
24
-
-
0016118725
-
Familial erythrocytosis among the residents of the Chuvash ASSR
-
Poliakova LA. Familial erythrocytosis among the residents of the Chuvash ASSR. Probl Gematol Pereliv Krovi 1974;19:30-3.
-
(1974)
Probl Gematol Pereliv Krovi
, vol.19
, pp. 30-33
-
-
Poliakova, L.A.1
-
25
-
-
0030985635
-
Congenital polycythemia in Chuvashia
-
Sergeyeva A, Gordeuk VR, Tokarev YN, Sokol L, Prchal JF, Prchal JT. Congenital polycythemia in Chuvashia. Blood 1997;89:2148-54.
-
(1997)
Blood
, vol.89
, pp. 2148-2154
-
-
Sergeyeva, A.1
Gordeuk, V.R.2
Tokarev, Y.N.3
Sokol, L.4
Prchal, J.F.5
Prchal, J.T.6
-
26
-
-
0036111623
-
Endemic polycythemia in Russia: Mutation in the VHL gene
-
Ang SO, Chen H, Gordeuk VR, et al. Endemic polycythemia in Russia: mutation in the VHL gene. Blood Cells Mol Dis 2002;28:57-62.
-
(2002)
Blood Cells Mol Dis
, vol.28
, pp. 57-62
-
-
Ang, S.O.1
Chen, H.2
Gordeuk, V.R.3
-
27
-
-
18744373593
-
Congenital Chuvash polycythemia: Altered oxygen homeostasis due to homozygosity for a hypomorphic VHL allele
-
Ang SO, Chen H, Hirota K, et al. Congenital Chuvash polycythemia: altered oxygen homeostasis due to homozygosity for a hypomorphic VHL allele. Nat Genet 2002;32:614-21.
-
(2002)
Nat Genet
, vol.32
, pp. 614-621
-
-
Ang, S.O.1
Chen, H.2
Hirota, K.3
-
28
-
-
79960970789
-
High mortality due to thrombosis and cerebral hemorrhage in Chuvash polycythemia
-
Gordeuk VR, Sergueeva AI, Miasnikova GY, Okhotin DJ, Prchal JT, Polyakova LA. High mortality due to thrombosis and cerebral hemorrhage in Chuvash polycythemia. Blood 2001;98:224a.
-
(2001)
Blood
, vol.98
-
-
Gordeuk, V.R.1
Sergueeva, A.I.2
Miasnikova, G.Y.3
Okhotin, D.J.4
Prchal, J.T.5
Polyakova, L.A.6
-
29
-
-
0037441601
-
Mutations in the VHL gene in sporadic apparently congenital polycythemia
-
Pastore YD, Jelinek J, Ang S, et al. Mutations in the VHL gene in sporadic apparently congenital polycythemia. Blood 2003;101:1591-5.
-
(2003)
Blood
, vol.101
, pp. 1591-1595
-
-
Pastore, Y.D.1
Jelinek, J.2
Ang, S.3
-
30
-
-
0042744741
-
Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry
-
in press
-
Percy MJ, McMullin MF, Jowitt SN, Potter M, Treacy M, Watson WH, et al. Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry. Blood 2003; in press.
-
(2003)
Blood
-
-
Percy, M.J.1
McMullin, M.F.2
Jowitt, S.N.3
Potter, M.4
Treacy, M.5
Watson, W.H.6
-
31
-
-
0042665948
-
Mutations of von Hippel-Lindau tumor suppressor gene and congenital polycythemia
-
in press
-
Pastore Y, Jedlickova K, Guan YL, Liu E, Fahner J, Hasle H, et al. Mutations of von Hippel-Lindau tumor suppressor gene and congenital polycythemia. Am J Hum Genet 2003; in press.
-
(2003)
Am J Hum Genet
-
-
Pastore, Y.1
Jedlickova, K.2
Guan, Y.L.3
Liu, E.4
Fahner, J.5
Hasle, H.6
-
32
-
-
0031778819
-
Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis
-
Julian BA, Brantley Jr RR, Barker CV, et al. Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis. J Am Soc Nephrol 1998;9:1104-8.
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 1104-1108
-
-
Julian, B.A.1
Brantley R.R., Jr.2
Barker, C.V.3
-
33
-
-
0000191789
-
Angiotensin II facilitates erythropoietin mediated proliferation of normal early erythroid progenitors
-
Mrug M, Stopka T, Julian BA, Prchal JF, Prchal JT. Angiotensin II facilitates erythropoietin mediated proliferation of normal early erythroid progenitors. J Clin Invest 1997;115:508-22.
-
(1997)
J Clin Invest
, vol.115
, pp. 508-522
-
-
Mrug, M.1
Stopka, T.2
Julian, B.A.3
Prchal, J.F.4
Prchal, J.T.5
-
34
-
-
0028278002
-
Clinical evaluation of erythrocytosis in patients with hepatocellular carcinoma
-
Hwang SJ, Lee SD, Wu JC, et al. Clinical evaluation of erythrocytosis in patients with hepatocellular carcinoma. Chung Hua I Hsueh Tsa Chih 1994;53:262-9.
-
(1994)
Chung Hua I Hsueh Tsa Chih
, vol.53
, pp. 262-269
-
-
Hwang, S.J.1
Lee, S.D.2
Wu, J.C.3
-
35
-
-
0035735611
-
Thrombocytosis and thrombocythemia
-
Schafer AI. Thrombocytosis and thrombocythemia. Blood Rev 2001;15:159-66.
-
(2001)
Blood Rev
, vol.15
, pp. 159-166
-
-
Schafer, A.I.1
-
36
-
-
0028350733
-
Occurrence, etiology, and clinical significance of extreme thrombocytosis: A study of 280 cases
-
Buss DH, Cashell QAW, Connor ML, Richards F. Occurrence, etiology, and clinical significance of extreme thrombocytosis: a study of 280 cases. Am J Med 1994;96:247-53.
-
(1994)
Am J Med
, vol.96
, pp. 247-253
-
-
Buss, D.H.1
Cashell, Q.A.W.2
Connor, M.L.3
Richards, F.4
-
37
-
-
0032322969
-
Clonality markers in polycythaemia and primary thrombocythaemia
-
Briere J, el-Kassar N. Clonality markers in polycythaemia and primary thrombocythaemia. Baillieres Clin Haematol 1998;11:787-801.
-
(1998)
Baillieres Clin Haematol
, vol.11
, pp. 787-801
-
-
Briere, J.1
El-Kassar, N.2
-
38
-
-
0033555392
-
A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications
-
Harrison CN, Gale RE, Machin SJ, Linch DC. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications. Blood 1999;93:417-24.
-
(1999)
Blood
, vol.93
, pp. 417-424
-
-
Harrison, C.N.1
Gale, R.E.2
Machin, S.J.3
Linch, D.C.4
-
39
-
-
0034669997
-
Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia
-
Axelrad AA, Eskinazi D, Correa PN, Amato D. Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia. Blood 2000;96:3310-21.
-
(2000)
Blood
, vol.96
, pp. 3310-3321
-
-
Axelrad, A.A.1
Eskinazi, D.2
Correa, P.N.3
Amato, D.4
-
40
-
-
0031975482
-
An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia
-
Wiestner A, Schlemper RJ, van der Maas AP, Skoda RC. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Nat Genet 1998;18:49-52.
-
(1998)
Nat Genet
, vol.18
, pp. 49-52
-
-
Wiestner, A.1
Schlemper, R.J.2
Van der Maas, A.P.3
Skoda, R.C.4
-
41
-
-
0035704766
-
Lack of pathogenic mutations in the 5′-untranslated region of the thrombopoietin gene in patients with non-familial essential thrombocythaemia
-
Allen AJ, Gale RE, Harrison CN, Machin SJ, Linch DC. Lack of pathogenic mutations in the 5′-untranslated region of the thrombopoietin gene in patients with non-familial essential thrombocythaemia. Eur J Haematol 2001;67:232-7.
-
(2001)
Eur J Haematol
, vol.67
, pp. 232-237
-
-
Allen, A.J.1
Gale, R.E.2
Harrison, C.N.3
Machin, S.J.4
Linch, D.C.5
-
42
-
-
0033897370
-
Hereditary thrombocythaemia is a genetically heterogeneous disorder: Exclusion of TPO and MPL in two families with hereditary thrombocythaemia
-
Wiestner A, Padosch SA, Ghilardi N, Cesar JM, Odriozola J, Shapiro A, Skoda RC. Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia. Br J Haematol 2000;110:104-9.
-
(2000)
Br J Haematol
, vol.110
, pp. 104-109
-
-
Wiestner, A.1
Padosch, S.A.2
Ghilardi, N.3
Cesar, J.M.4
Odriozola, J.5
Shapiro, A.6
Skoda, R.C.7
-
43
-
-
0035103996
-
Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab family
-
Stuhrmann M, Bashawri L, Ahmed MA, Al-Awamy BH, Kuhnau W, Schmidtke J, et al. Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab family. Br J Haematol 2001;112:616-20.
-
(2001)
Br J Haematol
, vol.112
, pp. 616-620
-
-
Stuhrmann, M.1
Bashawri, L.2
Ahmed, M.A.3
Al-Awamy, B.H.4
Kuhnau, W.5
Schmidtke, J.6
|