-
1
-
-
25844486924
-
Chronic myeloproliferative disorders-introduction
-
Skoda R., and Prchal J.T. Chronic myeloproliferative disorders-introduction. Semin Hematol 42 (2005) 181-183
-
(2005)
Semin Hematol
, vol.42
, pp. 181-183
-
-
Skoda, R.1
Prchal, J.T.2
-
2
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter E.J., Scott L.M., Campbell P.J., et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 365 (2005) 1054-1061
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
-
3
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James C., Ugo V., Le Couedic J.P., et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 434 (2005) 1144-1148
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.P.3
-
4
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics R., Passamonti F., Buser A.S., et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 352 (2005) 1779-1790
-
(2005)
N Engl J Med
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
-
5
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
Levine R.L., Wadleigh M., Cools J., et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 7 (2005) 387-397
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
-
6
-
-
20744460045
-
Identification of an acquired JAK2 mutation in polycythemia vera
-
Zhao R., Xing S., Li Z., et al. Identification of an acquired JAK2 mutation in polycythemia vera. J Biol Chem 280 (2005) 22788-22792
-
(2005)
J Biol Chem
, vol.280
, pp. 22788-22792
-
-
Zhao, R.1
Xing, S.2
Li, Z.3
-
7
-
-
0842309105
-
Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera
-
Ugo V., Marzac C., Teyssandier I., et al. Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera. Exp Hematol 32 (2004) 179-187
-
(2004)
Exp Hematol
, vol.32
, pp. 179-187
-
-
Ugo, V.1
Marzac, C.2
Teyssandier, I.3
-
8
-
-
33745721197
-
JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis
-
Lacout C., Pisani D.F., Tulliez M., Moreau Gachelin F., Vainchenker W., and Villeval J.L. JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis. Blood 108 (2006) 1652-1660
-
(2006)
Blood
, vol.108
, pp. 1652-1660
-
-
Lacout, C.1
Pisani, D.F.2
Tulliez, M.3
Moreau Gachelin, F.4
Vainchenker, W.5
Villeval, J.L.6
-
9
-
-
0036191941
-
Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
-
Kralovics R., Guan Y., and Prchal J.T. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Exp Hematol 30 (2002) 229-236
-
(2002)
Exp Hematol
, vol.30
, pp. 229-236
-
-
Kralovics, R.1
Guan, Y.2
Prchal, J.T.3
-
10
-
-
0242493826
-
Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease
-
Kralovics R., Stockton D.W., and Prchal J.T. Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease. Blood 102 (2003) 3793-3796
-
(2003)
Blood
, vol.102
, pp. 3793-3796
-
-
Kralovics, R.1
Stockton, D.W.2
Prchal, J.T.3
-
11
-
-
33747199312
-
Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders
-
Kralovics R., Teo S.S., Li S., et al. Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders. Blood 108 (2006) 1377-1380
-
(2006)
Blood
, vol.108
, pp. 1377-1380
-
-
Kralovics, R.1
Teo, S.S.2
Li, S.3
-
12
-
-
33745623666
-
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders
-
Bellanne-Chantelot C., Chaumarel I., Labopin M., et al. Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders. Blood 108 (2006) 346-352
-
(2006)
Blood
, vol.108
, pp. 346-352
-
-
Bellanne-Chantelot, C.1
Chaumarel, I.2
Labopin, M.3
-
13
-
-
0034090681
-
High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR
-
Germer S., Holland M.J., and Higuchi R. High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR. Genome Res 10 (2000) 258-266
-
(2000)
Genome Res
, vol.10
, pp. 258-266
-
-
Germer, S.1
Holland, M.J.2
Higuchi, R.3
-
14
-
-
1642565938
-
Oxygen-dependent regulation of erythropoiesis
-
Jelinek J., and Prchal J.T. Oxygen-dependent regulation of erythropoiesis. Methods Enzymol 381 (2004) 201-210
-
(2004)
Methods Enzymol
, vol.381
, pp. 201-210
-
-
Jelinek, J.1
Prchal, J.T.2
-
15
-
-
0024605518
-
Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
-
Newton C.R., Graham A., Heptinstall L.E., et al. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Res 17 (1989) 2503-2516
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 2503-2516
-
-
Newton, C.R.1
Graham, A.2
Heptinstall, L.E.3
-
17
-
-
25844447519
-
JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia
-
Jelinek J., Oki Y., Gharibyan V., et al. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. Blood 106 (2005) 3370-3373
-
(2005)
Blood
, vol.106
, pp. 3370-3373
-
-
Jelinek, J.1
Oki, Y.2
Gharibyan, V.3
-
18
-
-
0035894991
-
Genotyping by apyrase-mediated allele-specific extension
-
Ahmadian A., Gharizadeh B., O'Meara D., Odeberg J., and Lundeberg J. Genotyping by apyrase-mediated allele-specific extension. Nucleic Acids Res 29 (2001) E121
-
(2001)
Nucleic Acids Res
, vol.29
-
-
Ahmadian, A.1
Gharizadeh, B.2
O'Meara, D.3
Odeberg, J.4
Lundeberg, J.5
-
19
-
-
0027319769
-
PCR amplification of specific alleles: rapid detection of known mutations and polymorphisms
-
Bottema C.D., and Sommer S.S. PCR amplification of specific alleles: rapid detection of known mutations and polymorphisms. Mutat Res 288 (1993) 93-102
-
(1993)
Mutat Res
, vol.288
, pp. 93-102
-
-
Bottema, C.D.1
Sommer, S.S.2
-
20
-
-
0031914368
-
Differential amplification kinetics for point mutation analysis by PCR
-
202-204,206
-
Kaltenbock B., and Schneider R. Differential amplification kinetics for point mutation analysis by PCR. Biotechniques 24 (1998) 202-204,206
-
(1998)
Biotechniques
, vol.24
-
-
Kaltenbock, B.1
Schneider, R.2
-
21
-
-
0038723184
-
Enhanced allele-specific PCR discrimination in SNP genotyping using 3′ locked nucleic acid (LNA) primers
-
Latorra D., Campbell K., Wolter A., and Hurley J.M. Enhanced allele-specific PCR discrimination in SNP genotyping using 3′ locked nucleic acid (LNA) primers. Hum Mutat 22 (2003) 79-85
-
(2003)
Hum Mutat
, vol.22
, pp. 79-85
-
-
Latorra, D.1
Campbell, K.2
Wolter, A.3
Hurley, J.M.4
-
22
-
-
0038281343
-
Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietin
-
Liu E., Jelinek J., Pastore Y.D., Guan Y., Prchal J.F., and Prchal J.T. Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietin. Blood 101 (2003) 3294-3301
-
(2003)
Blood
, vol.101
, pp. 3294-3301
-
-
Liu, E.1
Jelinek, J.2
Pastore, Y.D.3
Guan, Y.4
Prchal, J.F.5
Prchal, J.T.6
-
23
-
-
0016391236
-
Letter: Bone-marrow responses in polycythemia vera
-
Prchal J.F., and Axelrad A.A. Letter: Bone-marrow responses in polycythemia vera. N Engl J Med 290 (1974) 1382
-
(1974)
N Engl J Med
, vol.290
, pp. 1382
-
-
Prchal, J.F.1
Axelrad, A.A.2
-
24
-
-
0017119808
-
Human erythroid colony formation in vitro: evidence for clonal origin
-
Prchal J.F., Adamson J.W., Steinmann L., and Fialkow P.J. Human erythroid colony formation in vitro: evidence for clonal origin. J Cell Physiol 89 (1976) 489-492
-
(1976)
J Cell Physiol
, vol.89
, pp. 489-492
-
-
Prchal, J.F.1
Adamson, J.W.2
Steinmann, L.3
Fialkow, P.J.4
-
25
-
-
0032525158
-
Human hematopoietic progenitors express erythropoietin
-
Stopka T., Zivny J.H., Stopkova P., Prchal J.F., and Prchal J.T. Human hematopoietic progenitors express erythropoietin. Blood 91 (1998) 3766-3772
-
(1998)
Blood
, vol.91
, pp. 3766-3772
-
-
Stopka, T.1
Zivny, J.H.2
Stopkova, P.3
Prchal, J.F.4
Prchal, J.T.5
-
26
-
-
0242352640
-
Design considerations and effects of LNA in PCR primers
-
Latorra D., Arar K., and Hurley J.M. Design considerations and effects of LNA in PCR primers. Mol Cell Probes 17 (2003) 253-259
-
(2003)
Mol Cell Probes
, vol.17
, pp. 253-259
-
-
Latorra, D.1
Arar, K.2
Hurley, J.M.3
-
27
-
-
33749358349
-
Progenitors homozygous for the V617F mutation occur in most patients with polycythemia vera, but not essential thrombocythemia
-
Scott L.M., Scott M.A., Campbell P.J., and Green A.R. Progenitors homozygous for the V617F mutation occur in most patients with polycythemia vera, but not essential thrombocythemia. Blood 108 (2006) 2435-2437
-
(2006)
Blood
, vol.108
, pp. 2435-2437
-
-
Scott, L.M.1
Scott, M.A.2
Campbell, P.J.3
Green, A.R.4
-
28
-
-
14644441737
-
Polycythemia vera and other primary polycythemias
-
Prchal J.T. Polycythemia vera and other primary polycythemias. Curr Opin Hematol 12 (2005) 112-116
-
(2005)
Curr Opin Hematol
, vol.12
, pp. 112-116
-
-
Prchal, J.T.1
|