-
1
-
-
0017174101
-
Polycythemia vera: Stem-cell and probable clonal origin of the disease
-
Adamson, J.W., Fialkow, P.J., Murphy, S., Prchal, J.F. & Steinmann, L. (1976) Polycythemia vera: stem-cell and probable clonal origin of the disease. New England Journal of Medicine, 295, 913-916.
-
(1976)
New England Journal of Medicine
, vol.295
, pp. 913-916
-
-
Adamson, J.W.1
Fialkow, P.J.2
Murphy, S.3
Prchal, J.F.4
Steinmann, L.5
-
2
-
-
0025233815
-
Clonal analysis of chronic myeloproliferative disorders using X-linked DNA polymorphisms
-
Anger, B., Janssen, J.W., Schrezenmeier, H., Hehlmann, R., Heimpel, H. & Bartram, C.R. (1990) Clonal analysis of chronic myeloproliferative disorders using X-linked DNA polymorphisms. Leukemia, 4, 258-261.
-
(1990)
Leukemia
, vol.4
, pp. 258-261
-
-
Anger, B.1
Janssen, J.W.2
Schrezenmeier, H.3
Hehlmann, R.4
Heimpel, H.5
Bartram, C.R.6
-
3
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter, E.J., Scott, L.M., Campbell, P.J., East, C., Fourouclas, N., Swanton, S., Vassiliou, G.S., Bench, A.J., Boyd, E.M., Curtin, N., Scott, M.A., Erber, W.N. & Green, A.R. (2005) Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet, 365, 1054-1061.
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
East, C.4
Fourouclas, N.5
Swanton, S.6
Vassiliou, G.S.7
Bench, A.J.8
Boyd, E.M.9
Curtin, N.10
Scott, M.A.11
Erber, W.N.12
Green, A.R.13
-
4
-
-
0023753816
-
Evidence for pluripotent stem cell origin of idiopathic myelofibrosis: Clonal analysis of a case characterized by a N-ras gene mutation
-
Buschle, M., Janssen, J.W., Drexler, H., Lyons, J., Anger, B. & Bartram, C.R. (1988) Evidence for pluripotent stem cell origin of idiopathic myelofibrosis: clonal analysis of a case characterized by a N-ras gene mutation. Leukemia, 2, 658-660.
-
(1988)
Leukemia
, vol.2
, pp. 658-660
-
-
Buschle, M.1
Janssen, J.W.2
Drexler, H.3
Lyons, J.4
Anger, B.5
Bartram, C.R.6
-
5
-
-
28244442441
-
Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: A prospective study
-
Campbell, P.J., Scott, L.M., Buck, G., Wheatley, K., East, C.L., Marsden, J.T., Duffy, A., Boyd, E.M., Bench, A.J., Scott, M.A., Vassiliou, G.S., Milligan, D.W., Smith, S.R., Erber, W.N., Bareford, D., Wilkins, B.S., Reilly, J.T., Harrison, C.N. & Green, A.R. (2005) Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study. Lancet, 366, 1945-1953.
-
(2005)
Lancet
, vol.366
, pp. 1945-1953
-
-
Campbell, P.J.1
Scott, L.M.2
Buck, G.3
Wheatley, K.4
East, C.L.5
Marsden, J.T.6
Duffy, A.7
Boyd, E.M.8
Bench, A.J.9
Scott, M.A.10
Vassiliou, G.S.11
Milligan, D.W.12
Smith, S.R.13
Erber, W.N.14
Bareford, D.15
Wilkins, B.S.16
Reilly, J.T.17
Harrison, C.N.18
Green, A.R.19
-
6
-
-
0020083461
-
Erythroid progenitors in polycythemia vera: Demonstration of their hypersensitivity to erythropoietin using serum free cultures
-
Casadevall, N., Vainchenker, W., Lacombe, C., Vinci, G., Chapman, J., Breton-Gorius, J. & Varet, B. (1982) Erythroid progenitors in polycythemia vera: demonstration of their hypersensitivity to erythropoietin using serum free cultures. Blood, 59, 447-451.
-
(1982)
Blood
, vol.59
, pp. 447-451
-
-
Casadevall, N.1
Vainchenker, W.2
Lacombe, C.3
Vinci, G.4
Chapman, J.5
Breton-Gorius, J.6
Varet, B.7
-
7
-
-
33846007215
-
Evidence that the JAK2 G1849T (V617F) mutation occurs in a lympho-myeloid progenitor in polycythemia vera and idiopathic myelofibrosis
-
Delhommeau, F., Dupont, S., Tonetti, C., Masse, A., Godin, I., Le Couedic, J.P., Debili, N., Saulnier, P., Casadevall, N., Vainchenker, W. & Giraudier, S. (2006) Evidence that the JAK2 G1849T (V617F) mutation occurs in a lympho-myeloid progenitor in polycythemia vera and idiopathic myelofibrosis. Blood, 109, 71-77.
-
(2006)
Blood
, vol.109
, pp. 71-77
-
-
Delhommeau, F.1
Dupont, S.2
Tonetti, C.3
Masse, A.4
Godin, I.5
Le Couedic, J.P.6
Debili, N.7
Saulnier, P.8
Casadevall, N.9
Vainchenker, W.10
Giraudier, S.11
-
8
-
-
0031019581
-
Clonality analysis of hematopoiesis in essential thrombocythemia: Advantages of studying T lymphocytes and platelets
-
el-Kassar, N., Hetet, G., Briere, J. & Grandchamp, B. (1997) Clonality analysis of hematopoiesis in essential thrombocythemia: advantages of studying T lymphocytes and platelets. Blood, 89, 128-134.
-
(1997)
Blood
, vol.89
, pp. 128-134
-
-
el-Kassar, N.1
Hetet, G.2
Briere, J.3
Grandchamp, B.4
-
9
-
-
0018079901
-
Chronic myelocytic leukemia. Origin of some lymphocytes from leukemic stem cells
-
Fialkow, P.J., Denman, A.M., Jacobson, R.J. & Lowenthal, M.N. (1978) Chronic myelocytic leukemia. Origin of some lymphocytes from leukemic stem cells. Journal of Clinical Investigation, 62, 815-823.
-
(1978)
Journal of Clinical Investigation
, vol.62
, pp. 815-823
-
-
Fialkow, P.J.1
Denman, A.M.2
Jacobson, R.J.3
Lowenthal, M.N.4
-
10
-
-
0019818299
-
Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell
-
Fialkow, P.J., Faguet, G.B., Jacobson, R.J., Vaidya, K. & Murphy, S. (1981) Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood, 58, 916-919.
-
(1981)
Blood
, vol.58
, pp. 916-919
-
-
Fialkow, P.J.1
Faguet, G.B.2
Jacobson, R.J.3
Vaidya, K.4
Murphy, S.5
-
11
-
-
0026075627
-
Clonality in myeloproliferative disorders: Analysis by means of the polymerase chain reaction
-
Gilliland, D.G., Blanchard, K.L., Levy, J., Perrin, S. & Bunn, H.F. (1991) Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction. Proceedings of the National Academy of Sciences of the United States of America, 88, 6848-6852.
-
(1991)
Proceedings of the National Academy of Sciences of the United States of America
, vol.88
, pp. 6848-6852
-
-
Gilliland, D.G.1
Blanchard, K.L.2
Levy, J.3
Perrin, S.4
Bunn, H.F.5
-
12
-
-
18244384493
-
Identification of a human B-cell/myeloid common progenitor by the absence of CXCR4
-
Hou, Y.H., Srour, E.F., Ramsey, H., Dahl, R., Broxmeyer, H.E. & Hromas, R. (2005) Identification of a human B-cell/myeloid common progenitor by the absence of CXCR4. Blood, 105, 3488-3492.
-
(2005)
Blood
, vol.105
, pp. 3488-3492
-
-
Hou, Y.H.1
Srour, E.F.2
Ramsey, H.3
Dahl, R.4
Broxmeyer, H.E.5
Hromas, R.6
-
13
-
-
33750611344
-
Involvement of various hematopoietic cell lineages by the JAK2V617F mutation in polycythemia vera
-
Ishii, T., Bruno, E., Hoffman, R. & Xu, M. (2006) Involvement of various hematopoietic cell lineages by the JAK2V617F mutation in polycythemia vera. Blood, 108, 3128-3134.
-
(2006)
Blood
, vol.108
, pp. 3128-3134
-
-
Ishii, T.1
Bruno, E.2
Hoffman, R.3
Xu, M.4
-
14
-
-
0017812507
-
Agnogenic myeloid metaplasia: A clonal proliferation of hematopoietic stem cells with secondary myelofibrosis
-
Jacobson, R.J., Salo, A. & Fialkow, P.J. (1978) Agnogenic myeloid metaplasia: a clonal proliferation of hematopoietic stem cells with secondary myelofibrosis. Blood, 51, 189-194.
-
(1978)
Blood
, vol.51
, pp. 189-194
-
-
Jacobson, R.J.1
Salo, A.2
Fialkow, P.J.3
-
15
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James, C., Ugo, V., Le Couedic, J.P., Staerk, J., Delhommeau, F., Lacout, C., Garcon, L., Raslova, H., Berger, R., Naceur-Griscelli, A., Villeval, J.L., Constantinescu, S.N., Casadevall, N. & Vainchenker, W. (2005) A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature, 434, 1144-1148.
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.P.3
Staerk, J.4
Delhommeau, F.5
Lacout, C.6
Garcon, L.7
Raslova, H.8
Berger, R.9
Naceur-Griscelli, A.10
Villeval, J.L.11
Constantinescu, S.N.12
Casadevall, N.13
Vainchenker, W.14
-
16
-
-
0036485175
-
Redefinition of lymphoid progenitors
-
Katsura, Y. (2002) Redefinition of lymphoid progenitors. Nature Reviews Immunology, 2, 127-132.
-
(2002)
Nature Reviews Immunology
, vol.2
, pp. 127-132
-
-
Katsura, Y.1
-
17
-
-
0036191941
-
Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
-
Kralovics, R., Guan, Y. & Prchal, J.T. (2002) Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Experimental Hematology, 30, 229-236.
-
(2002)
Experimental Hematology
, vol.30
, pp. 229-236
-
-
Kralovics, R.1
Guan, Y.2
Prchal, J.T.3
-
18
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics, R., Passamonti, F., Buser, A.S., Teo, S.S., Tiedt, R., Passweg, J.R., Tichelli, A., Cazzola, M. & Skoda, R.C. (2005) A gain-of-function mutation of JAK2 in myeloproliferative disorders. New England Journal of Medicine, 352, 1779-1790.
-
(2005)
New England Journal of Medicine
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
Teo, S.S.4
Tiedt, R.5
Passweg, J.R.6
Tichelli, A.7
Cazzola, M.8
Skoda, R.C.9
-
19
-
-
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., Theocharides, A., Buser, A.S., Tichelli, A. & Skoda, R.C. (2006) Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders. Blood, 108, 1377-1380.
-
(2006)
Blood
, vol.108
, pp. 1377-1380
-
-
Kralovics, R.1
Teo, S.S.2
Li, S.3
Theocharides, A.4
Buser, A.S.5
Tichelli, A.6
Skoda, R.C.7
-
20
-
-
33745721197
-
JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis
-
Lacout, C., Pisani, D.F., Tulliez, M., Gachelin, F.M., Vainchenker, W. & Villeval, J.L. (2006) JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis. Blood, 108, 1652-1660.
-
(2006)
Blood
, vol.108
, pp. 1652-1660
-
-
Lacout, C.1
Pisani, D.F.2
Tulliez, M.3
Gachelin, F.M.4
Vainchenker, W.5
Villeval, J.L.6
-
21
-
-
27244432586
-
Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes
-
Lasho, T.L., Mesa, R., Gilliland, D.G. & Tefferi, A. (2005) Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes. British Journal of Haematology, 130, 797-799.
-
(2005)
British Journal of Haematology
, vol.130
, pp. 797-799
-
-
Lasho, T.L.1
Mesa, R.2
Gilliland, D.G.3
Tefferi, A.4
-
22
-
-
20244369569
-
-
Levine, R.L., Wadleigh, M., Cools, J., Ebert, B.L., Wernig, G., Huntly, B.J., Boggon, T.J., Wlodarska, I., Clark, J.J., Moore, S., Adelsperger, J., Koo, S., Lee, J.C., Gabriel, S., Mercher, T., D'Andrea, A., Frohling, S., Dohner, K., Marynen, P., Vandenberghe, P., Mesa, R.A., Tefferi, A., Griffin, J.D., Eck, M.J., Sellers, W.R., Meyerson, M., Golub, T.R., Lee, S.J. & Gilliland, D.G. (2005) Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell, 7, 387-397.
-
Levine, R.L., Wadleigh, M., Cools, J., Ebert, B.L., Wernig, G., Huntly, B.J., Boggon, T.J., Wlodarska, I., Clark, J.J., Moore, S., Adelsperger, J., Koo, S., Lee, J.C., Gabriel, S., Mercher, T., D'Andrea, A., Frohling, S., Dohner, K., Marynen, P., Vandenberghe, P., Mesa, R.A., Tefferi, A., Griffin, J.D., Eck, M.J., Sellers, W.R., Meyerson, M., Golub, T.R., Lee, S.J. & Gilliland, D.G. (2005) Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell, 7, 387-397.
-
-
-
-
23
-
-
0019307897
-
Involvement of the B-lymphoid system in chronic myelogenous leukaemia
-
Martin, P.J., Najfeld, V., Hansen, J.A., Penfold, G.K., Jacobson, R.J. & Fialkow, P.J. (1980) Involvement of the B-lymphoid system in chronic myelogenous leukaemia. Nature, 287, 49-50.
-
(1980)
Nature
, vol.287
, pp. 49-50
-
-
Martin, P.J.1
Najfeld, V.2
Hansen, J.A.3
Penfold, G.K.4
Jacobson, R.J.5
Fialkow, P.J.6
-
24
-
-
0021956939
-
Evidence for the involvement of B lymphoid cells in polycythemia vera and essential thrombocythemia
-
Raskind, W.H., Jacobson, R., Murphy, S., Adamson, J.W. & Fialkow, P.J. (1985) Evidence for the involvement of B lymphoid cells in polycythemia vera and essential thrombocythemia. Journal of Clinical Investigation, 75, 1388-1390.
-
(1985)
Journal of Clinical Investigation
, vol.75
, pp. 1388-1390
-
-
Raskind, W.H.1
Jacobson, R.2
Murphy, S.3
Adamson, J.W.4
Fialkow, P.J.5
-
25
-
-
0037372287
-
Both B and T lymphocytes may be clonally involved in myelofibrosis with myeloid metaplasia
-
Reeder, T.L., Bailey, R.J., Dewald, G.W. & Tefferi, A. (2003) Both B and T lymphocytes may be clonally involved in myelofibrosis with myeloid metaplasia. Blood, 101, 1981-1983.
-
(2003)
Blood
, vol.101
, pp. 1981-1983
-
-
Reeder, T.L.1
Bailey, R.J.2
Dewald, G.W.3
Tefferi, A.4
-
26
-
-
33645074137
-
Trafficking from the bone marrow to the thymus: A prerequisite for thymopoiesis
-
Schwarz, B.A. & Bhandoola, A. (2006) Trafficking from the bone marrow to the thymus: a prerequisite for thymopoiesis. Immunological Reviews, 209, 47-57.
-
(2006)
Immunological Reviews
, vol.209
, pp. 47-57
-
-
Schwarz, B.A.1
Bhandoola, A.2
-
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. & Green, A.R. (2006) Progenitors homozygous for the V617F mutation occur in most patients with polycythemia vera, but not essential thrombocythemia. Blood, 108, 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
-
-
0028362575
-
Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: Demonstration of heterogeneity in lineage involvement
-
Tsukamoto, N., Morita, K., Maehara, T., Okamoto, K., Sakai, H., Karasawa, M., Naruse, T. & Omine, M. (1994) Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: demonstration of heterogeneity in lineage involvement. British Journal of Haematology, 86, 253-258.
-
(1994)
British Journal of Haematology
, vol.86
, pp. 253-258
-
-
Tsukamoto, N.1
Morita, K.2
Maehara, T.3
Okamoto, K.4
Sakai, H.5
Karasawa, M.6
Naruse, T.7
Omine, M.8
-
29
-
-
33744490974
-
Expression of Jak2V617F causes a polycythemia veralike disease with associated myelofibrosis in a murine bone marrow transplant model
-
Wernig, G., Mercher, T., Okabe, R., Levine, R.L., Lee, B.H. & Gilliland, D.G. (2006) Expression of Jak2V617F causes a polycythemia veralike disease with associated myelofibrosis in a murine bone marrow transplant model. Blood, 107, 4274-4281.
-
(2006)
Blood
, vol.107
, pp. 4274-4281
-
-
Wernig, G.1
Mercher, T.2
Okabe, R.3
Levine, R.L.4
Lee, B.H.5
Gilliland, D.G.6
-
30
-
-
27744606173
-
JAK2 mutation in essential thrombocythaemia: Clinical associations and long-term prognostic relevance
-
Wolanskyj, A.P., Lasho, T.L., Schwager, S.M., McClure, R.F., Wadleigh, M., Lee, S.J., Gilliland, D.G. & Tefferi, A. (2005) JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance. British Journal of Haematology, 131, 208-213.
-
(2005)
British Journal of Haematology
, vol.131
, pp. 208-213
-
-
Wolanskyj, A.P.1
Lasho, T.L.2
Schwager, S.M.3
McClure, R.F.4
Wadleigh, M.5
Lee, S.J.6
Gilliland, D.G.7
Tefferi, A.8
|