Chronic myeloproliferative disorders: molecular markers and pathogenesis

被引：3
作者：
Skoda, RC [1 ]
机构：
[1] Univ Basel Hosp, Dept Res, CH-4031 Basel, Switzerland
来源：
HEMATOLOGY JOURNAL | 2004年 / 5卷
关键词：
D O I：
10.1038/sj.thj.6200437
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：S122 / S125
页数：4
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共 31 条
  • [1] Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia
    Andrieux, J
    Demory, JL
    Dupriez, B
    Quief, S
    Plantier, I
    Roumier, C
    Bauters, F
    Laï, JL
    Kerckaert, JP
    [J]. GENES CHROMOSOMES & CANCER, 2004, 39 (01) : 82 - 87
  • [2] Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
    Ang, SO
    Chen, H
    Hirota, K
    Gordeuk, VR
    Jelinek, J
    Guan, YL
    Liu, EL
    Sergueeva, AI
    Miasnikova, GY
    Mole, D
    Maxwell, PH
    Stockton, DW
    Semenza, GL
    Prchal, JT
    [J]. NATURE GENETICS, 2002, 32 (04) : 614 - 621
  • [3] Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes
    Bench, AJ
    Nacheva, EP
    Hood, TL
    Holden, JL
    French, L
    Swanton, S
    Champion, KM
    Li, J
    Whittaker, P
    Stavrides, G
    Hunt, AR
    Huntly, BJP
    Campbell, LJ
    Bentley, DR
    Deloukas, P
    Green, AR
    [J]. ONCOGENE, 2000, 19 (34) : 3902 - 3913
  • [4] The polycythaemia rubra vera-1 gene is constitutively expressed by bone marrow cells and does not discriminate polycythaemia vera from reactive and other chronic myeloproliferative disorders
    Bock, O
    Serinsöz, E
    Neusch, M
    Schlué, J
    Kreipe, H
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2003, 123 (03) : 472 - 474
  • [5] Translational pathophysiology: a novel molecular mechanism of human disease
    Cazzola, M
    Skoda, RC
    [J]. BLOOD, 2000, 95 (11) : 3280 - 3288
  • [6] SOME SPECULATIONS ON THE MYELOPROLIFERATIVE SYNDROMES
    DAMESHEK, W
    [J]. BLOOD, 1951, 6 (04) : 372 - 375
  • [7] DING J, 2004, BLOOD 0205
  • [8] The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non-familial essential thrombocythaemia
    Harrison, CN
    Gale, RE
    Wiestner, AC
    Skoda, RC
    Linch, DC
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1998, 102 (05) : 1341 - 1343
  • [9] Platelet c-mpl expression is dysregulated in patients with essential thrombocythaemia but this is not of diagnostic value
    Harrison, CN
    Gale, RE
    Pezella, F
    Mire-Sluis, A
    Machin, SJ
    Linch, DC
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 107 (01) : 139 - 147
  • [10] Markedly reduced expression of platelet c-mpl receptor in essential thrombocythemia
    Horikawa, Y
    Matsumura, I
    Hashimoto, K
    Shiraga, M
    Kosugi, S
    Tadokoro, S
    Kato, T
    Miyazaki, H
    Tomiyama, Y
    Kurata, Y
    Matsuzawa, Y
    Kanakura, Y
    [J]. BLOOD, 1997, 90 (10) : 4031 - 4038
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