Characterization of four novel β3 integrin defects associated with Glanzmann's thrombasthenia

被引:0
|
作者
Sabi, E. M. [1 ]
Stockley, J. [1 ]
Al-Marwani, A. [1 ]
Kiss-Toth, E. [1 ]
Makris, M. [1 ]
Daly, M. E. [1 ]
机构
[1] Univ Sheffield, Sheffield, S Yorkshire, England
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:224 / 224
页数:1
相关论文
共 50 条
  • [1] Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia
    Tokgoz, Huseyin
    Ozkan, Didem Torun
    Caliskan, Umran
    Akar, Nejat
    PLATELETS, 2015, 26 (08) : 779 - 782
  • [2] Glanzmann thrombasthenia:: Integrin αIIbβ3 deficiency
    Tomiyama, Y
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2000, 72 (04) : 448 - 454
  • [3] A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patient
    Nair, S
    Ghosh, K
    Shetty, S
    Mohanty, D
    HAEMATOLOGICA, 2004, 89 (12) : 1529 - 1530
  • [4] Identification of four novel mutations in three patients with Glanzmann's Thrombasthenia.
    Bourdon, L
    Cutler, J
    Savidge, GF
    BLOOD, 2005, 106 (11) : 614A - 615A
  • [5] β3-integrin-deficient mice are a model for Glanzmann thrombasthenia showing placental defects and reduced survival
    Hodivala-Dilke, KM
    McHugh, KP
    Tsakiris, DA
    Rayburn, H
    Crowley, D
    Ullman-Culleré, M
    Ross, FP
    Coller, BS
    Teitelbaum, S
    Hynes, RO
    JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (02): : 229 - 238
  • [6] Molecular characterization of Glanzmann's thrombasthenia in Iran: identification of three novel mutations
    Kazemi, Ahmad
    Abolghasemi, Hassan
    Kazemzadeh, Shima
    Vahidi, Reza
    Faranoush, Mohammad
    Farsinejad, Alireza
    Ala, Fereydoun
    BLOOD COAGULATION & FIBRINOLYSIS, 2017, 28 (08) : 681 - 686
  • [7] Triple heterozygosity in the integrin αIIb subunit in a patient with Glanzmann's thrombasthenia
    Nurden, AT
    Breillat, C
    Jacquelin, B
    Combrié, R
    Freedman, J
    Blanchette, VS
    Schmugge, M
    Rand, ML
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (05) : 813 - 819
  • [8] MOLECULAR CHARACTERIZATION OF GLANZMANN'S THROMBASTHENIA IN IRAN: IDENTIFICATION OF THREE NOVEL MUTATIONS
    Kazemzadeh, S. H.
    Farsinejad, A. R.
    Kazemi, A.
    Abolghasemi, H.
    Faranoush, M.
    Ala, F.
    HAEMATOLOGICA, 2016, 101 : 5 - 6
  • [9] Glanzmann Thrombasthenia-Like Syndromes Associated with Macrothrombocytopenias and Mutations in the Genes Encoding the αIIbβ3 Integrin
    Nurden, Alan T.
    Pillois, Xavier
    Fiore, Mathieu
    Heilig, Roland
    Nurden, Paquita
    SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2011, 37 (06): : 698 - 706
  • [10] Characterization of six alterations in ITGA2B and ITGB3 associated with glanzmann's thrombasthenia
    Sabi, E.
    Leo, V. C.
    Al-Musbahi, A.
    Al-Marwani, A.
    Makris, M.
    Daly, M. E.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2015, 13 : 938 - 938