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
  • [31] Phenotypic correction of Glanzmann's thrombasthenia following megakaryocyte-targeted synthesis of the integrin beta(3)-subunit.
    Wilcox, DA
    Olsen, JC
    Ishizawa, L
    Bray, PF
    French, DL
    Bell, WR
    Griffith, M
    White, GC
    BLOOD, 1997, 90 (10) : 1236 - 1236
  • [32] Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the αIIbβ3 integrin
    Nurden, A. T.
    Kunicki, T.
    Nurden, P.
    Fiore, M.
    Martins, N.
    Heilig, R.
    Pillois, X.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (08) : 1866 - 1868
  • [33] Itgb3-integrin-deficient mice may not be a sufficient model for patients with Glanzmann thrombasthenia
    Li, Dongya
    Peng, Jie
    Li, Tiantian
    Liu, Yichen
    Chen, Min
    Shi, Xiaofeng
    MOLECULAR MEDICINE REPORTS, 2021, 23 (06)
  • [34] A novel Phe171Cys mutation in integrin αIIb causes Glanzmann thrombasthenia by abrogating αIIbβ3 complex formation
    Rosenberg, N
    Landau, M
    Luboshitz, J
    Rechavi, G
    Seligsohn, U
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (07) : 1167 - 1175
  • [35] Sheehan's Syndrome Associated with Glanzmann's Thrombasthenia: Case Report and Literatur Review
    Bayraktaroglu, T.
    Colak, N.
    Nalcaci, M.
    Yenerel, M. N.
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2008, 116 (09) : 549 - 553
  • [36] First description of an IgM monoclonal antibody causing IIb3 integrin activation and acquired Glanzmann thrombasthenia associated with macrothrombocytopenia
    Pillois, Xavier
    Guy, Alexandre
    Choquet, Emeline
    James, Chloe
    Tuffigo, Marie
    Viallard, Jean-Francois
    Garcia, Cedric
    Bordet, Jean-claude
    Jandrot-Perrus, Martine
    Payrastre, Bernard
    Fiore, Mathieu
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2019, 17 (05) : 795 - 802
  • [37] A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia
    Koukouritaki, Sevasti B.
    Thinn, Aye Myat M.
    Ashworth, Katrina J.
    Fang, Juan
    Slater, Haley S.
    Du, Lily M.
    Nguyen, Huong Thi Thu
    Pillois, Xavier
    Nurden, Alan T.
    Ng, Christopher J.
    Di Paola, Jorge
    Zhu, Jieqing
    Wilcox, David A.
    BLOOD ADVANCES, 2023, 7 (13) : 3180 - 3191
  • [38] Defects in Glanzmann thrombasthenia and LAD-III (LAD-1/v) syndrome: the role of integrin β1 and β3 in platelet adhesion to collagen
    van de Vijver, Edith
    De Cuyper, Iris M.
    Gerrits, Anja J.
    Verhoeven, Arthur J.
    Seeger, Karl
    Gutierrez, Laura
    van den Berg, Timo K.
    Kuijpers, Taco W.
    BLOOD, 2012, 119 (02) : 583 - 586
  • [39] A novel (288delC) mutation in exon 2 of GPIIb associated with type I Glanzmann's thrombasthenia
    Tao, JM
    Arias-Salgado, EG
    González-Manchón, C
    Díaz-Cremades, J
    Ayuso, MS
    Parrilla, R
    BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) : 96 - 103
  • [40] A polyadenylation signal mutation in the GPIIb gene associated with Glanzmann's thrombasthenia.
    Tomiyama, Y
    Honda, S
    Tadokoro, S
    Kashiwagi, H
    Shiraga, M
    Kosugi, S
    Kanakura, Y
    Kurata, Y
    Matsuzawa, Y
    BLOOD, 1995, 86 (10) : 313 - 313