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用SDS—PAGE和免疫印迹技术检测血小板无力症 被引量:3

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出处 《中华血液学杂志》 CAS CSCD 北大核心 1990年第4期205-206,共2页 Chinese Journal of Hematology
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  • 1包承鑫,中华血液学杂志,1985年,6期,599页

同被引文献11

  • 1袁小瑜,陈方平,解勤之,蹇在伏,王光平.αⅡbA477P(A446P)——发生于血小板无力症患者的新突变[J].医学临床研究,2004,21(11):1238-1241. 被引量:4
  • 2付斌,陈方平,夏昆,傅敢,刘巍,黄细莲,肖广芬.血小板膜糖蛋白αⅡ b基因A2334C突变对αⅡ bβ3复合物合成及转运的影响——附一例报告[J].中华血液学杂志,2005,26(3):157-162. 被引量:7
  • 3沈卫章,李淑梅,姜玉珍,王学锋,丁秋兰,王鸿利.一种新的整合素α_(Ⅱb)Pro126His突变导致的遗传性血小板无力症[J].诊断学理论与实践,2005,4(6):451-454. 被引量:3
  • 4Nelson E J R, Nair S C, Peretz H, et al. Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients [ J ]. J Thromb Haemost,2006,4 (8) :1730-1737.
  • 5Hantgan R R, Stable M C, Jerome W C, et al. Tirofiban blocks platdet adhesion to fibrin with minimal perturbation of GPⅡ b/Ⅲ a structure [ J ] . Thromb Haemost, 2002, 87 (5) :910-917.
  • 6Xiong J P, Stehle T, Diefenbach B, et al. Crystal structure of the extracellular segment of integrin αvβ3 [ J ]. Science, 2001,294(5541) :339-345.
  • 7Rosenberg N, Yatur R, Sobolev V, et al. Major mutations in calf-1 and calf-2 domains of glycoprotein Ⅱb in patients with Glanzmann thrombasthenia enable GP Ⅱ b/Ⅲ a complex formation, but impair its transport from the endoplasmic reticulum to the golgi apparatus [ J]. Blood, 2003, 101 (12) :4808- 4815.
  • 8Beutler E, Lichtman M A, Coller B S, et al. Williams Hematology [ M ] . 6 th ed. New York : Mcgraw - hill Medical Publishing Division ,2001 : 1551-1558.
  • 9Rosenberg N, landau M, Luboshitz J, et al. A novel Phe- 171 Cys mutation in integrin ctllb causes Glanzmann thrombasthenia by abrogating αⅡbβ3 complex formation [ J ] . J Thromb Haemost,2004,2 (7) :1167-1175.
  • 10Westrup D, Santoso S, Katja F H, et al. Glanzmann thrombasthenia Frankfurt I is associated with a point mutation Thr176I1e in the N-terminal region of αⅡb subunit integrin [J]. Thromb Haemost, 2004, 92(5) : 1040-1051.

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