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325 related items for PubMed ID: 15583747
21. Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort. Nurden AT, Pillois X, Fiore M, Alessi MC, Bonduel M, Dreyfus M, Goudemand J, Gruel Y, Benabdallah-Guerida S, Latger-Cannard V, Négrier C, Nugent D, Oiron RD, Rand ML, Sié P, Trossaert M, Alberio L, Martins N, Sirvain-Trukniewicz P, Couloux A, Canault M, Fronthroth JP, Fretigny M, Nurden P, Heilig R, Vinciguerra C. Hum Mutat; 2015 May; 36(5):548-61. PubMed ID: 25728920 [Abstract] [Full Text] [Related]
23. Molecular genetic analysis of a compound heterozygote for the glycoprotein (GP) IIb gene associated with Glanzmann's thrombasthenia: disruption of the 674-687 disulfide bridge in GPIIb prevents surface exposure of GPIIb-IIIa complexes. González-Manchón C, Fernández-Pinel M, Arias-Salgado EG, Ferrer M, Alvarez MV, García-Muñoz S, Ayuso MS, Parrilla R. Blood; 1999 Feb 01; 93(3):866-75. PubMed ID: 9920835 [Abstract] [Full Text] [Related]
24. Heterozygous ITGA2B R995W mutation inducing constitutive activation of the αIIbβ3 receptor affects proplatelet formation and causes congenital macrothrombocytopenia. Kunishima S, Kashiwagi H, Otsu M, Takayama N, Eto K, Onodera M, Miyajima Y, Takamatsu Y, Suzumiya J, Matsubara K, Tomiyama Y, Saito H. Blood; 2011 May 19; 117(20):5479-84. PubMed ID: 21454453 [Abstract] [Full Text] [Related]
25. C560Rβ3 caused platelet integrin αII b β3 to bind fibrinogen continuously, but resulted in a severe bleeding syndrome and increased murine mortality. Fang J, Nurden P, North P, Nurden AT, Du LM, Valentin N, Wilcox DA. J Thromb Haemost; 2013 Jun 19; 11(6):1163-71. PubMed ID: 23551977 [Abstract] [Full Text] [Related]
26. A mutation in the extracellular cysteine-rich repeat region of the beta3 subunit activates integrins alphaIIbbeta3 and alphaVbeta3. Kashiwagi H, Tomiyama Y, Tadokoro S, Honda S, Shiraga M, Mizutani H, Handa M, Kurata Y, Matsuzawa Y, Shattil SJ. Blood; 1999 Apr 15; 93(8):2559-68. PubMed ID: 10194435 [Abstract] [Full Text] [Related]
27. A unique interaction between alphaIIb and beta3 in the head region is essential for outside-in signaling-related functions of alphaIIbbeta3 integrin. Hauschner H, Landau M, Seligsohn U, Rosenberg N. Blood; 2010 Jun 03; 115(22):4542-50. PubMed ID: 20308600 [Abstract] [Full Text] [Related]
31. A three amino acid deletion in glycoprotein IIIa is responsible for type I Glanzmann's thrombasthenia: importance of residues Ile325Pro326Gly327 for beta3 integrin subunit association. Morel-Kopp MC, Kaplan C, Proulle V, Jallu V, Melchior C, Peyruchaud O, Aurousseau MH, Kieffer N. Blood; 1997 Jul 15; 90(2):669-77. PubMed ID: 9226167 [Abstract] [Full Text] [Related]
32. Coated platelets function in platelet-dependent fibrin formation via integrin αIIbβ3 and transglutaminase factor XIII. Mattheij NJ, Swieringa F, Mastenbroek TG, Berny-Lang MA, May F, Baaten CC, van der Meijden PE, Henskens YM, Beckers EA, Suylen DP, Nolte MW, Hackeng TM, McCarty OJ, Heemskerk JW, Cosemans JM. Haematologica; 2016 Apr 15; 101(4):427-36. PubMed ID: 26721892 [Abstract] [Full Text] [Related]
34. Role of the alpha-subunit 326GRV sequence in the surface expression of fibrinogen and vitronectin receptors. Ferrer M, Ayuso MS, Butta N, Parrilla R, González-Manchón C. Am J Physiol; 1998 Nov 15; 275(5):C1239-46. PubMed ID: 9814972 [Abstract] [Full Text] [Related]
35. A Ser162-->Leu mutation within glycoprotein (GP) IIIa (integrin beta3) results in an unstable alphaIIbbeta3 complex that retains partial function in a novel form of type II Glanzmann thrombasthenia. Jackson DE, White MM, Jennings LK, Newman PJ. Thromb Haemost; 1998 Jul 15; 80(1):42-8. PubMed ID: 9684783 [Abstract] [Full Text] [Related]
37. Adhesive and signaling properties of a naturally occurring allele of glycoprotein IIIa with an amino acid substitution within the ligand binding domain-the Pena/Penb platelet alloantigenic epitopes. Wang R, Newman PJ. Blood; 1998 Nov 01; 92(9):3260-7. PubMed ID: 9787162 [Abstract] [Full Text] [Related]
39. Probing conformational changes in the I-like domain and the cysteine-rich repeat of human beta 3 integrins following disulfide bond disruption by cysteine mutations: identification of cysteine 598 involved in alphaIIbbeta3 activation. Chen P, Melchior C, Brons NH, Schlegel N, Caen J, Kieffer N. J Biol Chem; 2001 Oct 19; 276(42):38628-35. PubMed ID: 11507099 [Abstract] [Full Text] [Related]
40. Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients. Nelson EJ, Nair SC, Peretz H, Coller BS, Seligsohn U, Chandy M, Srivastava A. J Thromb Haemost; 2006 Aug 19; 4(8):1730-7. PubMed ID: 16879215 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]