215 related articles for article (PubMed ID: 16407493)
21. A 10-base-pair deletion in the gene encoding platelet glycoprotein IIb associated with Glanzmann thrombasthenia in a horse.
Christopherson PW; van Santen VL; Livesey L; Boudreaux MK
J Vet Intern Med; 2007; 21(1):196-8. PubMed ID: 17338169
[No Abstract] [Full Text] [Related]
22. Immunization against α
Fiore M; Bayat B; Phuangtham R; Blouin L; Huguenin Y; Bein G; Santoso S
J Thromb Haemost; 2021 Jan; 19(1):255-261. PubMed ID: 33090654
[TBL] [Abstract][Full Text] [Related]
23. 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; 80(1):42-8. PubMed ID: 9684783
[TBL] [Abstract][Full Text] [Related]
24. Analysis of platelet membrane glycoprotein polymorphisms in Glanzmann thrombasthenia showed the French gypsy mutation in the alphaIIb gene to be strongly linked to the HPA-1b polymorphism in beta3.
Jacquelin B; Tuleja E; Kunicki TJ; Nurden P; Nurden AT
J Thromb Haemost; 2003 Mar; 1(3):573-5. PubMed ID: 12871468
[TBL] [Abstract][Full Text] [Related]
25. A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.
Rosenberg N; Hauschner H; Peretz H; Mor-Cohen R; Landau M; Shenkman B; Kenet G; Coller BS; Awidi AA; Seligsohn U
J Thromb Haemost; 2005 Dec; 3(12):2764-72. PubMed ID: 16359514
[TBL] [Abstract][Full Text] [Related]
26. [Analysis of clinical features and genotype in three Chinese pedigrees with Glanzmann thrombasthenia].
Jin PP; Shen WZ; Yang F; Ding QL; Wang XF; Xi XD; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2008 Mar; 29(3):149-53. PubMed ID: 18788610
[TBL] [Abstract][Full Text] [Related]
27. Glanzmann thrombasthenia: integrin alpha IIb beta 3 deficiency.
Tomiyama Y
Int J Hematol; 2000 Dec; 72(4):448-54. PubMed ID: 11197210
[TBL] [Abstract][Full Text] [Related]
28. Three novel beta-propeller mutations causing Glanzmann thrombasthenia result in production of normally stable pro-alphaIIb, but variably impaired progression of pro-alphaIIbbeta3 from endoplasmic reticulum to Golgi.
Nelson EJ; Li J; Mitchell WB; Chandy M; Srivastava A; Coller BS
J Thromb Haemost; 2005 Dec; 3(12):2773-83. PubMed ID: 16359515
[TBL] [Abstract][Full Text] [Related]
29. Glanzmann thrombasthenia-like syndromes associated with Macrothrombocytopenias and mutations in the genes encoding the αIIbβ3 integrin.
Nurden AT; Pillois X; Fiore M; Heilig R; Nurden P
Semin Thromb Hemost; 2011 Sep; 37(6):698-706. PubMed ID: 22102273
[TBL] [Abstract][Full Text] [Related]
30. Disulfide bond disruption by a beta 3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active alpha IIb beta 3.
Mor-Cohen R; Rosenberg N; Peretz H; Landau M; Coller BS; Awidi A; Seligsohn U
Thromb Haemost; 2007 Dec; 98(6):1257-65. PubMed ID: 18064323
[TBL] [Abstract][Full Text] [Related]
31. Two genetic defects in alphaIIb are associated with type I Glanzmann's thrombasthenia in a Great Pyrenees dog: a 14-base insertion in exon 13 and a splicing defect of intron 13.
Lipscomb DL; Bourne C; Boudreaux MK
Vet Pathol; 2000 Nov; 37(6):581-8. PubMed ID: 11105947
[TBL] [Abstract][Full Text] [Related]
32. Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3).
Peretz H; Rosenberg N; Landau M; Usher S; Nelson EJ; Mor-Cohen R; French DL; Mitchell BW; Nair SC; Chandy M; Coller BS; Srivastava A; Seligsohn U
Hum Mutat; 2006 Apr; 27(4):359-69. PubMed ID: 16463284
[TBL] [Abstract][Full Text] [Related]
33. 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
[TBL] [Abstract][Full Text] [Related]
34. Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism.
D'Andrea G; Margaglione M;
Haematologica; 2003 Dec; 88(12):1378-82. PubMed ID: 14687991
[TBL] [Abstract][Full Text] [Related]
35. Glanzmann thrombasthenia in a 17-year-old Peruvian Paso mare.
Sanz MG; Wills TB; Christopherson P; Hines MT
Vet Clin Pathol; 2011 Mar; 40(1):48-51. PubMed ID: 21291483
[TBL] [Abstract][Full Text] [Related]
36. A Glanzmann thrombasthenia-like phenotype caused by a defect in inside-out signaling through the integrin alpha(IIb)beta3.
Tomiyama Y; Shiraga M; Kinoshita S; Ambo H; Kurata Y; Matsuzawa Y; Kunicki TJ
Thromb Haemost; 1998 Nov; 80(5):735-42. PubMed ID: 9843164
[TBL] [Abstract][Full Text] [Related]
37. Glanzmann thrombasthenia Frankfurt I is associated with a point mutation Thr176Ile in the N-terminal region of alpha IIb subunit integrin.
Westrup D; Santoso S; Follert-Hagendorff K; Bassus S; Just M; Jablonka B; Kirchmaier CM
Thromb Haemost; 2004 Nov; 92(5):1040-51. PubMed ID: 15543332
[TBL] [Abstract][Full Text] [Related]
38. Two new beta3 integrin mutations in Indian patients with Glanzmann thrombasthenia: localization of mutations affecting cysteine residues in integrin beta3.
Nair S; Li J; Mitchell WB; Mohanty D; Coller BS; French DL
Thromb Haemost; 2002 Sep; 88(3):503-9. PubMed ID: 12353082
[TBL] [Abstract][Full Text] [Related]
39. Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome.
Hauschner H; Mor-Cohen R; Messineo S; Mansour W; Seligsohn U; Savoia A; Rosenberg N
Blood Coagul Fibrinolysis; 2015 Apr; 26(3):302-8. PubMed ID: 25806962
[TBL] [Abstract][Full Text] [Related]
40. Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal.
Garcia LC; Breillat C; Lima M; Combrié R; Morais S; Teixera Mdos A; Campos M; Justica B; Nurden AT
Platelets; 2004 Feb; 15(1):15-22. PubMed ID: 14985172
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
