These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 8317479)
21. Glanzmann thrombasthenia resulting from a single amino acid substitution between the second and third calcium-binding domains of GPIIb. Role of the GPIIb amino terminus in integrin subunit association. Wilcox DA; Paddock CM; Lyman S; Gill JC; Newman PJ J Clin Invest; 1995 Apr; 95(4):1553-60. PubMed ID: 7706461 [TBL] [Abstract][Full Text] [Related]
22. Single-strand conformation polymorphism analysis is a rapid and effective method for the identification of mutations and polymorphisms in the gene for glycoprotein IIIa. Jin Y; Dietz HC; Nurden A; Bray PF Blood; 1993 Oct; 82(8):2281-8. PubMed ID: 8400280 [TBL] [Abstract][Full Text] [Related]
23. Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I. Vannier C; Behnisch W; Bartsch I; Sandrock K; Ertle F; Schmidt K; Busse A; Superti-Furga A; Kulozik A; Santoso S; Zieger B Klin Padiatr; 2010 May; 222(3):150-3. PubMed ID: 20514618 [TBL] [Abstract][Full Text] [Related]
25. Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families. Sandrock K; Halimeh S; Wiegering V; Kappert G; Sauer K; Deeg N; Busse E; Zieger B Klin Padiatr; 2012 Apr; 224(3):174-8. PubMed ID: 22513797 [TBL] [Abstract][Full Text] [Related]
26. A nonsense mutation in the GPIIb heavy chain (Ser 870-->stop) impairs platelet GPIIb-IIIa expression. Vinciguerra C; Khelif A; Alemany M; Morle F; Grenier C; Uzan G; Gulino D; Dechavanne M; Negrier C Br J Haematol; 1996 Nov; 95(2):399-407. PubMed ID: 8904900 [TBL] [Abstract][Full Text] [Related]
27. Structure of platelet glycoprotein IIIa. A common subunit for two different membrane receptors. Zimrin AB; Eisman R; Vilaire G; Schwartz E; Bennett JS; Poncz M J Clin Invest; 1988 May; 81(5):1470-5. PubMed ID: 2452834 [TBL] [Abstract][Full Text] [Related]
28. Ser-752-->Pro mutation in the cytoplasmic domain of integrin beta 3 subunit and defective activation of platelet integrin alpha IIb beta 3 (glycoprotein IIb-IIIa) in a variant of Glanzmann thrombasthenia. Chen YP; Djaffar I; Pidard D; Steiner B; Cieutat AM; Caen JP; Rosa JP Proc Natl Acad Sci U S A; 1992 Nov; 89(21):10169-73. PubMed ID: 1438206 [TBL] [Abstract][Full Text] [Related]
29. Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin. Ruan C; Gu J; Wang X; Chu X; Pan J Thromb Haemost; 1993 Jan; 69(1):64-9. PubMed ID: 8095357 [TBL] [Abstract][Full Text] [Related]
30. Organization of the gene for platelet glycoprotein IIb. Heidenreich R; Eisman R; Surrey S; Delgrosso K; Bennett JS; Schwartz E; Poncz M Biochemistry; 1990 Feb; 29(5):1232-44. PubMed ID: 2322558 [TBL] [Abstract][Full Text] [Related]
31. [Rapid detection of platelet glycoprotein IIb, IIIA gene variety by single strand conformation polymorphism analysis]. Chen F; Coller B; French D Zhonghua Yi Xue Za Zhi; 1995 Jun; 75(6):341-3, 382. PubMed ID: 7553144 [TBL] [Abstract][Full Text] [Related]
32. A Val193Met mutation in GPIIIa results in a GPIIb/IIIa receptor with a constitutively high affinity for a small ligand. Fullard J; Murphy R; O'Neill S; Moran N; Ottridge B; Fitzgerald DJ Br J Haematol; 2001 Oct; 115(1):131-9. PubMed ID: 11722423 [TBL] [Abstract][Full Text] [Related]
33. A dinucleotide deletion in exon 4 of the PlA2 allelic form of glycoprotein IIIa: implications for the correlation of serologic versus genotypic analysis of human platelet alloantigens. Skogen B; Wang R; McFarland JG; Newman PJ Blood; 1996 Nov; 88(10):3831-6. PubMed ID: 8916947 [TBL] [Abstract][Full Text] [Related]
34. Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients. Nair S; Ghosh K; Shetty S; Mohanty D J Thromb Haemost; 2005 Mar; 3(3):482-8. PubMed ID: 15748237 [TBL] [Abstract][Full Text] [Related]
35. Homozygous Cys542-->Arg substitution in GPIIIa in a Swiss patient with type I Glanzmann's thrombasthenia. Ruan J; Schmugge M; Clemetson KJ; Cazes E; Combrie R; Bourre F; Nurden AT Br J Haematol; 1999 May; 105(2):523-31. PubMed ID: 10233432 [TBL] [Abstract][Full Text] [Related]
36. [Molecular pathology of inherited Glanzmann's thrombasthenia. Report of 11 cases]. Ruan CG; Gu JM; Li JY Zhonghua Nei Ke Za Zhi; 1992 Oct; 31(10):639-41, 659. PubMed ID: 1306460 [TBL] [Abstract][Full Text] [Related]
37. Cloning of glycoprotein IIIa cDNA from human erythroleukemia cells and localization of the gene to chromosome 17. Rosa JP; Bray PF; Gayet O; Johnston GI; Cook RG; Jackson KW; Shuman MA; McEver RP Blood; 1988 Aug; 72(2):593-600. PubMed ID: 3165296 [TBL] [Abstract][Full Text] [Related]
38. Abnormal processing of the glycoprotein IIb transcript due to a nonsense mutation in exon 17 associated with Glanzmann's thrombasthenia. Tomiyama Y; Kashiwagi H; Kosugi S; Shiraga M; Kanayama Y; Kurata Y; Matsuzawa Y Thromb Haemost; 1995 May; 73(5):756-62. PubMed ID: 7482399 [TBL] [Abstract][Full Text] [Related]
39. The genomic organization of platelet glycoprotein IIIa. Zimrin AB; Gidwitz S; Lord S; Schwartz E; Bennett JS; White GC; Poncz M J Biol Chem; 1990 May; 265(15):8590-5. PubMed ID: 2341395 [TBL] [Abstract][Full Text] [Related]
40. Physical linkage of the genes for platelet membrane glycoproteins IIb and IIIa. Bray PF; Barsh G; Rosa JP; Luo XY; Magenis E; Shuman MA Proc Natl Acad Sci U S A; 1988 Nov; 85(22):8683-7. PubMed ID: 3186752 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]