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Journal Abstract Search

267 related items for PubMed ID: 17018384

  • 1. Type II Glanzmann thrombasthenia in a compound heterozygote for the alpha IIb gene. A novel missense mutation in exon 27.
    Jayo A, Pabón D, Lastres P, Jiménez-Yuste V, González-Manchón C.
    Haematologica; 2006 Oct; 91(10):1352-9. PubMed ID: 17018384
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  • 2. A novel Pro126His beta propeller mutation in integrin alphaIIb causes Glanzmann thrombasthenia by impairing progression of pro-alphaIIbbeta3 from endoplasmic reticulum to Golgi.
    Shen WZ, Ding QL, Jin PP, Wang XF, Jiang YZ, Li SM, Wang HL.
    Blood Cells Mol Dis; 2009 Oct; 42(1):44-50. PubMed ID: 18976939
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  • 3. AlphaIIbG236E causes Glanzmann thrombasthenia by impairing association with beta3.
    Afrasiabi A, Gelain F, Artoni A, Mannucci PM.
    Platelets; 2008 Aug; 19(5):322-7. PubMed ID: 18791937
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  • 4. Type I Glanzmann thrombasthenia caused by an apparently silent beta3 mutation that results in aberrant splicing and reduced beta3 mRNA.
    Xie J, Pabón D, Jayo A, Butta N, González-Manchón C.
    Thromb Haemost; 2005 May; 93(5):897-903. PubMed ID: 15886806
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  • 5. Characterization of the cDNA Encoding alphaIIb and beta3 in normal horses and two horses with Glanzmann thrombasthenia.
    Christopherson PW, Insalaco TA, van Santen VL, Livesey L, Bourne C, Boudreaux MK.
    Vet Pathol; 2006 Jan; 43(1):78-82. PubMed ID: 16407493
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  • 6. [Novel frame-shift mutation of 540 A deletion in GP IIb gene from a patient with Glanzmann thrombasthenia].
    Jian ZF, Tang FQ, Chen FP, Xie QZ, Wang GP.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2008 Feb; 33(2):165-8. PubMed ID: 18326913
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  • 7. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
    Tokgoz H, Torun Ozkan D, Caliskan U, Akar N.
    Platelets; 2015 Feb; 26(8):779-82. PubMed ID: 25734216
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  • 8. AlphaIIbbeta3 integrin: new allelic variants in Glanzmann thrombasthenia, effects on ITGA2B and ITGB3 mRNA splicing, expression, and structure-function.
    Jallu V, Dusseaux M, Panzer S, Torchet MF, Hezard N, Goudemand J, de Brevern AG, Kaplan C.
    Hum Mutat; 2010 Mar; 31(3):237-46. PubMed ID: 20020534
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  • 10. 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
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  • 12. 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
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  • 20. Three novel integrin beta3 subunit missense mutations (H280P, C560F, and G579S) in thrombasthenia, including one (H280P) prevalent in Japanese patients.
    Ambo H, Kamata T, Handa M, Taki M, Kuwajima M, Kawai Y, Oda A, Murata M, Takada Y, Watanabe K, Ikeda Y.
    Biochem Biophys Res Commun; 1998 Oct 29; 251(3):763-8. PubMed ID: 9790984
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