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Journal Abstract Search

357 related items for PubMed ID: 27098940

  • 21.
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  • 23. Classification of Iranian patients with Glanzmann's Thrombasthenia using a flow cytometric method.
    Farsinejad A, Abolghasemi H, Kazemi A, Aghaiipour M, Hadjati E, Faranoush M, Jazebi M, Ala F.
    Platelets; 2011; 22(5):321-7. PubMed ID: 21526886
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  • 24. In silico analysis of structural modifications in and around the integrin αIIb genu caused by ITGA2B variants in human platelets with emphasis on Glanzmann thrombasthenia.
    Pillois X, Peters P, Segers K, Nurden AT.
    Mol Genet Genomic Med; 2018 Mar; 6(2):249-260. PubMed ID: 29385657
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  • 25. Glanzmann's thrombasthenia due to a point mutation within intron 10 results in aberrant splicing of the beta3 gene.
    Tanaka S, Hayashi T, Terada C, Hori Y, Han KS, Ahn HS, Bourre F, Tani Y.
    J Thromb Haemost; 2003 Nov; 1(11):2427-33. PubMed ID: 14629479
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  • 26. Are bone defects in rare patients with Glanzmann's thrombasthenia associated with ITGB3 or ITGA2B mutations?
    Nurden AT, Fiore M, Nurden P, Heilig R, Pillois X.
    Platelets; 2011 Nov; 22(7):547-51. PubMed ID: 21557682
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  • 29. A variant thrombasthenic phenotype associated with compound heterozygosity of integrin beta3-subunit: (Met124Val)beta3 alters the subunit dimerization rendering a decreased number of constitutive active alphaIIbbeta3 receptors.
    González-Manchón C, Butta N, Larrucea S, Arias-Salgado EG, Alonso S, López A, Parrilla R.
    Thromb Haemost; 2004 Dec; 92(6):1377-86. PubMed ID: 15583747
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  • 31. 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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  • 33. Molecular characterization of Glanzmann's thrombasthenia in Iran: identification of three novel mutations.
    Kazemi A, Abolghasemi H, Kazemzadeh S, Vahidi R, Faranoush M, Farsinejad A, Ala F.
    Blood Coagul Fibrinolysis; 2017 Dec; 28(8):681-686. PubMed ID: 29084015
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  • 37. Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations.
    Sandrock-Lang K, Oldenburg J, Wiegering V, Halimeh S, Santoso S, Kurnik K, Fischer L, Tsakiris DA, Sigl-Kraetzig M, Brand B, Bührlen M, Kraetzer K, Deeg N, Hund M, Busse E, Kahle A, Zieger B.
    Thromb Haemost; 2015 Apr; 113(4):782-91. PubMed ID: 25373348
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  • 38. Naturally occurring point mutation Cys460Trp located in the I-EGF1 domain of integrin β3 alters the binding of some anti-HPA-1a antibodies.
    Holzwarth ST, Bayat B, Zhu J, Phuangtham R, Fischer L, Boeckelmann D, Röder L, Berghöfer H, Schmidt S, Bein G, Santoso S.
    Transfusion; 2020 Sep; 60(9):2097-2107. PubMed ID: 32770549
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  • 40. [Effects of the ITGA2B Nonsense Mutation (c.2659C > T, p.Q887X) on Platelet Function in a Mouse Model of Glanzmann's Thrombasthenia Generated with CRISPR/Cas9 Technology].
    Yang F, Jiang M, Lin ZH, Xie ZL, Ma ZN, Yang L, Liu H, Wang ZY, Zhou L.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Apr; 30(2):559-564. PubMed ID: 35395997
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