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Journal Abstract Search

253 related items for PubMed ID: 8095357

  • 1. 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 11; 69(1):64-9. PubMed ID: 8095357
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  • 2. [Carrier detection of Glanzmann's thrombasthenia by Taq I restriction fragment length polymorphism of GPIIIa gene].
    Gu J.
    Zhonghua Yi Xue Za Zhi; 1991 Dec 11; 71(12):680-2, 46. PubMed ID: 1687449
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  • 5. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann's thrombasthenia.
    Bray PF, Shuman MA.
    Blood; 1990 Feb 15; 75(4):881-8. PubMed ID: 1967954
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  • 6. Role of RFLP using TspRI for carrier detection in Glanzmann's thrombasthenia: a report on two families.
    Kannan M, Yadav BK, Ahmad F, Saxena R.
    Int J Lab Hematol; 2010 Feb 15; 32(1 Pt 1):e158-62. PubMed ID: 19170775
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  • 7. Biochemical and molecular basis of Glanzmann's thrombasthenia.
    Perutelli P, Mori PG.
    Haematologica; 1992 Feb 15; 77(5):421-6. PubMed ID: 1483593
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  • 9. Prenatal diagnosis of Glanzmann thrombasthenia.
    Srivastava A, Usher S, Nelson EJ, Jayandharan G, Shaji RV, Chandy M, Seligsohn U, Peretz H.
    Natl Med J India; 2003 Feb 15; 16(4):207-8. PubMed ID: 14606769
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  • 11. [Glanzmann's thrombasthenia: a rare example of an integrin deficit].
    Perutelli P, Mori PG.
    Recenti Prog Med; 1992 Oct 15; 83(10):577-81. PubMed ID: 1462042
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  • 12. 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 15; 73(5):756-62. PubMed ID: 7482399
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  • 13. Glanzmann's thrombasthenia: updated.
    Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D.
    Platelets; 2002 Nov 15; 13(7):387-93. PubMed ID: 12487785
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  • 14. Bone marrow transplantation for Glanzmann's thrombasthenia.
    Johnson A, Goodall AH, Downie CJ, Vellodi A, Michael DP.
    Bone Marrow Transplant; 1994 Jul 15; 14(1):147-50. PubMed ID: 7951102
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  • 16. [Mutation screening and prenatal diagnosis of a pedigree with Glanzmann's thrombasthenia].
    Li W, Liu JL, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun 15; 28(3):251-5. PubMed ID: 21644217
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  • 18. [Familial occurrence of Glanzmann thrombasthenia].
    Musiał J, Krzanowski M, Judkiewicz L, Cierniewski C.
    Pol Tyg Lek; 2011 Jun 15; 47(5-6):138-40. PubMed ID: 1437802
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  • 19. A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia.
    Burk CD, Newman PJ, Lyman S, Gill J, Coller BS, Poncz M.
    J Clin Invest; 1991 Jan 15; 87(1):270-6. PubMed ID: 1702098
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  • 20. 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
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