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Volumn 7, Issue 11, 2009, Pages 1875-1877

Glanzmann thrombasthenia: The need for epidemiological studies

Author keywords

[No Author keywords available]

Indexed keywords

BETA3 INTEGRIN; BLOOD CLOTTING FACTOR 7; FIBRINOGEN RECEPTOR; VON WILLEBRAND FACTOR;

EID: 70449455550     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2009.03597.x     Document Type: Note
Times cited : (9)

References (17)
  • 1
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    • Inherited abnormalities of the platelet membrane: Glanzmann Thrombasthenia, Bernard-Soulier syndrome, and other disorders
    • In, eds, 4th edn, Philadelpia, Lippincott, Williams & Wilkins
    • Nurden AT, George JN, Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber S. Inherited abnormalities of the platelet membrane: Glanzmann Thrombasthenia, Bernard-Soulier syndrome, and other disorders. Hemostasis and Thrombosis 2006, 987-1010. In, eds, 4th edn, Philadelpia, Lippincott, Williams & Wilkins
    • (2006) Hemostasis and Thrombosis , pp. 987-1010
    • Nurden, A.T.1    George, J.N.2    Colman, R.W.3    Marder, V.J.4    Clowes, A.W.5    George, J.N.6    Goldhaber, S.7
  • 2
    • 0025178671 scopus 로고
    • Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann thrombasthenia
    • Bray PF, Shuman MA. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann thrombasthenia. Blood 1990, 75:881-8.
    • (1990) Blood , vol.75 , pp. 881-888
    • Bray, P.F.1    Shuman, M.A.2
  • 3
    • 0026356066 scopus 로고
    • The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel
    • Newman PJ, Seligsohn U, Lyman S, Coller BS. The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel. Proc Natl Acad Sci USA 1991, 88:3160-4.
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 3160-3164
    • Newman, P.J.1    Seligsohn, U.2    Lyman, S.3    Coller, B.S.4
  • 4
    • 0037443402 scopus 로고    scopus 로고
    • Two novel mutations in the alphaIIb calcium-binding domains identify hydrophobic regions essential for alphaIIbbeta3 biogenesis
    • Mitchell WB, Li J, Singh F, Michelson AD, Bussel J, Coller BS, French DL. Two novel mutations in the alphaIIb calcium-binding domains identify hydrophobic regions essential for alphaIIbbeta3 biogenesis. Blood 2003, 101:2268-76.
    • (2003) Blood , vol.101 , pp. 2268-2276
    • Mitchell, W.B.1    Li, J.2    Singh, F.3    Michelson, A.D.4    Bussel, J.5    Coller, B.S.6    French, D.L.7
  • 8
    • 33746618745 scopus 로고    scopus 로고
    • Diversity of Glanzmann thrombasthenia in Southern India: 10 novel mutations identified among 15 unrelated patients
    • Nelson EJ, Nair SC, Peretz H, Coller BS, Seligsohn U, Chandy M, Srivastava A. Diversity of Glanzmann thrombasthenia in Southern India: 10 novel mutations identified among 15 unrelated patients. J Thromb Haemost 2006, 4:1730-7.
    • (2006) J Thromb Haemost , vol.4 , pp. 1730-1737
    • Nelson, E.J.1    Nair, S.C.2    Peretz, H.3    Coller, B.S.4    Seligsohn, U.5    Chandy, M.6    Srivastava, A.7
  • 11
    • 18844417181 scopus 로고    scopus 로고
    • Type I Glanzmann thrombasthenia caused by an apparently silent β3 mutation that results in aberrant splicing and reduced β3 mRNA
    • Xie J, Pabon D, Jayo A, Butta N, Gonzalez-Manchon C. Type I Glanzmann thrombasthenia caused by an apparently silent β3 mutation that results in aberrant splicing and reduced β3 mRNA. Thromb Haemost 2005, 93:897-903.
    • (2005) Thromb Haemost , vol.93 , pp. 897-903
    • Xie, J.1    Pabon, D.2    Jayo, A.3    Butta, N.4    Gonzalez-Manchon, C.5
  • 12
    • 0642372604 scopus 로고    scopus 로고
    • Analysis of platelet membrane glycoprotein polymorphisms in Glanzmann thrombasthenia showed the French gypsy mutation in the αIIb gene to be strongly linked to the HPA-1b polymorphism in β3
    • Jacquelin B, Tuleja E, Kunicki TJ, Nurden P, Nurden AT. Analysis of platelet membrane glycoprotein polymorphisms in Glanzmann thrombasthenia showed the French gypsy mutation in the αIIb gene to be strongly linked to the HPA-1b polymorphism in β3. J Thromb Haemost 2003, 1:573-5.
    • (2003) J Thromb Haemost , vol.1 , pp. 573-575
    • Jacquelin, B.1    Tuleja, E.2    Kunicki, T.J.3    Nurden, P.4    Nurden, A.T.5
  • 17
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    • Therapeutic expression of the platelet-specific integrin, αIIbβ3, in a murine model for Glanzmann thrombasthenia
    • Fang J, Hodivala-Dilke K, Johnson BD, Lu LM, Hynes RO, White GC, Wilcox DA. Therapeutic expression of the platelet-specific integrin, αIIbβ3, in a murine model for Glanzmann thrombasthenia. Blood 2005, 106:2671-9.
    • (2005) Blood , vol.106 , pp. 2671-2679
    • Fang, J.1    Hodivala-Dilke, K.2    Johnson, B.D.3    Lu, L.M.4    Hynes, R.O.5    White, G.C.6    Wilcox, D.A.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.