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Thromb Haemost 1992; 68(05): 615-616
DOI: 10.1055/s-0038-1646326
Letter to the Editor
Schattauer GmbH Stuttgart

Classification of Glanzmann's Thrombasthenia Based on the Intracellular Transport Pathway of GPIIb-IIIa

Atsushi Kato
The First Department of Internal Medicine, Tokyo Medical and Dental University, Tokyo, Japan
,
Koh Yamamoto
The First Department of Internal Medicine, Tokyo Medical and Dental University, Tokyo, Japan
,
Nobuo Aoki
The First Department of Internal Medicine, Tokyo Medical and Dental University, Tokyo, Japan
› Author Affiliations
Further Information

Publication History

Received 27 April 1992

Accepted 27 May 1992

Publication Date:
04 July 2018 (online)

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  • REFERENCES

  • 1 Caen JP. Glanzmann thrombasthenia. Clin Haematol 1972; 1: 383-392
    PubMedGoogle Scholar
  • 2 George JN, Caen JP, Nurden AT. Glanzmann's thrombasthenia: The spectrum of clinical disease. Blood 1990; 75: 1383-1395
    PubMedGoogle Scholar
  • 3 Hurtley SM, Helenius A. Protein oligomerization in the endoplasmic reticulum. Annu Rev Cell Biol 1989; 5: 277-307
    CrossrefPubMedGoogle Scholar
  • 4 Duperray A, Troesch A, Berthier R, Chagnon E, Frachet P, Uzan G, Marguerie G. Biosynthesis and assembly of platelet GPIIb-IIIa in human megakaryocytes: Evidence that assembly between pro-GPIIb and GPIIIa is a prerequisite for expression of the complex on the cell surface. Blood 1989; 74: 1603-1611
    PubMedGoogle Scholar
  • 5 Kolodziej MA, Vilaire G, Rifat S, Poncz M, Bennett JS. Effect of deletion of glycoprotein II b exon 28 on the expression of the platelet glycoprotein IIb/IIIa complex. Blood 1991; 78: 2344-2353
    PubMedGoogle Scholar
  • 6 Bray PF, Shuman MA. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann's thrombasthenia. Blood 1990; 75: 881-888
    PubMedGoogle Scholar
  • 7 Burk CD, Newman PJ, Lyman S, Gill J, Coller BS, Poncz M. A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia. J Clin Invest 1991; 87: 270-276
    CrossrefPubMedGoogle Scholar
  • 8 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: 3160-3164
    CrossrefPubMedGoogle Scholar
  • 9 Kato A, Yamamoto K, Miyazaki S, Jung SM, Moroi M, Aoki N. Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: A proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex. Blood 1992; 79: 3212-3218
    PubMedGoogle Scholar
  • 10 Loftus JC, O'Toole TE, Plow EF, Glass A, Frelinger AL III, Ginsberg MH. A β3 integrin mutation abolishes ligand binding and alters divalent cation-dependent conformation. Science. 1990; 249: 915-918
    PubMedGoogle Scholar
  • 11 Kunicki TJ (chairman). The report of the platelet subcommittee on the Classification of Glanzmann's thrombasthenia. 36th Annual Meeting of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Barcelona, Spain: 1990
    Google Scholar
  • 12 Kieffer N, Phillips DR. Platelet membrane glycoproteins: Functions in cellular interactions. Annu Rev Cell Biol 1990; 6: 329-357
    CrossrefPubMedGoogle Scholar