4.5 Article Proceedings Paper

The annexinopathies: a new category of diseases

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
Volume 1498, Issue 2-3, Pages 169-173

Publisher

ELSEVIER
DOI: 10.1016/S0167-4889(00)00093-8

Keywords

annexin; acute promyelocytic leukemia; fibrinolysis; antiphospholipid antibody; antiphospholipid syndrome; placenta; endothelium; phospholipid

Funding

  1. NHLBI NIH HHS [HL-61331] Funding Source: Medline

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The annexins are a family of highly homologous phospholipid binding proteins, which share a four-domain structure, with one member of the family - annexin VI - having a duplication consisting of eight domains. Thus far, ten annexins have been described in mammals. Although the biological functions of the annexins have not been definitively established, two human diseases involving annexin abnormalities ('annexinopathies') have been identified as of the time of writing. Overexpression of annexin II occurs in the leukocytes of a subset of patients having a hemorrhagic form of acute promyelocytic leukemia. Underexpression of annexin V occurs on placental trophoblasts in the antiphospholipid syndrome and in preeclampsia. Also, an animal model has been described in which annexin VII is underexpressed and is associated with disease, but the relevance of this animal model to human disease is not yet understood. Future research is likely to elucidate additional 'annexinopathies'. (C) 2000 Elsevier Science B.V. All rights reserved.

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