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Defective Angiogenesis in Mice Lacking Endoglin.

Authors :
Li, Dean Y.
Sorensen, Lise K.
Brooke, Benjamin S.
Urness, Lise D.
Davis, Elaine C.
Taylor, Douglas G.
Boak, Beth B.
Wendel, Daniel P.
Source :
Science. 5/28/1999, Vol. 284 Issue 5419, p1534-1537. 4p. 38 Color Photographs, 2 Black and White Photographs, 1 Diagram.
Publication Year :
1999

Abstract

Reports that loss-of-function mutations in the human endoglin gene ENG causes hereditary hemorrhagic telangiectasis (HHT1), a disease characterized by vascular malformations. Shows that by gestational day 11.5 mice lacking endoglin die from defective vascular development; Vasculogenesis unaffected in mice lacking transforming growth factor-beta (TGF-beta); Results of loss of endoglin; Need for endoglin for angiogenesis.

Details

Language :
English
ISSN :
00368075
Volume :
284
Issue :
5419
Database :
Academic Search Index
Journal :
Science
Publication Type :
Academic Journal
Accession number :
1903635