A Rac/Cdc42 exchange factor complex promotes formation of lateral filopodia and blood vessel lumen morphogenesis

Abraham, S, Scarcia, M, Bagshaw, R et al. (15 more authors) (2015) A Rac/Cdc42 exchange factor complex promotes formation of lateral filopodia and blood vessel lumen morphogenesis. Nature Communications, 6. 7286. ISSN 2041-1723

Abstract

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Authors/Creators:
  • Abraham, S
  • Scarcia, M
  • Bagshaw, R
  • McMahon, K
  • Grant, G
  • Harvey, T
  • Yeo, M
  • Esteves, FOG
  • Thygesen, HH
  • Jones, PF
  • Spiers, V
  • Hanby, AM
  • Selby, PJ
  • Lorger, M
  • Dear, TN
  • Pawson, T
  • Marshall, CJ
  • Mavria, G
Copyright, Publisher and Additional Information: (c) 2015 Macmillan Publishers Limited. All rights reserved.This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
Keywords: angiogenesis; Rho GTPase; guanine nucleotide exchange factor; filopodia
Dates:
  • Accepted: 26 April 2015
  • Published: 1 July 2015
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Molecular Gastroenterology (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Experimental Oncology (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Leeds Institute of Cancer and Pathology (LICAP) > Section of Experimental Oncology (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 19 Jun 2015 12:48
Last Modified: 17 Mar 2016 15:50
Published Version: http://dx.doi.org/10.1038/ncomms8286
Status: Published
Publisher: Nature Publishing Group
Identification Number: https://doi.org/10.1038/ncomms8286

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