Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome-Reference-Cited by-同舟云学术

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Published:2006-03-19 Issue:4 Volume:38 Page:452-457
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Coucke Paul J,Willaert Andy,Wessels Marja W,Callewaert Bert,Zoppi Nicoletta,De Backer Julie,Fox Joyce E,Mancini Grazia M S,Kambouris Marios,Gardella Rita,Facchetti Fabio,Willems Patrick J,Forsyth Ramses,Dietz Harry C,Barlati Sergio,Colombi Marina,Loeys Bart,De Paepe Anne

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1764.pdf

Reference27 articles.

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2. Coucke, P.J. et al. Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13. J. Med. Genet. 40, 747–751 (2003).

3. Loeys, B.L. et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat. Genet. 37, 275–281 (2005).

4. Dawson, P.A. et al. Sequence and functional analysis of GLUT10: a glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12–13.1. Mol. Genet. Metab. 74, 186–199 (2001).

5. McVie-Wylie, A.J., Lamson, D.R. & Chen, Y.T. Molecular cloning of a novel member of the GLUT family of transporters, SLC2a10 (GLUT10), localized on chromosome 20q13.1: a candidate gene for NIDDM susceptibility. Genomics 72, 113–117 (2001).

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