Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome-Reference-Cited by-同舟云学术

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Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome

Published:2010-11-10 Issue:1 Volume:90 Page:182-190
ISSN:1755-3245
Container-title:Cardiovascular Research
language:en
Short-container-title:

Author:

Smith Lee B.,Hadoke Patrick W.F.,Dyer Emma,Denvir Martin A.,Brownstein David,Miller Eileen,Nelson Nancy,Wells Sara,Cheeseman Michael,Greenfield Andy

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Link

http://academic.oup.com/cardiovascres/article-pdf/90/1/182/17235497/cvq356.pdf

Reference24 articles.

1. Heritable diseases of collagen;Prockop;N Engl J Med,1984

2. A mutation in the gene for type-III procollagen (Col3A1) in a family with aortic-aneurysms;Kontusaari;J Clin Invest,1990

3. Ehlers–Danlos-syndrome type-IV—a single-base substitution of the last nucleotide of exon-34 in Col3A1 leads to exon skipping;Kuivaniemi;J Invest Dermatol,1995

4. Synthesis of Type-1 and Type-3 procollagen and collagen by monkey aortic smooth-muscle cells in vitro;Burke;Biochemistry,1977

5. Collagen characterization and cell transformation in human atherosclerosis;Mccullagh;Nature,1975

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