Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis-Reference-Cited by-同舟云学术

Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis

Published:2011-01-09 Issue:2 Volume:43 Page:121-126
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

van de Laar Ingrid M B H,Oldenburg Rogier A,Pals Gerard,Roos-Hesselink Jolien W,de Graaf Bianca M,Verhagen Judith M A,Hoedemaekers Yvonne M,Willemsen Rob,Severijnen Lies-Anne,Venselaar Hanka,Vriend Gert,Pattynama Peter M,Collée Margriet,Majoor-Krakauer Danielle,Poldermans Don,Frohn-Mulder Ingrid M E,Micha Dimitra,Timmermans Janneke,Hilhorst-Hofstee Yvonne,Bierma-Zeinstra Sita M,Willems Patrick J,Kros Johan M,Oei Edwin H G,Oostra Ben A,Wessels Marja W,Bertoli-Avella Aida M

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.744.pdf

Reference28 articles.

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2. Massague, J., Seoane, J. & Wotton, D. Smad transcription factors. Genes Dev. 19, 2783–2810 (2005).

3. Datto, M.B. et al. Targeted disruption of Smad3 reveals an essential role in transforming growth factor beta-mediated signal transduction. Mol. Cell. Biol. 19, 2495–2504 (1999).

4. Lilienfeld, D.E., Gunderson, P.D., Sprafka, J.M. & Vargas, C. Epidemiology of aortic aneurysms: I. Mortality trends in the United States, 1951 to 1981. Arteriosclerosis 7, 637–643 (1987).

5. 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).

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