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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2009 | 1 |
2011 | 2 |
2013 | 1 |
2015 | 2 |
2024 | 0 |
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Page 1
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
Am J Hum Genet. 2009 May;84(5):617-27. doi: 10.1016/j.ajhg.2009.04.007. Epub 2009 Apr 30.
Am J Hum Genet. 2009.
PMID: 19409525
Free PMC article.
Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2).
Disabella E, Grasso M, Gambarin FI, Narula N, Dore R, Favalli V, Serio A, Antoniazzi E, Mosconi M, Pasotti M, Odero A, Arbustini E.
Disabella E, et al.
Heart. 2011 Feb;97(4):321-6. doi: 10.1136/hrt.2010.204388. Epub 2011 Jan 6.
Heart. 2011.
PMID: 21212136
Item in Clipboard
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections.
Hoffjan S, Waldmüller S, Blankenfeldt W, Kötting J, Gehle P, Binner P, Epplen JT, Scheffold T.
Hoffjan S, et al.
Eur J Hum Genet. 2011 May;19(5):520-4. doi: 10.1038/ejhg.2010.239. Epub 2011 Jan 19.
Eur J Hum Genet. 2011.
PMID: 21248741
Free PMC article.
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Iris Flocculi as an ocular marker of ACTA2 mutation in familial thoracic aortic aneurysms and dissections.
Chamney S, McGimpsey S, McConnell V, Willoughby CE.
Chamney S, et al.
Ophthalmic Genet. 2015 Mar;36(1):86-8. doi: 10.3109/13816810.2013.833634. Epub 2013 Sep 10.
Ophthalmic Genet. 2015.
PMID: 24020716
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Gene panel sequencing in heritable thoracic aortic disorders and related entities - results of comprehensive testing in a cohort of 264 patients.
Campens L, Callewaert B, Muiño Mosquera L, Renard M, Symoens S, De Paepe A, Coucke P, De Backer J.
Campens L, et al.
Orphanet J Rare Dis. 2015 Feb 3;10:9. doi: 10.1186/s13023-014-0221-6.
Orphanet J Rare Dis. 2015.
PMID: 25644172
Free PMC article.
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