441 related articles for article (PubMed ID: 21212136)
1. 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
Heart; 2011 Feb; 97(4):321-6. PubMed ID: 21212136
[TBL] [Abstract][Full Text] [Related]
2. Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.
Renard M; Callewaert B; Baetens M; Campens L; MacDermot K; Fryns JP; Bonduelle M; Dietz HC; Gaspar IM; Cavaco D; Stattin EL; Schrander-Stumpel C; Coucke P; Loeys B; De Paepe A; De Backer J
Int J Cardiol; 2013 May; 165(2):314-21. PubMed ID: 21937134
[TBL] [Abstract][Full Text] [Related]
3. 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
Eur J Hum Genet; 2011 May; 19(5):520-4. PubMed ID: 21248741
[TBL] [Abstract][Full Text] [Related]
4. Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD).
Morisaki H; Akutsu K; Ogino H; Kondo N; Yamanaka I; Tsutsumi Y; Yoshimuta T; Okajima T; Matsuda H; Minatoya K; Sasaki H; Tanaka H; Ishibashi-Ueda H; Morisaki T
Hum Mutat; 2009 Oct; 30(10):1406-11. PubMed ID: 19639654
[TBL] [Abstract][Full Text] [Related]
5. Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunction.
Milewicz DM; Guo DC; Tran-Fadulu V; Lafont AL; Papke CL; Inamoto S; Kwartler CS; Pannu H
Annu Rev Genomics Hum Genet; 2008; 9():283-302. PubMed ID: 18544034
[TBL] [Abstract][Full Text] [Related]
6. Clinical, pathological, and genetic analysis of a Korean family with thoracic aortic aneurysms and dissections carrying a novel Asp26Tyr mutation.
Yoo EH; Choi SH; Jang SY; Suh YL; Lee I; Song JK; Choe YH; Kim JW; Ki CS; Kim DK
Ann Clin Lab Sci; 2010; 40(3):278-84. PubMed ID: 20689142
[TBL] [Abstract][Full Text] [Related]
7. [Familial thoracic aortic aneurysms and dissections can be divided into three different main categories].
Hannuksela M; Stattin EL; Nyberg P; Carlberg B
Lakartidningen; 2014 Feb; 111(9-10):399-403. PubMed ID: 24570135
[TBL] [Abstract][Full Text] [Related]
8. Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
Guo DC; Papke CL; Tran-Fadulu V; Regalado ES; Avidan N; Johnson RJ; Kim DH; Pannu H; Willing MC; Sparks E; Pyeritz RE; Singh MN; Dalman RL; Grotta JC; Marian AJ; Boerwinkle EA; Frazier LQ; LeMaire SA; Coselli JS; Estrera AL; Safi HJ; Veeraraghavan S; Muzny DM; Wheeler DA; Willerson JT; Yu RK; Shete SS; Scherer SE; Raman CS; Buja LM; Milewicz DM
Am J Hum Genet; 2009 May; 84(5):617-27. PubMed ID: 19409525
[TBL] [Abstract][Full Text] [Related]
9. Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections.
Prakash S; Kuang SQ; ; Regalado E; Guo D; Milewicz D
PLoS One; 2016; 11(4):e0153543. PubMed ID: 27092555
[TBL] [Abstract][Full Text] [Related]
10. The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys-Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD).
Lerner-Ellis JP; Aldubayan SH; Hernandez AL; Kelly MA; Stuenkel AJ; Walsh J; Joshi VA
Mol Genet Metab; 2014 Jun; 112(2):171-6. PubMed ID: 24793577
[TBL] [Abstract][Full Text] [Related]
11. The non-syndromic familial thoracic aortic aneurysms and dissections maps to 15q21 locus.
Keramati AR; Sadeghpour A; Farahani MM; Chandok G; Mani A
BMC Med Genet; 2010 Oct; 11():143. PubMed ID: 20937124
[TBL] [Abstract][Full Text] [Related]
12. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
Guo DC; Pannu H; Tran-Fadulu V; Papke CL; Yu RK; Avidan N; Bourgeois S; Estrera AL; Safi HJ; Sparks E; Amor D; Ades L; McConnell V; Willoughby CE; Abuelo D; Willing M; Lewis RA; Kim DH; Scherer S; Tung PP; Ahn C; Buja LM; Raman CS; Shete SS; Milewicz DM
Nat Genet; 2007 Dec; 39(12):1488-93. PubMed ID: 17994018
[TBL] [Abstract][Full Text] [Related]
13. Iris Flocculi as an ocular marker of ACTA2 mutation in familial thoracic aortic aneurysms and dissections.
Chamney S; McGimpsey S; McConnell V; Willoughby CE
Ophthalmic Genet; 2015 Mar; 36(1):86-8. PubMed ID: 24020716
[TBL] [Abstract][Full Text] [Related]
14. Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.
Poninska JK; Bilinska ZT; Franaszczyk M; Michalak E; Rydzanicz M; Szpakowski E; Pollak A; Milanowska B; Truszkowska G; Chmielewski P; Sioma A; Janaszek-Sitkowska H; Klisiewicz A; Michalowska I; Makowiecka-Ciesla M; Kolsut P; Stawinski P; Foss-Nieradko B; Szperl M; Grzybowski J; Hoffman P; Januszewicz A; Kusmierczyk M; Ploski R
J Transl Med; 2016 May; 14(1):115. PubMed ID: 27146836
[TBL] [Abstract][Full Text] [Related]
15. Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromes.
Hillebrand M; Millot N; Sheikhzadeh S; Rybczynski M; Gerth S; Kölbel T; Keyser B; Kutsche K; Robinson PN; Berger J; Mir TS; Zeller T; Blankenberg S; von Kodolitsch Y; Goldmann B
Clin Cardiol; 2014 Nov; 37(11):672-9. PubMed ID: 25113270
[TBL] [Abstract][Full Text] [Related]
16. Familial non-syndromal thoracic aortic aneurysms and dissections - Incidence and family screening outcomes.
Robertson EN; van der Linde D; Sherrah AG; Vallely MP; Wilson M; Bannon PG; Jeremy RW
Int J Cardiol; 2016 Oct; 220():43-51. PubMed ID: 27372041
[TBL] [Abstract][Full Text] [Related]
17. Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm.
Ke T; Han M; Zhao M; Wang QK; Zhang H; Zhao Y; Ruan X; Li H; Xu C; Sun T
BMC Med Genet; 2016 Jul; 17(1):45. PubMed ID: 27431987
[TBL] [Abstract][Full Text] [Related]
18. Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutation.
Ware SM; Shikany A; Landis BJ; James JF; Hinton RB
Pediatrics; 2014 Oct; 134(4):e1218-23. PubMed ID: 25225139
[TBL] [Abstract][Full Text] [Related]
19. Novel variants in the ACTA2 and MYH11 genes in a Cypriot family with thoracic aortic aneurysms: a case report.
Keravnou A; Bashiardes E; Michailidou K; Soteriou M; Moushi A; Cariolou M
BMC Med Genet; 2018 Dec; 19(1):208. PubMed ID: 30526509
[TBL] [Abstract][Full Text] [Related]
20. Clinical outcomes of aortic repair in young adult patients with ACTA2 mutations.
Seike Y; Minatoya K; Sasaki H; Tanaka H; Itonaga T; Inoue Y; Morisaki H; Morisaki T; Ishibashi-Ueda H; Kobayashi J
Gen Thorac Cardiovasc Surg; 2017 Dec; 65(12):686-691. PubMed ID: 28808903
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]