231 related articles for article (PubMed ID: 24570135)
1. [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]
2. 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]
3. 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]
4. Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.
Regalado ES; Guo DC; Villamizar C; Avidan N; Gilchrist D; McGillivray B; Clarke L; Bernier F; Santos-Cortez RL; Leal SM; Bertoli-Avella AM; Shendure J; Rieder MJ; Nickerson DA; ; Milewicz DM
Circ Res; 2011 Sep; 109(6):680-6. PubMed ID: 21778426
[TBL] [Abstract][Full Text] [Related]
5. [Familial thoracic aortic aneurysms and dissections (FTAAD)].
Milanowska B; Michalak E; Janaszek-Sitkowska H; Franaszczyk M; Płoski R; Bilińska ZT
Kardiol Pol; 2011; 69(12):1291-7. PubMed ID: 22219111
[No Abstract] [Full Text] [Related]
6. 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]
7. Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.
Hasham SN; Willing MC; Guo DC; Muilenburg A; He R; Tran VT; Scherer SE; Shete SS; Milewicz DM
Circulation; 2003 Jul; 107(25):3184-90. PubMed ID: 12821554
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Pathogenic FBN1 variants in familial thoracic aortic aneurysms and dissections.
Regalado ES; Guo DC; Santos-Cortez RL; Hostetler E; Bensend TA; Pannu H; Estrera A; Safi H; Mitchell AL; Evans JP; Leal SM; Bamshad M; Shendure J; Nickerson DA; ; Milewicz DM
Clin Genet; 2016 Jun; 89(6):719-23. PubMed ID: 26621581
[TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms.
Regalado E; Medrek S; Tran-Fadulu V; Guo DC; Pannu H; Golabbakhsh H; Smart S; Chen JH; Shete S; Kim DH; Stern R; Braverman AC; Milewicz DM
Am J Med Genet A; 2011 Sep; 155A(9):2125-30. PubMed ID: 21815248
[TBL] [Abstract][Full Text] [Related]
12. Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections.
Pannu H; Fadulu VT; Chang J; Lafont A; Hasham SN; Sparks E; Giampietro PF; Zaleski C; Estrera AL; Safi HJ; Shete S; Willing MC; Raman CS; Milewicz DM
Circulation; 2005 Jul; 112(4):513-20. PubMed ID: 16027248
[TBL] [Abstract][Full Text] [Related]
13. The Expanding Clinical Spectrum of Extracardiovascular and Cardiovascular Manifestations of Heritable Thoracic Aortic Aneurysm and Dissection.
Bradley TJ; Bowdin SC; Morel CF; Pyeritz RE
Can J Cardiol; 2016 Jan; 32(1):86-99. PubMed ID: 26724513
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic variability and diffuse arterial lesions in a family with Loeys-Dietz syndrome type 4.
Mazzella JM; Frank M; Collignon P; Langeois M; Legrand A; Jeunemaitre X; Albuisson J
Clin Genet; 2017 Mar; 91(3):458-462. PubMed ID: 27440102
[TBL] [Abstract][Full Text] [Related]
15. The genetic message of a sudden, unexpected death due to thoracic aortic dissection.
Ripperger T; Tröger HD; Schmidtke J
Forensic Sci Int; 2009 May; 187(1-3):1-5. PubMed ID: 19285815
[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. Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.
Tran-Fadulu V; Pannu H; Kim DH; Vick GW; Lonsford CM; Lafont AL; Boccalandro C; Smart S; Peterson KL; Hain JZ; Willing MC; Coselli JS; LeMaire SA; Ahn C; Byers PH; Milewicz DM
J Med Genet; 2009 Sep; 46(9):607-13. PubMed ID: 19542084
[TBL] [Abstract][Full Text] [Related]
18. MicroRNA-21 Knockout Exacerbates Angiotensin II-Induced Thoracic Aortic Aneurysm and Dissection in Mice With Abnormal Transforming Growth Factor-β-SMAD3 Signaling.
Huang X; Yue Z; Wu J; Chen J; Wang S; Wu J; Ren L; Zhang A; Deng P; Wang K; Wu C; Ding X; Ye P; Xia J
Arterioscler Thromb Vasc Biol; 2018 May; 38(5):1086-1101. PubMed ID: 29519942
[TBL] [Abstract][Full Text] [Related]
19. Characterization of syndromic, nonsyndromic familial, and sporadic type B aortic dissection.
Shalhub S; Rah JY; Campbell R; Sweet MP; Quiroga E; Starnes BW
J Vasc Surg; 2021 Jun; 73(6):1906-1914.e2. PubMed ID: 33249204
[TBL] [Abstract][Full Text] [Related]
20. Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections.
Meester JA; Vandeweyer G; Pintelon I; Lammens M; Van Hoorick L; De Belder S; Waitzman K; Young L; Markham LW; Vogt J; Richer J; Beauchesne LM; Unger S; Superti-Furga A; Prsa M; Dhillon R; Reyniers E; Dietz HC; Wuyts W; Mortier G; Verstraeten A; Van Laer L; Loeys BL
Genet Med; 2017 Apr; 19(4):386-395. PubMed ID: 27632686
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
