151 related articles for article (PubMed ID: 21270064)
1. Mutations in TGFBR2 gene cause spontaneous cervical artery dissection.
Pezzini A; Drera B; Del Zotto E; Ritelli M; Carletti M; Tomelleri G; Bovi P; Giossi A; Volonghi I; Costa P; Magoni M; Padovani A; Barlati S; Colombi M
J Neurol Neurosurg Psychiatry; 2011 Dec; 82(12):1372-4. PubMed ID: 21270064
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.
Mátyás G; Arnold E; Carrel T; Baumgartner D; Boileau C; Berger W; Steinmann B
Hum Mutat; 2006 Aug; 27(8):760-9. PubMed ID: 16791849
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Exon 47 skipping of fibrillin-1 leads preferentially to cardiovascular defects in patients with thoracic aortic aneurysms and dissections.
Wang WJ; Han P; Zheng J; Hu FY; Zhu Y; Xie JS; Guo J; Zhang Z; Dong J; Zheng GY; Cao H; Liu TS; Fu Q; Sun L; Yang BB; Tian XL
J Mol Med (Berl); 2013 Jan; 91(1):37-47. PubMed ID: 22772377
[TBL] [Abstract][Full Text] [Related]
6. TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections.
Inamoto S; Kwartler CS; Lafont AL; Liang YY; Fadulu VT; Duraisamy S; Willing M; Estrera A; Safi H; Hannibal MC; Carey J; Wiktorowicz J; Tan FK; Feng XH; Pannu H; Milewicz DM
Cardiovasc Res; 2010 Dec; 88(3):520-9. PubMed ID: 20628007
[TBL] [Abstract][Full Text] [Related]
7. Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.
Drera B; Ritelli M; Zoppi N; Wischmeijer A; Gnoli M; Fattori R; Calzavara-Pinton PG; Barlati S; Colombi M
Orphanet J Rare Dis; 2009 Nov; 4():24. PubMed ID: 19883511
[TBL] [Abstract][Full Text] [Related]
8. TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.
Singh KK; Rommel K; Mishra A; Karck M; Haverich A; Schmidtke J; Arslan-Kirchner M
Hum Mutat; 2006 Aug; 27(8):770-7. PubMed ID: 16799921
[TBL] [Abstract][Full Text] [Related]
9. Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Loeys BL; Schwarze U; Holm T; Callewaert BL; Thomas GH; Pannu H; De Backer JF; Oswald GL; Symoens S; Manouvrier S; Roberts AE; Faravelli F; Greco MA; Pyeritz RE; Milewicz DM; Coucke PJ; Cameron DE; Braverman AC; Byers PH; De Paepe AM; Dietz HC
N Engl J Med; 2006 Aug; 355(8):788-98. PubMed ID: 16928994
[TBL] [Abstract][Full Text] [Related]
10. Three Novel Mutations in FBN1 and TGFBR2 in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections.
Cao Y; Tan H; Li Z; Linpeng S; Long X; Liang D; Wu L
Int Heart J; 2018 Sep; 59(5):1059-1068. PubMed ID: 30101859
[TBL] [Abstract][Full Text] [Related]
11. Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome.
De Cario R; Sticchi E; Lucarini L; Attanasio M; Nistri S; Marcucci R; Pepe G; Giusti B
J Vasc Surg; 2018 Jul; 68(1):225-233.e5. PubMed ID: 28847661
[TBL] [Abstract][Full Text] [Related]
12. Comparison of clinical presentations and outcomes between patients with TGFBR2 and FBN1 mutations in Marfan syndrome and related disorders.
Attias D; Stheneur C; Roy C; Collod-Béroud G; Detaint D; Faivre L; Delrue MA; Cohen L; Francannet C; Béroud C; Claustres M; Iserin F; Khau Van Kien P; Lacombe D; Le Merrer M; Lyonnet S; Odent S; Plauchu H; Rio M; Rossi A; Sidi D; Steg PG; Ravaud P; Boileau C; Jondeau G
Circulation; 2009 Dec; 120(25):2541-9. PubMed ID: 19996017
[TBL] [Abstract][Full Text] [Related]
13. Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders.
Stheneur C; Collod-Béroud G; Faivre L; Gouya L; Sultan G; Le Parc JM; Moura B; Attias D; Muti C; Sznajder M; Claustres M; Junien C; Baumann C; Cormier-Daire V; Rio M; Lyonnet S; Plauchu H; Lacombe D; Chevallier B; Jondeau G; Boileau C
Hum Mutat; 2008 Nov; 29(11):E284-95. PubMed ID: 18781618
[TBL] [Abstract][Full Text] [Related]
14. Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2 genes in familial cases of bicuspid aortic valve.
Foffa I; Ait Alì L; Panesi P; Mariani M; Festa P; Botto N; Vecoli C; Andreassi MG
BMC Med Genet; 2013 Apr; 14():44. PubMed ID: 23578328
[TBL] [Abstract][Full Text] [Related]
15. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium).
Jondeau G; Ropers J; Regalado E; Braverman A; Evangelista A; Teixedo G; De Backer J; Muiño-Mosquera L; Naudion S; Zordan C; Morisaki T; Morisaki H; Von Kodolitsch Y; Dupuis-Girod S; Morris SA; Jeremy R; Odent S; Adès LC; Bakshi M; Holman K; LeMaire S; Milleron O; Langeois M; Spentchian M; Aubart M; Boileau C; Pyeritz R; Milewicz DM;
Circ Cardiovasc Genet; 2016 Dec; 9(6):548-558. PubMed ID: 27879313
[TBL] [Abstract][Full Text] [Related]
16. Mutations of the TGFBR2 gene in Chinese patients with Marfan-related syndrome.
Chen J; Li B; Yang Y; Hu J; Zhao T; Gong Y; Tan Z
Clin Invest Med; 2010 Feb; 33(1):E14-21. PubMed ID: 20144264
[TBL] [Abstract][Full Text] [Related]
17. Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?
Waldmüller S; Müller M; Warnecke H; Rees W; Schöls W; Walterbusch G; Ennker J; Scheffold T
Eur J Cardiothorac Surg; 2007 Jun; 31(6):970-5. PubMed ID: 17418587
[TBL] [Abstract][Full Text] [Related]
18. Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome.
Breckpot J; Budts W; De Zegher F; Vermeesch JR; Devriendt K
Eur J Med Genet; 2010; 53(6):408-10. PubMed ID: 20813212
[TBL] [Abstract][Full Text] [Related]
19. Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations.
Teekakirikul P; Milewicz DM; Miller DT; Lacro RV; Regalado ES; Rosales AM; Ryan DP; Toler TL; Lin AE
Am J Med Genet A; 2013 Jan; 161A(1):185-91. PubMed ID: 23239472
[TBL] [Abstract][Full Text] [Related]
20. Identification and surgical repair of familial thoracic aortic aneurysm and dissection caused by TGFBR1 mutation.
Dong SB; Zheng J; Ma WG; Chen MJ; Cheng LJ; He L; Xing QH; Sun LZ
Ann Vasc Surg; 2014 Nov; 28(8):1909-12. PubMed ID: 25110237
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
