These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
292 related articles for article (PubMed ID: 26446364)
1. Genetics of hereditary large vessel diseases. Morisaki T; Morisaki H J Hum Genet; 2016 Jan; 61(1):21-6. PubMed ID: 26446364 [TBL] [Abstract][Full Text] [Related]
2. Genetic basis of hereditary thoracic aortic aneurysms and dissections. Takeda N; Komuro I J Cardiol; 2019 Aug; 74(2):136-143. PubMed ID: 31000321 [TBL] [Abstract][Full Text] [Related]
3. 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]
5. Hereditary Influence in Thoracic Aortic Aneurysm and Dissection. Isselbacher EM; Lino Cardenas CL; Lindsay ME Circulation; 2016 Jun; 133(24):2516-28. PubMed ID: 27297344 [TBL] [Abstract][Full Text] [Related]
6. TGF-β Signaling-Related Genes and Thoracic Aortic Aneurysms and Dissections. Takeda N; Hara H; Fujiwara T; Kanaya T; Maemura S; Komuro I Int J Mol Sci; 2018 Jul; 19(7):. PubMed ID: 30037098 [TBL] [Abstract][Full Text] [Related]
7. Marfan syndrome: from gene to therapy. Bolar N; Van Laer L; Loeys BL Curr Opin Pediatr; 2012 Aug; 24(4):498-504. PubMed ID: 22705998 [TBL] [Abstract][Full Text] [Related]
8. Recent progress in genetics of Marfan syndrome and Marfan-associated disorders. Mizuguchi T; Matsumoto N J Hum Genet; 2007; 52(1):1-12. PubMed ID: 17061023 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Aortopathy in a Mouse Model of Marfan Syndrome Is Not Mediated by Altered Transforming Growth Factor β Signaling. Wei H; Hu JH; Angelov SN; Fox K; Yan J; Enstrom R; Smith A; Dichek DA J Am Heart Assoc; 2017 Jan; 6(1):. PubMed ID: 28119285 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Association Between Genetic Diagnosis and Clinical Outcomes in Patients With Heritable Thoracic Aortic Disease. Yagyu T; Noguchi T; Asano Y; Ida K; Ogata S; Nishimura K; Matsuda H J Am Heart Assoc; 2023 Apr; 12(8):e028625. PubMed ID: 37042257 [TBL] [Abstract][Full Text] [Related]
14. Connective Tissue Disorders and Cardiovascular Complications: The Indomitable Role of Transforming Growth Factor-β Signaling. Wheeler JB; Ikonomidis JS; Jones JA Adv Exp Med Biol; 2021; 1348():161-184. PubMed ID: 34807419 [TBL] [Abstract][Full Text] [Related]
15. Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes. Cook JR; Carta L; Galatioto J; Ramirez F Clin Genet; 2015; 87(1):11-20. PubMed ID: 24867163 [TBL] [Abstract][Full Text] [Related]
16. Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery. Verstraeten A; Alaerts M; Van Laer L; Loeys B Hum Mutat; 2016 Jun; 37(6):524-31. PubMed ID: 26919284 [TBL] [Abstract][Full Text] [Related]
17. Loeys-Dietz Syndrome. Velchev JD; Van Laer L; Luyckx I; Dietz H; Loeys B Adv Exp Med Biol; 2021; 1348():251-264. PubMed ID: 34807423 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis. Haller G; Alvarado DM; Willing MC; Braverman AC; Bridwell KH; Kelly M; Lenke LG; Luhmann SJ; Gurnett CA; Dobbs MB J Bone Joint Surg Am; 2015 Sep; 97(17):1411-7. PubMed ID: 26333736 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]