BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

344 related articles for article (PubMed ID: 16027248)

  • 21. [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]  

  • 22. 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]  

  • 23. TGFβRIIb mutations trigger aortic aneurysm pathogenesis by altering transforming growth factor β2 signal transduction.
    Bee KJ; Wilkes DC; Devereux RB; Basson CT; Hatcher CJ
    Circ Cardiovasc Genet; 2012 Dec; 5(6):621-9. PubMed ID: 23099432
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection.
    Guo DC; Regalado ES; Minn C; Tran-Fadulu V; Coney J; Cao J; Wang M; Yu RK; Estrera AL; Safi HJ; Shete SS; Milewicz DM
    Circ Cardiovasc Genet; 2011 Feb; 4(1):36-42. PubMed ID: 21163914
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm.
    Leutermann R; Sheikhzadeh S; Brockstädt L; Rybczynski M; van Rahden V; Kutsche K; von Kodolitsch Y; Rosenberger G
    Eur J Hum Genet; 2014 Jul; 22(7):944-8. PubMed ID: 24193348
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. Dexamethasone attenuated thoracic aortic aneurysm and dissection in vascular smooth muscle cell Tgfbr2-disrupted mice with CCL8 suppression.
    Wang X; Li Q; Li W; Zhang T; Li X; Jiao Y; Zhang X; Jiang J; Zhang X; Zhang X
    Exp Physiol; 2022 Jun; 107(6):631-645. PubMed ID: 35344629
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Familial aortic dissection of non-Marfan syndrome with mutations in the transforming growth factor-beta receptor type 1 genes].
    Suzuki R; Mikamo A; Kurazumi H; Sato M; Ikeda Y; Shirasawa B; Hamano K
    Kyobu Geka; 2011 Feb; 64(2):99-104. PubMed ID: 21387612
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pharmacologically Improved Contractility Protects Against Aortic Dissection in Mice With Disrupted Transforming Growth Factor-β Signaling Despite Compromised Extracellular Matrix Properties.
    Ferruzzi J; Murtada SI; Li G; Jiao Y; Uman S; Ting MY; Tellides G; Humphrey JD
    Arterioscler Thromb Vasc Biol; 2016 May; 36(5):919-27. PubMed ID: 26988590
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. 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]  

  • 39. Genotype-phenotype analysis of F-helix mutations at the kinase domain of TGFBR2, including a type 2 Marfan syndrome familial study.
    Zhang L; Gao LG; Zhang M; Zhou XL
    Mol Vis; 2012; 18():55-63. PubMed ID: 22259224
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Non-syndromic thoracic aortic aneurysms and dissections--a genetic review.
    Zhang P; Zhang E; Fan J; Gu J
    Front Biosci (Landmark Ed); 2013 Jan; 18(1):305-11. PubMed ID: 23276923
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.