BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 25113270)

  • 1. 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]  

  • 2. 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]  

  • 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]  

  • 4. Identification of fibrillin 1 gene mutations in patients with bicuspid aortic valve (BAV) without Marfan syndrome.
    Pepe G; Nistri S; Giusti B; Sticchi E; Attanasio M; Porciani C; Abbate R; Bonow RO; Yacoub M; Gensini GF
    BMC Med Genet; 2014 Feb; 15():23. PubMed ID: 24564502
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of 15 novel mutations in 52 children from 40 families with the Marfan or Loeys-Dietz syndrome and phenotype-genotype correlations.
    Pees C; Michel-Behnke I; Hagl M; Laccone F
    Clin Genet; 2014 Dec; 86(6):552-7. PubMed ID: 24199744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.
    Lindsay ME; Schepers D; Bolar NA; Doyle JJ; Gallo E; Fert-Bober J; Kempers MJ; Fishman EK; Chen Y; Myers L; Bjeda D; Oswald G; Elias AF; Levy HP; Anderlid BM; Yang MH; Bongers EM; Timmermans J; Braverman AC; Canham N; Mortier GR; Brunner HG; Byers PH; Van Eyk J; Van Laer L; Dietz HC; Loeys BL
    Nat Genet; 2012 Jul; 44(8):922-7. PubMed ID: 22772368
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations.
    Söylen B; Singh KK; Abuzainin A; Rommel K; Becker H; Arslan-Kirchner M; Schmidtke J
    Clin Genet; 2009 Mar; 75(3):265-70. PubMed ID: 19159394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Genetic analysis of young adult patients with aortic disease not fulfilling the diagnostic criteria for Marfan syndrome.
    Akutsu K; Morisaki H; Okajima T; Yoshimuta T; Tsutsumi Y; Takeshita S; Nonogi H; Ogino H; Higashi M; Morisaki T
    Circ J; 2010 May; 74(5):990-7. PubMed ID: 20354336
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes.
    Sakai H; Visser R; Ikegawa S; Ito E; Numabe H; Watanabe Y; Mikami H; Kondoh T; Kitoh H; Sugiyama R; Okamoto N; Ogata T; Fodde R; Mizuno S; Takamura K; Egashira M; Sasaki N; Watanabe S; Nishimaki S; Takada F; Nagai T; Okada Y; Aoka Y; Yasuda K; Iwasa M; Kogaki S; Harada N; Mizuguchi T; Matsumoto N
    Am J Med Genet A; 2006 Aug; 140(16):1719-25. PubMed ID: 16835936
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Connective tissue disorders and cardiovascular complications: the indomitable role of transforming growth factor-beta signaling.
    Wheeler JB; Ikonomidis JS; Jones JA
    Adv Exp Med Biol; 2014; 802():107-27. PubMed ID: 24443024
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited.
    Adès LC; Sullivan K; Biggin A; Haan EA; Brett M; Holman KJ; Dixon J; Robertson S; Holmes AD; Rogers J; Bennetts B
    Am J Med Genet A; 2006 May; 140(10):1047-58. PubMed ID: 16596670
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Outcome of aortic surgery in patients with Loeys-Dietz syndrome primarily treated as having Marfan syndrome.
    Schoenhoff FS; Mueller C; Czerny M; Matyas G; Kadner A; Schmidli J; Carrel T
    Eur J Cardiothorac Surg; 2014 Sep; 46(3):444-9; discussion 449. PubMed ID: 24499874
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 14.