BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 37719708)

  • 1. Variable clinical expression of a Belgian
    Perik MHAM; Govaerts E; Laga S; Goovaerts I; Saenen J; Van Craenenbroeck E; Meester JAN; Luyckx I; Rodrigus I; Verstraeten A; Van Laer L; Loeys BL
    Front Genet; 2023; 14():1251675. PubMed ID: 37719708
    [No Abstract]   [Full Text] [Related]  

  • 2. Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient.
    Perik M; Verstraeten A; Nijak-Paeske A; Rabaut L; Van Laer L; Loeys B
    Stem Cell Res; 2022 Dec; 65():102956. PubMed ID: 36356561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient.
    Marsili L; Overwater E; Hanna N; Baujat G; Baars MJH; Boileau C; Bonneau D; Brehin AC; Capri Y; Cheung HY; Dulfer E; Gerard M; Gouya L; Hilhorst-Hofstee Y; Houweling AC; Isidor B; Le Gloan L; Menke LA; Odent S; Morice-Picard F; Vanlerberghe C; Voorhoeve E; van Tintelen JP; Maugeri A; Arnaud P
    Clin Genet; 2020 May; 97(5):723-730. PubMed ID: 31898322
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel pathogenic
    Cannaerts E; Kempers M; Maugeri A; Marcelis C; Gardeitchik T; Richer J; Micha D; Beauchesne L; Timmermans J; Vermeersch P; Meyten N; Chénier S; van de Beek G; Peeters N; Alaerts M; Schepers D; Van Laer L; Verstraeten A; Loeys B
    J Med Genet; 2019 Apr; 56(4):220-227. PubMed ID: 29967133
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections.
    Bertoli-Avella AM; Gillis E; Morisaki H; Verhagen JMA; de Graaf BM; van de Beek G; Gallo E; Kruithof BPT; Venselaar H; Myers LA; Laga S; Doyle AJ; Oswald G; van Cappellen GWA; Yamanaka I; van der Helm RM; Beverloo B; de Klein A; Pardo L; Lammens M; Evers C; Devriendt K; Dumoulein M; Timmermans J; Bruggenwirth HT; Verheijen F; Rodrigus I; Baynam G; Kempers M; Saenen J; Van Craenenbroeck EM; Minatoya K; Matsukawa R; Tsukube T; Kubo N; Hofstra R; Goumans MJ; Bekkers JA; Roos-Hesselink JW; van de Laar IMBH; Dietz HC; Van Laer L; Morisaki T; Wessels MW; Loeys BL
    J Am Coll Cardiol; 2015 Apr; 65(13):1324-1336. PubMed ID: 25835445
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature.
    Baldo F; Morra L; Feresin A; Faletra F; Al Naber Y; Memo L; Travan L
    Ital J Pediatr; 2022 Jun; 48(1):85. PubMed ID: 35668506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel pathogenic TGFBR1 and SMAD3 variants identified after cerebrovascular events in adult patients with Loeys-dietz syndrome.
    Laterza D; Ritelli M; Zini A; Colombi M; Dell'Acqua ML; Vandelli L; Bigliardi G; Verganti L; Vallone S; Vincenzi C; Rosafio F; Ciolli L; Calabrese O; Nichelli PF; Picchetto L
    Eur J Med Genet; 2019 Oct; 62(10):103727. PubMed ID: 31326520
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long-term risk of arch complications in Loeys Dietz syndrome patients undergoing proximal ascending aortic replacement.
    Weininger G; Zafar M; Ziganshin BA; Mori M; Papanikolaou D; Sekar RB; Amabile A; Degife E; O'Marr J; Geirsson A; Elefteriades JA; Assi R; Vallabhajosyula P
    J Card Surg; 2022 Nov; 37(11):3688-3692. PubMed ID: 35989525
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Novel SMAD3 p.Arg386Thr genetic variant co-segregating with thoracic aortic aneurysm and dissection.
    Engström K; Vánky F; Rehnberg M; Trinks C; Jonasson J; Green A; Gunnarsson C
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1089. PubMed ID: 32022471
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiovascular operations for Loeys-Dietz syndrome: Intermediate-term results.
    Patel ND; Crawford T; Magruder JT; Alejo DE; Hibino N; Black J; Dietz HC; Vricella LA; Cameron DE
    J Thorac Cardiovasc Surg; 2017 Feb; 153(2):406-412. PubMed ID: 27955909
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ectopia lentis in Loeys-Dietz syndrome type 4.
    Braverman AC; Blinder KJ; Khanna S; Willing M
    Am J Med Genet A; 2020 Aug; 182(8):1957-1959. PubMed ID: 32462795
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome.
    Kuechler A; Altmüller J; Nürnberg P; Kotthoff S; Kubisch C; Borck G
    Mol Cell Probes; 2015 Oct; 29(5):330-4. PubMed ID: 26184463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early surgical experience with Loeys-Dietz: a new syndrome of aggressive thoracic aortic aneurysm disease.
    Williams JA; Loeys BL; Nwakanma LU; Dietz HC; Spevak PJ; Patel ND; François K; DeBacker J; Gott VL; Vricella LA; Cameron DE
    Ann Thorac Surg; 2007 Feb; 83(2):S757-63; discussion S785-90. PubMed ID: 17257922
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Clinical features and complications of Loeys-Dietz syndrome: A systematic review.
    Gouda P; Kay R; Habib M; Aziz A; Aziza E; Welsh R
    Int J Cardiol; 2022 Sep; 362():158-167. PubMed ID: 35662564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The first reported case of Loeys-Dietz syndrome in a patient with biallelic SMAD3 variants.
    Baskin SM; Morris SA; Vara A; Hecht JT; Farach LS
    Am J Med Genet A; 2020 Nov; 182(11):2755-2760. PubMed ID: 32935439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Type A Aortic Dissection Caused by Loeys-Dietz Syndrome with Novel Variation.
    Skeik N; Golden M; Berg A; North M
    Ann Vasc Surg; 2020 Oct; 68():567.e1-567.e4. PubMed ID: 32339686
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-term outcomes in heritable thoracic aortic disease.
    Robertson EN; Bannon PG; Jeremy RW
    Front Cardiovasc Med; 2022; 9():1009947. PubMed ID: 36312254
    [TBL] [Abstract][Full Text] [Related]  

  • 20. hiPSC Modeling of Lineage-Specific Smooth Muscle Cell Defects Caused by
    Zhou D; Feng H; Yang Y; Huang T; Qiu P; Zhang C; Olsen TR; Zhang J; Chen YE; Mizrak D; Yang B
    Circulation; 2021 Oct; 144(14):1145-1159. PubMed ID: 34346740
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.