BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 16775108)

  • 1. Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndrome.
    De Backer J; Nollen GJ; Devos D; Pals G; Coucke P; Verstraete K; van der Wall EE; De Paepe A; Mulder BJ
    Heart; 2006 Jul; 92(7):977-8. PubMed ID: 16775108
    [No Abstract]   [Full Text] [Related]  

  • 2. A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.
    Pereira L; Levran O; Ramirez F; Lynch JR; Sykes B; Pyeritz RE; Dietz HC
    N Engl J Med; 1994 Jul; 331(3):148-53. PubMed ID: 8008028
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly.
    Hayward C; Porteous ME; Brock DJ
    Mol Cell Probes; 1994 Aug; 8(4):325-7. PubMed ID: 7870075
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.
    Hayward C; Brock DJ
    Hum Mutat; 1997; 10(6):415-23. PubMed ID: 9401003
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Contribution of genetics to pathogenicity and diagnosis of Marfan syndrome].
    Boileau C; Collod G; Bonnet D
    Arch Mal Coeur Vaiss; 1997 Dec; 90(12 Suppl):1707-12. PubMed ID: 9587455
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation of the fibrillin-1 gene in a newborn with severe Marfan syndrome.
    Kochilas L; Gundogan F; Atalay M; Bliss JM; Vatta M; Pena LS; Abuelo D
    J Perinatol; 2008 Apr; 28(4):303-5. PubMed ID: 18379569
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fibrillin-1 genetic deficiency leads to pathological ageing of arteries in mice.
    Mariko B; Pezet M; Escoubet B; Bouillot S; Andrieu JP; Starcher B; Quaglino D; Jacob MP; Huber P; Ramirez F; Faury G
    J Pathol; 2011 May; 224(1):33-44. PubMed ID: 21432852
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Marfan's syndrome.
    Judge DP; Dietz HC
    Lancet; 2005 Dec; 366(9501):1965-76. PubMed ID: 16325700
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Coexistent Marfan's syndrome and ankylosing spondylitis.
    Kiss C; Jónap I; Gergely P; Poór G
    J Rheumatol; 2006 Jun; 33(6):1199-200. PubMed ID: 16755670
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gene symbol: FBN1.
    Tinkle B
    Hum Genet; 2007 Apr; 121(2):294. PubMed ID: 17598213
    [No Abstract]   [Full Text] [Related]  

  • 11. Fibrillin (FBN1) mutations in Marfan syndrome.
    Hayward C; Keston M; Brock DJ; Dietz HC
    Hum Mutat; 1992; 1(1):79. PubMed ID: 1301195
    [No Abstract]   [Full Text] [Related]  

  • 12. The FBN1 (R2726W) mutation is not fully penetrant.
    Buoni S; Zannolli R; Macucci F; Ansaldi S; Grasso M; Arbustini E; Fois A
    Ann Hum Genet; 2004 Nov; 68(Pt 6):633-8. PubMed ID: 15598221
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Marfan's syndrome].
    Shinawi S; Mandel H
    Harefuah; 2000 Apr; 138(7):598-603. PubMed ID: 10883194
    [No Abstract]   [Full Text] [Related]  

  • 14. [Acute lymphoblastic leukemia in a pediatric patient with Marfan's syndrome].
    Miyajima Y; Kitase Y; Mizuno S; Sakai H; Matsumoto N; Ogawa A
    Rinsho Ketsueki; 2011 Jan; 52(1):28-31. PubMed ID: 21378479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscle fibrillin deficiency in Marfan's syndrome myopathy.
    Behan WM; Longman C; Petty RK; Comeglio P; Child AH; Boxer M; Foskett P; Harriman DG
    J Neurol Neurosurg Psychiatry; 2003 May; 74(5):633-8. PubMed ID: 12700307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome.
    Liu W; Qian C; Francke U
    Nat Genet; 1997 Aug; 16(4):328-9. PubMed ID: 9241263
    [No Abstract]   [Full Text] [Related]  

  • 17. Genetic fibrillinopathies: new insights in molecular diagnosis and clinical management.
    Loeys BL; Matthys DM; de Paepe AM
    Acta Clin Belg; 2003; 58(1):3-11. PubMed ID: 12723256
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular mechanisms for the improvement of wound healing ability of periodontal ligament in Marfan's syndrome].
    Saito M; Tsuji T
    Clin Calcium; 2012 Jan; 22(1):35-42. PubMed ID: 22201097
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 gene.
    Elçioglu NH; Akalin F; Elçioglu M; Comeglio P; Child AH
    Genet Couns; 2004; 15(2):219-25. PubMed ID: 15287423
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dermal fibroblast culture as a model system for studies of fibrillin assembly and pathogenetic mechanisms: defects in distinct groups of individuals with Marfan's syndrome.
    Brenn T; Aoyama T; Francke U; Furthmayr H
    Lab Invest; 1996 Sep; 75(3):389-402. PubMed ID: 8804362
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.