BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

326 related articles for article (PubMed ID: 20529844)

  • 1. In vivo studies of mutant fibrillin-1 microfibrils.
    Charbonneau NL; Carlson EJ; Tufa S; Sengle G; Manalo EC; Carlberg VM; Ramirez F; Keene DR; Sakai LY
    J Biol Chem; 2010 Aug; 285(32):24943-55. PubMed ID: 20529844
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Microfibrils: a cornerstone of extracellular matrix and a key to understand Marfan syndrome.
    Bonetti MI
    Ital J Anat Embryol; 2009; 114(4):201-24. PubMed ID: 20578676
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome.
    Beene LC; Wang LW; Hubmacher D; Keene DR; Reinhardt DP; Annis DS; Mosher DF; Mecham RP; Traboulsi EI; Apte SS
    Invest Ophthalmol Vis Sci; 2013 Dec; 54(13):8337-44. PubMed ID: 24265020
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New insights into the structure, assembly and biological roles of 10-12 nm connective tissue microfibrils from fibrillin-1 studies.
    Jensen SA; Handford PA
    Biochem J; 2016 Apr; 473(7):827-38. PubMed ID: 27026396
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.
    Ramirez F; Dietz HC
    J Cell Physiol; 2007 Nov; 213(2):326-30. PubMed ID: 17708531
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.
    Dietz HC; Pyeritz RE
    Hum Mol Genet; 1995; 4 Spec No():1799-809. PubMed ID: 8541880
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New insights into the assembly of extracellular microfibrils from the analysis of the fibrillin 1 mutation in the tight skin mouse.
    Gayraud B; Keene DR; Sakai LY; Ramirez F
    J Cell Biol; 2000 Aug; 150(3):667-80. PubMed ID: 10931876
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function.
    Hubmacher D; Apte SS
    Cell Mol Life Sci; 2011 Oct; 68(19):3137-48. PubMed ID: 21858451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The molecular genetics of Marfan syndrome and related microfibrillopathies.
    Robinson PN; Godfrey M
    J Med Genet; 2000 Jan; 37(1):9-25. PubMed ID: 10633129
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome.
    Judge DP; Biery NJ; Keene DR; Geubtner J; Myers L; Huso DL; Sakai LY; Dietz HC
    J Clin Invest; 2004 Jul; 114(2):172-81. PubMed ID: 15254584
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microfibril structure masks fibrillin-2 in postnatal tissues.
    Charbonneau NL; Jordan CD; Keene DR; Lee-Arteaga S; Dietz HC; Rifkin DB; Ramirez F; Sakai LY
    J Biol Chem; 2010 Jun; 285(26):20242-51. PubMed ID: 20404337
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia.
    Hubmacher D; Wang LW; Mecham RP; Reinhardt DP; Apte SS
    Dis Model Mech; 2015 May; 8(5):487-99. PubMed ID: 25762570
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microenvironmental regulation by fibrillin-1.
    Sengle G; Tsutsui K; Keene DR; Tufa SF; Carlson EJ; Charbonneau NL; Ono RN; Sasaki T; Wirtz MK; Samples JR; Fessler LI; Fessler JH; Sekiguchi K; Hayflick SJ; Sakai LY
    PLoS Genet; 2012 Jan; 8(1):e1002425. PubMed ID: 22242013
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias.
    Jensen SA; Iqbal S; Bulsiewicz A; Handford PA
    Hum Mol Genet; 2015 Aug; 24(15):4454-63. PubMed ID: 25979247
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ADAMTSL6β protein rescues fibrillin-1 microfibril disorder in a Marfan syndrome mouse model through the promotion of fibrillin-1 assembly.
    Saito M; Kurokawa M; Oda M; Oshima M; Tsutsui K; Kosaka K; Nakao K; Ogawa M; Manabe RI; Suda N; Ganjargal G; Hada Y; Noguchi T; Teranaka T; Sekiguchi K; Yoneda T; Tsuji T
    J Biol Chem; 2011 Nov; 286(44):38602-38613. PubMed ID: 21880733
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heparin/heparan sulfate controls fibrillin-1, -2 and -3 self-interactions in microfibril assembly.
    Sabatier L; Djokic J; Hubmacher D; Dzafik D; Nelea V; Reinhardt DP
    FEBS Lett; 2014 Aug; 588(17):2890-7. PubMed ID: 25034023
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Engineered mutations in fibrillin-1 leading to Marfan syndrome act at the protein, cellular and organismal levels.
    Zeyer KA; Reinhardt DP
    Mutat Res Rev Mutat Res; 2015; 765():7-18. PubMed ID: 26281765
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fibrillin: from microfibril assembly to biomechanical function.
    Kielty CM; Baldock C; Lee D; Rock MJ; Ashworth JL; Shuttleworth CA
    Philos Trans R Soc Lond B Biol Sci; 2002 Feb; 357(1418):207-17. PubMed ID: 11911778
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nanoscale Structural Comparison of Fibrillin-1 Microfibrils Isolated from Marfan and Non-Marfan Syndrome Human Aorta.
    Șulea CM; Mártonfalvi Z; Csányi C; Haluszka D; Pólos M; Ágg B; Stengl R; Benke K; Szabolcs Z; Kellermayer MSZ
    Int J Mol Sci; 2023 Apr; 24(8):. PubMed ID: 37108724
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.