BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 37469709)

  • 1. Role of fibrilins in human cancer: A narrative review.
    Mahdizadehi M; Saghaeian Jazi M; Mir SM; Jafari SM
    Health Sci Rep; 2023 Jul; 6(7):e1434. PubMed ID: 37469709
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structure and function of the mammalian fibrillin gene family: implications for human connective tissue diseases.
    Davis MR; Summers KM
    Mol Genet Metab; 2012 Dec; 107(4):635-47. PubMed ID: 22921888
    [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. Basic Components of Connective Tissues and Extracellular Matrix: Fibronectin, Fibrinogen, Laminin, Elastin, Fibrillins, Fibulins, Matrilins, Tenascins and Thrombospondins.
    Halper J
    Adv Exp Med Biol; 2021; 1348():105-126. PubMed ID: 34807416
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18.
    Li X; Pereira L; Zhang H; Sanguineti C; Ramirez F; Bonadio J; Francke U
    Genomics; 1993 Dec; 18(3):667-72. PubMed ID: 8307578
    [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. Basic components of connective tissues and extracellular matrix: elastin, fibrillin, fibulins, fibrinogen, fibronectin, laminin, tenascins and thrombospondins.
    Halper J; Kjaer M
    Adv Exp Med Biol; 2014; 802():31-47. PubMed ID: 24443019
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome.
    Goldstein C; Liaw P; Jimenez SA; Buchberg AM; Siracusa LD
    Mamm Genome; 1994 Nov; 5(11):696-700. PubMed ID: 7873879
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices.
    Zhang H; Apfelroth SD; Hu W; Davis EC; Sanguineti C; Bonadio J; Mecham RP; Ramirez F
    J Cell Biol; 1994 Mar; 124(5):855-63. PubMed ID: 8120105
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.
    Miller G; Neilan M; Chia R; Gheryani N; Holt N; Charbit A; Wells S; Tucci V; Lalanne Z; Denny P; Fisher EM; Cheeseman M; Askew GN; Dear TN
    PLoS One; 2010 Feb; 5(2):e9137. PubMed ID: 20161761
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Specificity of latent TGF-β binding protein (LTBP) incorporation into matrix: role of fibrillins and fibronectin.
    Zilberberg L; Todorovic V; Dabovic B; Horiguchi M; Couroussé T; Sakai LY; Rifkin DB
    J Cell Physiol; 2012 Dec; 227(12):3828-36. PubMed ID: 22495824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. ¹H, ¹³C and ¹⁵N assignments of the four N-terminal domains of human fibrillin-1.
    Yadin DA; Robertson IB; Jensen SA; Handford PA; Redfield C
    Biomol NMR Assign; 2014 Apr; 8(1):75-80. PubMed ID: 23264024
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Development, composition, and structural arrangements of the ciliary zonule of the mouse.
    Shi Y; Tu Y; De Maria A; Mecham RP; Bassnett S
    Invest Ophthalmol Vis Sci; 2013 Apr; 54(4):2504-15. PubMed ID: 23493297
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation of the gene encoding fibrillin-2 results in syndactyly in mice.
    Chaudhry SS; Gazzard J; Baldock C; Dixon J; Rock MJ; Skinner GC; Steel KP; Kielty CM; Dixon MJ
    Hum Mol Genet; 2001 Apr; 10(8):835-43. PubMed ID: 11285249
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The fibrillin microfibril/elastic fibre network: A critical extracellular supramolecular scaffold to balance skin homoeostasis.
    Adamo CS; Zuk AV; Sengle G
    Exp Dermatol; 2021 Jan; 30(1):25-37. PubMed ID: 32920888
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutant fibrillin 1 from tight skin mice increases extracellular matrix incorporation of microfibril-associated glycoprotein 2 and type I collagen.
    Lemaire R; Farina G; Kissin E; Shipley JM; Bona C; Korn JH; Lafyatis R
    Arthritis Rheum; 2004 Mar; 50(3):915-26. PubMed ID: 15022335
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues.
    Corson GM; Charbonneau NL; Keene DR; Sakai LY
    Genomics; 2004 Mar; 83(3):461-72. PubMed ID: 14962672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.