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498 related items for PubMed ID: 25957949

  • 1. ADAMTS proteins as modulators of microfibril formation and function.
    Hubmacher D, Apte SS.
    Matrix Biol; 2015 Sep; 47():34-43. PubMed ID: 25957949
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Similarity of geleophysic dysplasia and Weill-Marchesani syndrome.
    Kochhar A, Kirmani S, Cetta F, Younge B, Hyland JC, Michels V.
    Am J Med Genet A; 2013 Dec; 161A(12):3130-2. PubMed ID: 24214363
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis.
    Gabriel LA, Wang LW, Bader H, Ho JC, Majors AK, Hollyfield JG, Traboulsi EI, Apte SS.
    Invest Ophthalmol Vis Sci; 2012 Jan 31; 53(1):461-9. PubMed ID: 21989719
    [Abstract] [Full Text] [Related]

  • 6. Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia.
    Hubmacher D, Taye N, Balic Z, Thacker S, Adams SM, Birk DE, Schweitzer R, Apte SS.
    Matrix Biol; 2019 Sep 31; 82():38-53. PubMed ID: 30738849
    [Abstract] [Full Text] [Related]

  • 7. Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage.
    Wang LW, Kutz WE, Mead TJ, Beene LC, Singh S, Jenkins MW, Reinhardt DP, Apte SS.
    Matrix Biol; 2019 Apr 31; 77():117-128. PubMed ID: 30201140
    [Abstract] [Full Text] [Related]

  • 8. Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease.
    Hubmacher D, Schneider M, Berardinelli SJ, Takeuchi H, Willard B, Reinhardt DP, Haltiwanger RS, Apte SS.
    Sci Rep; 2017 Feb 08; 7():41871. PubMed ID: 28176809
    [Abstract] [Full Text] [Related]

  • 9. Geleophysic dysplasia and Weill-Marchesani syndrome: ADAMTSL2 a possible common gene.
    Duzenli T, Uysal BS, Ulas B, Kayhan G.
    Ophthalmic Genet; 2024 Oct 08; 45(5):499-505. PubMed ID: 39044700
    [Abstract] [Full Text] [Related]

  • 10. 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 23; 54(13):8337-44. PubMed ID: 24265020
    [Abstract] [Full Text] [Related]

  • 11. The ADAMTS/Fibrillin Connection: Insights into the Biological Functions of ADAMTS10 and ADAMTS17 and Their Respective Sister Proteases.
    Karoulias SZ, Taye N, Stanley S, Hubmacher D.
    Biomolecules; 2020 Apr 12; 10(4):. PubMed ID: 32290605
    [Abstract] [Full Text] [Related]

  • 12. Acromelic dysplasias: how rare musculoskeletal disorders reveal biological functions of extracellular matrix proteins.
    Stanley S, Balic Z, Hubmacher D.
    Ann N Y Acad Sci; 2021 Apr 12; 1490(1):57-76. PubMed ID: 32880985
    [Abstract] [Full Text] [Related]

  • 13. Adamts17 is involved in skeletogenesis through modulation of BMP-Smad1/5/8 pathway.
    Oichi T, Taniguchi Y, Soma K, Oshima Y, Yano F, Mori Y, Chijimatsu R, Kim-Kaneyama JR, Tanaka S, Saito T.
    Cell Mol Life Sci; 2019 Dec 12; 76(23):4795-4809. PubMed ID: 31201465
    [Abstract] [Full Text] [Related]

  • 14. 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 12; 8(1):e1002425. PubMed ID: 22242013
    [Abstract] [Full Text] [Related]

  • 15. Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: sibling case report and literature review.
    Reyes-Hernández OD, Palacios-Reyes C, Chávez-Ocaña S, Cortés-Malagón EM, Alonso-Themann PG, Ramos-Cano V, Ramírez-Bello J, Sierra-Martínez M.
    BMC Musculoskelet Disord; 2016 Feb 15; 17():79. PubMed ID: 26875674
    [Abstract] [Full Text] [Related]

  • 16. A disintegrin-like and metalloprotease domain containing thrombospondin type 1 motif-like 5 (ADAMTSL5) is a novel fibrillin-1-, fibrillin-2-, and heparin-binding member of the ADAMTS superfamily containing a netrin-like module.
    Bader HL, Wang LW, Ho JC, Tran T, Holden P, Fitzgerald J, Atit RP, Reinhardt DP, Apte SS.
    Matrix Biol; 2012 Feb 15; 31(7-8):398-411. PubMed ID: 23010571
    [Abstract] [Full Text] [Related]

  • 17. ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts.
    Kutz WE, Wang LW, Bader HL, Majors AK, Iwata K, Traboulsi EI, Sakai LY, Keene DR, Apte SS.
    J Biol Chem; 2011 May 13; 286(19):17156-67. PubMed ID: 21402694
    [Abstract] [Full Text] [Related]

  • 18. Fibrillin protein pleiotropy: Acromelic dysplasias.
    Sakai LY, Keene DR.
    Matrix Biol; 2019 Jul 13; 80():6-13. PubMed ID: 30219651
    [Abstract] [Full Text] [Related]

  • 19. Fibrillin-rich microfibrils of the extracellular matrix: ultrastructure and assembly.
    Sherratt MJ, Wess TJ, Baldock C, Ashworth J, Purslow PP, Shuttleworth CA, Kielty CM.
    Micron; 2001 Feb 13; 32(2):185-200. PubMed ID: 10936461
    [Abstract] [Full Text] [Related]

  • 20. The fibrillin microfibril scaffold: A niche for growth factors and mechanosensation?
    Sengle G, Sakai LY.
    Matrix Biol; 2015 Sep 13; 47():3-12. PubMed ID: 25957947
    [Abstract] [Full Text] [Related]

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