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Volumn 31, Issue 2, 1999, Pages 255-259

The fibrillins

Author keywords

Elastic fibres; Extracellular matrix; Fibrillin; Marfan syndrome (MFS)

Indexed keywords

CALCIUM; CYSTEINE DERIVATIVE; FIBRILLIN; GLYCOPROTEIN; MONOMER; PROTEIN PRECURSOR;

EID: 0032968124     PISSN: 13572725     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-2725(98)00109-5     Document Type: Article
Times cited : (96)

References (13)
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    • Fibrillin-2 (FBN2) mutations result in the Marfan-like disorders, congenital contractural arachnodactily
    • Putnam E.A., Zhang H., Ramirez F., Milewicz D.M. Fibrillin-2 (FBN2) mutations result in the Marfan-like disorders, congenital contractural arachnodactily. Nat. Genet. 11:1995;456-458.
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    • Putnam, E.A.1    Zhang, H.2    Ramirez, F.3    Milewicz, D.M.4
  • 6
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    • Ramirez F. Fibrillin mutations in Marfan syndrome and related phenotypes. Curr. Op. Genet. Dev. 6:1996;309-315.
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    • Ramirez, F.1
  • 7
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    • Solution structure of a pair of calcium-binding epidermal growth factor-like domains: Implications for the Marfan syndrome and other genetic disorders
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    • Downing, A.K.1    Knott, V.2    Werner, J.3    Cardy, C.4    Campbell, I.D.5    Handford, P.A.6
  • 8
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    • Fibrillin-containing microfibrils: Structure and function in health and disease
    • Kielty C.M., Shuttleworth C.A. Fibrillin-containing microfibrils: structure and function in health and disease. Int. J. Biochem. Cell Biol. 27:1995;747-760.
    • (1995) Int. J. Biochem. Cell Biol. , vol.27 , pp. 747-760
    • Kielty, C.M.1    Shuttleworth, C.A.2
  • 9
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    • Solution structure of the transforming growth factor β-binding protein-like molecule, a domain associated with matrix fibrils
    • Yuan X., Downing A.K., Knott V., Hanford A.P. Solution structure of the transforming growth factor β-binding protein-like molecule, a domain associated with matrix fibrils. EMBO J. 16:1997;6659-6666.
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    • Yuan, X.1    Downing, A.K.2    Knott, V.3    Hanford, A.P.4
  • 10
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    • A mutation on FBN1 disrupts pro-fibrillin processing and results in isolated skeletal features of the Marfan syndrome
    • Milewicz D.M., Grossfield J., Cao S.N., Kielty C., Covitz W., Jewett T. A mutation on FBN1 disrupts pro-fibrillin processing and results in isolated skeletal features of the Marfan syndrome. J. Clin. Invest. 95:1995;2372-2378.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.