메뉴 건너뛰기




Volumn 11, Issue 12, 2000, Pages 1087-1092

Abnormal growth plate function in pigs carrying a dominant mutation in type X collagen

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; COLLAGEN TYPE 10;

EID: 0033661507     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003350010212     Document Type: Article
Times cited : (28)

References (39)
  • 2
    • 0031879246 scopus 로고    scopus 로고
    • Phenotypic and biochemical consequences of collagen X mutations in mice and humans
    • (1998) Matrix Biol , vol.17 , pp. 169-184
    • Chan, D.1    Jacenko, O.2
  • 6
    • 0033531789 scopus 로고    scopus 로고
    • Interaction of collagen alpha 1 (X) containing engineered NC1 mutations with normal alpha 1 (X) in vitro. Implications for the molecular basis of Schmid metaphyseal chondrodysplasia
    • (1999) J Biol Chem , vol.274 , pp. 13091-13097
    • Chan, D.1    Freddi, S.2    Weng, Y.M.3    Bateman, J.F.4
  • 10
    • 0024406857 scopus 로고
    • A novel genetic system to detect protein-protein interactions
    • (1989) Nature , vol.340 , pp. 245-246
    • Fields, S.1    Song, O.2
  • 15
    • 0028067659 scopus 로고
    • Mechanism of longitudinal bone growth and its regulation by growth plate chondrocytes
    • (1994) Microsc Res Tech , vol.28 , pp. 505-519
    • Hunziker, E.B.1
  • 16
    • 0027488970 scopus 로고
    • Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition
    • (1993) Nature , vol.365 , pp. 56-61
    • Jacenko, O.1    LuValle, P.A.2    Olsen, B.R.3
  • 18
    • 0002097152 scopus 로고
    • The collagen family: Structure, assembly, and organization in the extracellular matrix
    • Connective Tissue and Its Heritable Disorders, Royce PM, Steiman B (eds), New York: Wiley-Liss
    • (1993) , pp. 103-147
    • Kielty, C.M.1    Hopkinson, I.2    Grant, M.E.3
  • 19
    • 0028292785 scopus 로고
    • Stimulation of calcification of growth plate cartilage matrix vesicles by binding to type II and X collagens
    • (1994) J Biol Chem , vol.269 , pp. 11462-11469
    • Kirsch, T.1    Wuthier, R.E.2
  • 26
    • 0033548550 scopus 로고    scopus 로고
    • Folding and assembly of type X collagen mutants that cause metaphyseal chondrodysplasia-type Schmid. Evidence for co-assembly of the mutant and wild-type chains and binding to molecular chaperones
    • (1999) J Biol Chem , vol.274 , pp. 7570-7575
    • McLaughlin, S.H.1    Conn, S.N.2    Bulleid, N.J.3
  • 27
    • 0031035441 scopus 로고    scopus 로고
    • Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development-transcription factors and signaling pathways
    • (1997) FASEB J , vol.11 , pp. 125-132
    • Mundlos, S.1    Olsen, B.R.2
  • 28
    • 0030894287 scopus 로고    scopus 로고
    • Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis
    • (1997) FASEB J , vol.11 , pp. 227-233
    • Mundlos, S.1    Olsen, B.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.