메뉴 건너뛰기




Volumn 16, Issue , 2000, Pages 191-220

Bone development

Author keywords

Chondrogenesis; Growth plate; Joints; Ossification; Patterning

Indexed keywords

TRANSCRIPTION FACTOR;

EID: 0034521277     PISSN: 10810706     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.cellbio.16.1.191     Document Type: Review
Times cited : (805)

References (206)
  • 11
    • 0028837742 scopus 로고
    • Hedgehog and Bmp genes are coexpressed at many diverse sites of cell-cell interaction in the mouse embryo
    • (1995) Dev. Biol. , vol.172 , pp. 126-138
    • Bitgood, M.J.1    McMahon, A.P.2
  • 15
  • 20
    • 0033531789 scopus 로고    scopus 로고
    • Interaction of collagen alpha1(X) containing engineered NC1 mutations with normal alphal(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
  • 26
    • 0031008068 scopus 로고    scopus 로고
    • Matrix metallopro teinases regulate morphogenesis, migration and remodeling of epithelium, tongue skeletal muscle and cartilage in the mandibular arch
    • (1997) Development , vol.124 , pp. 1519-1530
    • Chin, J.R.1    Werb, Z.2
  • 27
  • 30
    • 0030824271 scopus 로고    scopus 로고
    • The Nicholas Andry Award. The molecular pathology of osteogenesis imperfecta
    • (1997) Clin. Orthop. , vol.343 , pp. 235-248
    • Cole, W.G.1
  • 41
    • 0025925068 scopus 로고
    • Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
    • (1991) Cell , vol.67 , pp. 767-774
    • Epstein, D.J.1    Vekemans, M.2    Gros, P.3
  • 63
    • 0027478216 scopus 로고
    • A mouse model of Greig cephalopolysyndactyly syndrome: The extra- toes J mutation contains an intragenic deletion of the Gli3 gene
    • (1993) Nat. Genet. , vol.3 , pp. 241-246
    • Hui, C.C.1    Joyner, A.L.2
  • 69
    • 0027488970 scopus 로고
    • Spondylometaphyseal dysplasia in mice cartying 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
  • 86
    • 0002448814 scopus 로고
    • Differentiation of craniofacial mesenchyme
    • Differentiation and Morphogenesis of Bone, ed. BK Hall. Boca Raton, FL: CRC Press
    • (1994) , vol.9 , pp. 1-63
    • Langille, R.M.1
  • 95
    • 0033548659 scopus 로고    scopus 로고
    • Role of Pitx1 up stream of Tbx4 in specification of hindlimb identity
    • (1999) Science , vol.283 , pp. 1736-1739
    • Logan, M.1    Tabin, C.J.2
  • 107
    • 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
  • 108
    • 0030894287 scopus 로고    scopus 로고
    • Heritable dis eases of the skeleton. Part II: Molecular in sights into skeletal development-matrix components and their homeostasis
    • (1997) FASEB J. , vol.11 , pp. 227-233
    • Mundlos, S.1    Olsen, B.R.2
  • 109
    • 4244218899 scopus 로고    scopus 로고
    • Defects in skeletal morphogenesis
    • Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects., ed. P Royce, B Stein mann, New York: Wiley & Sons. In press
    • (2000)
    • Mundlos, S.1    Olsen, B.R.2
  • 117
    • 0020624879 scopus 로고
    • The role of the neural crest in patterning of avian cranial skeletal, connective, and muscle tissues
    • (1983) Dev. Biol. , vol.96 , pp. 144-165
    • Noden, D.M.1
  • 129
    • 0028951117 scopus 로고
    • Dorsalizing signal Wnt-7a required for normal polarity of D-V and A-P axes of mouse limb
    • (1995) Nature , vol.374 , pp. 350-353
    • Parr, B.A.1    McMahon, A.P.2
  • 138
    • 0030955889 scopus 로고    scopus 로고
    • Role of the Dlx home obox genes in proximodistal patterning of the branchial arches: Mutations of Dlx-1, Dlx 2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches
    • (1997) Dev. Biol. , vol.185 , pp. 165-184
    • Qiu, M.1    Bulfone, A.2    Ghattas, I.3    Meneses, J.J.4    Christensen, L.5
  • 149
    • 0033428617 scopus 로고    scopus 로고
    • Mice mutant for both Hoxa1 and Hoxb1 show extensive remodeling of the hindbrain and defects in craniofacial development
    • (1999) Development , vol.126 , pp. 5027-5040
    • Rossel, M.1    Capecchi, M.R.2
  • 151
    • 0028292605 scopus 로고
    • Msx1-deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
    • (1994) Nat. Genet. , vol.6 , pp. 348-356
    • Satokata, I.1    Maas, R.2
  • 153
    • 0031470553 scopus 로고    scopus 로고
    • Direct binding and activation of receptor tyrosine kinases by collagen
    • (1997) Cell , vol.91 , pp. 869-872
    • Schlessinger, J.1
  • 174
    • 0032787621 scopus 로고    scopus 로고
    • The mouse mutation Pdn (Polydactyly Nagoya) is caused by the integration of a retrotransposon into the Gli3 gene
    • (1999) Mamm. Genome. , vol.10 , pp. 205-209
    • Thien, H.1    Ruther, U.2
  • 178
    • 0026001235 scopus 로고
    • Immunohistochemical localization of chondroitin and heparan sulfate proteoglycans in pre-spina bifida splotch mouse embryos
    • (1991) Teratology , vol.44 , pp. 571-579
    • Trasler, D.G.1    Morriss-Kay, G.2
  • 191
    • 0027361307 scopus 로고
    • Two additional cases of osteogenesis imperfecta with substitutions for glycine in the alpha 2(I) collagen chain. A regional model relating mutation location with phenotype
    • (1993) J. Biol. Chem. , vol.268 , pp. 25162-25167
    • Wang, Q.1    Orrison, B.M.2    Marini, J.C.3
  • 203


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.