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Volumn 264, Issue 1, 2003, Pages 64-76

Radiographic analysis of zebrafish skeletal defects

Author keywords

Collagen; Osteogenesis imperfecta; X ray; Zebrafish

Indexed keywords

COLLAGEN TYPE 1;

EID: 0242606044     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0012-1606(03)00399-3     Document Type: Article
Times cited : (160)

References (51)
  • 2
    • 0032577276 scopus 로고    scopus 로고
    • Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton
    • Brunet L.J., McMahon J.A., McMahon A.P., Harland R.M. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science. 280:1998;1455-1457.
    • (1998) Science , vol.280 , pp. 1455-1457
    • Brunet, L.J.1    Mcmahon, J.A.2    Mcmahon, A.P.3    Harland, R.M.4
  • 4
    • 0029828972 scopus 로고    scopus 로고
    • Development of the cranium and paired fins in the zebrafish Danio rerio (Osariophysi, Cyprinidae)
    • Cubbage C.C., Mabee P.M. Development of the cranium and paired fins in the zebrafish Danio rerio (Osariophysi, Cyprinidae). J. Morphcol. 229:1996;121-160.
    • (1996) J. Morphcol. , vol.229 , pp. 121-160
    • Cubbage, C.C.1    Mabee, P.M.2
  • 6
    • 0031571651 scopus 로고    scopus 로고
    • Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4
    • Dunn N.R., Winnier G.E., Hargett L.K., Schrick J.J., Fogo A.B., Hogan B.L. Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4. Dev. Biol. 188:1997;235-247.
    • (1997) Dev. Biol. , vol.188 , pp. 235-247
    • Dunn, N.R.1    Winnier, G.E.2    Hargett, L.K.3    Schrick, J.J.4    Fogo, A.B.5    Hogan, B.L.6
  • 8
    • 0030990981 scopus 로고    scopus 로고
    • Loss of cerebum function ventralizes the zebrafish embryo
    • Fisher S., Amacher S.L., Halpern M.E. Loss of cerebum function ventralizes the zebrafish embryo. Development. 124:1997;1301-1311.
    • (1997) Development , vol.124 , pp. 1301-1311
    • Fisher, S.1    Amacher, S.L.2    Halpern, M.E.3
  • 9
    • 0032707236 scopus 로고    scopus 로고
    • Patterning the zebrafish axial skeleton requires early chordin function
    • Fisher S., Halpern M.E. Patterning the zebrafish axial skeleton requires early chordin function. Nat. Genet. 23:1999;442-446.
    • (1999) Nat. Genet. , vol.23 , pp. 442-446
    • Fisher, S.1    Halpern, M.E.2
  • 10
    • 0033621331 scopus 로고    scopus 로고
    • Use of the Cre/lox recombination system to develop a non-lethal knock-in murine model for osteogenesis imperfecta with an alpha1(I) G349C substitution. Variability in phenotype in BrtlIV mice
    • Forlino A., Porter F.D., Lee E.J., Westphal H., Marini J.C. Use of the Cre/lox recombination system to develop a non-lethal knock-in murine model for osteogenesis imperfecta with an alpha1(I) G349C substitution. Variability in phenotype in BrtlIV mice. J. Biol. Chem. 274:1999;37923-37931.
    • (1999) J. Biol. Chem. , vol.274 , pp. 37923-37931
    • Forlino, A.1    Porter, F.D.2    Lee, E.J.3    Westphal, H.4    Marini, J.C.5
  • 15
    • 0021395969 scopus 로고
    • Insertion of retrovirus into the first intron of alpha 1(I) collagen gene to embryonic lethal mutation in mice
    • Harbers K., Kuehn M., Delius H., Jaenisch R. Insertion of retrovirus into the first intron of alpha 1(I) collagen gene to embryonic lethal mutation in mice. Proc. Natl. Acad. Sci. USA. 81:1984;1504-1508.
    • (1984) Proc. Natl. Acad. Sci. USA , vol.81 , pp. 1504-1508
    • Harbers, K.1    Kuehn, M.2    Delius, H.3    Jaenisch, R.4
  • 20
    • 0027431005 scopus 로고
    • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
    • Jabs E.W., Muller U., Li X., Ma L., Luo W., Haworth I.S., Klisak I., Sparkes R., Warman M.L., Mulliken J.B., et al. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell. 75:1993;443-450.
    • (1993) Cell , vol.75 , pp. 443-450
    • Jabs, E.W.1    Muller, U.2    Li, X.3    Ma, L.4    Luo, W.5    Haworth, I.S.6    Klisak, I.7    Sparkes, R.8    Warman, M.L.9    Mulliken, J.B.10
  • 21
    • 0026327359 scopus 로고
    • Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta
    • Khillan J.S., Olsen A.S., Kontusaari S., Sokolov B., Prockop D.J. Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta. J. Biol. Chem. 266:1991;23373-23379.
    • (1991) J. Biol. Chem. , vol.266 , pp. 23373-23379
    • Khillan, J.S.1    Olsen, A.S.2    Kontusaari, S.3    Sokolov, B.4    Prockop, D.J.5
  • 23
  • 24
    • 0030955414 scopus 로고    scopus 로고
    • Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels
    • Kuivaniemi H., Tromp G., Prockop D.J. Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels. Hum. Mutat. 9:1997;300-315.
    • (1997) Hum. Mutat. , vol.9 , pp. 300-315
    • Kuivaniemi, H.1    Tromp, G.2    Prockop, D.J.3
  • 25
    • 0030927622 scopus 로고    scopus 로고
    • Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia
    • Lee B., Thirunavukkarasu K., Zhou L., Pastore L., Baldini A., Hecht J., Geoffroy V., Ducy P., Karsenty G. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. Nat. Genet. 16:1997;307-310.
    • (1997) Nat. Genet. , vol.16 , pp. 307-310
    • Lee, B.1    Thirunavukkarasu, K.2    Zhou, L.3    Pastore, L.4    Baldini, A.5    Hecht, J.6    Geoffroy, V.7    Ducy, P.8    Karsenty, G.9
  • 27
    • 0027468095 scopus 로고
    • The morbid anatomy of the human genome: Chromosomal location of mutations causing disease
    • McKusick V.A., Amberger J.S. The morbid anatomy of the human genome chromosomal location of mutations causing disease . J. Med. Genet. 30:1993;1-26.
    • (1993) J. Med. Genet. , vol.30 , pp. 1-26
    • Mckusick, V.A.1    Amberger, J.S.2
  • 28
    • 0028198185 scopus 로고
    • The morbid anatomy of the human genome: Chromosomal location of mutations causing disease (update 1 December 1993)
    • McKusick V.A., Amberger J.S. The morbid anatomy of the human genome chromosomal location of mutations causing disease (update 1 December 1993) . J. Med. Genet. 31:1994;265-279.
    • (1994) J. Med. Genet. , vol.31 , pp. 265-279
    • Mckusick, V.A.1    Amberger, J.S.2
  • 29
    • 0031016666 scopus 로고    scopus 로고
    • Sclerotome development and peripheral nervous system segmentation in embryonic zebrafish
    • Morin-Kensicki E.M., Eisen J.S. Sclerotome development and peripheral nervous system segmentation in embryonic zebrafish. Development. 124:1997;159-167.
    • (1997) Development , vol.124 , pp. 159-167
    • Morin-Kensicki, E.M.1    Eisen, J.S.2
  • 30
    • 0036671537 scopus 로고    scopus 로고
    • Segmental relationship between somites and vertebral column in zebrafish
    • Morin-Kensicki E.M., Melancon E., Eisen J.S. Segmental relationship between somites and vertebral column in zebrafish. Development. 129:2002;3851-3860.
    • (2002) Development , vol.129 , pp. 3851-3860
    • Morin-Kensicki, E.M.1    Melancon, E.2    Eisen, J.S.3
  • 31
    • 0028387996 scopus 로고
    • Large-scale mutagenesis in the zebrafish: In search of genes controlling development in a vertebrate
    • Mullins M.C., Hammerschmidt M., Haffter P., Nüsslein-Volhard C. Large-scale mutagenesis in the zebrafish in search of genes controlling development in a vertebrate . Curr. Biol. 4:1994;189-202.
    • (1994) Curr. Biol. , vol.4 , pp. 189-202
    • Mullins, M.C.1    Hammerschmidt, M.2    Haffter, P.3    Nüsslein-Volhard, C.4
  • 36
    • 0027511167 scopus 로고
    • Transgenic mice expressing a partially deleted gene for type I procollagen (COLIA1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral
    • Pereira R., Khillan J.S., Helminen H.J., Hume E.L., Prockop D.J. Transgenic mice expressing a partially deleted gene for type I procollagen (COLIA1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral. J. Clin. Invest. 91:1993;709-716.
    • (1993) J. Clin. Invest. , vol.91 , pp. 709-716
    • Pereira, R.1    Khillan, J.S.2    Helminen, H.J.3    Hume, E.L.4    Prockop, D.J.5
  • 39
    • 0034830878 scopus 로고    scopus 로고
    • Complete primary structure of rainbow trout type I collagen consisting of alpha1(I)alpha2(I)alpha3(I) heterotrimers
    • Saito M., Takenouchi Y., Kunisaki N., Kimura S. Complete primary structure of rainbow trout type I collagen consisting of alpha1(I)alpha2(I) alpha3(I) heterotrimers. Eur. J. Biochem. 268:2001;2817-2827.
    • (2001) Eur. J. Biochem. , vol.268 , pp. 2817-2827
    • Saito, M.1    Takenouchi, Y.2    Kunisaki, N.3    Kimura, S.4
  • 40
    • 0028292605 scopus 로고
    • Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
    • Satokata I., Maas R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat. Genet. 6:1994;348-356.
    • (1994) Nat. Genet. , vol.6 , pp. 348-356
    • Satokata, I.1    Maas, R.2
  • 41
    • 0031170969 scopus 로고    scopus 로고
    • Genetic analysis of craniofacial development in the vertebrate embryo
    • Schilling T.F. Genetic analysis of craniofacial development in the vertebrate embryo. Bioessays. 19:1997;459-468.
    • (1997) Bioessays , vol.19 , pp. 459-468
    • Schilling, T.F.1
  • 42
    • 0028256072 scopus 로고
    • Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo
    • Schilling T.F., Kimmel C.B. Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo. Development. 120:1994;483-494.
    • (1994) Development , vol.120 , pp. 483-494
    • Schilling, T.F.1    Kimmel, C.B.2
  • 44
    • 0002317346 scopus 로고    scopus 로고
    • Osteogenesis imperfecta: Current concepts
    • J.P. Belizikian, L.G. Raisz, & G.A. Rodan. San Diego: Academic Press
    • Shapiro J.R., Primorac D., Rowe D.W. Osteogenesis imperfecta current concepts . Belizikian J.P., Raisz L.G., Rodan G.A. Principles of Bone Biology. 1996;889-902 Academic Press, San Diego.
    • (1996) Principles of Bone Biology , pp. 889-902
    • Shapiro, J.R.1    Primorac, D.2    Rowe, D.W.3
  • 45
    • 0027404215 scopus 로고
    • Fragilitas ossium (fro/fro) in the mouse: A model for a recessively inherited type of osteogenesis imperfecta
    • Sillence D.O., Ritchie H.E., Dibbayawan T., Eteson D., Brown K. Fragilitas ossium (fro/fro) in the mouse a model for a recessively inherited type of osteogenesis imperfecta . Am. J. Med. Genet. 45:1993;276-283.
    • (1993) Am. J. Med. Genet. , vol.45 , pp. 276-283
    • Sillence, D.O.1    Ritchie, H.E.2    Dibbayawan, T.3    Eteson, D.4    Brown, K.5
  • 46
    • 0019452034 scopus 로고
    • Production of clones of homozygous diploid zebra fish (Brachydanio rerio)
    • Streisinger G., Walker C., Dower N., Knauber D., Singer F. Production of clones of homozygous diploid zebra fish (Brachydanio rerio). Nature. 291:1981;293-296.
    • (1981) Nature , vol.291 , pp. 293-296
    • Streisinger, G.1    Walker, C.2    Dower, N.3    Knauber, D.4    Singer, F.5
  • 47
    • 0034464005 scopus 로고    scopus 로고
    • The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: The achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans
    • Vajo Z., Francomano C.A., Wilkin D.J. The molecular and genetic basis of fibroblast growth factor receptor 3 disorders the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans . Endocr. Rev. 21:2000;23-39.
    • (2000) Endocr. Rev. , vol.21 , pp. 23-39
    • Vajo, Z.1    Francomano, C.A.2    Wilkin, D.J.3
  • 48
    • 0030027374 scopus 로고    scopus 로고
    • Teleost HoxD and HoxA genes: Comparison with tetrapods and functional evolution of the HOXD complex
    • van der Hoeven F., Sordino P., Fraudeau N., Izpisua-Belmonte J.C., Duboule D. Teleost HoxD and HoxA genes comparison with tetrapods and functional evolution of the HOXD complex . Mech. Dev. 54:1996;9-21.
    • (1996) Mech. Dev. , vol.54 , pp. 9-21
    • Van Der Hoeven, F.1    Sordino, P.2    Fraudeau, N.3    Izpisua-Belmonte, J.C.4    Duboule, D.5
  • 50
    • 0004113253 scopus 로고
    • M. Westerfield. Eugene, OR: University of Oregon Press
    • Westerfield M. The Zebrafish Book. 1995;University of Oregon Press, Eugene, OR.
    • (1995) The Zebrafish Book


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.