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Volumn 40, Issue 6, 1996, Pages 1185-1188

Developmental expression of splicing variants of fibroblast growth factor receptor 3 (FGFR3) in mouse

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 3; UNCLASSIFIED DRUG;

EID: 12644265399     PISSN: 02146282     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (49)

References (10)
  • 3
    • 0027344852 scopus 로고
    • Structural and functional diversity in the FGF receptor multigene family
    • JOHNSON, D.E. and WILLIAMS, L.T. (1993). Structural and functional diversity in the FGF receptor multigene family. Adv. Cancer Res. 60: 1-41.
    • (1993) Adv. Cancer Res. , vol.60 , pp. 1-41
    • Johnson, D.E.1    Williams, L.T.2
  • 4
    • 0026020296 scopus 로고
    • Isolation of an additional member of the fibroblast growth factor receptor family, FGFR3
    • KEEGAN, K., JOHNSON, D.E., WILLIAMS, L.T. and HAYMAN, M.J. (1991). Isolation of an additional member of the fibroblast growth factor receptor family, FGFR3. Proc. Natl. Acad. Sci. USA 88: 1095-1099.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 1095-1099
    • Keegan, K.1    Johnson, D.E.2    Williams, L.T.3    Hayman, M.J.4
  • 5
    • 0028793472 scopus 로고
    • Fibroblast growth factor receptor 3 (FGRF3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
    • MEYERS, G.A., ORLOW, S.J., MUNRO, I.R., PRZYLEPA, K.A. and JABS, E.W. (1995). Fibroblast growth factor receptor 3 (FGRF3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. Nature Genet 11: 462-464.
    • (1995) Nature Genet , vol.11 , pp. 462-464
    • Meyers, G.A.1    Orlow, S.J.2    Munro, I.R.3    Przylepa, K.A.4    Jabs, E.W.5
  • 6
    • 0027409017 scopus 로고
    • Unique expression pattern of the FGF Receptor 3 gene during mouse organogenesis
    • PETERS, K., ORNITZ, D., WERNER, S. and WILLIAMS, L (1993) Unique expression pattern of the FGF Receptor 3 gene during mouse organogenesis. Dev. Biol. 155: 423-430.
    • (1993) Dev. Biol. , vol.155 , pp. 423-430
    • Peters, K.1    Ornitz, D.2    Werner, S.3    Williams, L.4
  • 8
    • 0027964261 scopus 로고
    • Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
    • SHIANG, R., THOMPSON, L.M., ZHU, Y-Z, CHURCH, D.M., FIELDER, T.J., BOCIAN, M., WINOKUR, S.T and WASMUTH, J.J. (1994). Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78: 335-342.
    • (1994) Cell , vol.78 , pp. 335-342
    • Shiang, R.1    Thompson, L.M.2    Zhu, Y.-Z.3    Church, D.M.4    Fielder, T.J.5    Bocian, M.6    Winokur, S.T.7    Wasmuth, J.J.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.