The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
Fibroblast-growth-factor receptor mutations in human skeletal disorders
Open accessAbstract
Fibroblast-growth-factor receptors (FGFRs), members of the tyrosine-kinase receptor family, play a crucial role in signal transduction and development. Recently, unique mutations in three human FGFR-encoding genes (FGFR1-3) have been identified as the cause of a variety of skeletal disorders. Comparison of these specific mutations with the resulting phenotypes is now providing new insight into the role of these receptors in normal and abnormal bone development.
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Citations
Cites
Signal transduction by receptors with tyrosine kinase activity
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Dimerization of cell surface receptors in signal transduction
Heldin, C.-H. (1995) · Cell · doi:10.1016/0092-8674(95)90404-2 · Cited by 1,634
Shiang, R., Thompson, L. M., Zhu, Y.-Z., Church, D. M., Fielder, T. J., Bocian, M., Winokur, S. T., & Wasmuth, J. J. (1994) · Cell · doi:10.1016/0092-8674(94)90302-6 · Cited by 1,329
Structural and Functional Diversity in the FGf Receptor Multigene Family
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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
Wilkie, A. O. M., Slaney, S. F., Oldridge, M., Poole, M. D., Ashworth, G. J., Hockley, A. D., Hayward, R. D., David, D. J., Pulleyn, L. J., Rutland, P., et al. (1995) · Nature Genetics · doi:10.1038/ng0295-165 · Cited by 935
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
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fgfr-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation.
Yamaguchi, T. P., Harpal, K., Henkemeyer, M., & Rossant, J. (1994) · Genes & Development · doi:10.1101/gad.8.24.3032 · Cited by 778
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
Reardon, W., Winter, R. M., Rutland, P., Pulleyn, L. J., Jones, B. M., & Malcolm, S. (1994) · Nature Genetics · doi:10.1038/ng0994-98 · Cited by 758
Cited by
Rao, E., Weiss, B., Fukami, M., Rump, A., Niesler, B., Mertz, A., Muroya, K., Binder, G., Kirsch, S., Winkelmann, M., et al. (1997) · Nature Genetics · doi:10.1038/ng0597-54 · Cited by 943
Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3
Colvin, J. S., Bohne, B. A., Harding, G. W., McEwen, D. G., & Ornitz, D. M. (1996) · Nature Genetics · doi:10.1038/ng0496-390 · Cited by 873
Mechanisms underlying differential responses to FGF signaling
Dailey, L., Ambrosetti, D., Mansukhani, A., & Basilico, C. (2005) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2005.01.007 · Cited by 649
Chesi, M., Nardini, E., Brents, L. A., Schröck, E., Ried, T., Kuehl, W. M., & Bergsagel, P. L. (1997) · Nature Genetics · doi:10.1038/ng0797-260 · Cited by 637
Neuronal defects and delayed wound healing in mice lacking fibroblast growth factor 2
Ortega, S., Ittmann, M., Tsang, S. H., Ehrlich, M., & Basilico, C. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.10.5672 · Cited by 593
Metadata
- Authors
- Muenke, M., & Schell, U.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 1995-08
- Volume
- 11
- Issue
- 8
- Pages
- 308-313
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2043471588
- Cited by
- 295
- References
- 44
- FWCI
- 2.79
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Muenke, M., & Schell, U. (1995). Fibroblast-growth-factor receptor mutations in human skeletal disorders. Trends in Genetics. https://doi.org/10.1016/s0168-9525(00)89088-5
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
