The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Craniosynostosis: genes and mechanisms
Abstract
Enlargement of the skull vault occurs by appositional growth at the fibrous joints between the bones, termed cranial sutures. Relatively little is known about the developmental biology of this process, but genetically determined disorders of premature cranial suture fusion (craniosynostosis) provide one route to the identification of some of the key molecules involved. Mutations of the MSX2, FGFR1, FGFR2, FGFR3 and TWIST genes yield new insights, both into normal and abnormal cranial suture biogenesis and into problems of broad interest, such as the conservation of molecular pathways in development, and mechanisms of mutation and dominance.
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Citations
Cites
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
Muenke, M., Schell, U., Hehr, A., Robin, N. H., Losken, H. W., Schinzel, A., Pulleyn, L. J., Rutland, P., Reardon, W., Malcolm, S., et al. (1994) · Nature Genetics · doi:10.1038/ng1194-269 · Cited by 614
Intracranial pressure in craniostenosis
Renier, D., Sainte-Rose, C., Marchac, D., & Hirsch, J.-F. (1982) · Journal of neurosurgery · doi:10.3171/jns.1982.57.3.0370 · Cited by 591
msh may play a conserved role in dorsoventral patterning of the neuroectoderm and mesoderm
D'Alessio, M., & Frasch, M. (1996) · Mechanisms of Development · doi:10.1016/s0925-4773(96)00583-7 · Cited by 126
Cited by
Signaling and transcriptional regulation in osteoblast commitment and differentiation
Huang, W. (2007) · Frontiers in Bioscience · doi:10.2741/2296 · Cited by 649
Morriss‐Kay, G. M., & Wilkie, A. O. M. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00475.x · Cited by 483
Self-citationKinase mutations in human disease: interpreting genotype–phenotype relationships
Lahiry, P., Torkamani, A., Schork, N. J., & Hegele, R. A. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2707 · Cited by 420
Transcriptional Control of Skeletogenesis
Karsenty, G. (2008) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.9.081307.164437 · Cited by 391
FGF signaling in the developing endochondral skeleton
Ornitz, D. M. (2005) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2005.02.003 · Cited by 356
Metadata
- Authors
- Wilkie, A.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 1997-09-01
- Volume
- 6
- Issue
- 10
- Pages
- 1647-1656
- ISSN
- 0964-6906 (ISSN-L)
- 1460-2083
- OpenAlex
- W1988151099
- Cited by
- 529
- References
- 3
- FWCI
- 14.78
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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