Mechanisms of premature closure of cranial sutures

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

William Reardon, Robin M. Winter, Paul Rutland et al. · Nature Genetics · 1994 · 768 citations

Life Sciences, Genetics, Molecular Genetics +6

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Ethylin Wang Jabs, Ulrich Müller, Xiang Li et al. · Cell · 1993 · 680 citations

Medicine, Genetics, Molecular Genetics +14

Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA.

Raymond Evers, Marcel Kool, Liesbeth van Deemter et al. · Journal of Clinical Investigation · 1998 · 615 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

FGF-, BMP- and Shh-mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development

Hyun‐Jung Kim, David Rice, Päivi Kettunen et al. · Development · 1998 · 413 citations

Dentistry, Craniofacial Biology, Developmental Biology +17

Craniofacial Skeletal Measurements Based on Computed Tomography: Part I. Accuracy and Reproducibility

Ariel A. Waitzman, Jeffrey C. Posnick, Derek Armstrong et al. · The Cleft Palate-Craniofacial Journal · 1992 · 218 citations

Dentistry, Anatomy, Radiology +14