| P50 | author | Karen J. Liu | Q41841535 |
| | John B. Wallingford | Q67470063 |
| P2093 | author name string | Jacqueline M Tabler | |
| | Christopher P Rice | |
| P2860 | cites work | The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation | Q24292169 |
| | New insights into craniofacial malformations | Q28088384 |
| | A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene | Q28263330 |
| | Signaling from Smo to Ci/Gli: conservation and divergence of Hedgehog pathways from Drosophila to vertebrates | Q28285927 |
| | Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes | Q28504497 |
| | Planar cell polarity effector gene Fuzzy regulates cilia formation and Hedgehog signal transduction in mouse | Q28505727 |
| | Fgf8 is required for anterior heart field development | Q28511534 |
| | The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development | Q28584722 |
| | Cilia and Hedgehog responsiveness in the mouse | Q28585101 |
| | Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology | Q28585125 |
| | Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase | Q29615040 |
| | A global double-fluorescent Cre reporter mouse | Q29616157 |
| | Cellular dynamics and tissue interactions of the dura mater during head development | Q30445497 |
| | Activation of FGF signaling mediates proliferative and osteogenic differences between neural crest derived frontal and mesoderm parietal derived bone | Q33761333 |
| | Acalvaria and hydrocephalus: a case report and discussion of the literature | Q33765584 |
| | Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1. | Q35804668 |
| | Patterning the neural crest derivatives during development of the vertebrate head: insights from avian studies | Q36324999 |
| | Multiple developmental mechanisms regulate species-specific jaw size. | Q37507635 |
| | A Ser252Trp mutation in fibroblast growth factor receptor 2 (FGFR2) mimicking human Apert syndrome reveals an essential role for FGF signaling in the regulation of endochondral bone formation | Q37525589 |
| | Craniosynostosis genetics: The mystery unfolds | Q37957083 |
| | Common skeletal features in rare diseases: New links between ciliopathies and FGF-related syndromes | Q40206060 |
| | Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling | Q42491186 |
| | Origin matters: differences in embryonic tissue origin and Wnt signaling determine the osteogenic potential and healing capacity of frontal and parietal calvarial bones | Q42862039 |
| | Generation and characterization of Osterix-Cherry reporter mice | Q43224789 |
| | Tissue origins and interactions in the mammalian skull vault | Q43849664 |
| | Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes. | Q45974169 |
| | Twist is required for establishment of the mouse coronal suture. | Q46460319 |
| | Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis | Q48096170 |
| | Cell lineage in mammalian craniofacial mesenchyme | Q49100509 |
| | Distinct roles for Hedgehog and canonical Wnt signaling in specification, differentiation and maintenance of osteoblast progenitors. | Q50722204 |
| | Craniosynostosis | Q56262853 |
| | Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression? | Q56417109 |
| | Co-culture of osteoblasts with immature dural cells causes an increased rate and degree of osteoblast differentiation | Q77570972 |
| | Dura mater biology: autocrine and paracrine effects of fibroblast growth factor 2 | Q77570978 |
| | Global strategies to reduce the healthcare burden of craniofacial anomalies | Q79314699 |
| | Dura mater-derived FGF-2 mediates mitogenic signaling in calvarial osteoblasts | Q81391318 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | GLI-Kruppel family member GLI3 | Q14886933 |
| | Fuzzy planar cell polarity protein | Q21979952 |
| | Fibroblast growth factor 8 | Q21985352 |
| P304 | page(s) | 4-10 | |
| P577 | publication date | 2016-07-06 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | A novel ciliopathic skull defect arising from excess neural crest | |
| P478 | volume | 417 | |