| scholarly article | Q13442814 |
| P50 | author | Anita S Deshpande | Q92090269 |
| P2093 | author name string | Steven L Goudy | |
| P2860 | cites work | Cranial neural crest deletion of VEGFa causes cleft palate with aberrant vascular and bone development | Q41249705 |
| Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development | Q41478213 | ||
| Syndromes and anomalies associated with cleft | Q41761188 | ||
| Wnt/β-catenin signaling and Msx1 promote outgrowth of the maxillary prominences | Q41859335 | ||
| Nucleocytoplasmic shuttling of Smads 2, 3, and 4 permits sensing of TGF-beta receptor activity | Q42811215 | ||
| Etiology of facial clefts: prospective evaluation of 428 patients. | Q45949221 | ||
| Cell autonomous requirement for PDGFRalpha in populations of cranial and cardiac neural crest cells. | Q52111063 | ||
| Cranial neural crest cells on the move: their roles in craniofacial development. | Q55522032 | ||
| Rescue of cleft palate in Msx1-deficient mice by transgenic Bmp4 reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis | Q74578263 | ||
| Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome | Q24310222 | ||
| Linking Smads and transcriptional activation | Q24528159 | ||
| Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes | Q24600400 | ||
| Scar-free healing: from embryonic mechanisms to adult therapeutic intervention | Q24675326 | ||
| It's all in your head: new insights into craniofacial development and deformation | Q24675572 | ||
| Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6) | Q24675845 | ||
| Genetic Syndromes Associated with Craniosynostosis | Q26745874 | ||
| DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 | Q28204282 | ||
| Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch | Q28268504 | ||
| TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome | Q28512803 | ||
| A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling | Q28585038 | ||
| Sonic hedgehog signaling regulates reciprocal epithelial-mesenchymal interactions controlling palatal outgrowth | Q28590687 | ||
| Type III transforming growth factor beta receptor regulates vascular and osteoblast development during palatogenesis | Q28592403 | ||
| HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo | Q29618704 | ||
| Is craniofacial morphology in Apert and Crouzon syndromes the same? | Q33538476 | ||
| BMPR1B mutation causes Pierre Robin sequence | Q33688452 | ||
| Roles of PDGF in animal development | Q34227429 | ||
| Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans | Q34289809 | ||
| Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome | Q34308670 | ||
| The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms | Q34349039 | ||
| Wound Complications After Cleft Repair in Children With Van der Woude Syndrome | Q34479458 | ||
| Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities | Q35011856 | ||
| Transforming growth factor Beta family: insight into the role of growth factors in regulation of fracture healing biology and potential clinical applications. | Q35076034 | ||
| Palatogenesis: engineering, pathways and pathologies | Q35693868 | ||
| Transforming growth factor-beta and the initiation of chondrogenesis and osteogenesis in the rat femur | Q36223123 | ||
| Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. | Q37156054 | ||
| Transforming growth factor-beta 3 is required for secondary palate fusion | Q37373842 | ||
| Incidence of cleft lip, cleft palate, and cleft lip and palate among races: a review | Q39669111 | ||
| Syndromes with cleft lip and cleft palate | Q40566366 | ||
| Tbx1 is necessary for palatal elongation and elevation | Q40616720 | ||
| Review of the role of potential teratogens in the origin of human nonsyndromic oral clefts | Q41173904 | ||
| P433 | issue | 1 | |
| P921 | main subject | cleft palate | Q3889390 |
| P304 | page(s) | 160-164 | |
| P577 | publication date | 2018-11-15 | |
| P1433 | published in | Laryngoscope Investigative Otolaryngology | Q50817247 |
| P1476 | title | Cellular and molecular mechanisms of cleft palate development | |
| P478 | volume | 4 |
| Q92128752 | Spatial Clusters of Children with Cleft Lip and Palate and Their Association with Polluted Zones in the Monterrey Metropolitan Area |
| Q100381932 | The cleft palate candidate gene BAG6 supports FoxO1 acetylation to promote FasL-mediated apoptosis during palate fusion |
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