Cranial neural crest cell contribution to craniofacial formation, pathology, and future directions in tissue engineering
dc.contributor.author | Snider, Taylor Nicholas | en_US |
dc.contributor.author | Mishina, Yuji | en_US |
dc.date.accessioned | 2014-10-07T16:09:28Z | |
dc.date.available | WITHHELD_12_MONTHS | en_US |
dc.date.available | 2014-10-07T16:09:28Z | |
dc.date.issued | 2014-09 | en_US |
dc.identifier.citation | Snider, Taylor Nicholas; Mishina, Yuji (2014). "Cranial neural crest cell contribution to craniofacial formation, pathology, and future directions in tissue engineering." Birth Defects Research Part C: Embryo Today: Reviews 102(3): 324-332. | en_US |
dc.identifier.issn | 1542-975X | en_US |
dc.identifier.issn | 1542-9768 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/108634 | |
dc.publisher | Wiley Periodicals, Inc. | en_US |
dc.publisher | Cambridge University Press | en_US |
dc.subject.other | Craniofacial Abnormality | en_US |
dc.subject.other | Cranial Neural Crest Cell | en_US |
dc.subject.other | Gene Regulatory Networks | en_US |
dc.subject.other | Tissue Engineering | en_US |
dc.title | Cranial neural crest cell contribution to craniofacial formation, pathology, and future directions in tissue engineering | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Obstetrics and Gynecology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/108634/1/bdrc21075.pdf | |
dc.identifier.doi | 10.1002/bdrc.21075 | en_US |
dc.identifier.source | Birth Defects Research Part C: Embryo Today: Reviews | en_US |
dc.identifier.citedreference | Reardon W, Winter RM, Rutland P, et al. 1994. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nat Genet 8: 98 – 103. | en_US |
dc.identifier.citedreference | Pelaez D, Huang CY, Cheung HS. 2013. Isolation of pluripotent neural crest‐derived stem cells from adult human tissues by connexin‐43 enrichment. Stem Cells Dev 22: 2906 – 2914. | en_US |
dc.identifier.citedreference | Perez‐Alcala S, Nieto MA, Barbas JA. 2004. LSox5 regulates RhoB expression in the neural tube and promotes generation of the neural crest. Development 131: 4455 – 4465. | en_US |
dc.identifier.citedreference | Pingault V, Ente D, Dastot‐Le Moal F, et al. 2010. Review and update of mutations causing Waardenburg syndrome. Hum Mutat 31: 391 – 406. | en_US |
dc.identifier.citedreference | Rinon A, Molchadsky A, Nathan E, et al. 2011. p53 coordinates cranial neural crest cell growth and epithelial‐mesenchymal transition/delamination processes. Development 138: 1827 – 1838. | en_US |
dc.identifier.citedreference | Rogers CD, Saxena A, Bronner ME. 2013. Sip1 mediates an E‐cadherin‐to‐N‐cadherin switch during cranial neural crest EMT. J Cell Biol 203: 835 – 847. | en_US |
dc.identifier.citedreference | Roscioli T, Elakis G, Cox TC, et al. 2013. Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients. Am J Med Genet C Semin Med Genet 163C: 259 – 270. | en_US |
dc.identifier.citedreference | Sanger C, David L, Argenta L. 2014. Latest trends in minimally invasive synostosis surgery: a review. Curr Opin Otolaryngol Head Neck Surg 22: 316 – 321. | en_US |
dc.identifier.citedreference | Santagati F, Rijli FM. 2003. Cranial neural crest and the building of the vertebrate head. Nat Rev Neurosci 4: 806 – 818. | en_US |
dc.identifier.citedreference | Shprintzen RJ, Goldberg RB, Lewin ML, et al. 1978. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo‐cardio‐facial syndrome. Cleft Palate J 15: 56 – 62. | en_US |
dc.identifier.citedreference | Simoes‐Costa M, Tan‐Cabugao J, Antoshechkin I, et al. 2014. Transcriptome analysis reveals novel players in the cranial neural crest gene regulatory network. Genome Res 24: 281 – 290. | en_US |
dc.identifier.citedreference | Southard‐Smith EM, Angrist M, Ellison JS, et al. 1999. The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg‐Shah (WS4) syndrome. Genome Res 9: 215 – 225. | en_US |
dc.identifier.citedreference | Takahashi K, Nuckolls GH, Takahashi I, et al. 2001. Msx2 is a repressor of chondrogenic differentiation in migratory cranial neural crest cells. Dev Dyn 222: 252 – 262. | en_US |
dc.identifier.citedreference | Theveneau E, Mayor R. 2012. Neural crest migration: interplay between chemorepellents, chemoattractants, contact inhibition, epithelial‐mesenchymal transition, and collective cell migration. Wiley Interdiscip Rev Dev Biol 1: 435 – 445. | en_US |
dc.identifier.citedreference | Theveneau E, Duband JL, Altabef M. 2007. Ets‐1 confers cranial features on neural crest delamination. PLoS One 2: e1142. | en_US |
dc.identifier.citedreference | Trainor P. 2013. Neural crest cells: evolution, development and disease. In: Trainor P, editor. London, UK: Academic Press. p. 488. | en_US |
dc.identifier.citedreference | Wang Y, Cox MK, Coricor G, et al. 2013. Inactivation of Tgfbr2 in Osterix‐Cre expressing dental mesenchyme disrupts molar root formation. Dev Biol 382: 27 – 37. | en_US |
dc.identifier.citedreference | Winograd J, Reilly MP, Roe R, et al. 1997. Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. Hum Mol Genet 6: 369 – 379. | en_US |
dc.identifier.citedreference | Xu X, Chen C, Akiyama K, et al. 2013. Gingivae contain neural‐crest‐ and mesoderm‐derived mesenchymal stem cells. J Dent Res 92: 825 – 832. | en_US |
dc.identifier.citedreference | Young NM, Hu D, Lainoff AJ, et al. 2014. Embryonic bauplans and the developmental origins of facial diversity and constraint. Development 141: 1059 – 1063. | en_US |
dc.identifier.citedreference | Achilleos A, Trainor PA. 2012. Neural crest stem cells: discovery, properties and potential for therapy. Cell Res 22: 288 – 304. | en_US |
dc.identifier.citedreference | Ashokan CS, Sreenivasan A, Saraswathy GK. 2014. Goldenhar syndrome–review with case series. J Clin Diagn Res 8: ZD17 – ZD19. | en_US |
dc.identifier.citedreference | Bassett AS, McDonald‐McGinn DM, Devriendt K, et al. 2011. Practical guidelines for managing patients with 22q11.2 deletion syndrome. J Pediatr 159: 332 – 339. | en_US |
dc.identifier.citedreference | Boutros S, Shetye PR, Ghali S, et al. 2007. Morphology and growth of the mandible in Crouzon, Apert, and Pfeiffer syndromes. J Craniofac Surg 18: 146 – 150. | en_US |
dc.identifier.citedreference | Burstyn‐Cohen T, Stanleigh J, Sela‐Donenfeld D, Kalcheim C. 2004. Canonical Wnt activity regulates trunk neural crest delamination linking BMP/noggin signaling with G1/S transition. Development 131: 5327 – 5339. | en_US |
dc.identifier.citedreference | Cooper GM, Durham EL, Cray JJ Jr, et al. 2012. Tissue interactions between craniosynostotic dura mater and bone. J Craniofac Surg 23: 919 – 924. | en_US |
dc.identifier.citedreference | Creuzet S, Schuler B, Couly G, Le Douarin NM. 2004. Reciprocal relationships between Fgf8 and neural crest cells in facial and forebrain development. Proc Natl Acad Sci USA 101: 4843 – 4847. | en_US |
dc.identifier.citedreference | Dixon J, Jones NC, Sandell LL, et al. 2006. Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities. Proc Natl Acad Sci USA 103: 13403 – 13408. | en_US |
dc.identifier.citedreference | Dudas M, Kim J, Li WY, et al. 2006. Epithelial and ectomesenchymal role of the type I TGF‐beta receptor ALK5 during facial morphogenesis and palatal fusion. Dev Biol 296: 298 – 314. | en_US |
dc.identifier.citedreference | Ezaldein HH, Metzler P, Persing JA, Steinbacher DM. 2014. Three‐dimensional orbital dysmorphology in metopic synostosis. J Plast Reconstr Aesthet Surg 67: 900 – 905. | en_US |
dc.identifier.citedreference | Graham A, Francis‐West P, Brickell P, Lumsden A. 1994. The signalling molecule BMP4 mediates apoptosis in the rhombencephalic neural crest. Nature 372: 684 – 686. | en_US |
dc.identifier.citedreference | Green SA, Bronner ME. 2014. The lamprey: a jawless vertebrate model system for examining origin of the neural crest and other vertebrate traits. Differentiation 87: 44 – 51. | en_US |
dc.identifier.citedreference | Hou L, Pavan WJ. 2008. Transcriptional and signaling regulation in neural crest stem cell‐derived melanocyte development: do all roads lead to Mitf? Cell Res 18: 1163 – 1176. | en_US |
dc.identifier.citedreference | Hsu PD, Lander ES, Zhang F. 2014. Development and applications of CRISPR‐Cas9 for genome engineering. Cell 157: 1262 – 1278. | en_US |
dc.identifier.citedreference | Huang CY, Pelaez D, Dominguez‐Bendala J, et al. 2009. Plasticity of stem cells derived from adult periodontal ligament. Regen Med 4: 809 – 821. | en_US |
dc.identifier.citedreference | Ibrahimi OA, Zhang F, Eliseenkova AV, et al. 2004. Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity. Hum Mol Genet 13: 69 – 78. | en_US |
dc.identifier.citedreference | Ishii M, Arias AC, Liu L, et al. 2012. A stable cranial neural crest cell line from mouse. Stem Cells Dev 21: 3069 – 3080. | en_US |
dc.identifier.citedreference | Ito Y, Yeo JY, Chytil A, et al. 2003. Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects. Development 130: 5269 – 5280. | en_US |
dc.identifier.citedreference | Jabs EW, Li X, Scott AF, et al. 1994. Jackson‐Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nat Genet 8: 275 – 279. | en_US |
dc.identifier.citedreference | Jones NC, Lynn ML, Gaudenz K, et al. 2008. Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function. Nat Med 14: 125 – 133. | en_US |
dc.identifier.citedreference | Kaartinen V, Voncken JW, Shuler C, et al. 1995. Abnormal lung development and cleft palate in mice lacking TGF‐beta 3 indicates defects of epithelial‐mesenchymal interaction. Nat Genet 11: 415 – 421. | en_US |
dc.identifier.citedreference | Lalani SR, Safiullah AM, Fernbach SD, et al. 2006. Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype‐phenotype correlation. Am J Hum Genet 78: 303 – 314. | en_US |
dc.identifier.citedreference | Le Douarin N. 1973. A biological cell labeling technique and its use in expermental embryology. Dev Biol 30: 217 – 222. | en_US |
dc.identifier.citedreference | Le Douarin N, Kalcheim C. 1999. The neural crest. Cambridge, UK: Cambridge University Press. | en_US |
dc.identifier.citedreference | Loeys BL, Chen J, Neptune ER, et al. 2005. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet 37: 275 – 281. | en_US |
dc.identifier.citedreference | Matera I, Watkins‐Chow DE, Loftus SK, et al. 2008. A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy. Hum Mol Genet 17: 2118 – 2131. | en_US |
dc.identifier.citedreference | Minoux M, Kratochwil CF, Ducret S, et al. 2013. Mouse Hoxa2 mutations provide a model for microtia and auricle duplication. Development 140: 4386 – 4397. | en_US |
dc.identifier.citedreference | Mishina Y, Snider TN. 2014. Neural crest cell signaling pathways critical to cranial bone development and pathology. Exp Cell Res 325: 138 – 147. | en_US |
dc.identifier.citedreference | Miura M, Gronthos S, Zhao M, et al. 2003. SHED: stem cells from human exfoliated deciduous teeth. Proc Natl Acad Sci USA 100: 5807 – 5812. | en_US |
dc.identifier.citedreference | Nagashima H, Shibata M, Taniguchi M, et al. 2014. Comparative study of the shell development of hard‐ and soft‐shelled turtles. J Anat 225: 60 – 70. | en_US |
dc.identifier.citedreference | Noden DM, Trainor PA. 2005. Relations and interactions between cranial mesoderm and neural crest populations. J Anat 207: 575 – 601. | en_US |
dc.identifier.citedreference | Papangeli I, Scambler P. 2013. The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1. Wiley Interdiscip Rev Dev Biol 2: 393 – 403. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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