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Msx1 and Pax3 Cooperate to Mediate FGF8 and WNT Signals during Xenopus Neural Crest Induction
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/dvdy.10056openalex-snapshot
Region‐ and stage‐specific effects of FGFs and BMPs in chick mandibular morphogenesis
inferredcites →https://doi.org/10.1006/dbio.1996.0113openalex-snapshot
Overexpression of Xgsk-3 Disrupts Anterior Ectodermal Patterning inXenopus
inferredcites →https://doi.org/10.1006/dbio.1996.0187openalex-snapshot
Neural Crest Formation in Xenopus laevis: Mechanisms of Xslug Induction
inferredcites →https://doi.org/10.1006/dbio.1997.8634openalex-snapshot
Role of FGF andNogginin Neural Crest Induction
inferredcites →https://doi.org/10.1006/dbio.1997.8732openalex-snapshot
FGF-8Is Associated with Anteroposterior Patterning and Limb Regeneration inXenopus
inferredcites →https://doi.org/10.1006/dbio.1997.8820openalex-snapshot
Neural Crest Induction by Xwnt7B in Xenopus
inferredcites →https://doi.org/10.1006/dbio.1998.8902openalex-snapshot
The Inductive Properties of Mesoderm Suggest That the Neural Crest Cells Are Specified by a BMP Gradient
inferredcites →https://doi.org/10.1006/dbio.1998.8927openalex-snapshot
Ventral and Lateral Regions of the Zebrafish Gastrula, Including the Neural Crest Progenitors, Are Established by abmp2b/swirlPathway of Genes
inferredcites →https://doi.org/10.1006/dbio.1999.9319openalex-snapshot
Expression of Pax-3 in the Lateral Neural Plate Is Dependent on a Wnt-Mediated Signal from Posterior Nonaxial Mesoderm
inferredcites →https://doi.org/10.1006/dbio.2000.9722openalex-snapshot
Roles for Fgf Signaling during Zebrafish Fin Regeneration
inferredcites →https://doi.org/10.1006/dbio.2001.0356openalex-snapshot
NF-κB Mediates FGF Signal Regulation of msx-1 Expression
inferredcites →https://doi.org/10.1006/dbio.2001.0565openalex-snapshot
Morpholino Oligos: Making Sense of Antisense?
inferredcites →https://doi.org/10.1016/0092-8674(89)90612-0openalex-snapshot
A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest
inferredcites →https://doi.org/10.1016/0168-9525(93)90082-sopenalex-snapshot
Signals from the notochord and floor plate regulate the region-specific expression of two Pax genes in the developing spinal cord
inferredcites →https://doi.org/10.1016/0925-4773(95)00426-2openalex-snapshot
The developmental relationships of the neural tube and the notochord: short and long term effects of the notochord on the dorsal spinal cord
inferredcites →https://doi.org/10.1016/0925-4773(96)00505-9openalex-snapshot
The murine homeobox gene Msx-3 shows highly restricted expression in the developing neural tube
inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.157openalex-snapshot
Direct regulation of the Nrarp gene promoter by the Notch signaling pathway
inferredcites →https://doi.org/10.1016/j.devcel.2004.08.007openalex-snapshot
Gene-Regulatory Interactions in Neural Crest Evolution and Development
inferredcites →https://doi.org/10.1016/s0925-4773(00)00480-9openalex-snapshot
A novel member of the Xenopus Zic family, Zic5, mediates neural crest development
inferredcites →https://doi.org/10.1016/s0925-4773(00)00569-4openalex-snapshot
Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf
inferredcites →https://doi.org/10.1016/s0925-4773(97)00065-8openalex-snapshot
Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene
inferredcites →https://doi.org/10.1016/s0925-4773(99)00013-1openalex-snapshot
Establishment and maintenance of the border of the neural plate in the chick: involvement of FGF and BMP activity
inferredcites →https://doi.org/10.1038/376331a0openalex-snapshot
Induction of epidermis and inhibition of neural fate by Bmp-4
inferredcites →https://doi.org/10.1038/74231openalex-snapshot
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
inferredcites →https://doi.org/10.1038/nrg819openalex-snapshot
Induction of the neural crest: a multigene process
inferredcites →https://doi.org/10.1073/pnas.0237226100openalex-snapshot
Induction of neural crest in Xenopus by transcription factor AP2α
inferredcites →https://doi.org/10.1073/pnas.91.9.3685openalex-snapshot
Molecular basis of splotch and Waardenburg Pax-3 mutations.
inferredcites →https://doi.org/10.1073/pnas.94.25.13713openalex-snapshot
Regulation of dorsal fate in the neuraxis by Wnt-1 and Wnt-3a
inferredcites →https://doi.org/10.1093/hmg/ddg107openalex-snapshot
Sox10 and Pax3 physically interact to mediate activation of a conserved c-RET enhancer
inferredcites →https://doi.org/10.1101/gad.301004openalex-snapshot
Divergent functions of murine Pax3 and Pax7 in limb muscle development
inferredcites →https://doi.org/10.1126/science.1070824openalex-snapshot
Ectodermal Wnt Function as a Neural Crest Inducer
inferredcites →https://doi.org/10.1126/science.7513443openalex-snapshot
Control of Cell Behavior During Vertebrate Development by Slug , a Zinc Finger Gene
inferredcites →https://doi.org/10.1172/jci10828openalex-snapshot
Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret
inferredcites →https://doi.org/10.1242/dev.00238openalex-snapshot
Snail precedes Slug in the genetic cascade required for the specification and migration of the Xenopus neural crest
inferredcites →https://doi.org/10.1242/dev.00531openalex-snapshot
Neural crest induction by paraxial mesoderm inXenopusembryos requires FGF signals
inferredcites →https://doi.org/10.1242/dev.00878openalex-snapshot
Regulation of Msx genes by a Bmp gradient is essential for neural crest specification
inferredcites →https://doi.org/10.1242/dev.01007openalex-snapshot
Reiterated Wnt signaling during zebrafish neural crest development
inferredcites →https://doi.org/10.1242/dev.01129openalex-snapshot
Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation
inferredcites →https://doi.org/10.1242/dev.111.4.1045openalex-snapshot
Xwnt-8, a Xenopus Wnt-1/int-1-related gene responsive to mesoderminducing growth factors, may play a role in ventral mesodermal patterning during embryogenesis
inferredcites →https://doi.org/10.1242/dev.117.3.1001openalex-snapshot
Signals from the notochord and floor plate regulate the region-specific expression of two Pax genes in the developing spinal cord
inferredcites →https://doi.org/10.1242/dev.121.2.525openalex-snapshot
Origins of the avian neural crest: the role of neural plate-epidermal interactions
inferredcites →https://doi.org/10.1242/dev.124.10.2075openalex-snapshot
Expression of Pax-3 is initiated in the early neural plate by posteriorizing signals produced by the organizer and by posterior non-axial mesoderm
inferredcites →https://doi.org/10.1242/dev.124.12.2477openalex-snapshot
Mechanisms of dorsal-ventral patterning in noggin-induced neural tissue
inferredcites →https://doi.org/10.1242/dev.124.16.3037openalex-snapshot
Xenopus msx1 mediates epidermal induction and neural inhibition by BMP4
inferredcites →https://doi.org/10.1242/dev.125.13.2403openalex-snapshot
Neural crest induction in Xenopus: evidence for a two-signal model
inferredcites →https://doi.org/10.1242/dev.125.14.2687openalex-snapshot
Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis
inferredcites →https://doi.org/10.1242/dev.125.4.579openalex-snapshot
Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction
inferredcites →https://doi.org/10.1242/dev.128.14.2769openalex-snapshot
Suppression of head formation by Xmsx-1 through the inhibition of intracellular nodal signaling
inferredcites →https://doi.org/10.1242/dev.128.19.3655openalex-snapshot
A role for frizzled 3 in neural crest development
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4669820openalex-extracted
Dyrk1a is Required for Craniofacial Development in Xenopus Laevis
inferred← citeshttps://doi.org/10.1002/9781118492833.ch13openalex-snapshot
Development of Neural Tissues inXenopus laevis
inferred← citeshttps://doi.org/10.1002/9781118498026.ch1openalex-snapshot
Molecular Blueprint for Craniofacial Morphogenesis and Development
inferred← citeshttps://doi.org/10.1002/ajmg.a.31965openalex-snapshot
Sequence evaluation of FGF and FGFR gene conserved non‐coding elements in non‐syndromic cleft lip and palate cases
inferred← citeshttps://doi.org/10.1002/ajmg.a.33454openalex-snapshot
Craniofacial birth defects: The role of neural crest cells in the etiology and pathogenesis of Treacher Collins syndrome and the potential for prevention
inferred← citeshttps://doi.org/10.1002/bdr2.1644openalex-snapshot
The role of teratogens in neural crest development
inferred← citeshttps://doi.org/10.1002/bdr2.1802openalex-snapshot
Role of epigenetics and miRNAs in orofacial clefts
inferred← citeshttps://doi.org/10.1002/bdrc.20149openalex-snapshot
Gene regulatory networks in embryonic stem cells and brain development
inferred← citeshttps://doi.org/10.1002/bies.20775openalex-snapshot
Do vertebrate neural crest and cranial placodes have a common evolutionary origin?
inferred← citeshttps://doi.org/10.1002/cne.22548openalex-snapshot
Embryonic genoarchitecture of the pretectum in Xenopus laevis: A conserved pattern in tetrapods
inferred← citeshttps://doi.org/10.1002/dneu.22173openalex-snapshot
Transcription factor AP2 epsilon (Tfap2e) regulates neural crest specification in xenopus
inferred← citeshttps://doi.org/10.1002/dvdy.21098openalex-snapshot
Emerging roles for zic genes in early development
inferred← citeshttps://doi.org/10.1002/dvdy.21152openalex-snapshot
Xenopus hairy2 functions in neural crest formation by maintaining cells in a mitotic and undifferentiated state
inferred← citeshttps://doi.org/10.1002/dvdy.21384openalex-snapshot
Midkine‐b regulates cell specification at the neural plate border in zebrafish
inferred← citeshttps://doi.org/10.1002/dvdy.21881openalex-snapshot
Comprehensive spatiotemporal analysis of early chick neural crest network genes
inferred← citeshttps://doi.org/10.1002/dvdy.22028openalex-snapshot
Diversification of the expression patterns and developmental functions of the dishevelled gene family during chordate evolution
inferred← citeshttps://doi.org/10.1002/dvdy.22079openalex-snapshot
Cardiac neural crest and outflow tract defects in Lrp6 mutant mice
inferred← citeshttps://doi.org/10.1002/dvdy.24034openalex-snapshot
Role of Sp5 as an essential early regulator of neural crest specification in xenopus
inferred← citeshttps://doi.org/10.1002/dvdy.24295openalex-snapshot
Functional analysis of Hairy genes in Xenopus neural crest initial specification and cell migration
inferred← citeshttps://doi.org/10.1002/dvdy.70130openalex-snapshot
Role of SoxE transcription factors in development and disease
inferred← citeshttps://doi.org/10.1002/dvg.20436openalex-snapshot
Evolution of the neural crest viewed from a gene regulatory perspective
inferred← citeshttps://doi.org/10.1002/dvg.22403openalex-snapshot
Gene regulatory evolution and the origin of macroevolutionary novelties: Insights from the neural crest
inferred← citeshttps://doi.org/10.1002/dvg.22841openalex-snapshot
Xhe2 is a member of the astacin family of metalloproteases that promotes X enopus hatching
inferred← citeshttps://doi.org/10.1002/dvg.22883openalex-snapshot
Neural crest specification by Prohibitin1 depends on transcriptional regulation of prl3 and vangl1
inferred← citeshttps://doi.org/10.1002/dvg.23082openalex-snapshot
Znf703, a novel target of Pax3 and Zic1, regulates hindbrain and neural crest development in Xenopus
inferred← citeshttps://doi.org/10.1002/dvg.23276openalex-snapshot
Specification and formation of the neural crest: Perspectives on lineage segregation
inferred← citeshttps://doi.org/10.1002/dvg.23445openalex-snapshot
Genetic interaction of Pax3 mutation and canonical Wnt signaling modulates neural tube defects and neural crest abnormalities
inferred← citeshttps://doi.org/10.1002/jat.4263openalex-snapshot
Gene expression profiles of multiple brain regions in rats differ between developmental and postpubertal exposure to valproic acid
inferred← citeshttps://doi.org/10.1002/wdev.142openalex-snapshot
Early embryonic specification of vertebrate cranial placodes
inferred← citeshttps://doi.org/10.1002/wdev.322openalex-snapshot
Specifying neural crest cells: From chromatin to morphogens and factors in between
inferred← citeshttps://doi.org/10.1002/wdev.76openalex-snapshot
Signaling and transcriptional regulation in neural crest specification and migration: lessons from xenopus embryos
inferred← citeshttps://doi.org/10.1002/wdev.8openalex-snapshot
Neural crest specification: tissues, signals, and transcription factors
inferred← citeshttps://doi.org/10.1007/978-0-387-46954-6_14openalex-snapshot
Molecular Bases of Human Neurocristopathies
inferred← citeshttps://doi.org/10.1007/978-1-4614-3801-4_5openalex-snapshot
Neural Crest Formation and Diversification
inferred← citeshttps://doi.org/10.1007/978-3-030-46024-2_8openalex-snapshot
Fundamental Mechanisms of Orofacial Clefts
inferred← citeshttps://doi.org/10.1007/978-3-031-36962-9_276-1openalex-snapshot
Fundamentals of Embryology in Maxillofacial Development
inferred← citeshttps://doi.org/10.1007/978-4-431-54634-4_17openalex-snapshot
The Role of Tsukushi as an Extracellular Signaling Coordinator
inferred← citeshttps://doi.org/10.1007/978-94-007-2801-1_16openalex-snapshot
Neural Crest and Hirschsprung’s Disease
inferred← citeshttps://doi.org/10.1007/s00018-012-0991-8openalex-snapshot
Current perspectives of the signaling pathways directing neural crest induction
inferred← citeshttps://doi.org/10.1007/s00018-013-1285-5openalex-snapshot
The ZIC gene family encodes multi-functional proteins essential for patterning and morphogenesis
inferred← citeshttps://doi.org/10.1007/s00018-018-2974-xopenalex-snapshot
Hindbrain induction and patterning during early vertebrate development
inferred← citeshttps://doi.org/10.1007/s00441-017-2747-0openalex-snapshot
Neuroblastoma pathogenesis: deregulation of embryonic neural crest development
inferred← citeshttps://doi.org/10.1007/s12032-021-01639-yopenalex-snapshot
Bioinformatics analysis of recurrent deletion regions in neuroblastoma
inferred← citeshttps://doi.org/10.1007/s12035-014-8639-3openalex-snapshot
Roles for the TGFβ Superfamily in the Development and Survival of Midbrain Dopaminergic Neurons
inferred← citeshttps://doi.org/10.1007/s13577-025-01292-xopenalex-snapshot
Generation of human induced pluripotent stem cell lines derived from Wolf–Hirschhorn syndrome patients with chromosomal 4p deletion
inferred← citeshttps://doi.org/10.1016/b978-0-12-381332-9.00020-7openalex-snapshot
Role of Cardiac Neural Crest Cells in Morphogenesis of the Heart and Great Vessels
inferred← citeshttps://doi.org/10.1016/b978-0-12-397266-8.00036-3openalex-snapshot
Neuronal Migration and Brain Patterning
inferred← citeshttps://doi.org/10.1016/b978-0-12-401730-6.00002-8openalex-snapshot
Induction and Specification of Neural Crest Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-405945-0.00019-3openalex-snapshot
Development of the Pre-Placodal Ectoderm and Cranial Sensory Placodes
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.00004-0openalex-snapshot
Neural Crest Stem Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-817988-8.00011-7openalex-snapshot
Current insights into neural crest cell development and pathologies
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2014.11.009openalex-snapshot
Transcriptional Regulation of Cranial Sensory Placode Development
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2020.04.002openalex-snapshot
Cell fate decisions during the development of the peripheral nervous system in the vertebrate head
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2021.03.002openalex-snapshot
Xenopus, an emerging model for studying pathologies of the neural crest
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.01.015openalex-snapshot
Making developmental sense of the senses, their origin and function
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2010.09.002openalex-snapshot
Association of Wnt3A gene variants with non-syndromic cleft lip with or without cleft palate in Chinese population
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2008.03.006openalex-snapshot
Gene regulatory networks that control the specification of neural-crest cells in the lamprey
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2014.04.023openalex-snapshot
Induction and dorsal restriction of Paired-box 3 (Pax3) gene expression in the caudal neuroectoderm is mediated by integration of multiple pathways on a short neural crest enhancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.02.135openalex-snapshot
Normal forebrain development may require continual Wnt antagonism until mid-somitogenesis in zebrafish
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.05.104openalex-snapshot
Role of the Rap2/TNIK kinase pathway in regulation of LRP6 stability for Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.12.127openalex-snapshot
Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus
inferred← citeshttps://doi.org/10.1016/j.bone.2020.115409openalex-snapshot
The development, patterning and evolution of neural crest cell differentiation into cartilage and bone
inferred← citeshttps://doi.org/10.1016/j.ceb.2006.09.003openalex-snapshot
Development of the neural crest: achieving specificity in regulatory pathways
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.03.025openalex-snapshot
Modeling Neural Crest Induction, Melanocyte Specification, and Disease-Related Pigmentation Defects in hESCs and Patient-Specific iPSCs
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109289openalex-snapshot
BMP signaling is enhanced intracellularly by FHL3 controlling WNT-dependent spatiotemporal emergence of the neural crest
inferred← citeshttps://doi.org/10.1016/j.crvi.2007.04.004openalex-snapshot
Neural crest progenitors and stem cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.08.005openalex-snapshot
Ancient Evolutionary Origin of the Neural Crest Gene Regulatory Network
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.07.006openalex-snapshot
Extracellular Matrix Protein Anosmin Promotes Neural Crest Formation and Regulates FGF, BMP, and WNT Activities
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.02.006openalex-snapshot
Pax3 and Pax7 Play Essential Safeguard Functions against Environmental Stress-Induced Birth Defects
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.06.024openalex-snapshot
Axud1 Integrates Wnt Signaling and Transcriptional Inputs to Drive Neural Crest Formation
inferred← citeshttps://doi.org/10.1016/j.diff.2010.01.003openalex-snapshot
Involvement of Neptune in induction of the hatching gland and neural crest in the Xenopus embryo
inferred← citeshttps://doi.org/10.1016/j.gde.2006.06.006openalex-snapshot
Development and evolution of the migratory neural crest: a gene regulatory perspective
inferred← citeshttps://doi.org/10.1016/j.gendis.2014.09.005openalex-snapshot
Fibroblast growth factor (FGF) signaling in development and skeletal diseases
inferred← citeshttps://doi.org/10.1016/j.gene.2018.04.087openalex-snapshot
The expression and function of PAX3 in development and disease
inferred← citeshttps://doi.org/10.1016/j.humpath.2016.04.009openalex-snapshot
Biphenotypic sinonasal sarcoma: an expanded immunoprofile including consistent nuclear β-catenin positivity and absence of SOX10 expression
inferred← citeshttps://doi.org/10.1016/j.jid.2017.05.038openalex-snapshot
MSX1-Induced Neural Crest-Like Reprogramming Promotes Melanoma Progression
inferred← citeshttps://doi.org/10.1016/j.mod.2017.08.002openalex-snapshot
Neural crest and cancer: Divergent travelers on similar paths
inferred← citeshttps://doi.org/10.1016/j.mod.2018.07.010openalex-snapshot
Gli2 is required for the induction and migration of Xenopus laevis neural crest
inferred← citeshttps://doi.org/10.1016/j.modgep.2005.11.011openalex-snapshot
Expression of TFAP2β and TFAP2γ genes in Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2013.07.002openalex-snapshot
BMP-Smad 1/5/8 signalling in the development of the nervous system
inferred← citeshttps://doi.org/10.1016/j.semcdb.2005.06.001openalex-snapshot
Genetic network during neural crest induction: From cell specification to cell survival
inferred← citeshttps://doi.org/10.1016/j.semcdb.2005.06.003openalex-snapshot
How to become neural crest: From segregation to delamination
inferred← citeshttps://doi.org/10.1016/j.semcdb.2005.06.007openalex-snapshot
Specification of neural crest cell formation and migration in mouse embryos
inferred← citeshttps://doi.org/10.1016/j.semcdb.2005.06.008openalex-snapshot
Reiterated Wnt and BMP signals in neural crest development
inferred← citeshttps://doi.org/10.1016/j.semcdb.2012.03.010openalex-snapshot
What is bad in cancer is good in the embryo: Importance of EMT in neural crest development
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.09.015openalex-snapshot
PAX transcription factors in neural crest development
inferred← citeshttps://doi.org/10.1016/j.stem.2015.03.008openalex-snapshot
β-Catenin Regulates Primitive Streak Induction through Collaborative Interactions with SMAD2/SMAD3 and OCT4
inferred← citeshttps://doi.org/10.1016/j.tig.2005.09.001openalex-snapshot
msh/Msx gene family in neural development
inferred← citeshttps://doi.org/10.1016/j.tranon.2019.07.001openalex-snapshot
Emerging Pathogenic and Prognostic Significance of Paired Box 3 (PAX3) Protein in Adult Gliomas
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.02.041openalex-snapshot
Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.03.001openalex-snapshot
Zebrafish msxB, msxC and msxE function together to refine the neural–nonneural border and regulate cranial placodes and neural crest development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.03.009openalex-snapshot
Induction and specification of cranial placodes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.06.015openalex-snapshot
Neural induction in Xenopus requires inhibition of Wnt-β-catenin signaling
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.06.037openalex-snapshot
Frizzled7 mediates canonical Wnt signaling in neural crest induction
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.07.034openalex-snapshot
Components of both major axial patterning systems of the Bilateria are differentially expressed along the primary axis of a ‘radiate’ animal, the anthozoan cnidarian Acropora millepora
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.12.042openalex-snapshot
Redundant activities of Tfap2a and Tfap2c are required for neural crest induction and development of other non-neural ectoderm derivatives in zebrafish embryos
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.02.016openalex-snapshot
Prediction and characterisation of a highly conserved, remote and cAMP responsive enhancer that regulates Msx1 gene expression in cardiac neural crest and outflow tract
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.02.058openalex-snapshot
Sequential actions of Pax3 and Pax7 drive xanthophore development in zebrafish neural crest
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.08.003openalex-snapshot
Hairy2–Id3 interactions play an essential role in Xenopus neural crest progenitor specification
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.08.007openalex-snapshot
A new role for the Endothelin-1/Endothelin-A receptor signaling during early neural crest specification
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.11.024openalex-snapshot
Xenopus Meis3 protein lies at a nexus downstream to Zic1 and Pax3 proteins, regulating multiple cell-fates during early nervous system development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.01.013openalex-snapshot
A divergent Tbx6-related gene and Tbx6 are both required for neural crest and intermediate mesoderm development in Xenopus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.01.022openalex-snapshot
The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.04.029openalex-snapshot
Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.03.010openalex-snapshot
FGF8 signaling is chemotactic for cardiac neural crest cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.09.019openalex-snapshot
Tfap2a and Foxd3 regulate early steps in the development of the neural crest progenitor population
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.10.019openalex-snapshot
Influence of mesodermal Fgf8 on the differentiation of neural crest-derived postganglionic neurons
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.11.016openalex-snapshot
Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.01.013openalex-snapshot
Neural crest induction at the neural plate border in vertebrates
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.02.029openalex-snapshot
Early neural crest induction requires an initial inhibition of Wnt signals
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.02.038openalex-snapshot
Specification of neural crest into sensory neuron and melanocyte lineages
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.03.014openalex-snapshot
Induction of the neural crest state: Control of stem cell attributes by gene regulatory, post-transcriptional and epigenetic interactions
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.06.028openalex-snapshot
The peripheral sensory nervous system in the vertebrate head: A gene regulatory perspective
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.09.006openalex-snapshot
FGF signaling transforms non-neural ectoderm into neural crest
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.11.035openalex-snapshot
A novel FoxD3 gene trap line reveals neural crest precursor movement and a role for FoxD3 in their specification
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.11.027openalex-snapshot
Setting appropriate boundaries: Fate, patterning and competence at the neural plate border
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.12.010openalex-snapshot
Pax3 and Zic1 trigger the early neural crest gene regulatory network by the direct activation of multiple key neural crest specifiers
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.12.011openalex-snapshot
Identification of Pax3 and Zic1 targets in the developing neural crest
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.01.019openalex-snapshot
The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.02.011openalex-snapshot
Establishing the pre-placodal region and breaking it into placodes with distinct identities
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.09.034openalex-snapshot
Epigenetic regulation in neural crest development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.12.028openalex-snapshot
The requirement of histone modification by PRDM12 and Kdm4a for the development of pre-placodal ectoderm and neural crest in Xenopus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.01.014openalex-snapshot
Hmga2 is required for neural crest cell specification in Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.06.017openalex-snapshot
Epigenetics in ENS development and Hirschsprung disease
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.09.006openalex-snapshot
Neural crest stem cells and their potential therapeutic applications
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.02.020openalex-snapshot
Characterization of Pax3 and Sox10 transgenic Xenopus laevis embryos as tools to study neural crest development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.05.018openalex-snapshot
The neural border: Induction, specification and maturation of the territory that generates neural crest cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.05.023openalex-snapshot
AKT signaling displays multifaceted functions in neural crest development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.12.015openalex-snapshot
Heparan sulfate proteoglycans regulate BMP signalling during neural crest induction
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.08.013openalex-snapshot
Mcrs1 interacts with Six1 to influence early craniofacial and otic development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.03.024openalex-snapshot
Altered sacral neural crest development in Pax3 spina bifida mutants underlies deficits of bladder innervation and function
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.08.002openalex-snapshot
Zebrafish Cdx4 regulates neural crest cell specification and migratory behaviors in the posterior body
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.12.015openalex-snapshot
An efficient miRNA knockout approach using CRISPR-Cas9 in Xenopus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.09.008openalex-snapshot
Ash2l, an obligatory component of H3K4 methylation complexes, regulates neural crest development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2024.04.004openalex-snapshot
Dyrk1a is required for craniofacial development in Xenopus laevis.
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.10.003openalex-snapshot
MicroRNA miR-219 is required for neural border and neural crest development in Xenopus neurulas
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.12.008openalex-snapshot
The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta–Notch pathway in neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.zool.2009.06.001openalex-snapshot
The evolutionary origin of the vertebrate neural crest and its developmental gene regulatory network – insights from amphioxus
inferred← citeshttps://doi.org/10.1016/s0070-2153(05)73001-5openalex-snapshot
The Molecular Origins of Species‐Specific Facial Pattern
inferred← citeshttps://doi.org/10.1016/s1574-3349(06)17006-4openalex-snapshot
Multiple roles for Wnt signaling in the development of the vertebrate neural crest
inferred← citeshttps://doi.org/10.1038/cr.2012.122openalex-snapshot
AP2γ regulates neural and epidermal development downstream of the BMP pathway at early stages of ectodermal patterning
inferred← citeshttps://doi.org/10.1038/emboj.2009.313openalex-snapshot
Self‐regulation of Stat3 activity coordinates cell‐cycle progression and neural crest specification
inferred← citeshttps://doi.org/10.1038/nature04684openalex-snapshot
Specification of the neural crest occurs during gastrulation and requires Pax7
inferred← citeshttps://doi.org/10.1038/ncomms6953openalex-snapshot
PFKFB4 controls embryonic patterning via Akt signalling independently of glycolysis
inferred← citeshttps://doi.org/10.1038/ncomms8476openalex-snapshot
Zic1 controls placode progenitor formation non-cell autonomously by regulating retinoic acid production and transport
inferred← citeshttps://doi.org/10.1038/nrm2428openalex-snapshot
A gene regulatory network orchestrates neural crest formation
inferred← citeshttps://doi.org/10.1038/nrn1805openalex-snapshot
Bone morphogenetic protein signalling and vertebrate nervous system development
inferred← citeshttps://doi.org/10.1038/s41418-022-00956-7openalex-snapshot
Genome-wide screening for deubiquitinase subfamily identifies ubiquitin-specific protease 49 as a novel regulator of odontogenesis
inferred← citeshttps://doi.org/10.1038/s41467-025-62003-6openalex-snapshot
Determination of trunk neural crest cell fate and susceptibility to splicing perturbation by the DLC1-SF3B1-PHF5A splicing complex
inferred← citeshttps://doi.org/10.1038/s41467-026-68647-2openalex-snapshot
NR6A1 is essential for neural crest cell specification, formation and survival
inferred← citeshttps://doi.org/10.1038/s41559-024-02476-8openalex-snapshot
Shared features of blastula and neural crest stem cells evolved at the base of vertebrates
inferred← citeshttps://doi.org/10.1038/s41583-021-00503-2openalex-snapshot
Riding the crest to get a head: neural crest evolution in vertebrates
inferred← citeshttps://doi.org/10.1038/s41598-018-19579-5openalex-snapshot
Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling
inferred← citeshttps://doi.org/10.1038/s41598-022-27293-6openalex-snapshot
Chromatin remodeler CHD7 targets active enhancer region to regulate cell type-specific gene expression in human neural crest cells
inferred← citeshttps://doi.org/10.1038/srep07750openalex-snapshot
A novel function for Egr4 in posterior hindbrain development
inferred← citeshttps://doi.org/10.1038/srep43173openalex-snapshot
Nicotinic acid inhibits glioma invasion by facilitating Snail1 degradation
inferred← citeshttps://doi.org/10.1042/bst20211152openalex-snapshot
Shaping axial identity during human pluripotent stem cell differentiation to neural crest cells
inferred← citeshttps://doi.org/10.1042/cbi20090133openalex-snapshot
Wnt‐3 and Wnt‐3a play different region‐specific roles in neural crest development in avians
inferred← citeshttps://doi.org/10.1051/medsci/20153108007openalex-snapshot
Pax3 et Pax7 : gardiens du développement craniofacial
inferred← citeshttps://doi.org/10.1073/pnas.0806009105openalex-snapshot
Dissecting early regulatory relationships in the lamprey neural crest gene network
inferred← citeshttps://doi.org/10.1073/pnas.1010740107openalex-snapshot
Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network
inferred← citeshttps://doi.org/10.1073/pnas.1219124110openalex-snapshot
Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos
inferred← citeshttps://doi.org/10.1073/pnas.2311685121openalex-snapshot
A time-resolved single-cell roadmap of the logic driving anterior neural crest diversification from neural border to migration stages
inferred← citeshttps://doi.org/10.1074/jbc.m112.356394openalex-snapshot
Caudal-related Homeobox (Cdx) Protein-dependent Integration of Canonical Wnt Signaling on Paired-box 3 (Pax3) Neural Crest Enhancer
inferred← citeshttps://doi.org/10.1074/jbc.m115.644864openalex-snapshot
The Proto-oncogene Transcription Factor Ets1 Regulates Neural Crest Development through Histone Deacetylase 1 to Mediate Output of Bone Morphogenetic Protein Signaling
inferred← citeshttps://doi.org/10.1074/jbc.m512449200openalex-snapshot
Regulation of Murine TGFβ2 by Pax3 during Early Embryonic Development
inferred← citeshttps://doi.org/10.1080/15592294.2016.1226739openalex-snapshot
Stage 4S neuroblastoma tumors show a characteristic DNA methylation portrait
inferred← citeshttps://doi.org/10.1080/23262133.2017.1292783openalex-snapshot
Signaling pathways and tissue interactions in neural plate border formation
inferred← citeshttps://doi.org/10.1083/jcb.201709149openalex-snapshot
Draxin acts as a molecular rheostat of canonical Wnt signaling to control cranial neural crest EMT
inferred← citeshttps://doi.org/10.1089/scd.2017.0234openalex-snapshot
A Novel Human Pluripotent Stem Cell-Derived Neural Crest Model of Treacher Collins Syndrome Shows Defects in Cell Death and Migration
inferred← citeshttps://doi.org/10.1091/mbc.e05-03-0210openalex-snapshot
Dynamic Alterations in Gene Expression after Wnt-mediated Induction of Avian Neural Crest
inferred← citeshttps://doi.org/10.1091/mbc.e06-11-1047openalex-snapshot
The Activity of Pax3 and Zic1 Regulates Three Distinct Cell Fates at the Neural Plate Border
inferred← citeshttps://doi.org/10.1091/mbc.e08-03-0325openalex-snapshot
Tumor Necrosis Factor-Receptor–associated Factor-4 Is a Positive Regulator of Transforming Growth Factor-β Signaling That Affects Neural Crest Formation
inferred← citeshttps://doi.org/10.1093/jmcb/mjv052openalex-snapshot
FGF8 signaling sustains progenitor status and multipotency of cranial neural crest-derived mesenchymal cellsin vivoandin vitro
inferred← citeshttps://doi.org/10.1093/molbev/msm228openalex-snapshot
Conservation and Diversification of Msx Protein in Metazoan Evolution
inferred← citeshttps://doi.org/10.1093/molbev/msr114openalex-snapshot
Lack of In Vivo Functional Compensation Between Pax Family Groups II and III in Rodents
inferred← citeshttps://doi.org/10.1093/neuonc/nou268.12openalex-snapshot
PM-12 * Pax3 EXPRESSION ENHANCES PDGF-B-INDUCED BRAINSTEM GLIOMAGENESIS AND CHARACTERIZES A SUBSET OF BRAINSTEM GLIOMA
inferred← citeshttps://doi.org/10.1101/191056openalex-snapshot
Reconstruction of developmental landscapes by optimal-transport analysis of single-cell gene expression sheds light on cellular reprogramming
inferred← citeshttps://doi.org/10.1101/2021.10.06.463249openalex-snapshot
CHD8 -associated gastrointestinal complaints are caused by impaired vagal neural crest development and homeostatic imbalance
inferred← citeshttps://doi.org/10.1101/2022.03.23.485460openalex-snapshot
From neural border to migratory stage: A comprehensive single cell roadmap of the timing and regulatory logic driving cranial and vagal neural crest emergence
inferred← citeshttps://doi.org/10.1101/2025.07.28.667246openalex-snapshot
A novel function for Prdm12 during neural crest migration reveals a link between Wnt and N-cadherin
inferred← citeshttps://doi.org/10.1101/gr.161182.113openalex-snapshot
Transcriptome analysis reveals novel players in the cranial neural crest gene regulatory network
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2005.00473.xopenalex-snapshot
Relations and interactions between cranial mesoderm and neural crest populations
inferred← citeshttps://doi.org/10.1111/j.1600-0714.2007.00553.xopenalex-snapshot
Cranial suture biology and dental development: genetic and clinical perspectives
inferred← citeshttps://doi.org/10.1111/j.1601-0825.2005.01176.xopenalex-snapshot
FGF signalling in craniofacial development and developmental disorders
inferred← citeshttps://doi.org/10.1111/j.1755-148x.2008.00506.xopenalex-snapshot
The making of a melanocyte: the specification of melanoblasts from the neural crest
inferred← citeshttps://doi.org/10.1111/pcmr.13178openalex-snapshot
Xenopus as a model system for studying pigmentation and pigmentary disorders
inferred← citeshttps://doi.org/10.1126/sciadv.aaz1469openalex-snapshot
The vertebrate-specific VENTX/NANOG gene empowers neural crest with ectomesenchyme potential
inferred← citeshttps://doi.org/10.1126/science.aaa3655openalex-snapshot
Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells
inferred← citeshttps://doi.org/10.1134/s002689330702001xopenalex-snapshot
Neural induction: New achievements and prospects
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.042308.113245openalex-snapshot
Assembling Neural Crest Regulatory Circuits into a Gene Regulatory Network
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.22.010305.103814openalex-snapshot
Neural Crest Stem and Progenitor Cells
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.23.090506.123438openalex-snapshot
The Role ofPaxGenes in the Development of Tissues and Organs:Pax3andPax7Regulate Muscle Progenitor Cell Functions
inferred← citeshttps://doi.org/10.1155/2018/1095459openalex-snapshot
PAX3: A Molecule with Oncogenic or Tumor Suppressor Function Is Involved in Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-25-5299openalex-snapshot
GNAQ Induces Melanomagenesis in Mitfa-Independent Melanocyte Progenitors in a Zebrafish Model of Uveal Melanoma
inferred← citeshttps://doi.org/10.1159/000084506openalex-snapshot
Regulatory Mechanisms for Neural Crest Formation
inferred← citeshttps://doi.org/10.1159/000088130openalex-snapshot
Specification and Patterning of Neural Crest Cells During Craniofacial Development
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