scholarly article | Q13442814 |
P356 | DOI | 10.1002/WDEV.142 |
P698 | PubMed publication ID | 25124756 |
P2093 | author name string | Gerhard Schlosser | |
P2860 | cites work | Molecular anatomy of placode development in Xenopus laevis | Q47273875 |
Initiation of neural induction by FGF signalling before gastrulation. | Q47845943 | ||
Time of exposure to BMP signals plays a key role in the specification of the olfactory and lens placodes ex vivo | Q48117502 | ||
Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm | Q48668204 | ||
Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis | Q48705949 | ||
Origin and segregation of cranial placodes in Xenopus laevis | Q48850036 | ||
Progressive restriction of otic fate: the role of FGF and Wnt in resolving inner ear potential. | Q50776563 | ||
Wnt-regulated temporal control of BMP exposure directs the choice between neural plate border and epidermal fate. | Q51945248 | ||
Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm. | Q51979531 | ||
Lens specification is the ground state of all sensory placodes, from which FGF promotes olfactory identity. | Q52005744 | ||
An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation. | Q52042524 | ||
Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor. | Q52085976 | ||
The protooncogene c-myc is an essential regulator of neural crest formation in xenopus. | Q52104498 | ||
Analysis of spatial and temporal gene expression patterns in blastula and gastrula stage chick embryos. | Q52120947 | ||
Inhibitory patterning of the anterior neural plate in Xenopus by homeodomain factors Dlx3 and Msx1. | Q52175343 | ||
Neural induction: 10 years on since the 'default model'. | Q36625558 | ||
The eyes absent family of phosphotyrosine phosphatases: properties and roles in developmental regulation of transcription | Q36752910 | ||
Differential BMP signaling controls formation and differentiation of multipotent preplacodal ectoderm progenitors from human embryonic stem cells | Q37016339 | ||
BMP inhibition initiates neural induction via FGF signaling and Zic genes. | Q37394829 | ||
Neural induction and factors that stabilize a neural fate | Q37596311 | ||
Canonical Wnt signaling is required for ophthalmic trigeminal placode cell fate determination and maintenance | Q37698498 | ||
From shared lineage to distinct functions: the development of the inner ear and epibranchial placodes. | Q37749102 | ||
Making senses development of vertebrate cranial placodes | Q37783809 | ||
Parallels between neuron and lens fiber cell structure and molecular regulatory networks | Q38013940 | ||
The peripheral sensory nervous system in the vertebrate head: a gene regulatory perspective | Q38025839 | ||
Neural induction and early patterning in vertebrates. | Q38135361 | ||
Setting appropriate boundaries: fate, patterning and competence at the neural plate border. | Q38169872 | ||
Establishing the pre-placodal region and breaking it into placodes with distinct identities | Q38191727 | ||
Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion | Q38289851 | ||
Transcription factor AP-2 is an essential and direct regulator of epidermal development in Xenopus | Q38289930 | ||
Neural crest determination by co-activation of Pax3 and Zic1 genes in Xenopus ectoderm | Q38327715 | ||
Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction. | Q38330996 | ||
Dlx proteins position the neural plate border and determine adjacent cell fates | Q39517208 | ||
Activation of Six1 target genes is required for sensory placode formation | Q39944176 | ||
Fine-grained fate maps for the ophthalmic and maxillomandibular trigeminal placodes in the chick embryo. | Q40110265 | ||
The Genesis of Neural Crest and Epidermal Placodes: A Reinterpretation of Vertebrate Origins | Q40152120 | ||
Integration of IGF, FGF, and anti-BMP signals via Smad1 phosphorylation in neural induction | Q40385522 | ||
A balance of FGF, BMP and WNT signalling positions the future placode territory in the head | Q40398079 | ||
Segregation of lens and olfactory precursors from a common territory: cell sorting and reciprocity of Dlx5 and Pax6 expression. | Q40500216 | ||
Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals. | Q40584140 | ||
Extensive cell movements accompany formation of the otic placode | Q40634813 | ||
Eya1-Six1 interaction is sufficient to induce hair cell fate in the cochlea by activating Atoh1 expression in cooperation with Sox2. | Q41485484 | ||
Specification of functional cranial placode derivatives from human pluripotent stem cells | Q41863431 | ||
Xenopus Sox3 activates sox2 and geminin and indirectly represses Xvent2 expression to induce neural progenitor formation at the expense of non-neural ectodermal derivatives | Q41896090 | ||
Neural tube derived Wnt signals cooperate with FGF signaling in the formation and differentiation of the trigeminal placodes | Q41914000 | ||
Specification of GnRH-1 neurons by antagonistic FGF and retinoic acid signaling. | Q41989080 | ||
Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning. | Q42050037 | ||
Differential requirements of BMP and Wnt signalling during gastrulation and neurulation define two steps in neural crest induction | Q42067316 | ||
A BMP regulatory network controls ectodermal cell fate decisions at the neural plate border | Q42542456 | ||
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning | Q42743132 | ||
The BMP signaling gradient patterns dorsoventral tissues in a temporally progressive manner along the anteroposterior axis | Q43074864 | ||
Cooperative interaction of Xvent-2 and GATA-2 in the activation of the ventral homeobox gene Xvent-1B. | Q43966294 | ||
Interplay between Notch signaling and the homeoprotein Xiro1 is required for neural crest induction in Xenopus embryos. | Q44697354 | ||
The zebrafish dog-eared mutation disrupts eya1, a gene required for cell survival and differentiation in the inner ear and lateral line | Q45168505 | ||
Essential role for PDGF signaling in ophthalmic trigeminal placode induction. | Q45931416 | ||
Multiple evolutionarily conserved enhancers control expression of Eya1. | Q46347689 | ||
Gonadotropin-releasing hormone (gnrh) cells arise from cranial neural crest and adenohypophyseal regions of the neural plate in the zebrafish, danio rerio | Q47073441 | ||
Specification of epibranchial placodes in zebrafish | Q47073452 | ||
pitx3 defines an equivalence domain for lens and anterior pituitary placode | Q47073484 | ||
Zebrafish msxB, msxC and msxE function together to refine the neural-nonneural border and regulate cranial placodes and neural crest development | Q47074075 | ||
Chase-and-run between adjacent cell populations promotes directional collective migration | Q27313434 | ||
Identification of early requirements for preplacodal ectoderm and sensory organ development | Q27345912 | ||
The role of Six1 in mammalian auditory system development | Q28188638 | ||
Ventral mesodermal patterning in Xenopus embryos: expression patterns and activities of BMP-2 and BMP-4 | Q28288976 | ||
Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes | Q28508554 | ||
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia | Q28587212 | ||
Neuropeptides: developmental signals in placode progenitor formation | Q28681733 | ||
The sine oculis homeobox (SIX) family of transcription factors as regulators of development and disease | Q28752140 | ||
Sensational placodes: neurogenesis in the otic and olfactory systems | Q30439054 | ||
To proliferate or to die: role of Id3 in cell cycle progression and survival of neural crest progenitors | Q30448186 | ||
Redundant activities of Tfap2a and Tfap2c are required for neural crest induction and development of other non-neural ectoderm derivatives in zebrafish embryos. | Q30496555 | ||
Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos | Q30538511 | ||
Fgf8a induces neural crest indirectly through the activation of Wnt8 in the paraxial mesoderm | Q33922679 | ||
Identification of synergistic signals initiating inner ear development. | Q33927542 | ||
Neural crest and ectodermal cells intermix in the nasal placode to give rise to GnRH-1 neurons, sensory neurons, and olfactory ensheathing cells | Q34182740 | ||
Vertebrate cranial placodes I. Embryonic induction | Q34187076 | ||
Regulation of Msx genes by a Bmp gradient is essential for neural crest specification | Q34277895 | ||
Cerberus is a head-inducing secreted factor expressed in the anterior endoderm of Spemann's organizer. | Q34392431 | ||
Neural crest origin of olfactory ensheathing glia | Q34396998 | ||
Induction of neural crest in Xenopus by transcription factor AP2alpha | Q34470119 | ||
Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network | Q34471732 | ||
Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish | Q34641625 | ||
Comparative synteny cloning of zebrafish you-too: mutations in the Hedgehog target gli2 affect ventral forebrain patterning | Q35189275 | ||
RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm | Q35768103 | ||
The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border | Q35810702 | ||
Gene-regulatory interactions in neural crest evolution and development | Q35885247 | ||
Early development of the cranial sensory nervous system: from a common field to individual placodes | Q35942303 | ||
Sox3 expression is maintained by FGF signaling and restricted to the neural plate by Vent proteins in the Xenopus embryo | Q36397987 | ||
The amniote paratympanic organ develops from a previously undiscovered sensory placode. | Q36456560 | ||
Induction and specification of cranial placodes | Q36469493 | ||
The Eyes Absent proteins in development and disease | Q36597900 | ||
P433 | issue | 5 | |
P304 | page(s) | 349-363 | |
P577 | publication date | 2014-07-02 | |
P1433 | published in | Wiley interdisciplinary reviews. Developmental biology | Q26842107 |
P1476 | title | Early embryonic specification of vertebrate cranial placodes | |
P478 | volume | 3 |