| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/DVDY.20796 |
| P8608 | Fatcat ID | release_we4orrgavfgr3ih3rhyg5ghwnu |
| P698 | PubMed publication ID | 16598716 |
| P5875 | ResearchGate publication ID | 7180476 |
| P2093 | author name string | Michael J Depew | |
| Carol A Simpson | |||
| P2860 | cites work | Bmp4 and Morphological Variation of Beaks in Darwin's Finches | Q22065814 |
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| Novel mechanism of Wnt signalling inhibition mediated by Dickkopf-1 interaction with LRP6/Arrow | Q24291392 | ||
| Head inducer Dickkopf-1 is a ligand for Wnt coreceptor LRP6 | Q24291433 | ||
| Requirement for Lim1 in head-organizer function | Q24312737 | ||
| Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain | Q24314632 | ||
| Cloning and characterization of two members of the vertebrate Dlx gene family | Q24318837 | ||
| sprouty encodes a novel antagonist of FGF signaling that patterns apical branching of the Drosophila airways | Q24336220 | ||
| Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer | Q24600201 | ||
| The head inducer Cerberus is a multifunctional antagonist of Nodal, BMP and Wnt signals | Q24645277 | ||
| Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus | Q24796653 | ||
| Stages of embryonic development of the zebrafish | Q27860947 | ||
| LDL-receptor-related protein 6 is a receptor for Dickkopf proteins | Q28116567 | ||
| Embryonic retinoic acid synthesis is essential for early mouse post-implantation development | Q28140751 | ||
| The organizer factors Chordin and Noggin are required for mouse forebrain development | Q28145368 | ||
| Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse | Q28204667 | ||
| The hypoblast of the chick embryo positions the primitive streak by antagonizing nodal signaling | Q28214764 | ||
| Nodal antagonists in the anterior visceral endoderm prevent the formation of multiple primitive streaks | Q28214766 | ||
| Jaw transformation with gain of symmetry after Dlx5/Dlx6 inactivation: mirror of the past? | Q28215057 | ||
| Mouse Otx2 functions in the formation and patterning of rostral head. | Q52205211 | ||
| Bone morphogenetic protein-2 and -4 expression during murine orofacial development. | Q52206109 | ||
| c-otx2 is expressed in two different phases of gastrulation and is sensitive to retinoic acid treatment in chick embryo. | Q52211551 | ||
| Ectopic expression of Sonic hedgehog alters dorsal-ventral patterning of somites. | Q52212312 | ||
| Expression patterns of the bone morphogenetic protein genes Bmp-4 and Bmp-2 in the developing chick face suggest a role in outgrowth of the primordia. | Q52213892 | ||
| Mechanisms of limb patterning. | Q52215435 | ||
| Sprouty, an intracellular inhibitor of Ras signaling. | Q52569025 | ||
| Evolution of the Auditory System in Synapsida (“Mammal-Like Reptiles” and Primitive Mammals) as Seen in the Fossil Record | Q56031384 | ||
| Coordinate expression of the murine Hox-5 complex homoeobox-containing genes during limb pattern formation | Q59065602 | ||
| Head induction by simultaneous repression of Bmp and Wnt signalling in Xenopus | Q59095359 | ||
| Organizers in Mammalian Development | Q60249572 | ||
| Region- and stage-specific effects of FGFs and BMPs in chick mandibular morphogenesis | Q63225020 | ||
| Formation of ectopic neurepithelium in chick blastoderms: age-related capacities for induction and self-differentiation following transplantation of quail Hensen's nodes | Q68673992 | ||
| Identification of a retinoic acid-sensitive period during primary axis formation in Xenopus laevis | Q68883323 | ||
| Development of the chick embryo mesoblast: morphogenesis of the prechordal plate and cranial segments | Q70794265 | ||
| Expression of bone morphogenetic protein-4 (BMP-4), bone morphogenetic protein-7 (BMP-7), fibroblast growth factor-8 (FGF-8) and sonic hedgehog (SHH) during branchial arch development in the chick | Q71114331 | ||
| Signs of the principle body axes prior to primitive streak formation in the rabbit embryo | Q71554552 | ||
| Ontogeny of cranial ossification in the small-mouthed salamander,Ambystoma texanum (Matthes) | Q71754413 | ||
| Goosecoid expression in neurectoderm and mesendoderm is disrupted in zebrafish cyclops gastrulas | Q72093910 | ||
| Zebrafish Dkk1, induced by the pre-MBT Wnt signaling, is secreted from the prechordal plate and patterns the anterior neural plate | Q73109226 | ||
| Patterning the vertebrate heart | Q74399546 | ||
| Differential gene expression of Xenopus Pitx1, Pitx2b and Pitx2c during cement gland, stomodeum and pituitary development | Q74420233 | ||
| Otx2 is required to respond to signals from anterior neural ridge for forebrain specification | Q77577443 | ||
| Reorganizing the organizer 75 years on | Q78244445 | ||
| Retinoic acid and retinoic acid receptors in craniofacial development | Q79734463 | ||
| Larval cement gland of frogs: comparative development and morphology | Q81322752 | ||
| A new evolutionary scenario for the vertebrate jaw | Q81407737 | ||
| Development of the cranium and paired fins in the zebrafish Danio rerio (Ostariophysi, Cyprinidae) | Q88935202 | ||
| Early development of the actinopterygian head. I. External development and staging of the paddlefish Polyodon spathula | Q88980470 | ||
| Pitx homeobox genes in Ciona and amphioxus show left-right asymmetry is a conserved chordate character and define the ascidian adenohypophysis | Q34527817 | ||
| Induction and initial patterning of the nervous system - the chick embryo enters the scene | Q34723587 | ||
| Retinoids as teratogens | Q34731458 | ||
| Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives | Q35034771 | ||
| What's your position? the Xenopus cement gland as a paradigm of regional specification | Q35158121 | ||
| Vertebrate dentitions at the origin of jaws: when and how pattern evolved | Q35161288 | ||
| Early endoderm development in vertebrates: lineage differentiation and morphogenetic function | Q35187703 | ||
| Cranial neural crest and the building of the vertebrate head | Q35549127 | ||
| Significance of the cranial neural crest. | Q35618164 | ||
| Evolution of the mammalian middle ear | Q28218517 | ||
| Specification of jaw subdivisions by Dlx genes | Q28218878 | ||
| Fgf and Bmp signals repress the expression of Bapx1 in the mandibular mesenchyme and control the position of the developing jaw joint | Q28239307 | ||
| Transformation of tooth type induced by inhibition of BMP signaling | Q28287853 | ||
| Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse | Q28296363 | ||
| Active repression of RAR signaling is required for head formation | Q28346239 | ||
| Inhibition of Wnt activity induces heart formation from posterior mesoderm | Q28346509 | ||
| The transcription factor FoxH1 (FAST) mediates Nodal signaling during anterior-posterior patterning and node formation in the mouse | Q28365336 | ||
| Cripto is required for correct orientation of the anterior-posterior axis in the mouse embryo | Q28504851 | ||
| Isolation of novel cDNAs by subtractions between the anterior mesendoderm of single mouse gastrula stage embryos | Q28504903 | ||
| The mammalian twisted gastrulation gene functions in foregut and craniofacial development | Q28505603 | ||
| The BMP antagonists Chordin and Noggin have essential but redundant roles in mouse mandibular outgrowth | Q28505692 | ||
| Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest | Q28506270 | ||
| Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation | Q28506952 | ||
| Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis | Q28507650 | ||
| Combinatorial activities of Smad2 and Smad3 regulate mesoderm formation and patterning in the mouse embryo | Q28510693 | ||
| Function of Rieger syndrome gene in left-right asymmetry and craniofacial development | Q28511353 | ||
| Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation | Q28511870 | ||
| Multiple roles for Nodal in the epiblast of the mouse embryo in the establishment of anterior-posterior patterning | Q28513774 | ||
| Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo | Q28584770 | ||
| Distinct functions for Bmp signaling in lip and palate fusion in mice | Q28585153 | ||
| Nodal antagonists regulate formation of the anteroposterior axis of the mouse embryo | Q28585896 | ||
| Threshold-specific requirements for Bmp4 in mandibular development | Q28586072 | ||
| Different phenotypes for mice deficient in either activins or activin receptor type II | Q28587129 | ||
| Cerberus-like is a secreted factor with neutralizing activity expressed in the anterior primitive endoderm of the mouse gastrula | Q28587138 | ||
| Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development | Q28587312 | ||
| Cell fate decisions within the mouse organizer are governed by graded Nodal signals | Q28587363 | ||
| Nodal signalling in the epiblast patterns the early mouse embryo | Q28587896 | ||
| Murine cerberus homologue mCer-1: a candidate anterior patterning molecule | Q28588349 | ||
| Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches | Q28588808 | ||
| Craniofacial defects in mice lacking BMP type I receptor Alk2 in neural crest cells | Q28588988 | ||
| Smad2 and Smad3 coordinately regulate craniofacial and endodermal development | Q28589411 | ||
| Endothelin-A receptor-dependent and -independent signaling pathways in establishing mandibular identity | Q28591036 | ||
| The type II activin receptors are essential for egg cylinder growth, gastrulation, and rostral head development in mice | Q28592388 | ||
| A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene | Q28593109 | ||
| Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1 | Q28593256 | ||
| Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia | Q28594833 | ||
| Complementary functions of Otx2 and Cripto in initial patterning of mouse epiblast | Q28594848 | ||
| Conserved deployment of genes during odontogenesis across osteichthyans | Q28765393 | ||
| Neural crest patterning and the evolution of the jaw | Q28767335 | ||
| Reassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and development | Q28767452 | ||
| Evolution of the vertebrate jaw: comparative embryology and molecular developmental biology reveal the factors behind evolutionary novelty | Q28767490 | ||
| Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction | Q29616164 | ||
| HNF-3 beta is essential for node and notochord formation in mouse development | Q29616180 | ||
| Sonic hedgehog mediates the polarizing activity of the ZPA | Q29616565 | ||
| Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity | Q29616632 | ||
| Conversion of Xenopus ectoderm into neurons by NeuroD, a basic helix-loop-helix protein | Q29618504 | ||
| Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch | Q30500614 | ||
| Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice | Q30503216 | ||
| Evolutionary innovation in the vertebrate jaw: A derived morphology in anuran tadpoles and its possible developmental origin | Q33214069 | ||
| Teratology of retinoids | Q33636703 | ||
| Head in the WNT: the molecular nature of Spemann's head organizer | Q33702224 | ||
| Nodal signalling in vertebrate development. | Q33833716 | ||
| Anterior endoderm and head induction in early vertebrate embryos | Q33950730 | ||
| Nodal signaling in early vertebrate embryos: themes and variations | Q34101865 | ||
| Signalling pathways in Drosophila and vertebrate retinal development | Q34102511 | ||
| The role of prechordal mesendoderm in neural patterning | Q34141429 | ||
| Morphogen gradients, positional information, and Xenopus: interplay of theory and experiment. | Q34161204 | ||
| Vertebrate cranial placodes I. Embryonic induction | Q34187076 | ||
| Nodal Signaling in Vertebrate Development | Q34271462 | ||
| Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology | Q34294154 | ||
| Requirement of 19K form of Sonic hedgehog for induction of distinct ventral cell types in CNS explants. | Q34310844 | ||
| Fgf-8 expression in the post-gastrulation mouse suggests roles in the development of the face, limbs and central nervous system. | Q34319673 | ||
| Evolution of vertebrate forebrain development: how many different mechanisms? | Q34347339 | ||
| Allocation and early differentiation of cardiovascular progenitors in the mouse embryo | Q34399529 | ||
| Midline and laterality defects: left and right meet in the middle | Q34400224 | ||
| Neural induction: toward a unifying mechanism | Q34425366 | ||
| Mouse gastrulation: the formation of a mammalian body plan | Q34452578 | ||
| Hindbrain patterning revisited: timing and effects of retinoic acid signalling. | Q34464611 | ||
| Axis development and early asymmetry in mammals | Q34492466 | ||
| Early steps in the development of the forebrain | Q35666127 | ||
| Early development of the cranial sensory nervous system: from a common field to individual placodes | Q35942303 | ||
| Dkk1 and noggin cooperate in mammalian head induction | Q35971142 | ||
| Craniofacial development and the evolution of the vertebrates: the old problems on a new background | Q36026367 | ||
| Neural induction: old problem, new findings, yet more questions | Q36097576 | ||
| cyclops encodes a nodal-related factor involved in midline signaling | Q36280774 | ||
| Colocalization of BMP 7 and BMP 2 RNAs suggests that these factors cooperatively mediate tissue interactions during murine development | Q36686718 | ||
| Ectopic bone morphogenetic proteins 5 and 4 in the chicken forebrain lead to cyclopia and holoprosencephaly | Q37187365 | ||
| Expression of the mouse cerberus-related gene, Cerr1, suggests a role in anterior neural induction and somitogenesis | Q37388746 | ||
| Developmental processes, developmental sequences and early vertebrate phylogeny | Q38694351 | ||
| Homeobox genes and orofacial development. | Q40411519 | ||
| Sonic hedgehog: a key mediator of anterior-posterior patterning of the limb and dorso-ventral patterning of axial embryonic structures | Q40569337 | ||
| Vertebrate embryonic induction: mesodermal and neural patterning | Q40639590 | ||
| Ectodermally derived FGF8 defines the maxillomandibular region in the early chick embryo: epithelial-mesenchymal interactions in the specification of the craniofacial ectomesenchyme | Q40737788 | ||
| Retinoic acid perturbs Otx gene expression in the ascidian pharynx. | Q40827192 | ||
| Evolutionary alteration in anterior patterning: otx2 expression in the direct developing frog Eleutherodactylus coqui | Q40827538 | ||
| Retinoic acid and craniofacial development: molecules and morphogenesis | Q40852842 | ||
| Phenotypic effects in Xenopus and zebrafish suggest that one-eyed pinhead functions as antagonist of BMP signalling | Q40875538 | ||
| Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo | Q40922142 | ||
| Retinoic acid and pattern formation in vertebrates | Q40960548 | ||
| Morphogenesis of the murine node and notochordal plate | Q41013679 | ||
| Smad2 role in mesoderm formation, left-right patterning and craniofacial development | Q41027581 | ||
| Embryonic development and pattern formation | Q41108313 | ||
| Short historical survey of pattern formation in the endo-mesoderm and the neural anlage in the vertebrates: the role of vertical and planar inductive actions | Q41460160 | ||
| Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development | Q41478213 | ||
| RAR beta isoforms: distinct transcriptional control by retinoic acid and specific spatial patterns of promoter activity during mouse embryonic development | Q41485047 | ||
| Developmental patterning and evolution of the mammalian viscerocranium: genetic insights into comparative morphology | Q41500136 | ||
| Formation and function of Spemann's organizer | Q41689393 | ||
| Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos | Q41858943 | ||
| Retinoic acid causes an anteroposterior transformation in the developing central nervous system | Q41931859 | ||
| Molecular shaping of the beak | Q42181684 | ||
| Epithelial-mesenchymal transformation is the mechanism for fusion of the craniofacial primordia involved in morphogenesis of the chicken lip. | Q42497014 | ||
| Sonic hedgehog participates in craniofacial morphogenesis and is down-regulated by teratogenic doses of retinoic acid | Q42548680 | ||
| Epiblast and primitive-streak origins of the endoderm in the gastrulating chick embryo | Q43523171 | ||
| The status of Wnt signalling regulates neural and epidermal fates in the chick embryo | Q43611057 | ||
| Pitx1 and Pitx2c are required for ectopic cement gland formation in Xenopus laevis | Q43690951 | ||
| Noggin and retinoic acid transform the identity of avian facial prominences | Q43847132 | ||
| Axes establishment during eye morphogenesis in Xenopus by coordinate and antagonistic actions of BMP4, Shh, and RA. | Q44060754 | ||
| Deficits in the posterior pharyngeal endoderm in the absence of retinoids | Q44119981 | ||
| A novel role for retinoids in patterning the avian forebrain during presomite stages | Q44385742 | ||
| Retinoic acid-induced developmental defects are mediated by RARbeta/RXR heterodimers in the pharyngeal endoderm. | Q44385746 | ||
| The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system | Q44408464 | ||
| Insertional mutation of a gene involved in growth regulation of the early mouse embryo | Q44860550 | ||
| Fgf signaling is required for zebrafish tooth development | Q45050273 | ||
| A new origin for the maxillary jaw. | Q45142714 | ||
| Developmental origins and evolution of jaws: new interpretation of "maxillary" and "mandibular". | Q45142715 | ||
| Control of retinoic acid synthesis and FGF expression in the nasal pit is required to pattern the craniofacial skeleton | Q45175382 | ||
| A zone of frontonasal ectoderm regulates patterning and growth in the face. | Q45999105 | ||
| The cellular and molecular origins of beak morphology | Q46149530 | ||
| Coordinate expression of Fgf8, Otx2, Bmp4, and Shh in the rostral prosencephalon during development of the telencephalic and optic vesicles. | Q46173182 | ||
| Coordinate regulation and synergistic actions of BMP4, SHH and FGF8 in the rostral prosencephalon regulate morphogenesis of the telencephalic and optic vesicles | Q46351477 | ||
| Molecular interactions coordinating the development of the forebrain and face. | Q46567732 | ||
| Teratogenic effects of two antifungal triazoles, triadimefon and triadimenol, on Xenopus laevis development: craniofacial defects | Q46579142 | ||
| Tissue-specific expression of Fgfr2b and Fgfr2c isoforms, Fgf10 and Fgf9 in the developing chick mandible | Q46654753 | ||
| Fgf signalling controls the dorsoventral patterning of the zebrafish embryo | Q47073185 | ||
| An essential role for Fgfs in endodermal pouch formation influences later craniofacial skeletal patterning | Q47073360 | ||
| Roles for fgf8 signaling in left-right patterning of the visceral organs and craniofacial skeleton | Q47073509 | ||
| Zebrafish Dkk1 functions in forebrain specification and axial mesendoderm formation | Q47073690 | ||
| The function of silberblick in the positioning of the eye anlage in the zebrafish embryo | Q47073722 | ||
| Zebrafish nodal-related genes are implicated in axial patterning and establishing left-right asymmetry | Q47073917 | ||
| Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse | Q47194311 | ||
| Separate evolutionary origins of teeth from evidence in fossil jawed vertebrates. | Q47406883 | ||
| Signaling pathways crucial for craniofacial development revealed by endothelin-A receptor-deficient mice | Q47622053 | ||
| Anterior identity is established in chick epiblast by hypoblast and anterior definitive endoderm. | Q47659927 | ||
| Hypomorphic expression of Dkk1 in the doubleridge mouse: dose dependence and compensatory interactions with Lrp6. | Q47679349 | ||
| Molecular interactions continuously define the organizer during the cell movements of gastrulation | Q47927980 | ||
| Cloning and expression pattern of chicken Pitx2: a new component in the SHH signaling pathway controlling embryonic heart looping | Q47939390 | ||
| An early phase of embryonic Dlx5 expression defines the rostral boundary of the neural plate. | Q48018154 | ||
| Expression analysis of chick Wnt and frizzled genes and selected inhibitors in early chick patterning | Q48020237 | ||
| Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling | Q48021528 | ||
| Zebrafish organizer development and germ-layer formation require nodal-related signals | Q48021535 | ||
| Effects of redox reagents and arsenical compounds on [3H]-cytisine binding to immunoisolated nicotinic acetylcholine receptors from chick brain containing alpha 4 beta 2 subunits | Q48145506 | ||
| FGF17b and FGF18 have different midbrain regulatory properties from FGF8b or activated FGF receptors | Q48152543 | ||
| Heterotopic shift of epithelial-mesenchymal interactions in vertebrate jaw evolution. | Q48303673 | ||
| Nested expression domains of four homeobox genes in developing rostral brain | Q48444447 | ||
| Rostral truncation of a cyclostome, Lampetra japonica, induced by all-trans retinoic acid defines the head/trunk interface of the vertebrate body | Q48559762 | ||
| Role of the isthmus and FGFs in resolving the paradox of neural crest plasticity and prepatterning | Q48687225 | ||
| The cyclops mutation blocks specification of the floor plate of the zebrafish central nervous system | Q48766492 | ||
| Mesenchymal/epithelial induction mediates olfactory pathway formation | Q49110374 | ||
| The vertebrate skeleton | Q51413439 | ||
| Chordate morphology | Q51456350 | ||
| The life of vertebrates | Q51499536 | ||
| Regionalisation of early head ectoderm is regulated by endoderm and prepatterns the orofacial epithelium. | Q52087805 | ||
| Shh and Fgf8 act synergistically to drive cartilage outgrowth during cranial development. | Q52088188 | ||
| Neural crest cells provide species-specific patterning information in the developing branchial skeleton. | Q52090119 | ||
| Analysis of spatial and temporal gene expression patterns in blastula and gastrula stage chick embryos. | Q52120947 | ||
| otx2 expression in the ectoderm activates anterior neural determination and is required for Xenopus cement gland formation. | Q52125394 | ||
| The concept of developmental reprogramming and the quest for an inclusive theory of evolutionary mechanisms. | Q52138165 | ||
| The Mdm2 gene of zebrafish (Danio rerio): preferential expression during development of neural and muscular tissues, and absence of tumor formation after overexpression of its cDNA during early embryogenesis. | Q52144129 | ||
| Stage- and species-specific developmental toxicity of all-trans retinoic acid in four native North American ranids and Xenopus laevis. | Q52164974 | ||
| Coincidence of otx2 and BMP4 signaling correlates with Xenopus cement gland formation. | Q52169858 | ||
| Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage. | Q52171937 | ||
| Mouse Lefty2 and zebrafish antivin are feedback inhibitors of nodal signaling during vertebrate gastrulation. | Q52174020 | ||
| Spatially distinct head and heart inducers within the Xenopus organizer region. | Q52174781 | ||
| Anterior patterning in mouse. | Q52185823 | ||
| The Spemann organizer of Xenopus is patterned along its anteroposterior axis at the earliest gastrula stage. | Q52191291 | ||
| Mouse Otlx2/RIEG expression in the odontogenic epithelium precedes tooth initiation and requires mesenchyme-derived signals for its maintenance. | Q52192778 | ||
| Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene. | Q52193774 | ||
| Retinoic acid disturbs mouse middle ear development in a stage-dependent fashion. | Q52195437 | ||
| Specific craniofacial cartilage dysmorphogenesis coincides with a loss of dlx gene expression in retinoic acid-treated zebrafish embryos. | Q52197512 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 1256-1291 | |
| P577 | publication date | 2006-05-01 | |
| P1433 | published in | Developmental Dynamics | Q59752 |
| P1476 | title | 21st century neontology and the comparative development of the vertebrate skull | |
| P478 | volume | 235 |
| Q36029243 | A phenotype-driven ENU mutagenesis screen identifies novel alleles with functional roles in early mouse craniofacial development |
| Q36999856 | An endothelin-1 switch specifies maxillomandibular identity |
| Q41982436 | Asymmetric requirement of surface epithelial β-catenin during the upper and lower jaw development. |
| Q35197153 | Beyond the functional matrix hypothesis: a network null model of human skull growth for the formation of bone articulations |
| Q41355632 | Bite force in the horned frog (Ceratophrys cranwelli) with implications for extinct giant frogs |
| Q36350674 | Dinosaurs, Chameleons, Humans, and Evo-Devo Path: Linking Étienne Geoffroy's Teratology, Waddington's Homeorhesis, Alberch's Logic of "Monsters," and Goldschmidt Hopeful "Monsters". |
| Q28658047 | Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway |
| Q24596162 | Downregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesis |
| Q47795724 | Effects of aneuploidy on skull growth in a mouse model of Down syndrome |
| Q28742879 | Evolutionary patterns and processes in the radiation of phyllostomid bats |
| Q37086538 | Exclusion of Dlx5/6 expression from the distal-most mandibular arches enables BMP-mediated specification of the distal cap. |
| Q38641243 | Facial Morphogenesis: Physical and Molecular Interactions Between the Brain and the Face. |
| Q41854792 | Fate of cranial neural crest cells during craniofacial development in endothelin-A receptor-deficient mice |
| Q41845249 | Fgf8 dosage determines midfacial integration and polarity within the nasal and optic capsules |
| Q90517346 | Getting out of an egg: Merging of tooth germs to create an egg tooth in the snake |
| Q34341687 | Hand1 phosphoregulation within the distal arch neural crest is essential for craniofacial morphogenesis |
| Q35079847 | Interaction between Foxc1 and Fgf8 during mammalian jaw patterning and in the pathogenesis of syngnathia. |
| Q38206169 | Left-right asymmetry of the gnathostome skull: its evolutionary, developmental, and functional aspects |
| Q37143914 | Memory encoded throughout our bodies: molecular and cellular basis of tissue regeneration |
| Q33584477 | Morphological integration of the skull in craniofacial anomalies |
| Q46188964 | Negative regulation of endothelin signaling by SIX1 is required for proper maxillary development. |
| Q64999191 | Neural crest and the origin of species-specific pattern. |
| Q41934893 | Neural crest cells pattern the surface cephalic ectoderm during FEZ formation |
| Q28088384 | New insights into craniofacial malformations |
| Q33978601 | Overview of the transcriptome profiles identified in hagfish, shark, and bichir: current issues arising from some nonmodel vertebrate taxa |
| Q34331978 | Pattern and polarity in the development and evolution of the gnathostome jaw: both conservation and heterotopy in the branchial arches of the shark, Scyliorhinus canicula. |
| Q46754963 | Patterning of mammalian heterodont dentition within the upper and lower jaws |
| Q46526863 | Patterns of orofacial clefting in the facial morphology of bats: a possible naturally occurring model of cleft palate |
| Q52607888 | Pax6 regulates craniofacial form through its control of an essential cephalic ectodermal patterning center. |
| Q36670114 | Possible involvement of SINEs in mammalian-specific brain formation |
| Q57296246 | Probing the origin of matching functional jaws: roles of Dlx5/6 in cranial neural crest cells |
| Q28602486 | Recent insights into the morphological diversity in the amniote primary and secondary palates |
| Q28512086 | Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development |
| Q45864057 | Satb2, modularity, and the evolvability of the vertebrate jaw. |
| Q37461994 | Signaling integration in the rugae growth zone directs sequential SHH signaling center formation during the rostral outgrowth of the palate |
| Q29039455 | Spatio-temporal dynamics of gene expression of the Edn1-Dlx5/6 pathway during development of the lower jaw |
| Q42151105 | Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with hand2. |
| Q28751334 | The midline, oral ectoderm, and the arch-0 problem |
| Q41812833 | Unique organization of the frontonasal ectodermal zone in birds and mammals. |
| Q51562273 | Whole genome microarray analysis of chicken embryo facial prominences. |
| Q30496252 | hand2 and Dlx genes specify dorsal, intermediate and ventral domains within zebrafish pharyngeal arches |
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