| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/AJA.1001930302 |
| P8608 | Fatcat ID | release_l3k6nufbbvcozotqhaxrvizmca |
| P698 | PubMed publication ID | 1600240 |
| P5875 | ResearchGate publication ID | 21555971 |
| P2093 | author name string | Keller R | |
| Shih J | |||
| Sater A | |||
| P2860 | cites work | Homeogenetic neural induction in Xenopus. | Q30446899 |
| Mesodermal control of neural cell identity: floor plate induction by the notochord | Q34257473 | ||
| Mapping of the presumptive brain regions in the neural plate of Xenopus laevis | Q34334693 | ||
| Planar induction of convergence and extension of the neural plate by the organizer of Xenopus | Q34432075 | ||
| Neural fold formation at newly created boundaries between neural plate and epidermis in the axolotl | Q34522031 | ||
| Expression of Epi 1, an epidermis-specific marker in Xenopus laevis embryos, is specified prior to gastrulation | Q41266471 | ||
| Notochordal induction of cell wedging in the chick neural plate and its role in neural tube formation | Q41309512 | ||
| Signals from the dorsal blastopore lip region during gastrulation bias the ectoderm toward a nonepidermal pathway of differentiation in Xenopus laevis | Q42154751 | ||
| Shaping and bending of the avian neuroepithelium: morphometric analyses | Q42435346 | ||
| Changes in the shape of the developing vertebrate nervous system analyzed experimentally, mathematically and by computer simulation | Q43736996 | ||
| Mediolateral cell intercalation in the dorsal, axial mesoderm of Xenopus laevis | Q46131164 | ||
| Vital dye mapping of the gastrula and neurula of Xenopus laevis. II. Prospective areas and morphogenetic movements of the deep layer | Q46907145 | ||
| Expression of an epidermal antigen used to study tissue induction in the early Xenopus laevis embryo | Q51213201 | ||
| Die totale Exogastrulation, eine Selbstablösung des Ektoderms vom Entomesoderm : Entwicklung und funktionelles Verhalten nervenloser Organe | Q53057509 | ||
| Time-lapse cinemicrographic analysis of superficial cell behavior during and prior to gastrulation in Xenopus laevis | Q91585469 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 199-217 | |
| P577 | publication date | 1992-03-01 | |
| P1433 | published in | Developmental Dynamics | Q59752 |
| P1476 | title | The cellular basis of the convergence and extension of the Xenopus neural plate | |
| P478 | volume | 193 |
| Q60300597 | A role for the hypoblast (AVE) in the initiation of neural induction, independent of its ability to position the primitive streak |
| Q38016770 | Cadherin Function During Xenopus Gastrulation |
| Q34114814 | Cadherins and catenins, Wnts and SOXs: embryonic patterning in Xenopus |
| Q46769023 | Calcium signaling during convergent extension in Xenopus |
| Q53088604 | Calpain2 protease: A new member of the Wnt/Ca(2+) pathway modulating convergent extension movements in Xenopus. |
| Q47909589 | Calponin modulates the exclusion of Otx-expressing cells from convergence extension movements |
| Q37611224 | Cell adhesion in amphibian gastrulation |
| Q46571077 | Cell motility driving mediolateral intercalation in explants of Xenopus laevis |
| Q30410398 | Cell segregation, mixing, and tissue pattern in the spinal cord of the Xenopus laevis neurula |
| Q52697723 | Cell shape changes indicate a role for extrinsic tensile forces in Drosophila germ-band extension. |
| Q46650863 | Cellular Mechanism Underlying Neural Convergent Extension in Xenopus laevis Embryos |
| Q35483292 | Cellular basis of amphibian gastrulation |
| Q48826772 | Cellular mechanisms of posterior neural tube morphogenesis in the zebrafish |
| Q35006500 | Cellular patterning of the vertebrate embryo |
| Q41120576 | Changes in dorsoventral but not rostrocaudal regionalization of the chick neural tube in the absence of cranial notochord, as revealed by expression of engrailed-2. |
| Q42491186 | Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling |
| Q37571696 | Comparative analysis of neurulation: first impressions do not count |
| Q36042628 | Compartmentalized morphogenesis in epithelia: from cell to tissue shape |
| Q28204202 | Convergent extension: the molecular control of polarized cell movement during embryonic development |
| Q35777654 | Different strategies for midline formation in bilaterians |
| Q41141164 | Differentiation processes in the amphibian brain with special emphasis on heterochronies. |
| Q41390807 | Dorsal or ventral: similarities in fate maps and gastrulation patterns in annelids, arthropods and chordates |
| Q36874103 | Dorsal-Ventral Patterning during Neural Induction inXenopus:Assessment of Spinal Cord Regionalization withxHB9,a Marker for the Motor Neuron Region |
| Q30445378 | Dynamic determinations: patterning the cell behaviours that close the amphibian blastopore |
| Q36266874 | Dynamics of beta-catenin interactions with APC protein regulate epithelial tubulogenesis |
| Q40702301 | Early anteroposterior division of the presumptive neurectoderm in Xenopus |
| Q30434805 | Early development of Ensatina eschscholtzii: an amphibian with a large, yolky egg |
| Q30772857 | Early patterning of the prospective midbrain–hindbrain boundary by the HES-related gene XHR1 in Xenopus embryos |
| Q43679034 | Effects of retinoic acid upon eye field morphogenesis and differentiation |
| Q46100344 | Embryonic cells depleted of beta-catenin remain competent to differentiate into dorsal mesodermal derivatives. |
| Q44584332 | Epithelial Cell Wedging and Neural Trough Formation Are Induced Planarly inXenopus,without Persistent Vertical Interactions with Mesoderm |
| Q45263249 | Ethanol exposure affects gene expression in the embryonic organizer and reduces retinoic acid levels |
| Q41090586 | Evidence that the border of the neural plate may be positioned by the interaction between signals that induce ventral and dorsal mesoderm |
| Q72312541 | Experimental analyses of the rearrangement of ectodermal cells during gastrulation and neurulation in avian embryos |
| Q46552117 | FGF receptor signalling is required to maintain neural progenitors during Hensen's node progression. |
| Q30579259 | GEF-H1 functions in apical constriction and cell intercalations and is essential for vertebrate neural tube closure |
| Q41757735 | Genetic evidence for posterior specification by convergent extension in the Xenopus embryo |
| Q30436269 | Genetic locus half baked is necessary for morphogenesis of the ectoderm |
| Q48119260 | Histology Atlas of the Developing Prenatal and Postnatal Mouse Central Nervous System, with Emphasis on Prenatal Days E7.5 to E18.5. |
| Q52004444 | Hox genes, homology and axis formation--the application of morphological concepts to evolutionary developmental biology |
| Q40775363 | Induction and axial patterning of the neural plate: planar and vertical signals |
| Q46673000 | Induction of neuronal differentiation by planar signals in Xenopus embryos |
| Q52542676 | Inversion of dorsoventral axis? |
| Q46219921 | Involvement of AP-2rep in morphogenesis of the axial mesoderm in Xenopus embryo |
| Q48056993 | Involvement of Livertine, a hepatocyte growth factor family member, in neural morphogenesis |
| Q27339759 | Live imaging of Xwnt5A-ROR2 complexes |
| Q30306607 | Mechanisms of convergence and extension by cell intercalation |
| Q27331377 | Microtubule-associated protein 1b is required for shaping the neural tube |
| Q44856178 | Morphogenesis of the primitive gut tube is generated by Rho/ROCK/myosin II-mediated endoderm rearrangements |
| Q30436768 | Morphogenetic movements driving neural tube closure in Xenopus require myosin IIB. |
| Q46679500 | Morphogenetic movements during cranial neural tube closure in the chick embryo and the effect of homocysteine. |
| Q78029770 | Multistep role for actin in initial closure of the mesencephalic neural groove in the chick embryo |
| Q30487825 | N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements |
| Q51946032 | Neogenin and RGMa control neural tube closure and neuroepithelial morphology by regulating cell polarity. |
| Q36087230 | Neural tube closure and neural tube defects: studies in animal models reveal known knowns and known unknowns |
| Q47865557 | Neuroectodermal specification and regionalization of the Spemann organizer in Xenopus |
| Q40675177 | Neurogenesis in Xenopus: a molecular genetic perspective |
| Q34758596 | Non-canonical Wnt signalling and regulation of gastrulation movements |
| Q45990963 | Onset of electrical excitability during a period of circus plasma membrane movements in differentiating Xenopus neurons. |
| Q40976641 | Order and coherence in the fate map of the zebrafish nervous system |
| Q30435847 | PTK7 is essential for polarized cell motility and convergent extension during mouse gastrulation |
| Q45237825 | Patterns of cell motility in the organizer and dorsal mesoderm of Xenopus laevis |
| Q42515878 | Patterns of oriented cell division during the steady-state morphogenesis of the body column in hydra |
| Q38035934 | Planar Cell Polarity and the Developmental Control of Cell Behavior in Vertebrate Embryos |
| Q40775357 | Planar and vertical induction of anteroposterior pattern during the development of the amphibian central nervous system |
| Q36433141 | Planar cell polarity acts through septins to control collective cell movement and ciliogenesis. |
| Q24336656 | Planar cell polarity links axes of spatial dynamics in neural-tube closure |
| Q35741800 | Planar polarization of Vangl2 in the vertebrate neural plate is controlled by Wnt and Myosin II signaling |
| Q30794038 | Polarized basolateral cell motility underlies invagination and convergent extension of the ascidian notochord |
| Q30479061 | Polychaete trunk neuroectoderm converges and extends by mediolateral cell intercalation. |
| Q37686145 | RFX7 is required for the formation of cilia in the neural tube |
| Q36068399 | Regulation of distinct branches of the non-canonical Wnt-signaling network in Xenopus dorsal marginal zone explants |
| Q42855703 | Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein |
| Q47072149 | Serotonin synchronises convergent extension of ectoderm with morphogenetic gastrulation movements in Drosophila |
| Q35193899 | Shroom3 functions downstream of planar cell polarity to regulate myosin II distribution and cellular organization during neural tube closure |
| Q56530246 | Spatial and temporal analysis of PCP protein dynamics during neural tube closure |
| Q79676473 | Stem cell growth becomes predominant while neural plate progenitor pool decreases during spinal cord elongation |
| Q35695057 | Synthesis and Characterization of 8-O-Carboxymethylpyranine (CM-Pyranine) as a Bright, Violet-Emitting, Fluid-Phase Fluorescent Marker in Cell Biology |
| Q50420456 | The Birth of the Eye Vesicle: When Fate Decision Equals Morphogenesis |
| Q52190622 | The Role of Intracellular Alkalinization in the Establishment of Anterior Neural Fate inXenopus |
| Q38355008 | The function of Xenopus germ cell nuclear factor (xGCNF) in morphogenetic movements during neurulation |
| Q47073722 | The function of silberblick in the positioning of the eye anlage in the zebrafish embryo |
| Q34284889 | The larval ascidian nervous system: the chordate brain from its small beginnings |
| Q46059346 | The mechanism of gastrulation in the white sturgeon |
| Q30310700 | The midline (notochord and notoplate) patterns the cell motility underlying convergence and extension of the Xenopus neural plate |
| Q30441855 | The presumptive floor plate (notoplate) induces behaviors associated with convergent extension in medial but not lateral neural plate cells of Xenopus |
| Q52594235 | The radial-symmetric hydra and the evolution of the bilateral body plan: an old body became a young brain |
| Q52193879 | The role in neural patterning of translation initiation factor eIF4AII; induction of neural fold genes |
| Q42451571 | The role of F-cadherin in localizing cells during neural tube formation in Xenopus embryos |
| Q38781482 | Tissue morphodynamics: Translating planar polarity cues into polarized cell behaviors |
| Q27313958 | Tissue tectonics: morphogenetic strain rates, cell shape change and intercalation |
| Q34417533 | Transcription factors and head formation in vertebrates |
| Q52692294 | Two different mechanisms of planar cell intercalation leading to tissue elongation |
| Q91972811 | Vangl2 coordinates cell rearrangements during gut elongation |
| Q41496834 | Vertebrate neural induction: inducers, inhibitors, and a new synthesis |
| Q35152288 | Vertical versus planar neural induction in Rana pipiens embryos |
| Q39661503 | Wide and high resolution tension measurement using FRET in embryo |
| Q46706845 | Xenopus Gastrulation without a blastocoel roof |
| Q44247930 | Xenopus hoxc8 during early development |
| Q46132873 | Xenopus laevis as a Model Organism for the Study of Spinal Cord Formation, Development, Function and Regeneration |
| Q40872256 | XenopusHindbrain Patterning Requires Retinoid Signaling |
| Q47989507 | hmmr mediates anterior neural tube closure and morphogenesis in the frog Xenopus |
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