review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Kate Gillian Storey | Q21264119 |
Elsa Abranches | Q59702868 | ||
Laure Verrier | Q63386753 | ||
Domingos Henrique | Q57009307 | ||
P2860 | cites work | Requirement for Lim1 in head-organizer function | Q24312737 |
Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern | Q24319689 | ||
Tcf3: a transcriptional regulator of axis induction in the early embryo | Q28190724 | ||
Two distinct sources for a population of maturing axial progenitors | Q28235278 | ||
Brachyury cooperates with Wnt/β-catenin signalling to elicit primitive-streak-like behaviour in differentiating mouse embryonic stem cells | Q28245798 | ||
Symmetry breaking, germ layer specification and axial organisation in aggregates of mouse embryonic stem cells | Q28250962 | ||
Signaling by FGF4 and FGF8 is required for axial elongation of the mouse embryo | Q28274409 | ||
Wnt-3a regulates somite and tailbud formation in the mouse embryo | Q28504870 | ||
Churchill, a zinc finger transcriptional activator, regulates the transition between gastrulation and neurulation | Q28505236 | ||
Evidence that absence of Wnt-3a signaling promotes neuralization instead of paraxial mesoderm development in the mouse | Q28507549 | ||
Transcriptional regulatory networks in epiblast cells and during anterior neural plate development as modeled in epiblast stem cells | Q28511646 | ||
Cdx1 and Cdx2 have overlapping functions in anteroposterior patterning and posterior axis elongation | Q28512428 | ||
Inactivation of FGF8 in early mesoderm reveals an essential role in kidney development | Q28585034 | ||
BMP signalling inhibits premature neural differentiation in the mouse embryo | Q28585811 | ||
Cdx and Hox genes differentially regulate posterior axial growth in mammalian embryos | Q28585942 | ||
Wnt3a plays a major role in the segmentation clock controlling somitogenesis | Q28587356 | ||
Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling | Q29615601 | ||
Formation of ectopic neurepithelium in chick blastoderms: age-related capacities for induction and self-differentiation following transplantation of quail Hensen's nodes | Q68673992 | ||
Caudalization of neural fate by tissue recombination and bFGF | Q70935497 | ||
The spatial and temporal dynamics of Sax1 (CHox3) homeobox gene expression in the chick's spinal cord | Q72714701 | ||
A mitogen gradient of dorsal midline Wnts organizes growth in the CNS | Q77960718 | ||
Specification and maintenance of the spinal cord stem zone. | Q52040192 | ||
Acquisition of Hox codes during gastrulation and axial elongation in the mouse embryo. | Q52103471 | ||
A morphogen gradient of Wnt/beta-catenin signalling regulates anteroposterior neural patterning in Xenopus. | Q52128006 | ||
Reconciling different models of forebrain induction and patterning: a dual role for the hypoblast. | Q52166188 | ||
Early posterior neural tissue is induced by FGF in the chick embryo. | Q52191486 | ||
c-otx2 is expressed in two different phases of gastrulation and is sensitive to retinoic acid treatment in chick embryo. | Q52211551 | ||
Positive and negative signals from mesoderm regulate the expression of mouse Otx2 in ectoderm explants | Q52214147 | ||
A region of the vertebrate neural plate in which neighbouring cells can adopt neural or epidermal fates. | Q52580788 | ||
Clonal analysis in the intact mouse embryo by intragenic homologous recombination. | Q54042393 | ||
Compartment-dependent activities of Wnt3a/β-catenin signaling during vertebrate axial extension | Q58475639 | ||
Combinatorial analysis of developmental cues efficiently converts human pluripotent stem cells into multiple neuronal subtypes. | Q50624483 | ||
Regulation of mesodermal precursor production by low-level expression of B1 Sox genes in the caudal lateral epiblast. | Q50689834 | ||
The Pou5f1/Pou3f-dependent but SoxB-independent regulation of conserved enhancer N2 initiates Sox2 expression during epiblast to neural plate stages in vertebrates. | Q51892667 | ||
Redefining the progression of lineage segregations during mammalian embryogenesis by clonal analysis. | Q51926154 | ||
Localised axial progenitor cell populations in the avian tail bud are not committed to a posterior Hox identity. | Q51956205 | ||
Wnt signals provide a timing mechanism for the FGF-retinoid differentiation switch during vertebrate body axis extension. | Q51985699 | ||
Collinear activation of Hoxb genes during gastrulation is linked to mesoderm cell ingression. | Q52015694 | ||
Convergence of Wnt and FGF signals in the genesis of posterior neural plate through activation of the Sox2 enhancer N-1. | Q52031459 | ||
Charting Brachyury-mediated developmental pathways during early mouse embryogenesis | Q30574934 | ||
Integration of signals along orthogonal axes of the vertebrate neural tube controls progenitor competence and increases cell diversity | Q33904021 | ||
The regulation of Hox gene expression during animal development | Q34038204 | ||
In vitro generation of neuromesodermal progenitors reveals distinct roles for wnt signalling in the specification of spinal cord and paraxial mesoderm identity | Q34089469 | ||
Functional diversity of ESC-derived motor neuron subtypes revealed through intraspinal transplantation | Q34102851 | ||
Initial patterning of the central nervous system: how many organizers? | Q34185960 | ||
Pluripotency factors in embryonic stem cells regulate differentiation into germ layers | Q34191627 | ||
Concerted involvement of Cdx/Hox genes and Wnt signaling in morphogenesis of the caudal neural tube and cloacal derivatives from the posterior growth zone | Q34200190 | ||
The developmental dismantling of pluripotency is reversed by ectopic Oct4 expression | Q34279160 | ||
Induction of a second neural axis by the mouse node. | Q34339852 | ||
Major transcriptome re-organisation and abrupt changes in signalling, cell cycle and chromatin regulation at neural differentiation in vivo | Q34341301 | ||
Wnt/β-catenin and FGF signalling direct the specification and maintenance of a neuromesodermal axial progenitor in ensembles of mouse embryonic stem cells | Q34446332 | ||
Mesogenin 1 is a master regulator of paraxial presomitic mesoderm differentiation | Q34446339 | ||
Loss of FGF-dependent mesoderm identity and rise of endogenous retinoid signalling determine cessation of body axis elongation. | Q34464307 | ||
Generation of Aggregates of Mouse Embryonic Stem Cells that Show Symmetry Breaking, Polarization and Emergent Collective Behaviour In Vitro | Q34504594 | ||
Tbx6-dependent Sox2 regulation determines neural or mesodermal fate in axial stem cells | Q34588851 | ||
FGF4 and FGF8 comprise the wavefront activity that controls somitogenesis. | Q34652756 | ||
TCreERT2, a transgenic mouse line for temporal control of Cre-mediated recombination in lineages emerging from the primitive streak or tail bud. | Q34701581 | ||
Concordia discors: duality in the origin of the vertebrate tail | Q35114056 | ||
T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification. | Q35210431 | ||
Deterministic HOX patterning in human pluripotent stem cell-derived neuroectoderm | Q35453975 | ||
Lineage tracing of neuromesodermal progenitors reveals novel Wnt-dependent roles in trunk progenitor cell maintenance and differentiation | Q35568242 | ||
Clonal and molecular analysis of the prospective anterior neural boundary in the mouse embryo | Q35624855 | ||
Clonal analysis of cell fate during gastrulation and early neurulation in the mouse | Q35784893 | ||
Opposing FGF and retinoid pathways: a signalling switch that controls differentiation and patterning onset in the extending vertebrate body axis | Q35845613 | ||
Interaction of Wnt3a, Msgn1 and Tbx6 in neural versus paraxial mesoderm lineage commitment and paraxial mesoderm differentiation in the mouse embryo | Q36007876 | ||
Neural induction: old problem, new findings, yet more questions | Q36097576 | ||
Head-tail patterning of the vertebrate embryo: one, two or many unresolved problems? | Q36328935 | ||
Neural induction: 10 years on since the 'default model'. | Q36625558 | ||
Nkx1-2 is a transcriptional repressor and is essential for the activation of Brachyury in P19 mouse embryonal carcinoma cell | Q36661973 | ||
Generation of knock-in mice that express nuclear enhanced green fluorescent protein and tamoxifen-inducible Cre recombinase in the notochord from Foxa2 and T loci | Q36784040 | ||
In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency | Q37217485 | ||
Stem cells, signals and vertebrate body axis extension | Q37460556 | ||
Transcriptional profiling of Wnt3a mutants identifies Sp transcription factors as essential effectors of the Wnt/β-catenin pathway in neuromesodermal stem cells | Q37514374 | ||
Multipotent caudal neural progenitors derived from human pluripotent stem cells that give rise to lineages of the central and peripheral nervous system. | Q37696446 | ||
Developmental mechanisms directing early anterior forebrain specification in vertebrates | Q38080448 | ||
Region-specific regulation of posterior axial elongation during vertebrate embryogenesis. | Q38126445 | ||
Neural induction and early patterning in vertebrates. | Q38135361 | ||
Mapping the route from naive pluripotency to lineage specification. | Q38263165 | ||
An emerging molecular mechanism for the neural vs mesodermal cell fate decision | Q38857365 | ||
Erk signaling suppresses embryonic stem cell self-renewal to specify endoderm. | Q38926181 | ||
SMAD7 directly converts human embryonic stem cells to telencephalic fate by a default mechanism. | Q39266474 | ||
FGF signalling inhibits neural induction in human embryonic stem cells | Q39442630 | ||
Primary Induction in Birds | Q39998666 | ||
SoxB transcription factors specify neuroectodermal lineage choice in ES cells | Q40497549 | ||
FGF-dependent Notch signaling maintains the spinal cord stem zone | Q40648767 | ||
Visceral endoderm mediates forebrain development by suppressing posteriorizing signals | Q40748196 | ||
eFGF regulates Xbra expression during Xenopus gastrulation. | Q40793305 | ||
Sequential roles for Otx2 in visceral endoderm and neuroectoderm for forebrain and midbrain induction and specification. | Q41046046 | ||
An early role for WNT signaling in specifying neural patterns of Cdx and Hox gene expression and motor neuron subtype identity | Q41564030 | ||
Distinct Wnt-driven primitive streak-like populations reflect in vivo lineage precursors. | Q41812893 | ||
Saltatory remodeling of Hox chromatin in response to rostrocaudal patterning signals. | Q41839120 | ||
Assessing the bipotency of in vitro-derived neuromesodermal progenitors | Q41874256 | ||
Multiple roles of Activin/Nodal, bone morphogenetic protein, fibroblast growth factor and Wnt/β-catenin signalling in the anterior neural patterning of adherent human embryonic stem cell cultures | Q42076307 | ||
3D reconstitution of the patterned neural tube from embryonic stem cells. | Q42082421 | ||
Canonical Wnt signaling dynamically controls multiple stem cell fate decisions during vertebrate body formation | Q42496522 | ||
Conserved and divergent roles of FGF signaling in mouse epiblast stem cells and human embryonic stem cells | Q43140844 | ||
Regulation of canonical Wnt signaling by Brachyury is essential for posterior mesoderm formation | Q43228969 | ||
Cdx2 regulation of posterior development through non-Hox targets | Q43244137 | ||
Evolutionarily conserved requirement of Cdx for post-occipital tissue emergence | Q44007033 | ||
Fate mapping and cell lineage analysis of Hensen's node in the chick embryo | Q44476738 | ||
Opposing FGF and retinoid pathways control ventral neural pattern, neuronal differentiation, and segmentation during body axis extension | Q44607276 | ||
Initiation of neural induction by FGF signalling before gastrulation. | Q47845943 | ||
cash4, a novel achaete-scute homolog induced by Hensen's node during generation of the posterior nervous system | Q48052959 | ||
Expression of the novel murine homeobox gene Sax-1 in the developing nervous system. | Q48074068 | ||
Functional analysis of chicken Sox2 enhancers highlights an array of diverse regulatory elements that are conserved in mammals | Q48251434 | ||
Neural induction and regionalisation in the chick embryo | Q48512472 | ||
Progressive induction of caudal neural character by graded Wnt signaling | Q48607954 | ||
P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 17 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell | Q7868 |
embryonic structure | Q30062554 | ||
nervous system | Q9404 | ||
P304 | page(s) | 2864-75 | |
P577 | publication date | 2015-09-01 | |
P1433 | published in | Development | Q3025404 |
P1476 | title | Neuromesodermal progenitors and the making of the spinal cord | |
P478 | volume | 142 |
Q33658152 | A Gene Regulatory Network Balances Neural and Mesoderm Specification during Vertebrate Trunk Development |
Q51118312 | A Gradient of Glycolytic Activity Coordinates FGF and Wnt Signaling during Elongation of the Body Axis in Amniote Embryos. |
Q96769261 | A Tgfbr1/Snai1-dependent developmental module at the core of vertebrate axial elongation |
Q42417041 | A novel cold-sensitive mutant of ntla reveals temporal roles of brachyury in zebrafish |
Q47718096 | A stepwise model of reaction-diffusion and positional information governs self-organized human peri-gastrulation-like patterning |
Q49545312 | Antagonism between the transcription factors NANOG and OTX2 specifies rostral or caudal cell fate during neural patterning transition. |
Q99721478 | Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
Q97524919 | Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes |
Q39448322 | At the base of colinear Hox gene expression: cis-features and trans-factors orchestrating the initial phase of Hox cluster activation |
Q38859697 | Axial level-dependent molecular and cellular mechanisms underlying the genesis of the embryonic neural plate |
Q55346231 | BMP and FGF signaling interact to pattern mesoderm by controlling basic helix-loop-helix transcription factor activity. |
Q36399912 | Biomechanical coupling facilitates spinal neural tube closure in mouse embryos |
Q92067502 | CDX4 regulates the progression of neural maturation in the spinal cord |
Q33830443 | ChIP-seq analysis of genomic binding regions of five major transcription factors highlights a central role for ZIC2 in the mouse epiblast stem cell gene regulatory network. |
Q64093314 | Characterization and Therapeutic Application of Mesenchymal Stem Cells with Neuromesodermal Origin from Human Pluripotent Stem Cells |
Q37095287 | Co-expression of Foxa.a, Foxd and Fgf9/16/20 defines a transient mesendoderm regulatory state in ascidian embryos |
Q47587043 | Co-expression of Tbx6 and Sox2 identifies a novel transient neuromesoderm progenitor cell state |
Q90627425 | Comments on 'Molecular architecture of lineage allocation and tissue organization in early mouse embryo' |
Q42323938 | Defining recovery neurobiology of injured spinal cord by synthetic matrix-assisted hMSC implantation. |
Q37545446 | Early molecular events during retinoic acid induced differentiation of neuromesodermal progenitors |
Q64947950 | Efficient Generation of Trunk Neural Crest and Sympathetic Neurons from Human Pluripotent Stem Cells Via a Neuromesodermal Axial Progenitor Intermediate. |
Q91620991 | Eomes and Brachyury control pluripotency exit and germ-layer segregation by changing the chromatin state |
Q38964345 | Evo-engineering and the cellular and molecular origins of the vertebrate spinal cord. |
Q46411750 | FGF and canonical Wnt signaling cooperate to induce paraxial mesoderm from tailbud neuromesodermal progenitors through regulation of a two-step epithelial to mesenchymal transition. |
Q91614573 | Filling the Gap: Neural Stem Cells as A Promising Therapy for Spinal Cord Injury |
Q90788805 | Generation and post-injury integration of human spinal cord neural stem cells |
Q56529903 | Human axial progenitors generate trunk neural crest cells in vitro |
Q92503878 | In vitro characterization of the human segmentation clock |
Q96683897 | Intracellular pH controls WNT downstream of glycolysis in amniote embryos |
Q57045771 | Lineage tracing of axial progenitors using Nkx1-2CreER mice defines their trunk and tail contributions |
Q39188341 | Mapping body-building potential |
Q104515534 | Modeling mammalian trunk development in a dish |
Q92483967 | Molecular architecture of lineage allocation and tissue organization in early mouse embryo |
Q63090614 | Mouse but not zebrafish requires retinoic acid for control of neuromesodermal progenitors and body axis extension |
Q64892789 | Myc activity is required for maintenance of the neuromesodermal progenitor signalling network and for segmentation clock gene oscillations in mouse. |
Q47286671 | Myogenic progenitor specification from pluripotent stem cells. |
Q38998787 | Neural Subtype Specification from Human Pluripotent Stem Cells |
Q60609140 | Neural differentiation, selection and transcriptomic profiling of human neuromesodermal progenitor-like cells |
Q49346811 | Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues. |
Q39135434 | Neural tube closure: cellular, molecular and biomechanical mechanisms |
Q89721043 | Neural-fated self-renewing cells regulated by Sox2 during secondary neurulation in chicken tail bud |
Q92450893 | Neuro-mesodermal progenitors (NMPs): a comparative study between pluripotent stem cells and embryo-derived populations |
Q58563401 | Neurogenesis in the sea urchin embryo is initiated uniquely in three domains |
Q58563419 | Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
Q41639915 | Nuclear receptor corepressors Ncor1 and Ncor2 (Smrt) are required for retinoic acid-dependent repression of Fgf8 during somitogenesis |
Q64933040 | Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice. |
Q93074716 | Overview of Methods to Differentiate Sympathetic Neurons from Human Pluripotent Stem Cells |
Q38776431 | Playing with the cell cycle to build the spinal cord |
Q90163058 | Regulating Retinoic Acid Availability during Development and Regeneration: The Role of the CYP26 Enzymes |
Q97528953 | Regulation of Neurogenesis by FGF Signaling and Neurogenin in the Invertebrate Chordate Ciona |
Q48337799 | Regulation of posterior body and epidermal morphogenesis in zebrafish by localized Yap1 and Wwtr1. |
Q43227503 | Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism |
Q90629887 | Single-cell qPCR demonstrates that Repsox treatment changes cell fate from endoderm to neuroectoderm and disrupts epithelial-mesenchymal transition |
Q37534200 | Tet proteins influence the balance between neuroectodermal and mesodermal fate choice by inhibiting Wnt signaling |
Q90282727 | The Chick Caudolateral Epiblast Acts as a Permissive Niche for Generating Neuromesodermal Progenitor Behaviours |
Q39381816 | The Multiple Roles of FGF Signaling in the Developing Spinal Cord. |
Q92284678 | The interaction of maternal diabetes with mutations that affect folate metabolism and how they affect the development of neural tube defects in mice |
Q52325935 | The non-canonical Wnt-PCP pathway shapes the caudal neural plate. |
Q90321927 | The vertebrate tail: a gene playground for evolution |
Q36497733 | The zebrafish tailbud contains two independent populations of midline progenitor cells that maintain long-term germ layer plasticity and differentiate in response to local signaling cues |
Q61807528 | Transcriptionally dynamic progenitor populations organised around a stable niche drive axial patterning |
Q33364683 | Turn It Down a Notch |
Q98394731 | Understanding paraxial mesoderm development and sclerotome specification for skeletal repair |
Search more.