Tissue Rotation of the Xenopus Anterior–Posterior Neural Axis Reveals Profound but Transient Plasticity at the Mid-Gastrula Stage
暂无分享,去创建一个
[1] A. Wills,et al. Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration. , 2022, Developmental biology.
[2] C. Niehrs. The role of Xenopus developmental biology in unraveling Wnt signalling and antero-posterior axis formation. , 2021, Developmental biology.
[3] Jaebong Kim,et al. The Organizer and Its Signaling in Embryonic Development , 2021, Journal of developmental biology.
[4] Aditi Dubey,et al. Anterior patterning genes induced by Zic1 are sensitive to retinoic acid and its metabolite, 4‐oxo‐RA , 2021, Developmental dynamics : an official publication of the American Association of Anatomists.
[5] Andrew L. Miller,et al. Transmembrane H+ fluxes and the regulation of neural induction in Xenopus laevis. , 2021, Zygote.
[6] R. Krumlauf,et al. Segmentation and patterning of the vertebrate hindbrain. , 2021, Development.
[7] S. Sokol,et al. The dorsal blastopore lip is a source of signals inducing planar cell polarity in the Xenopus neural plate , 2021, Biology open.
[8] H. Willsey,et al. Xenopus leads the way: Frogs as a pioneering model to understand the human brain , 2020, Genesis.
[9] N. Sasai,et al. Neural induction: Historical views and application to pluripotent stem cells , 2020, Development, growth & differentiation.
[10] M. Lutolf,et al. Gastruloids generated without exogenous Wnt activation develop anterior neural tissues , 2020, bioRxiv.
[11] D. Stainier,et al. Transcriptional adaptation: a mechanism underlying genetic robustness , 2020, Development.
[12] R. Vadigepalli,et al. Retinoic Acid Fluctuation Activates an Uneven, Direction-Dependent Network-Wide Robustness Response in Early Embryogenesis , 2020, Frontiers in Cell and Developmental Biology.
[13] H. Vihinen,et al. Heterochromatin-Driven Nuclear Softening Protects the Genome against Mechanical Stress-Induced Damage , 2020, Cell.
[14] M. Levin,et al. Morphological Coordination: A Common Ancestral Function Unifying Neural and Non-Neural Signaling. , 2020, Physiology.
[15] Andrew D. Halleran,et al. Xenopus embryos show a compensatory response following perturbation of the Notch signaling pathway , 2019, Developmental biology.
[16] Troy J. Pells,et al. Xenbase: deep integration of GEO & SRA RNA-seq and ChIP-seq data in a model organism database , 2019, Nucleic Acids Res..
[17] O. Pourquié,et al. Mechanics of Anteroposterior Axis Formation in Vertebrates. , 2019, Annual review of cell and developmental biology.
[18] P. Beldade,et al. Genomics of Developmental Plasticity in Animals , 2019, Front. Genet..
[19] B. Martin,et al. Transformation of a neural activation and patterning model , 2019, EMBO reports.
[20] N. Ueno,et al. Cdc2‐like kinase 2 (Clk2) promotes early neural development in Xenopus embryos , 2019, Development, growth & differentiation.
[21] D. Frank,et al. New roles for Wnt and BMP signaling in neural anteroposterior patterning , 2019, EMBO reports.
[22] A. Qutub,et al. A novel self-organizing embryonic stem cell system reveals signaling logic underlying the patterning of human ectoderm , 2019, Development.
[23] R. Harland,et al. Integration of Wnt and FGF signaling in the Xenopus gastrula at TCF and Ets binding sites shows the importance of short-range repression by TCF in patterning the marginal zone , 2019, Development.
[24] S. Moody. Lineage Tracing and Fate Mapping in Xenopus Embryos. , 2018, Cold Spring Harbor protocols.
[25] R. Lovell-Badge,et al. Nervous System Regionalization Entails Axial Allocation before Neural Differentiation , 2018, Cell.
[26] Tim Ott,et al. Xenopus: An Undervalued Model Organism to Study and Model Human Genetic Disease , 2018, Cells Tissues Organs.
[27] Yi Zheng,et al. Mechanics-guided embryonic patterning of neuroectoderm tissue from human pluripotent stem cells , 2018, Nature Materials.
[28] A. Suzuki,et al. Coordinated regulation of the dorsal‐ventral and anterior‐posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14 , 2018, Development, growth & differentiation.
[29] A. Martinez Arias,et al. On the nature and function of organizers , 2018, Development.
[30] A. Streit,et al. Neural induction by the node and placode induction by head mesoderm share an initial state resembling neural plate border and ES cells , 2017, Proceedings of the National Academy of Sciences.
[31] L. N. Borodinsky. Xenopus laevis as a Model Organism for the Study of Spinal Cord Formation, Development, Function and Regeneration , 2017, Front. Neural Circuits.
[32] M. Eisen,et al. A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates , 2017, PLoS biology.
[33] M. Bronner,et al. Dynamic transcriptional signature and cell fate analysis reveals plasticity of individual neural plate border cells , 2017, eLife.
[34] S. Moody,et al. Using Xenopus to understand human disease and developmental disorders , 2017, Genesis.
[35] G. Ming,et al. Epigenetic mechanisms in neurogenesis , 2016, Nature Reviews Neuroscience.
[36] I. Daar,et al. Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm , 2016, Genesis.
[37] C. Carron,et al. Specification of anteroposterior axis by combinatorial signaling during Xenopus development , 2016, Wiley interdisciplinary reviews. Developmental biology.
[38] G. Blin,et al. Position-dependent plasticity of distinct progenitor types in the primitive streak , 2016, eLife.
[39] AnjaliL . Rao,et al. Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells , 2015, Science.
[40] M. Mullins,et al. Temporally coordinated signals progressively pattern the anteroposterior and dorsoventral body axes. , 2015, Seminars in cell & developmental biology.
[41] M. Zernicka-Goetz,et al. Developmental plasticity, cell fate specification and morphogenesis in the early mouse embryo , 2014, Philosophical Transactions of the Royal Society B: Biological Sciences.
[42] I. Arregi,et al. Active signals, gradient formation and regional specificity in neural induction. , 2014, Experimental cell research.
[43] J. Nichols,et al. A molecular basis for developmental plasticity in early mammalian embryos , 2013, Development.
[44] S. L. Klein,et al. On becoming neural: what the embryo can tell us about differentiating neural stem cells. , 2013, American journal of stem cells.
[45] M. Mullins,et al. Anteroposterior and dorsoventral patterning are coordinated by an identical patterning clock , 2013, Development.
[46] D. Kimelman,et al. Anterior–posterior patterning in early development: three strategies , 2012, Wiley interdisciplinary reviews. Developmental biology.
[47] R. Harland,et al. Microinjection of Xenopus embryos. , 2010, Cold Spring Harbor protocols.
[48] R. Harland,et al. Microinjection of RNA and preparation of secreted proteins from Xenopus oocytes. , 2010, Cold Spring Harbor protocols.
[49] R. Harland,et al. Calibration of the injection volume for microinjection of Xenopus oocytes and embryos. , 2010, Cold Spring Harbor protocols.
[50] S. Moody,et al. Neural induction and factors that stabilize a neural fate. , 2009, Birth defects research. Part C, Embryo today : reviews.
[51] J. I. Izpisúa Belmonte,et al. Beyond early development: Xenopus as an emerging model for the study of regenerative mechanisms , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[52] G. Crabtree,et al. ATP-dependent chromatin remodeling in neural development , 2009, Current Opinion in Neurobiology.
[53] N. Staudt,et al. The Prethalamus Is Established during Gastrulation and Influences Diencephalic Regionalization , 2007, PLoS biology.
[54] J. Krebs,et al. Neural and eye-specific defects associated with loss of the Imitation Switch (ISWI) chromatin remodeler in Xenopus laevis , 2005, Mechanisms of Development.
[55] M. Wullimann,et al. Secondary neurogenesis in the brain of the African clawed frog, Xenopus laevis, as revealed by PCNA, Delta‐1, Neurogenin‐related‐1, and NeuroD expression , 2005, The Journal of comparative neurology.
[56] C. Stern. Neural induction: old problem, new findings, yet more questions , 2005, Development.
[57] K. Kroll,et al. The SWI/SNF chromatin remodeling protein Brg1 is required for vertebrate neurogenesis and mediates transactivation of Ngn and NeuroD , 2004, Development.
[58] C. Niehrs. Regionally specific induction by the Spemann–Mangold organizer , 2004, Nature Reviews Genetics.
[59] S. Moody. Xenopus Embryo: Neural Induction , 2001 .
[60] V. Prince,et al. Plasticity in zebrafish hox expression in the hindbrain and cranial neural crest. , 2001, Developmental biology.
[61] H. Sive,et al. Vertebrate anteroposterior patterning: the Xenopus neurectoderm as a paradigm , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.
[62] R. Keller,et al. The role of planar and early vertical signaling in patterning the expression of Hoxb-1 in Xenopus. , 1997, Developmental biology.
[63] R. Krumlauf,et al. Rhombomere of origin determines autonomous versus environmentally regulated expression of Hoxa-3 in the avian embryo. , 1996, Development.
[64] R. Krumlauf,et al. Reprogramming Hox Expression in the Vertebrate Hindbrain: Influence of Paraxial Mesoderm and Rhombomere Transposition , 1996, Neuron.
[65] J. Gurdon,et al. Normal table of Xenopus laevis (Daudin) , 1995 .
[66] R. Krumlauf,et al. Plasticity of transposed rhombomeres: Hox gene induction is correlated with phenotypic modifications. , 1995, Development.
[67] A. Lumsden,et al. Independent assignment of antero-posterior and dorso-ventral positional values in the developing chick hindbrain , 1995, Current Biology.
[68] V. Prince,et al. Selective dispersal of avian rhombomere cells in orthotopic and heterotopic grafts. , 1993, Development.
[69] M. Saha,et al. A labile period in the determination of the anterior-posterior axis during early neural development in Xenopus , 1992, Neuron.
[70] R. Krumlauf,et al. Neuroectodermal autonomy of Hox-2.9 expression revealed by rhombomere transpositions , 1992, Nature.
[71] J. Slack,et al. Mechanism of anteroposterior axis specification in vertebrates. Lessons from the amphibians. , 1992, Development.
[72] R. Grainger,et al. Changes in neural and lens competence in Xenopus ectoderm: evidence for an autonomous developmental timer. , 1991, Development.
[73] H. Weintraub,et al. Progressive determination during formation of the anteroposterior axis in Xenopus laevis , 1989, Cell.
[74] B. Albers. Competence as the Main Factor Determining the Size of the Neural Plate , 1987, Development, growth & differentiation.
[75] C. Kaye,et al. Regulation in the neural plate of Xenopus laevis demonstrated by genetic markers. , 1985, The Journal of experimental zoology.
[76] A. Jacobson. THE DETERMINATION AND POSITIONING OF THE NOSE, LENS AND EAR. III. EFFECTS OF REVERSING THE ANTERO-POSTERIOR AXIS OF EPIDERMIS, NEURAL PLATE AND NEURAL FOLD. , 1963, The Journal of experimental zoology.
[77] J. S. Nicholas. RESULTS OF INVERSION OF NEURAL PLATE MATERIAL. , 1957, Proceedings of the National Academy of Sciences of the United States of America.
[78] P. Nieuwkoop,et al. Activation and organization of the central nervous system in amphibians. Part III. Synthesis of a new working hypothesis , 1952 .
[79] P. Nieuwkoop. Activation and organization of the central nervous system in amphibians.† Part I. Induction and activation , 1952 .
[80] C. Waddington,et al. Studies on regional specificity within the organization centre of urodeles. , 1950, The Journal of experimental biology.
[81] Frances Cummings Roach. Differentiation of the central nervous system after axial reversals of the medullary plate of Amblystoma , 1945 .
[82] Grace E Solini,et al. Embryonic transplantation experiments: Past, present, and future. , 2017, Trends in developmental biology.
[83] C. Joseph. Plasticity. , 2013, Handbook of clinical neurology.
[84] Noah W. Gray,et al. Plasticity , 2010, Nature.
[85] S. Gilbert. Continuity and change: paradigm shifts in neural induction. , 2001, The International journal of developmental biology.
[86] R. Harland,et al. Early development of Xenopus laevis : a laboratory manual , 2000 .
[87] G. Eichele,et al. Rhombomere transplantation repatterns the segmental organization of cranial nerves and reveals cell-autonomous expression of a homeodomain protein. , 1993, Development.