Spemann's organizer and self-regulation in amphibian embryos
暂无分享,去创建一个
[1] E. Robertis,et al. Embryonic Dorsal-Ventral Signaling: Secreted Frizzled-Related Proteins as Inhibitors of Tolloid Proteinases , 2006, Cell.
[2] E. Robertis,et al. Regulation of ADMP and BMP2/4/7 at Opposite Embryonic Poles Generates a Self-Regulating Morphogenetic Field , 2005, Cell.
[3] Robert W Cook,et al. The structure of the follistatin:activin complex reveals antagonism of both type I and type II receptor binding. , 2005, Developmental cell.
[4] E. D. De Robertis,et al. Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos , 2005, Development.
[5] C. Stern. Neural induction: old problem, new findings, yet more questions , 2005, Development.
[6] E. D. De Robertis,et al. Default neural induction: neuralization of dissociated Xenopus cells is mediated by Ras/MAPK activation. , 2005, Genes & development.
[7] M. Khokha,et al. Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures. , 2005, Developmental cell.
[8] S. Fisher,et al. Twisted gastrulation enhances BMP signaling through chordin dependent and independent mechanisms , 2005, Development.
[9] H. Spemann,et al. Versuche zur Analyse der Induktionsmittel in der Embryonalentwicklung , 1932, Naturwissenschaften.
[10] Shawn C. Little,et al. Twisted gastrulation promotes BMP signaling in zebrafish dorsal-ventral axial patterning , 2004, Development.
[11] E. D. De Robertis,et al. Dorsal-ventral patterning and neural induction in Xenopus embryos. , 2004, Annual review of cell and developmental biology.
[12] E. Robertis,et al. Neural Induction in Xenopus: Requirement for Ectodermal and Endomesodermal Signals via Chordin, Noggin, β-Catenin, and Cerberus , 2004, PLoS biology.
[13] J. Massagué. Integration of Smad and MAPK pathways: a link and a linker revisited. , 2003, Genes & development.
[14] E. D. De Robertis,et al. Integration of IGF, FGF, and anti-BMP signals via Smad1 phosphorylation in neural induction. , 2003, Genes & development.
[15] S. Schulte-Merker,et al. The ventralized ogon mutant phenotype is caused by a mutation in the zebrafish homologue of Sizzled, a secreted Frizzled-related protein. , 2003, Developmental biology.
[16] T. Hirano,et al. Ogon/Secreted Frizzled functions as a negative feedback regulator of Bmp signaling , 2003, Development.
[17] M. Kirschner,et al. The secreted Frizzled-related protein Sizzled functions as a negative feedback regulator of extreme ventral mesoderm , 2003, Development.
[18] E. D. De Robertis,et al. Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos. , 2003, Developmental cell.
[19] L. Dale,et al. Xolloid-related: a novel BMP1/Tolloid-related metalloprotease is expressed during early Xenopus development , 2002, Mechanisms of Development.
[20] Christof Niehrs,et al. Kremen proteins are Dickkopf receptors that regulate Wnt/β-catenin signalling , 2002, Nature.
[21] J. Heasman. Morpholino oligos: making sense of antisense? , 2002, Developmental biology.
[22] H. Spemann,et al. Induction of embryonic primordia by implantation of organizers from a different species. 1923. , 2001, The International journal of developmental biology.
[23] M. Oelgeschläger,et al. The establishment of spemann's organizer and patterning of the vertebrate embryo , 2000, Nature Reviews Genetics.
[24] E. Robertis,et al. The evolutionarily conserved BMP-binding protein Twisted gastrulation promotes BMP signalling , 2000, Nature.
[25] Ryan M. Anderson,et al. The organizer factors Chordin and Noggin are required for mouse forebrain development , 2000, Nature.
[26] C. Niehrs,et al. Requirement for anti-dorsalizing morphogenetic protein in organizer patterning , 2000, Mechanisms of Development.
[27] C. Niehrs,et al. Synexpression groups in eukaryotes , 1999, Nature.
[28] C. Niehrs,et al. Silencing of TGF-β signalling by the pseudoreceptor BAMBI , 1999, Nature.
[29] R. Beddington,et al. Axis Development and Early Asymmetry in Mammals , 1999, Cell.
[30] C. Niehrs,et al. Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction , 1998, Nature.
[31] Leslie Dale,et al. Cleavage of Chordin by Xolloid Metalloprotease Suggests a Role for Proteolytic Processing in the Regulation of Spemann Organizer Activity , 1997, Cell.
[32] R. Harland,et al. The Spemann Organizer Signal noggin Binds and Inactivates Bone Morphogenetic Protein 4 , 1996, Cell.
[33] Y. Sasai,et al. Dorsoventral Patterning in Xenopus: Inhibition of Ventral Signals by Direct Binding of Chordin to BMP-4 , 1996, Cell.
[34] T. Bouwmeester,et al. Cerberus is a head-inducing secreted factor expressed in the anterior endoderm of Spemann's organizer , 1996, Nature.
[35] B. Stillman,et al. Cold Spring Harbor Laboratory , 1995, Molecular medicine.
[36] M. Krinks,et al. Anti-dorsalizing morphogenetic protein is a novel TGF-beta homolog expressed in the Spemann organizer. , 1995, Development.
[37] Y. Sasai,et al. Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus , 1995, Nature.
[38] P. Wilson,et al. Induction of epidermis and inhibition of neural fate by Bmp-4 , 1995, Nature.
[39] Y. Sasai,et al. Xenopus chordin: A novel dorsalizing factor activated by organizer-specific homeobox genes , 1994, Cell.
[40] D. Melton,et al. Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity , 1994, Cell.
[41] R. Harland,et al. Neural induction by the secreted polypeptide noggin. , 1993, Science.
[42] Ken W. Y. Cho,et al. The homeobox gene goosecoid controls cell migration in Xenopus embryos , 1993, Cell.
[43] William C. Smith,et al. Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos , 1992, Cell.
[44] M. Jamrich,et al. A novel, activin-inducible, blastopore lip-specific gene of Xenopus laevis contains a fork head DNA-binding domain. , 1992, Genes & development.
[45] P. Good,et al. The LIM domain-containing homeo box gene Xlim-1 is expressed specifically in the organizer region of Xenopus gastrula embryos. , 1992, Genes & development.
[46] Ken W. Y. Cho,et al. Molecular nature of Spemann's organizer: the role of the Xenopus homeobox gene goosecoid , 1991, Cell.
[47] E. D. De Robertis,et al. Gradient fields and homeobox genes. , 1991, Development.
[48] Gillian M. Morriss-Kay,et al. Langman's Medical Embryology , 1991 .
[49] J. Gurdon,et al. The heritage of experimental embryology: Hans Spemann and the organizer by Viktor Hamburger, Oxford University Press, 1988. £22.50/$29.95 (196 pages) ISBN 0 19505 110 6 , 1989, Trends in Neurosciences.
[50] L. Tacke,et al. Neural differentiation of Xenopus laevis ectoderm takes place after disaggregation and delayed reaggregation without inducer. , 1989, Cell differentiation and development : the official journal of the International Society of Developmental Biologists.
[51] J. Slack. The heritage of experimental embryology: Hans Spemann and the organizer , 1989, Medical History.
[52] J. Saint-Jeannet,et al. Neural induction. , 1986, Archives d'anatomie microscopique et de morphologie experimentale.
[53] William McGinnis,et al. Cloning of an X. laevis gene expressed during early embryogenesis coding for a peptide region homologous to Drosophila homeotic genes , 1984, Cell.
[54] T.W.Sadler. Langman's Medical Embryology , 1969 .
[55] Arthur Hughes,et al. Analysis of Development , 1955 .
[56] Viktor Hamburger,et al. Analysis of development , 1955 .
[57] A. M. Turing,et al. The chemical basis of morphogenesis , 1952, Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences.
[58] J. Holtfreter. Neural differentiation of ectoderm through exposure to saline solution , 1944 .
[59] L. G. Barth. Neural differentiation without organizer , 1941 .
[60] R. R. Bensley,et al. Embryonic Development and Induction , 1938, The Yale Journal of Biology and Medicine.
[61] T. Morgan. Embryology And Genetics , 1934 .
[62] R. G. Harrison,et al. Experiments on the development of the fore limb of Amblystoma, a self‐differentiating equipotential system , 1918 .