How does Fgf signaling from the isthmic organizer induce midbrain and cerebellum development?
暂无分享,去创建一个
Harukazu Nakamura | A. Joyner | Alexandra L. Joyner | Harukazu Nakamura | Tatsuya Sato | Tatsuya Sato
[1] H. Ohuchi,et al. Role of Pax‐5 in the regulation of a mid‐hindbrain organizer’s activity , 1999, Development, growth & differentiation.
[2] M. Ekker,et al. fgfr3 and regionalization of anterior neural tube in zebrafish , 2001, Mechanisms of Development.
[3] D. Ornitz,et al. Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18. , 2002, Genes & development.
[4] A. Joyner,et al. Cell Behaviors and Genetic Lineages of the Mesencephalon and Rhombomere 1 , 2004, Neuron.
[5] Francis Vella,et al. Distinct regulators control the expression of the mid-hindbrain organizer signal FGF8 , 2001, Nature Neuroscience.
[6] C. MacArthur,et al. Genomic structure, mapping, activity and expression of fibroblast growth factor 17 , 1999, Mechanisms of Development.
[7] M. Wassef,et al. Relationship between Wnt-1 and En-2 expression domains during early development of normal and ectopic met-mesencephalon. , 1992, Development.
[8] Wolfgang Wurst,et al. FGFR1 is independently required in both developing mid‐ and hindbrain for sustained response to isthmic signals , 2003, The EMBO journal.
[9] Harukazu Nakamura. Regionalization of the optic tectum: combinations of gene expression that define the tectum , 2001, Trends in Neurosciences.
[10] C. Irving,et al. Regeneration of isthmic tissue is the result of a specific and direct interaction between rhombomere 1 and midbrain. , 1999, Development.
[11] M. Hatten,et al. The role of the rhombic lip in avian cerebellum development. , 1999, Development.
[12] A. Joyner,et al. En-1 and En-2, two mouse genes with sequence homology to the Drosophila engrailed gene: expression during embryogenesis. , 1987, Genes & development.
[13] Harukazu Nakamura,et al. Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development. , 2002, Development.
[14] Mario R. Capecchi,et al. Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development , 1990, Nature.
[15] Salvador Martinez,et al. Midbrain development induced by FGF8 in the chick embryo , 1996, Nature.
[16] M. Wassef,et al. Induction of a mesencephalic phenotype in the 2-day-old chick prosencephalon is preceded by the early expression of the homeobox gene en , 1991, Neuron.
[17] G. Martin,et al. The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo. , 1995, Development.
[18] C. Sotelo,et al. Homotopic and heterotopic transplantations of quail tectal primordia in chick embryos: organization of the retinotectal projections in the chimeric embryos. , 1984, Developmental biology.
[19] A. Joyner,et al. Engrailed, Wnt and Pax genes regulate midbrain--hindbrain development. , 1996, Trends in genetics : TIG.
[20] A. Simeone,et al. Fgf8 and Gbx2 induction concomitant with Otx2 repression is correlated with midbrain-hindbrain fate of caudal prosencephalon. , 1999, Development.
[21] Wolfgang Wurst,et al. Neural plate patterning: Upstream and downstream of the isthmic organizer , 2001, Nature Reviews Neuroscience.
[22] Michael Brand,et al. The Midbrain–hindbrain Boundary Organizer , 2022 .
[23] Y. Maeda,et al. The prepattern transcription factor Irx2, a target of the FGF8/MAP kinase cascade, is involved in cerebellum formation , 2004, Nature Neuroscience.
[24] C. A. Gardner,et al. The cellular environment controls the expression of engrailed-like protein in the cranial neuroepithelium of quail-chick chimeric embryos. , 1991, Development.
[25] A. Joyner,et al. Expression patterns of the homeo box-containing genes En-1 and En-2 and the proto-oncogene int-1 diverge during mouse development. , 1988, Genes & development.
[26] Peter Gruss,et al. Pax in development , 1992, Cell.
[27] Wolfgang Wurst,et al. The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum , 2003, Development.
[28] P. Gruss,et al. Conserved biological function between Pax-2 and Pax-5 in midbrain and cerebellum development: evidence from targeted mutations. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[29] M. Brand,et al. Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis. , 1998, Development.
[30] A. Joyner,et al. Early anterior/posterior patterning of the midbrain and cerebellum. , 2001, Annual review of neuroscience.
[31] H. Nakamura,et al. Inductive signal and tissue responsiveness defining the tectum and the cerebellum. , 2001, Development.
[32] J M Slack,et al. Spatial response to fibroblast growth factor signalling in Xenopus embryos. , 1999, Development.
[33] D. Ornitz,et al. Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures. , 2000, Development.
[34] Andrew P. McMahon,et al. Pax-2 expression in the murine neural plate precedes and encompasses the expression domains of Wnt-1 and En-1 , 1995, Mechanisms of Development.
[35] B. Hogan,et al. Comparison of the expression of three highly related genes, Fgf8, Fgf17 and Fgf18, in the mouse embryo , 1998, Mechanisms of Development.
[36] Alexandra L. Joyner,et al. A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer , 1999, Nature.
[37] K. G. Coleman,et al. Expression during embryogenesis of a mouse gene with sequence homology to the Drosophila engrailed gene , 1985, Cell.
[38] I. Mason,et al. Expression of FGFR1, FGFR2 and FGFR3 during early neural development in the chick embryo , 2000, Mechanisms of Development.
[39] P Gruss,et al. Pax: gene regulators in the developing nervous system. , 1993, Journal of neurobiology.
[40] Wolfgang Wurst,et al. The caudal limit of Otx2 expression positions the isthmic organizer , 1999, Nature.
[41] E. Hafen,et al. Ras--a versatile cellular switch. , 1998, Current opinion in genetics & development.
[42] Tobias Langenberg,et al. Isthmus-to-midbrain transformation in the absence of midbrain-hindbrain organizer activity , 2003, Development.
[43] A. Joyner,et al. Otx2 and Gbx2 are required for refinement and not induction of mid-hindbrain gene expression. , 2001, Development.
[44] A. Simeone,et al. The caudal limit of Otx2 gene expression as a marker of the midbrain/hindbrain boundary: a study using in situ hybridisation and chick/quail homotopic grafts. , 1996, Development.
[45] J. Rossant,et al. Spatial and temporal patterns of ERK signaling during mouse embryogenesis , 2003, Development.
[46] A. Joyner,et al. EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region. , 2001, Development.
[47] I. Cobos,et al. FGF 8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx 2 expression , 1999 .
[48] Andrew P. McMahon,et al. The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain , 1990, Cell.
[49] H. Nakamura,et al. Antagonizing activity of chick Grg4 against tectum-organizing activity. , 2000, Developmental biology.
[50] A. Simeone,et al. Positioning the isthmic organizer where Otx2 and Gbx2meet. , 2000, Trends in genetics : TIG.
[51] B. Bruneau,et al. The Iroquois Homeobox Gene Irx2 Is Not Essential for Normal Development of the Heart and Midbrain-Hindbrain Boundary in Mice , 2003, Molecular and Cellular Biology.
[52] A. Joyner,et al. Two Pax-binding sites are required for early embryonic brain expression of an Engrailed-2 transgene. , 1996, Development.
[53] N. Itoh,et al. FGF18 is required for normal cell proliferation and differentiation during osteogenesis and chondrogenesis. , 2002, Genes & development.
[54] A. Joyner,et al. Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2. , 1995, Science.
[55] A. McMahon,et al. Evidence that FGF8 signalling from the midbrain-hindbrain junction regulates growth and polarity in the developing midbrain. , 1997, Development.
[56] Harukazu Nakamura. Do CNS anlagen have plasticity in differentiation? Analysis in quail-chick chimera , 1990, Brain Research.
[57] F. McCormick,et al. Signal transduction from multiple Ras effectors. , 1997, Current opinion in genetics & development.
[58] A. Aguzzi,et al. Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis. , 1992, Genes & development.
[59] Jeffrey A. Golden,et al. The transcription factor Lmx1b maintains Wnt1 expression within the isthmic organizer. , 2000, Development.
[60] A. Simeone,et al. Regionalisation of anterior neuroectoderm and its competence in responding to forebrain and midbrain inducing activities depend on mutual antagonism between OTX2 and GBX2. , 2001, Development.
[61] The Fgf8 signal causes cerebellar differentiation by activating the Ras-ERK signaling pathway , 2004, Development.
[62] H. Nakamura,et al. Plasticity and rigidity of differentiation of brain vesicles studied in quail-chick chimeras. , 1986, Cell differentiation.
[63] S. Sugiyama,et al. Interaction between Otx2 and Gbx2 defines the organizing center for the optic tectum , 2000, Mechanisms of Development.
[64] N. Itasaki,et al. Expression of en in the Prosencephalon Heterotopically Transplanted into the Mesencephalon , 1992, Development, growth & differentiation.
[65] A. Joyner,et al. Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer. , 2000, Current opinion in cell biology.
[66] P. Doherty,et al. Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain. , 1999, Development.
[67] C. MacArthur,et al. FGF-8 isoforms differ in NIH3T3 cell transforming potential. , 1995, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[68] B. Shilo,et al. In situ activation pattern of Drosophila EGF receptor pathway during development. , 1997, Science.
[69] N. Itoh,et al. Involvement of fibroblast growth factor (FGF)18-FGF8 signaling in specification of left-right asymmetry and brain and limb development of the chick embryo , 2000, Mechanisms of Development.
[70] A. Kuroiwa,et al. Fgf signalling through MAPK cascade is required for development of the subpallial telencephalon in zebrafish embryos. , 2001, Development.
[71] Harukazu Nakamura. Regionalisation and acquisition of polarity in the optic tectum , 2001, Progress in Neurobiology.
[72] L. Puelles,et al. Induction of ectopic engrailed expression and fate change in avian rhombomeres: intersegmental boundaries as barriers , 1995, Mechanisms of Development.
[73] A. Joyner,et al. FGF17b and FGF18 have different midbrain regulatory properties from FGF8b or activated FGF receptors , 2003, Development.
[74] A. Joyner,et al. Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function. , 1997, Development.
[75] K. Losos,et al. FGF8 can activate Gbx2 and transform regions of the rostral mouse brain into a hindbrain fate. , 1999, Development.
[76] I. Cobos,et al. FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. , 1999, Development.
[77] G. Martin,et al. An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination , 1998, Nature Genetics.
[78] A. Joyner,et al. Changing Requirements for Gbx2 in Development of the Cerebellum and Maintenance of the Mid/Hindbrain Organizer , 2002, Neuron.