Inductive signal and tissue responsiveness defining the tectum and the cerebellum.
暂无分享,去创建一个
H. Nakamura | T. Sato | Harukazu Nakamura | I. Araki | I Araki | H Nakamura | T Sato | Tatsuya Sato
[1] C. Irving,et al. Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression. , 2000, Development.
[2] Harukazu Nakamura,et al. A Role for Gradient en Expression in Positional Specification on the Optic Tectum , 1996, Neuron.
[3] K. Losos,et al. FGF8 can activate Gbx2 and transform regions of the rostral mouse brain into a hindbrain fate. , 1999, Development.
[4] I. Cobos,et al. FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. , 1999, Development.
[5] G. Martin,et al. An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination , 1998, Nature Genetics.
[6] 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.
[7] Wolfgang Wurst,et al. The caudal limit of Otx2 expression positions the isthmic organizer , 1999, Nature.
[8] A. Simeone,et al. Fgf8 and Gbx2 induction concomitant with Otx2 repression is correlated with midbrain-hindbrain fate of caudal prosencephalon. , 1999, Development.
[9] A. Simeone,et al. Positioning the isthmic organizer where Otx2 and Gbx2meet. , 2000, Trends in genetics : TIG.
[10] M. Hatten,et al. The role of the rhombic lip in avian cerebellum development. , 1999, Development.
[11] Salvador Martinez,et al. Midbrain development induced by FGF8 in the chick embryo , 1996, Nature.
[12] H. Nakamura,et al. Regulation of the neural crest cell fate by N-myc: promotion of ventral migration and neuronal differentiation. , 1997, Development.
[13] Harukazu Nakamura. Regionalization of the optic tectum: combinations of gene expression that define the tectum , 2001, Trends in Neurosciences.
[14] 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.
[15] K. Umesono,et al. Efficient targeting of gene expression in chick embryos by microelectroporation , 1999, Development, growth & differentiation.
[16] D A Kane,et al. Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain. , 1996, Development.
[17] H. Ohuchi,et al. Role of Pax‐5 in the regulation of a mid‐hindbrain organizer’s activity , 1999, Development, growth & differentiation.
[18] A. Joyner,et al. Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum. , 1994, Development.
[19] H. Nakamura,et al. Pax6 defines the di-mesencephalic boundary by repressing En1 and Pax2. , 2000, Development.
[20] Viktor Hamburger,et al. A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.
[21] S. Martinez,et al. Transplanted mesencephalic quail cells colonize selectively all primary visual nuclei of chick diencephalon: a study using heterotopic transplants. , 1989, Brain research. Developmental brain research.
[22] M. Brand,et al. Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function. , 1998, Development.
[23] G. Arbuthnott. Fundamental Neuroscience edited by M.J. Zigmond, F.E. Bloom, S.C. Landis, J.L. Roberts and L.R. Squire , 2000, Trends in Neurosciences.
[24] A. Joyner,et al. Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2. , 1995, Science.
[25] 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.
[26] A. McMahon,et al. Evidence that FGF8 signalling from the midbrain-hindbrain junction regulates growth and polarity in the developing midbrain. , 1997, Development.
[27] Harukazu Nakamura,et al. Rostrocaudal polarity of the tectum in birds: Correlation of en gradient and topographic order in retinotectal projection , 1992, Neuron.
[28] C. MacArthur,et al. FGF-8 isoforms activate receptor splice forms that are expressed in mesenchymal regions of mouse development. , 1995, Development.
[29] J. Funahashi,et al. Misexpression of genes in brain vesicles by in ovo electroporation , 2000, Development, growth & differentiation.
[30] C. MacArthur,et al. Genomic structure, mapping, activity and expression of fibroblast growth factor 17 , 1999, Mechanisms of Development.
[31] 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.
[32] Alexandra L. Joyner,et al. A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer , 1999, Nature.
[33] L. Puelles,et al. Induction of ectopic engrailed expression and fate change in avian rhombomeres: intersegmental boundaries as barriers , 1995, Mechanisms of Development.
[34] M. Wassef,et al. Involvement of Wnt-1 in the formation of the mes/metencephalic boundary , 1995, Mechanisms of Development.
[35] 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 .
[36] 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.
[37] D. Ornitz,et al. Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures. , 2000, Development.
[38] H. Nakamura,et al. Plasticity and rigidity of differentiation of brain vesicles studied in quail-chick chimeras. , 1986, Cell differentiation.
[39] S. Sugiyama,et al. Interaction between Otx2 and Gbx2 defines the organizing center for the optic tectum , 2000, Mechanisms of Development.
[40] H. Nakamura,et al. Pax6 defines the di-mesencephalic boundary by repressing En1 and Pax2. , 2000, Development.
[41] N. Itasaki,et al. Expression of en in the Prosencephalon Heterotopically Transplanted into the Mesencephalon , 1992, Development, growth & differentiation.
[42] H. Nakamura,et al. Roles of Pax-2 in initiation of the chick tectal development. , 1999, Brain research. Developmental brain research.
[43] N. Nakatsuji,et al. A mouse embryonic stem cell line showing pluripotency of differentiation in early embryos and ubiquitous beta-galactosidase expression. , 1990, Cell differentiation and development : the official journal of the International Society of Developmental Biologists.
[44] Stephen W. Wilson,et al. Zebrafish pax[b] is involved in the formation of the midbrain–hindbrain boundary , 1992, Nature.
[45] W. Cowan,et al. The development of the chick optic tectum. I. Normal morphology and cytoarchitectonic development. , 1971, Brain research.
[46] P. Doherty,et al. Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain. , 1999, Development.
[47] 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.
[48] H. Nakamura,et al. Engrailed defines the position of dorsal di-mesencephalic boundary by repressing diencephalic fate. , 1999, Development.