Notch is required for outgrowth of the Xenopus tail bud.
暂无分享,去创建一个
[1] J. Slack,et al. The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud. , 2001, Developmental Biology.
[2] Joseph L Goldstein,et al. Regulated Intramembrane Proteolysis A Control Mechanism Conserved from Bacteria to Humans , 2000, Cell.
[3] Raphael Kopan,et al. A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1. , 2000, Molecular cell.
[4] Julian Lewis,et al. Sequence and embryonic expression of deltaC in the zebrafish , 2000, Mechanisms of Development.
[5] A. Bernstein,et al. Mice lacking both presenilin genes exhibit early embryonic patterning defects. , 1999, Genes & development.
[6] S. Lincoln,et al. A Loss of Function Mutation of Presenilin-2 Interferes with Amyloid β-Peptide Production and Notch Signaling* , 1999, The Journal of Biological Chemistry.
[7] B. Yankner,et al. Proteolytic release and nuclear translocation of Notch-1 are induced by presenilin-1 and impaired by pathogenic presenilin-1 mutations. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[8] J M Slack,et al. A developmental pathway controlling outgrowth of the Xenopus tail bud. , 1999, Development.
[9] Iva Greenwald,et al. Presenilin is required for activity and nuclear access of Notch in Drosophila , 1999, Nature.
[10] William J. Ray,et al. A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain , 1999, Nature.
[11] Julian Lewis,et al. Vertebrate segmentation: The clock is linked to Notch signalling , 1998, Current Biology.
[12] P. Simpson. Introduction: Notch signalling and choice of cell fates in development. , 1998, Seminars in cell & developmental biology.
[13] Nigel A. Brown,et al. Waves of mouse Lunatic fringe expression, in four-hour cycles at two-hour intervals, precede somite boundary formation , 1998, Current Biology.
[14] J. Slack,et al. Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth , 1998, Mechanisms of Development.
[15] Hugo Vanderstichele,et al. Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein , 1998, Nature.
[16] R. Beddington,et al. Mouse Dll3: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo. , 1997, Development.
[17] T. Yamaguchi. New insights into segmentation and patterning during vertebrate somitogenesis. , 1997, Current opinion in genetics & development.
[18] S. Tonegawa,et al. Skeletal and CNS Defects in Presenilin-1-Deficient Mice , 1997, Cell.
[19] D. Price,et al. Presenilin 1 is required for Notch 1 and Dll1 expression in the paraxial mesoderm , 1997, Nature.
[20] M. Lardelli,et al. Three novel Notch genes in zebrafish: implications for vertebrate Notch gene evolution and function , 1997, Development Genes and Evolution.
[21] D. Simon,et al. Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta. , 1995, Development.
[22] Jonathan M.W. Slack,et al. Tail bud determination in the vertebrate embryo , 1995, Current Biology.
[23] David Ish-Horowicz,et al. Primary neurogenesis in Xenopus embryos regulated by a homologue of the Drosophila neurogenic gene Delta , 1995, Nature.
[24] J. Slack,et al. The Xenopus laevis tail-forming region , 1995 .
[25] J. Slack. Inducing factors in Xenopus early embryos , 1994, Current Biology.
[26] J. Faber,et al. Normal table of Xenopus laevis. , 1994 .
[27] J. Rossant,et al. Expression analysis of a Notch homologue in the mouse embryo. , 1992, Developmental biology.
[28] J. Brockes,et al. Monoclonal antibodies identify blastemal cells derived from dedifferentiating muscle in newt limb regeneration , 1984, Nature.