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Summary Anatomy Item Literature (1054) Expression Attributions Wiki
XB-ANAT-200

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Mesodermal cell migration during Xenopus gastrulation., Winklbauer R., Dev Biol. November 1, 1990; 142 (1): 155-68.


A mesoderm-inducing factor produced by WEHI-3 murine myelomonocytic leukemia cells is activin A., Albano RM., Development. October 1, 1990; 110 (2): 435-43.


Two types of intrinsic muscarinic responses in Xenopus oocytes. II. Hemispheric asymmetry of responses and receptor distribution., Matus-Leibovitch N., Pflugers Arch. October 1, 1990; 417 (2): 194-9.


Graded changes in dose of a Xenopus activin A homologue elicit stepwise transitions in embryonic cell fate., Green JB., Nature. September 27, 1990; 347 (6291): 391-4.


Studies on the expression of intracellular and surface polarity in animal pole cells of Xenopus embryos cultured on various substrata., Asada-Kubota M., J Struct Biol. April 1, 1990; 103 (2): 113-23.


The Xenopus MyoD gene: an unlocalised maternal mRNA predates lineage-restricted expression in the early embryo., Harvey RP., Development. April 1, 1990; 108 (4): 669-80.


Mesoderm induction by fibroblast growth factor in early Xenopus development., Slack JM., Philos Trans R Soc Lond B Biol Sci. March 12, 1990; 327 (1239): 75-84.


Fibronectin-rich fibrillar extracellular matrix controls cell migration during amphibian gastrulation., Boucaut JC., Int J Dev Biol. March 1, 1990; 34 (1): 139-47.              


A two-step model for the localization of maternal mRNA in Xenopus oocytes: involvement of microtubules and microfilaments in the translocation and anchoring of Vg1 mRNA., Yisraeli JK., Development. February 1, 1990; 108 (2): 289-98.              


Mesoderm induction and the control of gastrulation in Xenopus laevis: the roles of fibronectin and integrins., Smith JC., Development. February 1, 1990; 108 (2): 229-38.


Effect of microinjection of a low-Mr human placenta protein tyrosine phosphatase on induction of meiotic cell division in Xenopus oocytes., Tonks NK., Mol Cell Biol. February 1, 1990; 10 (2): 458-63.


Differential keratin gene expression during the differentiation of the cement gland of Xenopus laevis., LaFlamme SE., Dev Biol. February 1, 1990; 137 (2): 414-8.        


The biological effects of XTC-MIF: quantitative comparison with Xenopus bFGF., Green JB., Development. January 1, 1990; 108 (1): 173-83.


Segregation of fate during cleavage of frog (Xenopus laevis) blastomeres., Moody SA., Anat Embryol (Berl). January 1, 1990; 182 (4): 347-62.


Inositol 1,4,5-trisphosphate-induced calcium mobilization is localized in Xenopus oocytes., Berridge MJ., Proc R Soc Lond B Biol Sci. December 22, 1989; 238 (1292): 235-43.


Cellular polarity in cultured animal pole cells of Xenopus embryos., Asada-Kubota M., J Ultrastruct Mol Struct Res. December 1, 1989; 102 (3): 265-75.


Spatial aspects of neural induction in Xenopus laevis., Jones EA., Development. December 1, 1989; 107 (4): 785-91.          


Tissue-specific processing and polarized compartmentalization of clone-produced cholinesterase in microinjected Xenopus oocytes., Dreyfus PA., Cell Mol Neurobiol. September 1, 1989; 9 (3): 323-41.


Clonal analysis of mesoderm induction in Xenopus laevis., Godsave SF., Dev Biol. August 1, 1989; 134 (2): 486-90.


Latencies of membrane currents evoked in Xenopus oocytes by receptor activation, inositol trisphosphate and calcium., Miledi R., J Physiol. August 1, 1989; 415 189-210.


MPF-induced breakdown of cytokeratin filament organization in the maturing Xenopus oocyte depends upon the translation of maternal mRNAs., Klymkowsky MW., Dev Biol. August 1, 1989; 134 (2): 479-85.      


Induction of mesoderm by a viral oncogene in early Xenopus embryos., Whitman M., Science. May 19, 1989; 244 (4906): 803-6.


Analysis of competence: receptors for fibroblast growth factor in early Xenopus embryos., Gillespie LL., Development. May 1, 1989; 106 (1): 203-8.


Mesoderm-inducing properties of INT-2 and kFGF: two oncogene-encoded growth factors related to FGF., Paterno GD., Development. May 1, 1989; 106 (1): 79-83.


Developmental expression of the protein product of Vg1, a localized maternal mRNA in the frog Xenopus laevis., Dale L., EMBO J. April 1, 1989; 8 (4): 1057-65.


Potentiation by the lithium ion of morphogenetic responses to a Xenopus inducing factor., Cooke J., Development. March 1, 1989; 105 (3): 549-58.


Inducing factors and the control of mesodermal pattern in Xenopus laevis., Smith JC., Development. January 1, 1989; 107 Suppl 149-59.


Mesoderm induction in Xenopus laevis: responding cells must be in contact for mesoderm formation but suppression of epidermal differentiation can occur in single cells., Symes K., Development. December 1, 1988; 104 (4): 609-18.


Nuclear protein synthesis in animal and vegetal hemispheres of Xenopus oocytes., Feldherr CM., Exp Cell Res. December 1, 1988; 179 (2): 527-34.


Localization of c-myc expression during oogenesis and embryonic development in Xenopus laevis., Hourdry J., Development. December 1, 1988; 104 (4): 631-41.          


Hemispheric asymmetry of rapid chloride responses to inositol trisphosphate and calcium in Xenopus oocytes., Lupu-Meiri M., FEBS Lett. November 21, 1988; 240 (1-2): 83-7.


Expression of Epi 1, an epidermis-specific marker in Xenopus laevis embryos, is specified prior to gastrulation., London C., Dev Biol. October 1, 1988; 129 (2): 380-9.              


Expression of a histone H1-like protein is restricted to early Xenopus development., Smith RC., Genes Dev. October 1, 1988; 2 (10): 1284-95.              


Inositol trisphosphate-induced membrane potential oscillations in Xenopus oocytes., Berridge MJ., J Physiol. September 1, 1988; 403 589-99.


Patterns of junctional communication during development of the early amphibian embryo., Guthrie S., Development. August 1, 1988; 103 (4): 769-83.


Purification, partial characterization and biological effects of the XTC mesoderm-inducing factor., Smith JC., Development. July 1, 1988; 103 (3): 591-600.


Maitotoxin triggers the cortical reaction and phosphatidylinositol-4,5-bisphosphate breakdown in amphibian oocytes., Bernard V., Eur J Biochem. July 1, 1988; 174 (4): 655-62.


Vimentin expression in oocytes, eggs and early embryos of Xenopus laevis., Tang P., Development. June 1, 1988; 103 (2): 279-87.              


Differences in receptor-evoked membrane electrical responses in native and mRNA-injected Xenopus oocytes., Oron Y., Proc Natl Acad Sci U S A. June 1, 1988; 85 (11): 3820-4.


The function of the nuclear envelope in nuclear protein accumulation., Zimmer FJ., J Cell Biol. May 1, 1988; 106 (5): 1435-44.            


Analysis of proteins in the peripheral and central regions of amphibian oocytes and eggs., Capco DG., Cell Differ. April 1, 1988; 23 (3): 155-64.


Dorsal and ventral cells of cleavage-stage Xenopus embryos show the same ability to induce notochord and somite formation., Pierce KE., Dev Biol. April 1, 1988; 126 (2): 228-32.


Regulatory factors of embryonic stem cells., Heath JK., J Cell Sci Suppl. January 1, 1988; 10 257-66.


Expression and segregation of nucleoplasmin during development in Xenopus., Litvin J., Development. January 1, 1988; 102 (1): 9-21.                    


Synergistic induction of mesoderm by FGF and TGF-beta and the identification of an mRNA coding for FGF in the early Xenopus embryo., Kimelman D., Cell. December 4, 1987; 51 (5): 869-77.


A maternal mRNA localized to the vegetal hemisphere in Xenopus eggs codes for a growth factor related to TGF-beta., Weeks DL., Cell. December 4, 1987; 51 (5): 861-7.        


The organization of mesodermal pattern in Xenopus laevis: experiments using a Xenopus mesoderm-inducing factor., Cooke J., Development. December 1, 1987; 101 (4): 893-908.            


The development of an assay to detect mRNAs that affect early development., Woodland HR., Development. December 1, 1987; 101 (4): 925-30.


The Xenopus animal pole blastomere., Smith JC., Bioessays. November 1, 1987; 7 (5): 229-34.


The involvement of inositol 1,4,5-trisphosphate and calcium in the two-component response to acetylcholine in Xenopus oocytes., Gillo B., J Physiol. November 1, 1987; 392 349-61.

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