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Summary Anatomy Item Literature (10397) Expression Attributions Wiki
XB-ANAT-111

Papers associated with embryo

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The effect of egg rotation on the differentiation of primordial germ cells in Xenopus laevis., Cleine JH., J Embryol Exp Morphol. December 1, 1985; 90 79-99.


Cytological analyses of factors which determine the number of primordial germ cells (PGCs) in Xenopus laevis., Akita Y., J Embryol Exp Morphol. December 1, 1985; 90 251-65.


Map formation in the developing Xenopus retinotectal system: an examination of ganglion cell terminal arborizations., Sakaguchi DS., J Neurosci. December 1, 1985; 5 (12): 3228-45.


Developmental changes in keratin patterns during epidermal maturation., Ellison TR., Dev Biol. December 1, 1985; 112 (2): 329-37.


Different conformations of ribosomal DNA in active and inactive chromatin in Xenopus laevis., Spadafora C., J Mol Biol. December 20, 1985; 186 (4): 743-58.


[Distribution of differentiation potentials and the conditions for their realization in the amphibian neuroectoderm]., Golubeva ON., Ontogenez. January 1, 1986; 17 (6): 648-54.


[Effect of a short-term disturbance of the cell contacts on the mesodermal differentiation of clawed toad embryos]., Georgiev PG., Ontogenez. January 1, 1986; 17 (3): 256-62.


The time course of the changes in axon number of both oculomotor nerves in normal and unilaterally enucleated Xenopus laevis., Schönenberger N., Dev Biol. January 1, 1986; 389 (1-2): 169-77.


The migration of amphibian primordial germ cells in the chick embryo., England MA., Scan Electron Microsc. January 1, 1986; (Pt 3): 1175-82.


Developmental changes in P-face and E-face particle densities of Xenopus cardiac muscle plasma membrane., Kordylewski L., Tissue Cell. January 1, 1986; 18 (5): 793-801.


The coelomic envelope to vitelline envelope conversion in eggs of Xenopus laevis., Gerton GL., J Cell Biochem. January 1, 1986; 30 (4): 341-50.


Naturally occurring and induced ganglion cell death. A retinal whole-mount autoradiographic study in Xenopus., Jenkins S., Anat Embryol (Berl). January 1, 1986; 174 (1): 59-66.


Explanted and implanted notochord of amphibian anuran embryos. Histofluorescence study on the ability to synthesize catecholamines., Godin I., Anat Embryol (Berl). January 1, 1986; 173 (3): 393-9.


[Movements of cellular material of the dorsal wall in clawed-toad embryos during gastrulation and neurulation]., Petrov KV., Ontogenez. January 1, 1986; 17 (1): 78-83.


The development of serotonergic raphespinal projections in Xenopus laevis., van Mier P., Int J Dev Neurosci. January 1, 1986; 4 (5): 465-75.


Cytoskeletal changes during oogenesis and early development of Xenopus laevis., Wylie CC., J Cell Sci Suppl. January 1, 1986; 5 329-41.          


Ionophore-induced cell shape changes in Xenopus early embryos., Stanisstreet M., Cytobios. January 1, 1986; 46 (186-187): 155-65.


Spatial domains within the early Xenopus laevis embryo revealed by in situ hybridization and monoclonal antibodies., Phillips CR., Acta Histochem Suppl. January 1, 1986; 32 21-7.


Synaptic organization of dorsal root projections to lumbar motoneurons in the clawed toad (Xenopus laevis)., Shiriaev BI., Exp Brain Res. January 1, 1986; 63 (1): 135-42.


Involvement of calcium in the regulation of serotonin N-acetyltransferase in retina., Iuvone PM., J Neurochem. January 1, 1986; 46 (1): 82-8.


Cyclic AMP stimulates serotonin N-acetyltransferase activity in Xenopus retina in vitro., Iuvone PM., J Neurochem. January 1, 1986; 46 (1): 33-9.


Tissue interactions during axial structure pattern formation in amphibia., Malacinski GM., Scan Electron Microsc. January 1, 1986; (Pt 2): 307-18.


Permanent distortion of positional system of Xenopus embryo by brief early perturbation in gravity., Cooke J., Nature. January 2, 1986; 319 (6048): 60-3.


Evidence for a D2 dopamine receptor in frog retina that decreases cyclic AMP accumulation and serotonin N-acetyltransferase activity., Iuvone PM., Life Sci. January 27, 1986; 38 (4): 331-42.


Development of the ectoderm in Xenopus: tissue specification and the role of cell association and division., Jones EA., Cell. January 31, 1986; 44 (2): 345-55.                


Kinematics of gray crescent formation in Xenopus eggs: the displacement of subcortical cytoplasm relative to the egg surface., Vincent JP., Dev Biol. February 1, 1986; 113 (2): 484-500.


Pattern formation in 8-cell composite embryos of Xenopus laevis., Kageura H., J Embryol Exp Morphol. February 1, 1986; 91 79-100.


An examination of the evidence for the existence of preformed pathways in the neural tube of Xenopus laevis., Scott TM., J Embryol Exp Morphol. February 1, 1986; 91 181-95.


Localization of specific mRNA sequences in Xenopus laevis embryos by in situ hybridization., Dworkin-Rastl E., J Embryol Exp Morphol. February 1, 1986; 91 153-68.            


Expression of an epidermal antigen used to study tissue induction in the early Xenopus laevis embryo., Akers RM., Science. February 7, 1986; 231 (4738): 613-6.


Noncoordinate synthesis of the fibrinogen subunits in hepatocytes cultured under hormone-deficient conditions., Plant PW., J Biol Chem. February 15, 1986; 261 (5): 2331-6.


Cell interactions and the control of gene activity during early development of Xenopus laevis., Sargent TD., Dev Biol. March 1, 1986; 114 (1): 238-46.


Ocular migration and the metamorphic and postmetamorphic maturation of the retinotectal system in Xenopus laevis: an autoradiographic and morphometric study., Grant S., J Embryol Exp Morphol. March 1, 1986; 92 43-69.


The role of glycosaminoglycans in anuran pigment cell migration., Tucker RP., J Embryol Exp Morphol. March 1, 1986; 92 145-64.


Expression and modulation of voltage-gated calcium channels after RNA injection in Xenopus oocytes., Dascal N., Science. March 7, 1986; 231 (4742): 1147-50.


Dopamine receptor-mediated inhibition of serotonin N-acetyltransferase activity in retina., Iuvone PM., Dev Biol. March 26, 1986; 369 (1-2): 168-76.


Embryonic and regenerating Xenopus retinal fibers are intrinsically different., Grant P., Dev Biol. April 1, 1986; 114 (2): 475-91.


Pattern regulation in the eyebud of Xenopus studied with a vital-dye fiber-tracing technique., O'Rourke NA., Dev Biol. April 1, 1986; 114 (2): 277-88.


Dynamic aspects of retinotectal map formation revealed by a vital-dye fiber-tracing technique., O'Rourke NA., Dev Biol. April 1, 1986; 114 (2): 265-76.


Myoblasts and notochord influence the orientation of somitic myoblasts from Xenopus laevis., McCaig CD., J Embryol Exp Morphol. April 1, 1986; 93 121-31.


Use of Hybrids between Xenopus laevis and Xenopus borealis in Chimera Formation: Dorsalization of Ventral Cells: (cell lineage/chimera/hybrid/Xenopus/dorsalization)., Koga M., Dev Growth Differ. April 1, 1986; 28 (2): 177-183.


Observations on the mitochondrial distribution in normal, rotated and cold-treated 2-cell stage embryos of Xenopus laevis., Marinos E., Cell Differ. May 1, 1986; 18 (3): 163-71.


Control of the development of the ipsilateral retinothalamic projection in Xenopus laevis by thyroxine: results and speculation., Hoskins SG., J Neurobiol. May 1, 1986; 17 (3): 203-29.


Cell surface carbohydrate involvement in controlling the adhesion and morphology of neural crest cells and melanophores of Xenopus laevis., Milos NC., J Exp Zool. May 1, 1986; 238 (2): 211-24.


Myoblasts and myoblast-conditioned medium attract the earliest spinal neurites from frog embryos., McCaig CD., J Physiol. June 1, 1986; 375 39-54.


Replacement of posterior by anterior endoderm reduces sterility in embryos from inverted eggs of Xenopus laevis., Cleine JH., J Embryol Exp Morphol. June 1, 1986; 94 83-93.


Membrane protein redistribution during Xenopus first cleavage., Byers TJ., J Cell Biol. June 1, 1986; 102 (6): 2176-84.


Acquisition of developmental autonomy in the equatorial region of the Xenopus embryo., Gimlich RL., Dev Biol. June 1, 1986; 115 (2): 340-52.


Ammonium ion as a possible regulator of the commencement of rRNA synthesis in Xenopus laevis embryogenesis., Shiokawa K., Dev Biol. June 1, 1986; 115 (2): 380-91.


The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis., Eagleson GW., J Embryol Exp Morphol. June 1, 1986; 95 1-14.              

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