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Summary Anatomy Item Literature (6290) Expression Attributions Wiki
XB-ANAT-475

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Protein synthesis and messenger RNA levels along the animal-vegetal axis during early Xenopus development., Smith RC., J Embryol Exp Morphol. June 1, 1986; 95 15-35.


Peptide C-terminal alpha-amidating enzyme purified to homogeneity from Xenopus laevis skin., Mizuno K., Biochem Biophys Res Commun. June 30, 1986; 137 (3): 984-91.


Characterization of a high-Mr plasma-membrane-bound protein and assessment of its role as a constituent of hyaluronate synthase complex., Mian N., Biochem J. July 15, 1986; 237 (2): 343-57.


Analysis of cell-growth-phase-related variations in hyaluronate synthase activity of isolated plasma-membrane fractions of cultured human skin fibroblasts., Mian N., Biochem J. July 15, 1986; 237 (2): 333-42.


Induction of neural cell adhesion molecule (NCAM) in Xenopus embryos., Jacobson M., Dev Biol. August 1, 1986; 116 (2): 524-31.            


Covalent coupling of neuralizing factors from Xenopus to Sepharose beads: no decrease of inducing activity., Born J., Cell Differ. September 1, 1986; 19 (2): 97-101.


Sequential expression of murine homeo box genes during F9 EC cell differentiation., Breier G., EMBO J. September 1, 1986; 5 (9): 2209-15.


The appearance and distribution of intermediate filament proteins during differentiation of the central nervous system, skin and notochord of Xenopus laevis., Godsave SF., J Embryol Exp Morphol. September 1, 1986; 97 201-23.              


The inducing capacity of the presumptive endoderm of Xenopus laevis studied by transfilter experiments., Grunz H., Rouxs Arch Dev Biol. September 1, 1986; 195 (7): 467-473.


[Analytical study of Xenopus hindlimb regenerate with special reference to muscle regeneration]., Fujikura K., Jikken Dobutsu. October 1, 1986; 35 (4): 421-32.


Isolation of a dipeptidyl aminopeptidase, a putative processing enzyme, from skin secretion of Xenopus laevis., Mollay C., Eur J Biochem. October 1, 1986; 160 (1): 31-5.


Cell proliferation in the ectoderm of the Xenopus embryo: development of substratum requirements for cytokinesis., Winklbauer R., Dev Biol. November 1, 1986; 118 (1): 70-81.


Pigment cell pattern formation in amphibian embryos: a reexamination of the dopa technique., Tucker RP., J Exp Zool. November 1, 1986; 240 (2): 173-82.


Prospective Neural Areas and Their Morphogenetic Movements during Neural Plate Formation of Xenopus Embryos. I. Development of Vegetal Half Embryos and Chimera Embryos: (developmental fates/cell marker, quinacrine/Xenopus embryo)., Suzuki AS., Dev Growth Differ. November 1, 1986; 28 (6): 519-529.


Skin peptides in Xenopus laevis: morphological requirements for precursor processing in developing and regenerating granular skin glands., Flucher BE., J Cell Biol. December 1, 1986; 103 (6 Pt 1): 2299-309.                


Presumptive mesoderm cells from Xenopus laevis gastrulae attach to and migrate on substrata coated with fibronectin or laminin., Nakatsuji N., J Cell Sci. December 1, 1986; 86 109-18.


Expression of the c-myc proto-oncogene during development of Xenopus laevis., King MW, King MW., Mol Cell Biol. December 1, 1986; 6 (12): 4499-508.


[Rearrangement of the morphological structure and degradation of the extracellular matrix in amphibian embryos after short-term disruption of cell contacts]., Georgiev PG., Ontogenez. January 1, 1987; 18 (5): 535-40.


A mesoderm-inducing factor is produced by Xenopus cell line., Smith JC., Development. January 1, 1987; 99 (1): 3-14.              


Prolactin binding sites in Xenopus laevis tissues: comparison between normal and dehydrated animals., Guardabassi A., Gen Comp Endocrinol. January 1, 1987; 65 (1): 40-7.


The development of the Merkel cells in the tentacles of Xenopus laevis larvae., Eglmeier W., Anat Embryol (Berl). January 1, 1987; 176 (4): 493-500.


Cell behaviour during active cell rearrangement: evidence and speculations., Keller R., J Cell Sci Suppl. January 1, 1987; 8 369-93.


The histone H1(0)/H5 variant and terminal differentiation of cells during development of Xenopus laevis., Moorman AF., Differentiation. January 1, 1987; 35 (2): 100-7.            


Assessment of TRH as a potential MSH release stimulating factor in Xenopus laevis., Verburg-van Kemenade BM., Peptides. January 1, 1987; 8 (1): 69-76.


Tolerance induced by grafting semi-allogeneic adult skin to larval Xenopus laevis: possible involvement of specific suppressor cell activity., Nakamura T., Differentiation. January 1, 1987; 35 (2): 108-14.


Amino acids, including neurotransmitter candidates, in a hair cell-enriched fraction from the lateral line of Xenopus laevis., Drescher MJ., Comp Biochem Physiol A Comp Physiol. January 1, 1987; 86 (3): 553-8.


Fates of the blastomeres of the 16-cell stage Xenopus embryo., Moody SA., Dev Biol. February 1, 1987; 119 (2): 560-78.        


Changes in states of commitment of single animal pole blastomeres of Xenopus laevis., Snape A., Dev Biol. February 1, 1987; 119 (2): 503-10.


Vegetal pole cells and commitment to form endoderm in Xenopus laevis., Wylie CC., Dev Biol. February 1, 1987; 119 (2): 496-502.


Neural cell adhesion molecule expression in Xenopus embryos., Balak K., Dev Biol. February 1, 1987; 119 (2): 540-50.              


The midblastula cell cycle transition and the character of mesoderm in u.v.-induced nonaxial Xenopus development., Cooke J., Development. February 1, 1987; 99 (2): 197-210.              


Expression of Xenopus N-CAM RNA in ectoderm is an early response to neural induction., Kintner CR., Development. March 1, 1987; 99 (3): 311-25.                  


Mesoderm induction in early Xenopus embryos by heparin-binding growth factors., Slack JM., Nature. March 12, 1987; 326 (6109): 197-200.


Fate map for the 32-cell stage of Xenopus laevis., Dale L., Development. April 1, 1987; 99 (4): 527-51.                


Biosynthesis and degradation of peptides derived from Xenopus laevis prohormones., Giovannini MG., Biochem J. April 1, 1987; 243 (1): 113-20.


Expression of the Ca2+-binding protein, parvalbumin, during embryonic development of the frog, Xenopus laevis., Kay BK., J Cell Biol. April 1, 1987; 104 (4): 841-7.              


Cell-type-specific expression of epidermal cytokeratin genes during gastrulation of Xenopus laevis., Jamrich M., Genes Dev. April 1, 1987; 1 (2): 124-32.                


Binding of anti-fibronectin to early amphibian ectoderm does not result in inhibition of neural induction under in vitro conditions., Grunz H., Rouxs Arch Dev Biol. April 1, 1987; 196 (4): 203-209.


Cytoplasmic effect on gene function in Xenopus laevis., Yu HJ., Sci Sin B. May 1, 1987; 30 (5): 487-94.


Localization of Xenopus homoeo-box gene transcripts during embryogenesis and in the adult nervous system., Carrasco AE., Dev Biol. May 1, 1987; 121 (1): 69-81.              


Regional specification within the mesoderm of early embryos of Xenopus laevis., Dale L., Development. June 1, 1987; 100 (2): 279-95.


Epidermal capillariasis in South African clawed frogs (Xenopus laevis)., Stephens LC., Lab Anim Sci. June 1, 1987; 37 (3): 341-4.


Neurotensin receptors on the rat liver plasma membranes., Muraki K., Biochem Biophys Res Commun. June 30, 1987; 145 (3): 1071-9.


Cerulein mRNA and peptide alpha-amidation activity in the skin of Xenopus laevis: stimulation by norepinephrine., Spindel ER., Gen Comp Endocrinol. July 1, 1987; 67 (1): 67-76.


Functional gametes derived from explants of single blastomeres containing the "germ plasm" in Xenopus laevis: a genetic marker study., Ikenishi K., Dev Biol. July 1, 1987; 122 (1): 35-8.


Fates of the blastomeres of the 32-cell-stage Xenopus embryo., Moody SA., Dev Biol. August 1, 1987; 122 (2): 300-19.      


Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor., Zasloff M., Proc Natl Acad Sci U S A. August 1, 1987; 84 (15): 5449-53.


Hormone action in newt limb regeneration: insulin and endorphins., Vethamany-Globus S., Biochem Cell Biol. August 1, 1987; 65 (8): 730-8.


Analysis of allotolerance in thymectomized Xenopus restored with semiallogeneic thymus grafts., Maéno M., Transplantation. August 1, 1987; 44 (2): 308-14.


A homeobox-containing marker of posterior neural differentiation shows the importance of predetermination in neural induction., Sharpe CR., Cell. August 28, 1987; 50 (5): 749-58.

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