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Summary Anatomy Item Literature (1563) Expression Attributions Wiki
XB-ANAT-55

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Expression sequences and distribution of two primary cell adhesion molecules during embryonic development of Xenopus laevis., Levi G., J Cell Biol. November 1, 1987; 105 (5): 2359-72.                  


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 restrictive effect of early exposure to lithium upon body pattern in Xenopus development, studied by quantitative anatomy and immunofluorescence., Cooke J., Development. January 1, 1988; 102 (1): 85-99.          


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


The distribution of tenascin coincides with pathways of neural crest cell migration., Mackie EJ., Development. January 1, 1988; 102 (1): 237-50.              


Regulation of acetylcholine receptor transcript expression during development in Xenopus laevis., Baldwin TJ., J Cell Biol. February 1, 1988; 106 (2): 469-78.              


Mesoderm-inducing factors: a small class of molecules., Godsave SF., Development. March 1, 1988; 102 (3): 555-66.


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.


Lack of keratan sulphate in the human notochord., Salisbury JR., J Anat. April 1, 1988; 157 175-9.


The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos., Kao KR., Dev Biol. May 1, 1988; 127 (1): 64-77.                      


Mapping of neural crest pathways in Xenopus laevis using inter- and intra-specific cell markers., Krotoski DM., Dev Biol. May 1, 1988; 127 (1): 119-32.


Microinjection of synthetic Xhox-1A homeobox mRNA disrupts somite formation in developing Xenopus embryos., Harvey RP., Cell. June 3, 1988; 53 (5): 687-97.              


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


Xenopus endo B is a keratin preferentially expressed in the embryonic notochord., LaFlamme SE., Genes Dev. July 1, 1988; 2 (7): 853-62.            


Differential expression of the Ca2+-binding protein parvalbumin during myogenesis in Xenopus laevis., Schwartz LM., Dev Biol. August 1, 1988; 128 (2): 441-52.              


The distribution of fibronectin and tenascin along migratory pathways of the neural crest in the trunk of amphibian embryos., Epperlein HH., Development. August 1, 1988; 103 (4): 743-56.                  


Effect of antibodies against the gap junction protein on differentiation of induced embryonic cells., Zeng MB., Sci Sin B. November 1, 1988; 31 (11): 1315-8.


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


A community effect in animal development., Gurdon JB., Nature. December 22, 1988; 336 (6201): 772-4.


A gradient of homeodomain protein in developing forelimbs of Xenopus and mouse embryos., Oliver G., Cell. December 23, 1988; 55 (6): 1017-24.        


A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus., Dent JA., Development. January 1, 1989; 105 (1): 61-74.                      


Cell rearrangement and segmentation in Xenopus: direct observation of cultured explants., Wilson PA., Development. January 1, 1989; 105 (1): 155-66.


Embryonic development of Xenopus studied in a cell culture system with tissue-specific monoclonal antibodies., Mitani S., Development. January 1, 1989; 105 (1): 53-9.        


A comparison of the distribution of muscle type in the tadpole tails of Xenopus laevis and Rana temporaria: an histological and ultrastructural study., Muntz L., Tissue Cell. January 1, 1989; 21 (5): 773-81.


Expression of intermediate filament proteins during development of Xenopus laevis. II. Identification and molecular characterization of desmin., Herrmann H., Development. February 1, 1989; 105 (2): 299-307.              


Expression of intermediate filament proteins during development of Xenopus laevis. I. cDNA clones encoding different forms of vimentin., Herrmann H., Development. February 1, 1989; 105 (2): 279-98.                      


Mediolateral cell intercalation in the dorsal, axial mesoderm of Xenopus laevis., Keller R., Dev Biol. February 1, 1989; 131 (2): 539-49.


Amphibian (urodele) myotomes display transitory anterior/posterior and medial/lateral differentiation patterns., Neff AW., Dev Biol. April 1, 1989; 132 (2): 529-43.  


Differential gene expression in the anterior neural plate during gastrulation of Xenopus laevis., Jamrich M., Development. April 1, 1989; 105 (4): 779-86.            


Lithium-induced teratogenesis in frog embryos prevented by a polyphosphoinositide cycle intermediate or a diacylglycerol analog., Busa WB., Dev Biol. April 1, 1989; 132 (2): 315-24.


Bimodal and graded expression of the Xenopus homeobox gene Xhox3 during embryonic development., Ruiz i Altaba A., Development. May 1, 1989; 106 (1): 173-83.                  


Hyperdorsoanterior embryos from Xenopus eggs treated with D2O., Scharf SR., Dev Biol. July 1, 1989; 134 (1): 175-88.


Cell intercalation during notochord development in Xenopus laevis., Keller R., J Exp Zool. August 1, 1989; 251 (2): 134-54.


The appearance of neural and glial cell markers during early development of the nervous system in the amphibian embryo., Messenger NJ., Development. September 1, 1989; 107 (1): 43-54.                      


Mesoderm induction by the mesoderm of Xenopus neurulae., Represa J., Int J Dev Biol. September 1, 1989; 33 (3): 397-401.


Ectopic expression of the proto-oncogene int-1 in Xenopus embryos leads to duplication of the embryonic axis., McMahon AP., Cell. September 22, 1989; 58 (6): 1075-84.                


Interference with function of a homeobox gene in Xenopus embryos produces malformations of the anterior spinal cord., Wright CV., Cell. October 6, 1989; 59 (1): 81-93.              


Ontogeny and tissue distribution of leukocyte-common antigen bearing cells during early development of Xenopus laevis., Ohinata H., Development. November 1, 1989; 107 (3): 445-52.              


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


Neural differentiation of Xenopus laevis ectoderm takes place after disaggregation and delayed reaggregation without inducer., Grunz H., Cell Differ Dev. December 1, 1989; 28 (3): 211-7.


A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest., Hopwood ND., Cell. December 1, 1989; 59 (5): 893-903.                    


The cell junctions of the notochord of Xenopus laevis tadpoles., Honer W., Tissue Cell. January 1, 1990; 22 (2): 149-55.


Critical time periods and the effect of tryptophan in malathion-induced developmental defects in Xenopus embryos., Snawder JE., Life Sci. January 1, 1990; 46 (23): 1635-42.


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.


Mesoderm-inducing factor from bovine amniotic fluid: purification and N-terminal amino acid sequence determination., Chertov OYu., Biomed Sci. January 1, 1990; 1 (5): 499-506.


Origin and distribution of enteric neurones in Xenopus., Epperlein HH., Anat Embryol (Berl). January 1, 1990; 182 (1): 53-67.


Appearance and distribution of laminin during development of Xenopus laevis., Fey J., Differentiation. February 1, 1990; 42 (3): 144-52.            


Distribution of integrins and their ligands in the trunk of Xenopus laevis during neural crest cell migration., Krotoski D., J Exp Zool. February 1, 1990; 253 (2): 139-50.


Expression pattern of the mouse T gene and its role in mesoderm formation., Wilkinson DG., Nature. February 15, 1990; 343 (6259): 657-9.

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