Papers associated with notochord

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	Dimensions of the notochord and somites in embryos of Xenopus laevis treated with thiocyanate., RANZI S., J Embryol Exp Morphol. June 1, 1959; 7 117-21.
	Similar pattern of fine structure in the basement lamella of the skin and the external sheath of the notochord in Xenopus larvae., WEBER R., Experientia. August 15, 1961; 17 365-6.
	Physical properties and protein constituents fo cytoplasmic and mitochondrial ribosomes of Xenopus laevis., Leister DE., J Biol Chem. August 25, 1974; 249 (16): 5108-18.
	Regeneration of the tail bud in Xenopus embryos., Deuchar EM., J Exp Zool. June 1, 1975; 192 (3): 381-90.
	The developmental capacity of nuclei transplanted from keratinized skin cells of adult frogs., Gurdon JB., J Embryol Exp Morphol. August 1, 1975; 34 (1): 93-112.
	Melanoblast-tissue interactions and the development of pigment pattern in Xenopus larvae., Macmillan GJ., J Embryol Exp Morphol. June 1, 1976; 35 (3): 463-84.
	Development of the urostyle during metamorphosis in five species of anurans., Branham AE., J Morphol. March 1, 1979; 159 (3): 311-329.
	The mechanism of somite segmentation in the chick embryo., Bellairs R., J Embryol Exp Morphol. June 1, 1979; 51 227-43.
	Cell number in relation to primary pattern formation in the embryo of Xenopus laevis. II. Sequential cell recruitment, and control of the cell cycle, during mesoderm formation., Cooke J., J Embryol Exp Morphol. October 1, 1979; 53 269-89.
	An atlas of notochord and somite morphogenesis in several anuran and urodelean amphibians., Youn BW., J Embryol Exp Morphol. October 1, 1980; 59 223-47.
	[Study of the catecholamines in the notochord of Anura Amphibia embryos. Its possible relationships with the adenyl-cyclase activity and the primordial germ cells migration (author's transl)]., Raïs R., Arch Anat Microsc Morphol Exp. January 1, 1981; 70 (3): 149-60.
	Effects of fenitrothion and carbaryl on Xenopus laevis development., Elliott-Feeley E., Toxicology. January 1, 1981; 22 (4): 319-35.
	Axial structure development in ultraviolet-irradiated (notochord-defective) amphibian embryos., Youn BW., Dev Biol. April 30, 1981; 83 (2): 339-52.
	Somitogenesis in the amphibian Xenopus laevis: scanning electron microscopic analysis of intrasomitic cellular arrangements during somite rotation., Youn BW., J Embryol Exp Morphol. August 1, 1981; 64 23-43.
	The structure of the anuran amphibian Notochord and a re-evaluation of its presumed role in early embryogenesis., Malacinski GM., Differentiation. January 1, 1982; 21 (1): 13-21.
	[Detection of collagen by immunofluorescence during development of Xenopus (Xenopus laevis Daud.)]., Bride M., C R Seances Soc Biol Fil. January 1, 1982; 176 (4): 494-502.
	Effects of inducers on inner and outer gastrula ectoderm layers of Xenopus laevis., Asashima M., Differentiation. January 1, 1983; 23 (3): 206-12.
	Changes in the ultrastructure of neural tube cells and the notochordal sheath of ultraviolet irradiated Xenopus laevis embryos., Jurand A., Acta Embryol Morphol Exp. May 1, 1983; 4 (1): 3-16.
	Change in the differentiation pattern ofXenopus laevis ectoderm by variation of the incubation time and concentration of vegetalizing factor., Grunz H., Wilehm Roux Arch Dev Biol. May 1, 1983; 192 (3-4): 130-137.
	On the role of the notochord in somite formation and the possible evolutionary significance of the concomitant cell re-orientation., Burgess AM., J Anat. June 1, 1983; 136 (Pt 4): 829-35.
	Aggregates of acetylcholine receptors are associated with plaques of a basal lamina heparan sulfate proteoglycan on the surface of skeletal muscle fibers., Anderson MJ., J Cell Biol. November 1, 1983; 97 (5 Pt 1): 1396-411.
	Neural tube (canal) morphogenesis in notochordless amphibian (Xenopus laevis) embryos., Malacinski GM., Proc Soc Exp Biol Med. December 1, 1983; 174 (3): 316-21.
	Dorsalization and neural induction: properties of the organizer in Xenopus laevis., Smith JC., J Embryol Exp Morphol. December 1, 1983; 78 299-317.
	Cell lineage analysis of neural induction: origins of cells forming the induced nervous system., Jacobson M., Dev Biol. March 1, 1984; 102 (1): 122-9.
	CNS effects of mechanically produced spina bifida., Katz MJ., Dev Med Child Neurol. October 1, 1984; 26 (5): 617-31.
	Biochemical specificity of Xenopus notochord., Smith JC., Differentiation. January 1, 1985; 29 (2): 109-15.
	Dynamics of the control of body pattern in the development of Xenopus laevis. II. Timing and pattern in the development of single blastomeres (presumptive lateral halves) isolated at the 2-cell stage., Cooke J., J Embryol Exp Morphol. August 1, 1985; 88 113-33.
	The embryotoxic and osteolathyrogenic effects of semicarbazide., Schultz TW., Toxicology. August 1, 1985; 36 (2-3): 183-98.
	Mesoderm induction in Xenopus laevis: a quantitative study using a cell lineage label and tissue-specific antibodies., Dale L., J Embryol Exp Morphol. October 1, 1985; 89 289-312.
	Regional specificity of glycoconjugates in Xenopus and axolotl embryos., Slack JM., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 137-53.
	Effects of minute doses of ethylenebisdithiocarbamate disodium salt (nabam) and its degradative products on connective tissue envelopes of the notochord in Xenopus: an ultrastructural study., Birch WX., Cytobios. January 1, 1986; 48 (194-195): 175-84.
	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.
	Tissue interactions during axial structure pattern formation in amphibia., Malacinski GM., Scan Electron Microsc. January 1, 1986; (Pt 2): 307-18.
	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.
	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.
	Myoblasts and notochord influence the orientation of somitic myoblasts from Xenopus laevis., McCaig CD., J Embryol Exp Morphol. April 1, 1986; 93 121-31.
	Developmental Fates of Blastomeres of Eight-Cell-Stage Xenopus laevis Embryos: (intracellular injection/horseradish peroxidase/developmental fate/Xenopus embryo)., Masho R., Dev Growth Differ. April 1, 1986; 28 (2): 113-123.
	Acquisition of developmental autonomy in the equatorial region of the Xenopus embryo., Gimlich RL., Dev Biol. June 1, 1986; 115 (2): 340-52.
	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.
	A mesoderm-inducing factor is produced by Xenopus cell line., Smith JC., Development. January 1, 1987; 99 (1): 3-14.
	Fates of the blastomeres of the 16-cell stage Xenopus embryo., Moody SA., Dev Biol. February 1, 1987; 119 (2): 560-78.
	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.
	Fate map for the 32-cell stage of Xenopus laevis., Dale L., Development. April 1, 1987; 99 (4): 527-51.
	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.
	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.
	Fates of the blastomeres of the 32-cell-stage Xenopus embryo., Moody SA., Dev Biol. August 1, 1987; 122 (2): 300-19.
	An amphibian cytoskeletal-type actin gene is expressed exclusively in muscle tissue., Mohun TJ., Development. October 1, 1987; 101 (2): 393-402.

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