Papers associated with ectoderm

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	The anatomy and function of ''free'' nerve endings in an amphibian skin sensory system., Roberts A., Proc R Soc Lond B Biol Sci. April 1, 1977; 196 (1125): 415-29.
	Filaments of the vertebrate lens., Maisel H., Experientia. April 15, 1977; 33 (4): 525.
	In vitro studies on the effects on granular gland secretion in Xenopus laevis skin of stimulation and blockade of alpha and beta adrenoceptors of myoepithelial cells., Holmes CH., Cell Biol Int Rep. May 1, 1977; 1 (3): 263-70.
	An SEM study of cellular morphology, contact, and arrangement, as related to gastrulation inXenopus laevis., Keller RE., Wilehm Roux Arch Dev Biol. June 1, 1977; 182 (2): 165-186.
	Biosynthesis, processing, and control of release of melanotropic peptides in the neurointermediate lobe of Xenopus laevis., Loh YP., J Gen Physiol. July 1, 1977; 70 (1): 37-58.
	Variations in differentiation in the regenerating lens of Xenopus laevis., Campbell JC., Exp Eye Res. July 1, 1977; 25 (1): 99-100.
	Localization of myosin and actin in ocular nonmuscle cells. Immunofluorescence-microscopic, biochemical, and electron-microscopic studies., Drenckhahn D., Cell Tissue Res. July 19, 1977; 181 (4): 493-503.
	Treatment of skin-invading capillarid nematode in a colony of South African clawed frogs (Xenopus laevis)., Cosgrove GE., Lab Anim Sci. August 1, 1977; 27 (4): 526-7.
	In vitro studies of frog mucous glands., Skoglund CR., Acta Physiol Scand. August 1, 1977; 100 (4): 457-70.
	Monoaminergic fluorescence in frog skin., Sjöberg E., Acta Physiol Scand. August 1, 1977; 100 (4): 452-6.
	Lens regeneration from cornea in tail ectopic eyes of Xenopus laevis tadpoles., Reeve JG., Experientia. September 15, 1977; 33 (9): 1210-1.
	Hormonal regulation of epidermis-specific protein and messenger RNA synthesis in amphibian metamorphosis., Reeves R., Dev Biol. October 1, 1977; 60 (1): 163-79.
	Splenic involvement in amphibian transplantation immunity., Horton JD., Transplantation. October 1, 1977; 24 (4): 247-55.
	The action of melatonin on single amphibian pigment cells in tissue culture., Messenger EA., Br J Pharmacol. December 1, 1977; 61 (4): 607-14.
	[Transfer of behavior patterns through transplantation of systems of neuroanatomic structures in amphibian larvae. II. Xenoplastic transplantation of hind brain systems between Xenopus laevis (Daud.) as well as Hymenochirus boettgeri (Torn.) and Triturus vulgaris]., Rössler E., Z Tierpsychol. January 1, 1978; 46 (1): 1-13.
	Histological changes in Xenopus laevis Daudin adult specimens kept under dry conditions, then moved back to their natural aquatic environment. II. Skin, kidney and interrenal tissue., Campantico E., Arch Sci Biol (Bologna). January 1, 1978; 62 (1-4): 63-76.
	Na+/K+-dependent adenosinetriphosphatase activity in the skin, kidney and muscle in Xenopus laevis (Daud.) adult specimens under different experimental conditions., Giunta C., Arch Sci Biol (Bologna). January 1, 1978; 62 (1-4): 21-30.
	[Histochemistry of the ball cell in larval epidermis of Xenopus laevis Daudin]., Fröhlich J., Acta Histochem. January 1, 1978; 61 (1): 155-61.
	The permeability of the skin of the aquatic anuran Xenopus laevis (Pipidae)., Yorio T., J Exp Biol. February 1, 1978; 72 285-9.
	Neural transduction in Xenopus laevis lateral line system., Strelioff D., J Neurophysiol. March 1, 1978; 41 (2): 432-44.
	Calcium dependence of alpha-adrenoreceptor stimulation of myoepithelial cell contraction in the granular glands of Xenopus laevis skin [proceedings]., Balls M., J Physiol. March 1, 1978; 276 30P-31P.
	Lack of effect of blood-volume expansion on short-circuit current across an isolated toad skin incorporated in the circulation of a rat., Querido D., Clin Sci Mol Med. July 1, 1978; 55 (1): 15-21.
	Synthesis of lens crystallins in Xenopus oocytes as determined by quantitative immunoprecipitation., Asselbergs FA., Eur J Biochem. July 3, 1978; 87 (3): 517-24.
	Quinacrine fluorescence of Merkel cells in Xenopus laevis., Crowe R., Cell Tissue Res. July 5, 1978; 190 (2): 273-83.
	Further characterization of the effects of ultraviolet irradiation of the amphibian egg., Malacinski GM., Experientia. July 15, 1978; 34 (7): 883-4.
	Frequency response of the lateral-line organ of Xenopus laevis., Kroese AB., Pflugers Arch. July 18, 1978; 375 (2): 167-75.
	Biochemical changes in developmentally retarded Xenopus laevis larvae. I. The lens crystallin transition., Doyle MJ., J Embryol Exp Morphol. August 1, 1978; 46 215-25.
	Changes in the cell surface coat during the development ofXenopus laevis embryos, detected by lectins., Nosek J., Wilehm Roux Arch Dev Biol. September 1, 1978; 184 (3): 181-193.
	Rod-shaped particles in the plasma membrane of the mitochondria-rich cell of amphibian epidermis., Brown D., Anat Rec. October 1, 1978; 192 (2): 269-75.
	In vitro studies on the control of myoepithelial cell contraction in the granular glands of Xenopus laevis skin., Holmes C., Gen Comp Endocrinol. October 1, 1978; 36 (2): 255-63.
	Post-translational assembly of lens alpha-crystallin in the reticulocyte lysate and in Xenopus laevis oocytes., Asselbergs FA., Eur J Biochem. November 2, 1978; 91 (1): 65-72.
	Scanning electron microscopy of cells isolated from amphibian early embryos., Stanisstreet M., J Embryol Exp Morphol. December 1, 1978; 48 215-23.
	Nerve supply as a stimulator of the growth of tissues including skin. II. Animal evidence., Whimster IW., Clin Exp Dermatol. December 1, 1978; 3 (4): 389-410.
	Lens regeneration from cornea of larval Xenopus laevis in the presence of the lens., Reeve JG., J Embryol Exp Morphol. December 1, 1978; 48 205-14.
	The localisation of lead in the skin of light- and dark-adapted Xenopus laevis., Ireland MP., Histochemistry. January 1, 1979; 65 (1): 31-9.
	Embryonic appearance of alpha, beta, and gamma crystallins in the periodic albinism (ap) mutant of Xenopus laevis., McDevitt DS., Differentiation. January 1, 1979; 14 (1-2): 107-12.
	Differential response of embryonic cells to culture on tissue matrices., Overton J., Tissue Cell. January 1, 1979; 11 (1): 89-98.
	[Immunochemical study of the water-soluble lens proteins in the embryo of Xenopus laevis with the mutation of periodic albinism]., Mikhailov AT., Ontogenez. January 1, 1979; 10 (3): 220-30.
	Photoreceptor outer segment development: light and dark regulate the rate of membrane addition and loss., Hollyfield JG., Invest Ophthalmol Vis Sci. February 1, 1979; 18 (2): 117-32.
	The time of origin of the mesencephalic trigeminal neurons in Xenopus., Lewis S., J Comp Neurol. February 1, 1979; 183 (3): 633-45.
	Messenger RNA competition in living Xenopus oocytes., Asselbergs FA., Eur J Biochem. February 15, 1979; 94 (1): 249-54.
	Tissue distribution of immunoreactive somatostatin in the South African clawed toad (Xenopus laevis)., Shapiro B., J Endocrinol. March 1, 1979; 80 (3): 407-8.
	Freeze-fracture differences in plasma membranes of the stratum corneum and replacement layer cells of amphibian epidermis., Brown D., J Ultrastruct Res. April 1, 1979; 67 (1): 55-64.
	The mechanism of somite segmentation in the chick embryo., Bellairs R., J Embryol Exp Morphol. June 1, 1979; 51 227-43.
	The function of the sodium pump during differentiation of amphibian embryonic neurones., Messenger EA., J Physiol. July 1, 1979; 292 85-105.
	An analysis of pigment cell development in the periodic albino mutant of Xenopus., MacMillan GJ., J Embryol Exp Morphol. August 1, 1979; 52 165-70.
	Relationships between eye factors and lens-forming transformations in the cornea and pericorneal epidermis of larval Xenopus laevis., Bosco L., J Exp Zool. August 1, 1979; 209 (2): 261-82.
	[Immunohistochemical identification of specific antigens in stained and balsam-embedded eye lens sections]., Mikhaĭlov AT., Biull Eksp Biol Med. September 1, 1979; 88 (9): 367-9.
	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.
	Endorphins supersensitize frog skin melanophores to isoproterenol, but subsensitize them to alpha-melanocyte-stimulating hormone., Novales RR., Gen Comp Endocrinol. December 1, 1979; 39 (4): 481-9.

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