Papers associated with pronephric kidney

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	Experimental studies on the development of the pronephric duct in anuran embryos., Tung TC., J Anat. January 1, 1944; 78 (Pt 1-2): 52-7.
	ORIGIN OF THE PRONEPHRIC DUCT IN XENOPUS LAEVIS., FOX H., Arch Biol (Liege). January 1, 1964; 75 245-51.
	Stimulation of cell division in pronephros of embryonic grafts following partial nephrectomy in the host (Xenopus laevis)., Chopra DP., J Embryol Exp Morphol. November 1, 1970; 24 (3): 525-33.
	An histochemical investigation of acid phosphatase activity in the pronephros of the developing Xenopus laevis tadpole., Goldin G., Acta Embryol Exp (Palermo). January 1, 1973; 1 31-9.
	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.
	The glomus cell of the carotid labyrinth of Xenopus laevis., Ishii K., Cell Tissue Res. January 1, 1982; 224 (2): 459-63.
	T-lymphocyte and B-lymphocyte dichotomy in anuran amphibians: I. T-lymphocyte proportions, distribution and ontogeny, as measured by E-rosetting, nylon wool adherence, postmetamorphic thymectomy, and non-specific esterase staining., Klempau AE., Dev Comp Immunol. January 1, 1983; 7 (1): 99-110.
	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.
	Evidence for specific feedback signals underlying pattern control during vertebrate embryogenesis., Cooke J., J Embryol Exp Morphol. August 1, 1983; 76 95-114.
	Different modes of pronephric duct origin among vertebrates., Poole TJ., Scan Electron Microsc. January 1, 1984; (Pt 1): 475-82.
	[Glomus cell in controlling vascular tone of the carotid labyrinth (Xenopus laevis)]., Kusakabe T., Nihon Seirigaku Zasshi. January 1, 1984; 46 (10): 623-33.
	Regional specificity of glycoconjugates in Xenopus and axolotl embryos., Slack JM., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 137-53.
	Principles of organization of the vertebrate olfactory glomerulus: an hypothesis., Graziadei PP., Neuroscience. December 1, 1986; 19 (4): 1025-35.
	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.
	Fate map for the 32-cell stage of Xenopus laevis., Dale L., Development. April 1, 1987; 99 (4): 527-51.
	A possible role of the glomus cell in controlling vascular tone of the carotid labyrinth of Xenopus laevis., Kusakabe T., Tohoku J Exp Med. April 1, 1987; 151 (4): 395-408.
	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.
	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.
	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.
	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.
	XlHbox 8: a novel Xenopus homeo protein restricted to a narrow band of endoderm., Wright CV., Development. April 1, 1989; 105 (4): 787-94.
	Translation of the human C3b/C4b receptor mRNA in a cell-free system and by Xenopus oocytes., Kumar V., Biochemistry. May 2, 1989; 28 (9): 4040-6.
	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.
	The biological effects of XTC-MIF: quantitative comparison with Xenopus bFGF., Green JB., Development. January 1, 1990; 108 (1): 173-83.
	Cell migration in the formation of the pronephric duct in Xenopus laevis., Lynch K., Dev Biol. December 1, 1990; 142 (2): 283-92.
	The distribution of E-cadherin during Xenopus laevis development., Levi G., Development. January 1, 1991; 111 (1): 159-69.
	Localization of substance P, CGRP, VIP, neuropeptide Y, and somatostatin immunoreactive nerve fibers in the carotid labyrinths of some amphibian species., Kusakabe T., Histochemistry. January 1, 1991; 96 (3): 255-60.
	Immunoglobulin heavy chain cDNA from the teleost Atlantic cod (Gadus morhua L.): nucleotide sequences of secretory and membrane form show an unusual splicing pattern., Bengtén E., Eur J Immunol. December 1, 1991; 21 (12): 3027-33.
	Retinoic acid induces changes in the localization of homeobox proteins in the antero-posterior axis of Xenopus laevis embryos., López SL., Mech Dev. February 1, 1992; 36 (3): 153-64.
	Xlcaax-1 is localized to the basolateral membrane of kidney tubule and other polarized epithelia during Xenopus development., Cornish JA., Dev Biol. March 1, 1992; 150 (1): 108-20.
	The marginal zone of the 32-cell amphibian embryo contains all the information required for chordamesoderm development., Pierce KE., J Exp Zool. April 15, 1992; 262 (1): 40-50.
	Analysis of Xwnt-4 in embryos of Xenopus laevis: a Wnt family member expressed in the brain and floor plate., McGrew LL., Development. June 1, 1992; 115 (2): 463-73.
	Wasting disease associated with cutaneous and renal nematodes, in commercially obtained Xenopus laevis., Brayton C., Ann N Y Acad Sci. June 16, 1992; 653 197-201.
	N-cadherin transcripts in Xenopus laevis from early tailbud to tadpole., Simonneau L., Dev Dyn. August 1, 1992; 194 (4): 247-60.
	Developmental regulation and tissue distribution of the liver transcription factor LFB1 (HNF1) in Xenopus laevis., Bartkowski S., Mol Cell Biol. January 1, 1993; 13 (1): 421-31.
	Changes in contractile properties by androgen hormones in sexually dimorphic muscles of male frogs (Xenopus laevis)., Regnier M., J Physiol. February 1, 1993; 461 565-81.
	Secreted noggin protein mimics the Spemann organizer in dorsalizing Xenopus mesoderm., Smith WC., Nature. February 11, 1993; 361 (6412): 547-9.
	Catenins in Xenopus embryogenesis and their relation to the cadherin-mediated cell-cell adhesion system., Schneider S., Development. June 1, 1993; 118 (2): 629-40.
	Vital dye labelling of Xenopus laevis trunk neural crest reveals multipotency and novel pathways of migration., Collazo A., Development. June 1, 1993; 118 (2): 363-76.
	The formation of the pronephric duct in Xenopus involves recruitment of posterior cells by migrating pronephric duct cells., Cornish JA., Dev Biol. September 1, 1993; 159 (1): 338-45.
	Expression of Xenopus snail in mesoderm and prospective neural fold ectoderm., Essex LJ., Dev Dyn. October 1, 1993; 198 (2): 108-22.
	[Ontogeny of the pronephros and mesonephros in the South African clawed frog, Xenopus laevis Daudin, with special reference to the appearance and movement of the renin-immunopositive cells]., Tahara T., Jikken Dobutsu. October 1, 1993; 42 (4): 601-10.
	Distinct elements of the xsna promoter are required for mesodermal and ectodermal expression., Mayor R., Development. November 1, 1993; 119 (3): 661-71.
	Expression patterns of the murine LIM class homeobox gene lim1 in the developing brain and excretory system., Fujii T., Dev Dyn. January 1, 1994; 199 (1): 73-83.
	Parvalbumin-immunoreactive material in the kidney of Xenopus laevis., Kerschbaum HH., Tissue Cell. February 1, 1994; 26 (1): 75-81.
	Pagliaccio, a member of the Eph family of receptor tyrosine kinase genes, has localized expression in a subset of neural crest and neural tissues in Xenopus laevis embryos., Winning RS., Mech Dev. June 1, 1994; 46 (3): 219-29.

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