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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.
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.
Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity. , Hemmati-Brivanlou A ., Cell. April 22, 1994; 77 (2): 283-95.
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.