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Summary Anatomy Item Literature (34) Expression Attributions Wiki
XB-ANAT-136

Papers associated with mesentery

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Na+-dependent intestinal glucose absorption mechanisms and its luminal Na+ homeostasis across metamorphosis from tadpoles to frogs., Ishizuka N., Am J Physiol Regul Integr Comp Physiol. May 1, 2023; 324 (5): R645-R655.              


Development of Xenopus laevis bipotential gonads into testis or ovary is driven by sex-specific cell-cell interactions, proliferation rate, cell migration and deposition of extracellular matrix., Piprek RP., Dev Biol. December 15, 2017; 432 (2): 298-310.                        


Identification of anti-cancer chemical compounds using Xenopus embryos., Tanaka M., Cancer Sci. June 1, 2016; 107 (6): 803-11.            


Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints., Genikhovich G., Cell Rep. March 17, 2015; 10 (10): 1646-1654.            


Left-right asymmetry: lessons from Cancún., Burdine RD., Development. November 1, 2013; 140 (22): 4465-70.    


Sexual dimorphism of AMH, DMRT1 and RSPO1 localization in the developing gonads of six anuran species., Piprek RP., Int J Dev Biol. January 1, 2013; 57 (11-12): 891-5.        


Germ plasm in Eleutherodactylus coqui, a direct developing frog with large eggs., Elinson RP., Evodevo. October 6, 2011; 2 20.              


A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.                            


The mRNA coding for Xenopus glutamate receptor interacting protein 2 (XGRIP2) is maternally transcribed, transported through the late pathway and localized to the germ plasm., Kaneshiro K., Biochem Biophys Res Commun. April 20, 2007; 355 (4): 902-6.          


Identification of mannose moieties in N- and O-linked oligosaccharides of the primordial germ cells of Xenopus embryos., Alonso E., Microsc Res Tech. July 1, 2006; 69 (7): 595-9.


Tracing of Xenopus tropicalis germ plasm and presumptive primordial germ cells with the Xenopus tropicalis DAZ-like gene., Sekizaki H., Dev Dyn. February 1, 2004; 229 (2): 367-72.      


Using Xenopus as a model system for an undergraduate laboratory course in vertebrate development at the University of Bordeaux, France., Olive M., Int J Dev Biol. January 1, 2003; 47 (2-3): 153-60.          


Downregulation of Hedgehog signaling is required for organogenesis of the small intestine in Xenopus., Zhang J., Dev Biol. January 1, 2001; 229 (1): 188-202.                  


The vegetally localized mRNA fatvg is associated with the germ plasm in the early embryo and is later expressed in the fat body., Chan AP., Mech Dev. January 1, 2001; 100 (1): 137-40.          


A critical role for Xdazl, a germ plasm-localized RNA, in the differentiation of primordial germ cells in Xenopus., Houston DW., Development. February 1, 2000; 127 (3): 447-56.          


Xpat, a gene expressed specifically in germ plasm and primordial germ cells of Xenopus laevis., Hudson C., Mech Dev. May 1, 1998; 73 (2): 159-68.        


Involvement of the protein of Xenopus vasa homolog (Xenopus vasa-like gene 1, XVLG1) in the differentiation of primordial germ cells., Ikenishi K., Dev Growth Differ. October 1, 1997; 39 (5): 625-33.            


Expression of Xenopus snail in mesoderm and prospective neural fold ectoderm., Essex LJ., Dev Dyn. October 1, 1993; 198 (2): 108-22.              


Distinct distribution of vimentin and cytokeratin in Xenopus oocytes and early embryos., Torpey NP., J Cell Sci. January 1, 1992; 101 ( Pt 1) 151-60.                


Distribution and migration pathways of HNK-1-immunoreactive neural crest cells in teleost fish embryos., Sadaghiani B., Development. September 1, 1990; 110 (1): 197-209.


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.


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


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.


Occurrence of a species-specific nuclear antigen in the germ line of Xenopus and its expression from paternal genes in hybrid frogs., Wedlich D., Dev Biol. March 1, 1985; 108 (1): 220-34.                


Further analysis of the effect of ultra-violet irradiation on the formation of the germ line in Xenopus laevis., Thomas V., J Embryol Exp Morphol. August 1, 1983; 76 67-81.


Primordial germ cells of Xenopus embryos: the role of fibronectin in their adhesion during migration., Heasman J., Cell. December 1, 1981; 27 (3 Pt 2): 437-47.


Contact relations and guidance of primordial germ cells on their migratory route in embryos of Xenopus laevis., Heasman J., Proc R Soc Lond B Biol Sci. September 17, 1981; 213 (1190): 41-58.


The invasion of cultured cell layers and intact epithelia., Swan AP., Scan Electron Microsc. January 1, 1981; 4 99-104.


[Effects of cyclic AMP treatment on the migration of primordial germ cells in the embryo of Xenopus laevis]., Gipouloux JD., C R Acad Hebd Seances Acad Sci D. December 1, 1978; 287 (16): 1425-7.


Electron microscopic studies on the structure of motile primordial germ cells of Xenopus laevis in vitro., Heasman J., J Embryol Exp Morphol. August 1, 1978; 46 119-33.        


Observations on the migration and proliferation of gonocytes in Xenopus laevis., Kamimura M., J Embryol Exp Morphol. August 1, 1976; 36 (1): 197-207.


The formation of the gonadal ridge in Xenopus laevis. II. A scanning electron microscope study., Wylie CC., J Embryol Exp Morphol. February 1, 1976; 35 (1): 139-48.


The formation of the gonadal ridge in Xenopus laevis. I. A light and transmission electron microscope study., Wylie CC., J Embryol Exp Morphol. February 1, 1976; 35 (1): 125-38.


Quantitative studies of germ plasm and germ cells during early embryogenesis of Xenopus laevis., Whitington PM., J Embryol Exp Morphol. February 1, 1975; 33 (1): 57-74.            

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