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Summary Anatomy Item Literature (2238) Expression Attributions Wiki
XB-ANAT-3835

Papers associated with posterior foregut (and tff3.7)

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Cystic fibrosis transmembrane conductance regulator (CFTR) potentiators protect G551D but not ΔF508 CFTR from thermal instability., Liu X., Biochemistry. September 9, 2014; 53 (35): 5613-8.        

Myb promotes centriole amplification and later steps of the multiciliogenesis program., Tan FE., Development. October 1, 2013; 140 (20): 4277-86.                

Retinoic acid-activated Ndrg1a represses Wnt/β-catenin signaling to allow Xenopus pancreas, oesophagus, stomach, and duodenum specification., Zhang T., PLoS One. May 15, 2013; 8 (5): e65058.                  

Identification and characterization of alternative promoters of zebrafish Rtn-4/Nogo genes in cultured cells and zebrafish embryos., Chen YC., Nucleic Acids Res. August 1, 2010; 38 (14): 4635-50.              

Structural and biological properties of erythropoietin in Xenopus laevis., Nogawa-Kosaka N., Exp Hematol. May 1, 2010; 38 (5): 363-72.

Regulation of ALF promoter activity in Xenopus oocytes., Li D., PLoS One. August 17, 2009; 4 (8): e6664.                

The adaptor molecule FADD from Xenopus laevis demonstrates evolutionary conservation of its pro-apoptotic activity., Sakamaki K., Genes Cells. December 1, 2004; 9 (12): 1249-64.                

A novel G protein-coupled P2 purinoceptor (P2Y3) activated preferentially by nucleoside diphosphates., Webb TE., Mol Pharmacol. August 1, 1996; 50 (2): 258-65.

Cloning of rat and mouse P2Y purinoceptors., Tokuyama Y., Biochem Biophys Res Commun. June 6, 1995; 211 (1): 211-8.

xP2, a new member of the P-domain peptide family of potential growth factors, is synthesized in Xenopus laevis skin., Hauser F., J Biol Chem. July 15, 1992; 267 (20): 14451-5.            

Dermal glands of Xenopus laevis contain a polypeptide with a highly repetitive amino acid sequence., Gmachl M., FEBS Lett. January 15, 1990; 260 (1): 145-8.

Subnuclear fractionation by mild micrococcal-nuclease treatment of nuclei of different transcriptional activities causes a partition of expressed and non-expressed genes., Dimitriadis GJ., Biochem J. May 1, 1980; 187 (2): 467-77.

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