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Summary Expression Phenotypes Gene Literature (9) GO Terms (1) Nucleotides (43) Proteins (26) Interactants (25) Wiki
XB-GENEPAGE-6051230

Papers associated with tmem158



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Amphibian Metamorphosis Assay: Investigation of the potential effects of five chemicals on the hypothalamic-pituitary thyroid axis of Xenopus laevis., Kamel A, Matten SR, Lynn SG, Wolf JC, Fort DJ., Regul Toxicol Pharmacol. October 1, 2022; 134 105241.

The Xenopus laevis teratogenesis assay for developmental toxicity of phthalate plasticizers and alternatives., Xu Y, Jang J, Gye MC., Environ Pollut. May 1, 2022; 300 118985.

p27(BBP)/eIF6 acts as an anti-apoptotic factor upstream of Bcl-2 during Xenopus laevis development., De Marco N, Iannone L, Carotenuto R, Biffo S, Vitale A, Campanella C., Cell Death Differ. February 1, 2010; 17 (2): 360-72.

Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ, Moers V, Yan J, Souopgui J, Quan XJ, De Geest N, Kricha S, Hassan BA, Bellefroid EJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.              

Estrogenic activity of phthalate esters by in vitro VTG assay using primary-cultured Xenopus hepatocytes., Nomura Y, Mitsui N, Bhawal UK, Sawajiri M, Tooi O, Takahashi T, Okazaki M., Dent Mater J. September 1, 2006; 25 (3): 533-7.

Phosphorylation of p27(BBP)/eIF6 and its association with the cytoskeleton are developmentally regulated in Xenopus oogenesis., Carotenuto R, De Marco N, Biffo S, Wilding M, Vaccaro MC, Marchisio PC, Capriglione T, Russo GL, Campanella C., Cell Mol Life Sci. July 1, 2005; 62 (14): 1641-52.

Beta-amyloid peptide binding protein does not couple to G protein in a heterologous Xenopus expression system., Lee Y, Chang DJ, Lee YS, Chang KA, Kim H, Yoon JS, Lee S, Suh YH, Kaang BK., J Neurosci Res. July 15, 2003; 73 (2): 255-9.

Isolation of a novel beta4 integrin-binding protein (p27(BBP)) highly expressed in epithelial cells., Biffo S, Sanvito F, Costa S, Preve L, Pignatelli R, Spinardi L, Marchisio PC., J Biol Chem. November 28, 1997; 272 (48): 30314-21.

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