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Summary Anatomy Item Literature (6624) Expression Attributions Wiki
XB-ANAT-718

Papers associated with anatomical region (and bax)

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Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB., iScience. September 15, 2023; 26 (9): 107665.                          


Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax., Wang S., Cell Biosci. February 23, 2023; 13 (1): 40.              


Bisphenol A exposure induces apoptosis and impairs early embryonic development in Xenopus laevis., Ge Y., Environ Pollut. July 1, 2021; 280 116901.


Developmental toxicity of dibutyl phthalate and citrate ester plasticizers in Xenopus laevis embryos., Xu Y, Xu Y., Chemosphere. August 1, 2018; 204 523-534.


Alterations in gene expression levels provide early indicators of chemical stress during Xenopus laevis embryo development: A case study with perfluorooctane sulfonate (PFOS)., San-Segundo L., Ecotoxicol Environ Saf. May 1, 2016; 127 51-60.


Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3., Juraver-Geslin HA., Genesis. February 1, 2015; 53 (2): 203-24.          


Visual and functional demonstration of growing Bax-induced pores in mitochondrial outer membranes., Gillies LA., Mol Biol Cell. January 15, 2015; 26 (2): 339-49.          


Eukaryotic initiation factor 6 (eif6) overexpression affects eye development in Xenopus laevis., De Marco N., Differentiation. September 1, 2011; 82 (2): 108-15.          


Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53., Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.                


Unfertilized Xenopus eggs die by Bad-dependent apoptosis under the control of Cdk1 and JNK., Du Pasquier D., PLoS One. January 1, 2011; 6 (8): e23672.              


Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.                    


Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus., Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.                        


Differential subcellular sequestration of proapoptotic and antiapoptotic proteins and colocalization of Bcl-x(L) with the germ plasm, in Xenopus laevis oocytes., Kloc M., Genesis. August 1, 2007; 45 (8): 523-31.          


Developmental cell death during Xenopus metamorphosis involves BID cleavage and caspase 2 and 8 activation., Du Pasquier D., Dev Dyn. August 1, 2006; 235 (8): 2083-94.                  


Apoptosis of tail muscle during amphibian metamorphosis involves a caspase 9-dependent mechanism., Rowe I., Dev Dyn. May 1, 2005; 233 (1): 76-87.


Implication of bax in Xenopus laevis tail regression at metamorphosis., Sachs LM., Dev Dyn. December 1, 2004; 231 (4): 671-82.          


Xenopus Bcl-X(L) selectively protects Rohon-Beard neurons from metamorphic degeneration., Coen L., Proc Natl Acad Sci U S A. July 3, 2001; 98 (14): 7869-74.


Apoptosis in Xenopus tadpole tail muscles involves Bax-dependent pathways., Sachs LM., FASEB J. August 1, 1997; 11 (10): 801-8.

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