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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ, Rajasekaran A, Jusić N, Taylor L , Read M, Alfandari D , Alfandari D , Pignoni F, Moody SA ., J Exp Zool B Mol Dev Evol. October 13, 2023;
Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis. , Harata A, Hirakawa M, Sakuma T, Yamamoto T , Hashimoto C., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
Developmental role of plk4 in Xenopus laevis and Danio rerio: implications for Seckel Syndrome. , Rapchak CE, Patel N , Hudson J, Crawford M ., Biochem Cell Biol. August 1, 2015; 93 (4): 396-404.
Rett syndrome: clinical review and genetic update. , Weaving LS, Ellaway CJ, Gécz J, Christodoulou J., J Med Genet. January 1, 2005; 42 (1): 1-7.
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. , Stancheva I , Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR ., Mol Cell. August 1, 2003; 12 (2): 425-35.