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Summary Expression Phenotypes Gene Literature (107) GO Terms (21) Nucleotides (442) Proteins (58) Interactants (1019) Wiki
XB--487829

Papers associated with hes4 (and Disease Ontology)



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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.                          

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.

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.  

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.                                

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;             

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