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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.
A potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome. , Tanaka K, Kato A, Angelocci C, Watanabe M, Kato Y ., Dev Biol. March 1, 2014; 387 (1): 28-36.
BMP signalling controls the construction of vertebrate mucociliary epithelia. , Cibois M, Luxardi G , Chevalier B, Thomé V, Mercey O, Zaragosi LE , Barbry P, Pasini A, Marcet B, Kodjabachian L ., Development. July 1, 2015; 142 (13): 2352-63.
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.
Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndrome. , Johnston JJ , Lee C , Wentzensen IM, Parisi MA, Crenshaw MM, Sapp JC, Gross JM, Wallingford JB , Biesecker LG., Cold Spring Harb Mol Case Stud. July 1, 2017; 3 (4):
A convergent molecular network underlying autism and congenital heart disease. , Rosenthal SB, Willsey HR , Xu Y , Xu Y , Mei Y, Dea J, Wang S, Curtis C, Sempou E, Khokha MK , Chi NC, Willsey AJ, Fisch KM, Ideker T., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.