Papers associated with wnt11 (and Disease Ontology)

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referenced by:

	A homozygous human WNT11 variant is associated with laterality, heart and renal defects., Berns H, Weber D, Haas M, Bakey Z, Brislinger-Engelhardt MM, Schmidts M, Walentek P., Dis Model Mech. April 9, 2025;
	RAD21 deficiency drives corneal to scleral differentiation fate switching via upregulating WNT9B., Liu H, Qi B, Liu G, Duan H, Li Z, Shi Z, Chen Y, Chu WK, Zhou Q, Zhang BN., iScience. June 21, 2024; 27 (6): 109875.
	Dishevelled Paralogs in Vertebrate Development: Redundant or Distinct?, Gentzel M, Schambony A., Front Cell Dev Biol. May 26, 2017; 5 59.
	Aberrant regulation of Wnt signaling in hepatocellular carcinoma., Liu LJ, Xie SX, Chen YT, Xue JL, Zhang CJ, Zhu F., World J Gastroenterol. September 7, 2016; 22 (33): 7486-99.
	The NIMA-like kinase Nek2 is a key switch balancing cilia biogenesis and resorption in the development of left-right asymmetry., Endicott SJ, Basu B, Khokha M, Brueckner M., Development. December 1, 2015; 142 (23): 4068-79.
	Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S, Cheng F, Liang J, Wu W, Zhang J., PLoS Biol. January 1, 2012; 10 (3): e1001286.
	Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S, Yabe S, Uchiyama H., Dev Biol. October 15, 2010; 346 (2): 170-80.
	Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos., Tao Q, Tao Q, Yokota C, Puck H, Kofron M, Birsoy B, Yan D, Asashima M, Wylie CC, Lin X, Heasman J., Cell. March 25, 2005; 120 (6): 857-71.

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