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Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.
Gibbs BC, Damerla RR, Vladar EK, Chatterjee B, Wan Y, Liu X, Cui C, Gabriel GC, Zahid M, Yagi H, Szabo-Rogers HL, Suyama KL, Axelrod JD, Lo CW. Gibbs BC, et al. Among authors: wan y. Biol Open. 2016 Feb 16;5(3):323-35. doi: 10.1242/bio.015750. Biol Open. 2016. PMID: 26883626 Free PMC article.
Finding the Unicorn, a New Mouse Model of Midfacial Clefting.
Lantz B, White C, Liu X, Wan Y, Gabriel G, Lo CWY, Szabo-Rogers HL. Lantz B, et al. Among authors: wan y. Genes (Basel). 2020 Jan 11;11(1):83. doi: 10.3390/genes11010083. Genes (Basel). 2020. PMID: 31940751 Free PMC article.
7,855 results