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DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes. , Marquez J ., J Med Genet. July 1, 2021; 58 (7): 453-464.
The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1. , Ott T., Front Physiol. January 1, 2019; 10 134.
The involvement of PCP proteins in radial cell intercalations during Xenopus embryonic development. , Ossipova O., Dev Biol. December 15, 2015; 408 (2): 316-27.
Mechanical strain determines the axis of planar polarity in ciliated epithelia. , Chien YH., Curr Biol. November 2, 2015; 25 (21): 2774-2784.
A novel serotonin-secreting cell type regulates ciliary motility in the mucociliary epidermis of Xenopus tadpoles. , Walentek P ., Development. April 1, 2014; 141 (7): 1526-33.
Ciliogenesis and cerebrospinal fluid flow in the developing Xenopus brain are regulated by foxj1. , Hagenlocher C., Cilia. April 29, 2013; 2 (1): 12.
Global hyper-synchronous spontaneous activity in the developing optic tectum. , Imaizumi K., Sci Rep. January 1, 2013; 3 1552.