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Mebendazole preferentially inhibits cilia formation and exerts anticancer activity by synergistically augmenting DNA damage. , Hong J., Biomed Pharmacother. March 20, 2024; 174 116434.
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa. , Bocquet B., JCI Insight. November 8, 2023; 8 (21):
CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability. , Deniz E ., Dev Biol. July 1, 2023; 499 75-88.
Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease. , Mishra-Gorur K., Proc Natl Acad Sci U S A. April 18, 2023; 120 (16): e2214997120.
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes. , Marquez J ., J Med Genet. July 1, 2021; 58 (7): 453-464.
Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility. , Robson A., Proc Natl Acad Sci U S A. July 9, 2019; 116 (28): 14049-14054.
Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development. , Konjikusic MJ., PLoS Genet. November 6, 2018; 14 (11): e1007817.
La-related protein 6 controls ciliated cell differentiation. , Manojlovic Z., Cilia. January 1, 2017; 6 4.
Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia. , Del Viso F., Dev Cell. September 12, 2016; 38 (5): 478-92.
The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin. , Epting D., Development. January 1, 2015; 142 (1): 174-84.
RFX2 is broadly required for ciliogenesis during vertebrate development. , Chung MI ., Dev Biol. March 1, 2012; 363 (1): 155-65.