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CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability. , Deniz E ., Dev Biol. July 1, 2023; 499 75-88.
Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR. , Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
Quantitative analysis of transcriptome dynamics provides novel insights into developmental state transitions. , Johnson K., BMC Genomics. October 23, 2022; 23 (1): 723.
RNA demethylation by FTO stabilizes the FOXJ1 mRNA for proper motile ciliogenesis. , Kim H ., Dev Cell. April 19, 2021; 56 (8): 1118-1130.e6.
Nucleoporin NUP205 plays a critical role in cilia and congenital disease. , Marquez J ., Dev Biol. January 1, 2021; 469 46-53.
CFAP43 modulates ciliary beating in mouse and Xenopus. , Rachev E., Dev Biol. March 15, 2020; 459 (2): 109-125.
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.
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.
Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral- right blastomere. , Tingler M., Genesis. June 1, 2014; 52 (6): 588-99.