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Developmentally-programmed cellular senescence is conserved and widespread in zebrafish. , Da Silva-Álvarez S., Aging (Albany NY). September 29, 2020; 12 (18): 17895-17901.
Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells. , Zhang Z ., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
Proteolysis of Xenopus Cip-type CDK inhibitor, p16Xic2, is regulated by PCNA binding and CDK2 phosphorylation. , Zhu XN., Cell Div. April 22, 2013; 8 (1): 5.
Xaml1/ Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus. , Park BY., Dev Biol. February 1, 2012; 362 (1): 65-75.
VentX trans-activates p53 and p16ink4a to regulate cellular senescence. , Wu X., J Biol Chem. April 8, 2011; 286 (14): 12693-701.
Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size. , Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
Tumorhead distribution to cytoplasmic membrane of neural plate cells is positively regulated by Xenopus p21-activated kinase 1 ( X- PAK1). , Wu CF ., Dev Biol. August 1, 2007; 308 (1): 169-86.
Mxi1 is essential for neurogenesis in Xenopus and acts by bridging the pan-neural and proneural genes. , Klisch TJ., Dev Biol. April 15, 2006; 292 (2): 470-85.
Identification of Xenopus cyclin-dependent kinase inhibitors, p16Xic2 and p17Xic3. , Daniels M., Gene. November 10, 2004; 342 (1): 41-7.