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Summary Attributions Wiki
XB-MORPHOLINO-17249271

Attributions for cdknx MO1

Papers


Ascl1 phospho-status regulates neuronal differentiation in a Xenopus developmental model of neuroblastoma., Wylie LA, Hardwick LJ, Papkovskaia TD, Thiele CJ, Philpott A., Dis Model Mech. May 1, 2015; 8 (5): 429-41.                

The phosphorylation status of Ascl1 is a key determinant of neuronal differentiation and maturation in vivo and in vitro., Ali FR, Cheng K, Kirwan P, Metcalfe S, Livesey FJ, Barker RA, Philpott A., Development. June 1, 2014; 141 (11): 2216-24.            

Cell cycle-regulated multi-site phosphorylation of Neurogenin 2 coordinates cell cycling with differentiation during neurogenesis., Ali F, Hindley C, McDowell G, Deibler R, Jones A, Kirschner M, Guillemot F, Philpott A., Development. October 1, 2011; 138 (19): 4267-77.      

Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW, Collins RJ, Philpott A, Jones EA., Organogenesis. October 1, 2009; 5 (4): 201-10.                                          

Xhairy2 functions in Xenopus lens development by regulating p27(xic1) expression., Murato Y, Hashimoto C., Dev Dyn. September 1, 2009; 238 (9): 2179-92.              

Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1., Movassagh M, Philpott A., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.                                

Notch targets the Cdk inhibitor Xic1 to regulate differentiation but not the cell cycle in neurons., Vernon AE, Movassagh M, Horan I, Wise H, Ohnuma S, Philpott A., EMBO Rep. June 1, 2006; 7 (6): 643-8.

The cdk inhibitor p27Xic1 is required for differentiation of primary neurones in Xenopus., Vernon AE, Devine C, Philpott A., Development. January 1, 2003; 130 (1): 85-92.          

A single cdk inhibitor, p27Xic1, functions beyond cell cycle regulation to promote muscle differentiation in Xenopus., Vernon AE, Philpott A., Development. January 1, 2003; 130 (1): 71-83.