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Summary Attributions Wiki
XB-MORPHOLINO-17250366

Attributions for sox11 MO1

Papers


Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome., Hempel A, Pagnamenta AT, Blyth M, Mansour S, McConnell V, Kou I, Ikegawa S, Tsurusaki Y, Matsumoto N, Lo-Castro A, Plessis G, Albrecht B, Battaglia A, Taylor JC, Howard MF, Keays D, Sohal AS, null null, Kühl SJ, Kini U, McNeill A., J Med Genet. March 1, 2016; 53 (3): 152-62.            


sox4 and sox11 function during Xenopus laevis eye development., Cizelsky W, Hempel A, Metzig M, Tao S, Hollemann T, Kühl M, Kühl SJ., PLoS One. January 1, 2013; 8 (7): e69372.              


WT1 and Sox11 regulate synergistically the promoter of the Wnt4 gene that encodes a critical signal for nephrogenesis., Murugan S, Shan J, Kühl SJ, Tata A, Pietilä I, Kühl M, Vainio SJ., Exp Cell Res. June 10, 2012; 318 (10): 1134-45.