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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, [Organization not found],
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. July 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.