Mice Lacking Zfhx1b, the Gene That Codes for Smad-Interacting Protein-1, Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation SyndromeTom Van de Putte, Yujiro Higashi, Mitsuji Maruhashi et al.|The American Journal of Human Genetics|2003Cited by 308
Generation of the floxed allele of the SIP1 (<i>Smad‐interacting protein 1</i>) gene for Cre‐mediated conditional knockout in the mouseYujiro Higashi, Danny Huylebroeck, Mitsuji Maruhashi et al.|genesis|2002Cited by 111
Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formationAmaya Miquelajáuregui, Victor Tarabykin, A. S. Polyakov et al.|Proceedings of the National Academy of Sciences|2007Cited by 89
Complementary expression pattern of <i>Zfhx1</i> genes <i>Sip1</i> and <i>δEF1</i> in the mouse embryo and their genetic interaction revealed by compound mutantsTomoya Miyoshi, Yujiro Higashi, Mitsuji Maruhashi et al.|Developmental Dynamics|2006Cited by 72
Involvement of SIP1 in positioning of somite boundaries in the mouse embryoMitsuji Maruhashi, Yujiro Higashi, Tom Van de Putte et al.|Developmental Dynamics|2005Cited by 60