Loss of CRMP1 and CRMP2 results in migration defects of Purkinje cells in the X lobule of the mouse cerebellum
Satoshi Akinaga(Waseda University), Toshio Ohshima(Waseda University), P.E. Kolattukudy(University of Central Florida), Aosa Kaneko(Waseda University), Yoshio Goshima(Yokohama University of Pharmacy), Sayaka Harada(Waseda University), Miyuki Takahashi(Waseda University)
Cited by 6
Related Papers
Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death.
|Proceedings of the National Academy of Sciences|1996|900
Semaphorin3A signalling is mediated via sequential Cdk5 and GSK3β phosphorylation of CRMP2: implication of common phosphorylating mechanism underlying axon guidance and Alzheimer's disease
|Genes to Cells|2005|411
α-Galactosidase A deficient mice: A model of Fabry disease
|Proceedings of the National Academy of Sciences|1997|370
Gene Expression Patterns of Murine Dentin Matrix Protein 1 (Dmp1) and Dentin Sialophosphoprotein (DSPP) Suggest Distinct Developmental Functions In Vivo
|Journal of Bone and Mineral Research|1997|348