Kazuhiro Ikenaka

Affiliations: 
Division of Neurobiology and Bioinformatics National Institute for Physiological Sciences, Okazaki-shi, Aichi-ken, Japan 
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"Kazuhiro Ikenaka"
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Publications

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Abdullah A, Hayashi Y, Morimura N, et al. (2022) Fut9 Deficiency Causes Abnormal Neural Development in the Mouse Cerebral Cortex and Retina. Neurochemical Research
Kunisawa K, Hatanaka N, Shimizu T, et al. (2020) Focal loss of the paranodal domain protein Neurofascin155 in the internal capsule impairs cortically induced muscle activity in vivo. Molecular Brain. 13: 159
Wisessmith W, Shimizu T, Li J, et al. (2018) Cathepsin C Modulates Myelin Oligodendrocyte Glycoprotein-induced Experimental Autoimmune Encephalomyelitis. Journal of Neurochemistry
Kunisawa K, Shimizu T, Kushima I, et al. (2018) Dysregulation of schizophrenia-related aquaporin 3 through disruption of paranode influences neuronal viability. Journal of Neurochemistry
Hashimoto H, Jiang W, Yoshimura T, et al. (2017) Strong sonic hedgehog signaling in the mouse ventral spinal cord is not required for oligodendrocyte precursor cell (OPC) generation but is necessary for correct timing of its generation. Neurochemistry International
Jiang W, Ishino Y, Hashimoto H, et al. (2017) Sulfatase 2 Modulates Fate Change from Motor Neurons to Oligodendrocyte Precursor Cells through Coordinated Regulation of Shh Signaling with Sulfatase 1. Developmental Neuroscience
Ikeda M, Hossain MI, Zhou L, et al. (2016) Histological detection of dynamic glial responses in the dysmyelinating Tabby-jimpy mutant brain. Anatomical Science International
Shimizu T, Smits R, Ikenaka K. (2016) Microglia-induced activation of non-canonical Wnt signaling aggravates neurodegeneration in demyelinating disorders. Molecular and Cellular Biology. 36: 2728-2741
Hashimoto H, Ishino Y, Jiang W, et al. (2016) Keratan Sulfate Regulates the Switch from Motor Neuron to Oligodendrocyte Generation During Development of the Mouse Spinal Cord. Neurochemical Research
Horie M, Watanabe K, Bepari AK, et al. (2014) Disruption of actin-binding domain-containing Dystonin protein causes dystonia musculorum in mice. The European Journal of Neuroscience. 40: 3458-71
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