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Acta Neuropathologica|June 19, 2002
Monoclonal antibody to stage-specific fetal brain 68-kDa glycoprotein (FGP68) revealed increased FGP68 expression in human primary brain tumorsShinsuke Kato, Takao Shinozawa, Hiroaki Nagashige, et al.Plos One|October 11, 2007
An in vitro model for Lewy body-like hyaline inclusion/astrocytic hyaline inclusion: induction by ER stress with an ALS-linked SOD1 mutationSatoru Yamagishi, Yoshihisa Koyama, Taiichi Katayama, et al.Acta Neuropathologica Communications|April 1, 2016
High expression of α-synuclein in damaged mitochondria with PLA2G6 dysfunctionHisae Sumi-Akamaru, Goichi Beck, Koei Shinzawa, et al.Journal of the Neurological Sciences|November 1, 2019
Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndromeShinobu Fukumura, Kosuke Yamauchi, Akira Kawanabe, et al.Journal of Neuroscience Research|August 19, 2005
Motoneuron degeneration after facial nerve avulsion is exacerbated in presymptomatic transgenic rats expressing human mutant Cu/Zn superoxide dismutaseKen Ikeda, Masashi Aoki, Yoko Kawazoe, et al.Acta Neuropathologica|June 29, 2005
Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal modelsShinsuke Kato, Masako Kato, Yasuko Abe, et al.Acta Neuropathologica|December 3, 2003
Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal modelsShinsuke Kato, Yusuke Saeki, Masashi Aoki, et al.The Journal of Biological Chemistry|December 20, 2003
NEDL1, a novel ubiquitin-protein isopeptide ligase for dishevelled-1, targets mutant superoxide dismutase-1Kou Miyazaki, Tomoyuki Fujita, Toshinori Ozaki, et al.Journal of Neuropathology and Experimental Neurology|August 11, 2012
FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutationNaoki Suzuki, Shinsuke Kato, Masako Kato, et al.Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|April 8, 2003
Altered expression of cardiac ankyrin repeat protein and its homologue, ankyrin repeat protein with PEST and proline-rich region, in atrophic muscles in amyotrophic lateral sclerosisKyoko Nakamura, Chisato Nakada, Kengo Takeuchi, et al.Pageof 6