Yokota, Takanori
Tokyo Medical and Dental University
5 papers on CoChatORCID 0000-0002-6490-3263
Most cited papers
- Verified
Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition
Yokota, T., Sugawara, K., Ito, K., Takahashi, R., Ariga, H., & Mizusawa, H. (2003) · Biochemical and Biophysical Research Communications
Parkinson's Disease Mechanisms and TreatmentsNuclear Receptors and Signaling
Cited by 356
- Verified
Delayed-onset ataxia in mice lacking α-tocopherol transfer protein: Model for neuronal degeneration caused by chronic oxidative stress
Yokota, T., Igarashi, K., Uchihara, T., Jishage, K.-I., Tomita, H., Inaba, A., Li, Y., Arita, M., Suzuki, H., Mizusawa, H., et al. (2001) · Proceedings of the National Academy of Sciences
Antioxidant Activity and Oxidative StressHereditary Neurological Disorders
Cited by 261
- Verified
Focal degeneration of astrocytes in amyotrophic lateral sclerosis
Rossi, D., Brambilla, L., Valori, C. F., Roncoroni, C., Crugnola, A., Yokota, T., Bredesen, D. E., & Volterra, A. (2008) · Cell Death & Differentiation
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 194
- Verified
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation
Guo, L., Bertola, D. R., Takanohashi, A., Saito, A., Segawa, Y., Yokota, T., Ishibashi, S., Nishida, Y., Yamamoto, G. L., Franco, J. F. D. S., et al. (2019) · The American Journal of Human Genetics
Bone Metabolism and DiseasesConnective tissue disorders research
Cited by 133
- Verified
A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34
Ozaki, K., Doi, H., Mitsui, J., Sato, N., Iikuni, Y., Majima, T., Yamane, K., Irioka, T., Ishiura, H., Doi, K., et al. (2015) · JAMA Neurology
Genetic Neurodegenerative DiseasesHereditary Neurological Disorders
Cited by 81
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