Aoki, Masashi

Mutations of optineurin in amyotrophic lateral sclerosis

Maruyama, H., Morino, H., Ito, H., Izumi, Y., Kato, H., Watanabe, Y., Kinoshita, Y., Kamada, M., Nodera, H., Suzuki, H., et al. (2010) · Nature

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 1,265

Distinction between MOG antibody-positive and AQP4 antibody-positive NMO spectrum disorders

Sato, D. K., Callegaro, D., Lana-Peixoto, M. A., Waters, P. J., Jorge, F. M. D. H., Takahashi, T., Nakashima, I., Apostolos-Pereira, S. L., Talim, N., Simm, R. F., et al. (2014) · Neurology

Multiple Sclerosis Research StudiesPeripheral Neuropathies and Disorders

Cited by 850

Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent

Fujimori, K., Ishikawa, M., Otomo, A., Atsuta, N., Nakamura, R., Akiyama, T., Hadano, S., Aoki, M., Saya, H., Sobue, G., et al. (2018) · Nature Medicine

Amyotrophic Lateral Sclerosis ResearchPluripotent Stem Cells Research

Cited by 494

Myelin injury without astrocytopathy in neuroinflammatory disorders with MOG antibodies

Kaneko, K., Sato, D. K., Nakashima, I., Nishiyama, S., Tanaka, S., Marignier, R., Hyun, J.-W., Oliveira, L. M. D., Reindl, M., Seifert-Held, T., et al. (2016) · Journal of Neurology, Neurosurgery & Psychiatry

Multiple Sclerosis Research StudiesAutoimmune Neurological Disorders and Treatments

Cited by 106

Proteasome dysfunction induces muscle growth defects and protein aggregation

Kitajima, Y., Tashiro, Y., Suzuki, N., Warita, H., Kato, M., Tateyama, M., Ando, R., Izumi, R., Yamazaki, M., Abe, M., et al. (2014) · Journal of Cell Science

Muscle Physiology and DisordersUbiquitin and proteasome pathways

Cited by 79

The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients

Ikeda, M., Sharma, V., Mark Sumi, S., Rogaeva, E. A., Poorkaj, P., Sherrington, R., Nee, L., Tsuda, T., Oda, N., Watanabe, M., et al. (1996) · Annals of Neurology

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 60

Glucokinase gene in gestational diabetes mellitus: population association study and molecular scanning

Chiu, K. C., Go, R. C. P., Aoki, M., Riggs, A. C., Tanizawa, Y., Acton, R. T., Bell, D. S. H., Goldenberg, R. L., Roseman, J. M., & Permutt, M. A. (1994) · Diabetologia

Pancreatic function and diabetesGestational Diabetes Research and Management

Cited by 49

ABCD1 translation–initiator mutation demonstrates genotype–phenotype correlation for AMN

O’Neill, G. N., Aoki, M., & Brown, R. H. (2001) · Neurology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 28

Inducible Rpt3, a Proteasome Component, Knockout in Adult Skeletal Muscle Results in Muscle Atrophy

Kitajima, Y., Suzuki, N., Yoshioka, K., Izumi, R., Tateyama, M., Tashiro, Y., Takahashi, R., Aoki, M., & Ono, Y. (2020) · Frontiers in Cell and Developmental Biology

Muscle Physiology and DisordersUbiquitin and proteasome pathways

Cited by 14