メンバーの研究業績
論文
Sato, H., Kasuga, K., Isoo, N., Hayashi, T., Ikeuchi, T., Hori, Y., Tomita, T.Soluble form of the APP fragment, sAPPβ, positively regulates tau secretion. Neuroscience Research, 193:63-70, 2023. DOI:10.1016/j.neures.2023.03.002
Nishikawa N, Murata M, Hatano T, Mukai Y, Saitoh Y, Sakamoto T, Hanakawa T, Kamei Y, Tachimori H, Hatano K, Matsuda H, Taruno Y, Sawamoto N, Kajiyama Y, Ikenaka K, Kawabata K, Nakamura T, Iwaki H, Kadotani H, Sumi Y, Inoue Y, Hayashi T, Ikeuchi T, Shimo Y, Mochizuki H, Watanabe H, Hattori N, Takahashi Y, Takahashi R, the Japan Parkinson's Progression Markers Initiative (J-PPMI) study group, Idiopathic rapid eye movement sleep behavior disorder in Japan: An observational study, Parkinsonism and Related Disorders, 103:129-135, 2022. doi:10.1016/j.parkreldis.2022.08.011.
Kameda, H., Murabe N., Mizukami H., Ozawa K., Hayashi T., Sakurai M. Parcellation of the murine cortical hindlimb area is demonstrated by its subcortical connectivity and cytoarchitecture. Journal of Comparative Neurology, 530:1950-1965, 2022. Doi:10.1002/cne.25313
Kurihara, M., Sugiyama, Y., Sato, K., Tanaka, M., Mano, T., Ishiura, H., Kubota, A., Hayashi, T., Iwata, A., Shimizu, J., Tsuji, S., Toda, T. Diagnostic values of venous peak lactate, lactate-to-pyruvate ratio, and fold increase in lactate from baseline in aerobic exercise tests in patients with mitochondrial diseases. Internal Medicine, Article ID 8629-21, 2021. DOI:10.2169/internalmedicine.8629-21
Ohno, T., Fukuda, S., Murabe, N., Niido, M., Sakurai, M. Temporal Course of Transient Direct Corticomotoneuronal Connections during Development in Rodents. Neuroscience,478:89-99, 2021. DOI:10.1016/j.neuroscience.2021.09.006
Fukuda, S., Murabe, N., Mizuta, H., Yamamoto, T., Nagai, T. Bio-electrical signal associated with sweet taste transduction in humans is a hyperpolarizing potential on the lingual epithelium. Chemical Senses, 2021;46:bjab040, DOI:10.1093/chemse/bjab040
Kikuchi, JK., Nagashima, Y., Mano, T., Ishiura, H., Hayashi, T., Shimizu, J., Matsukawa, T., Ichikawa, Y., Takahashi, Y., Karino, S., Kanbayashi, T., Kira, J., Goto, J., Tsuji, S. Cerebellar ataxia as a common clinical presentation associated with DNMT1 p.Y511H and a review of the literature. Journal of Molecular Neuroscience, 71(9):1796-1801, 2021. DOI:10.1007/s12031-020-01784-5
Murabe N., Okumura E., Chiba K., Hosoda E., Ikegami S., Kishimoto T. The Starfish Asterina pectinifera: Collection and Maintenance of Adults and Rearing and Metamorphosis of Larvae. In: Carroll D.J., Stricker S.A. (eds) Developmental Biology of the Sea Urchin and Other Marine Invertebrates. Methods in Molecular Biology, vol 2219. Humana, New York, NY, 2021. DOI:10.1007/978-1-0716-0974-3_3
Mimura, T., Mizota, A., Hayashi, T., Nishimura, S. In situ Observations of Porcine Ocular Surface Cells with Handheld 2K-pixel Microscope. The Open Ophthalmology Journal, 14(1), 66–69, 2020. DOI:10.2174/1874364102014010066
Kurihara, M., Orimo, K., Mano, T., Miyano, R., Kamisawa Sato, A., Sato, K., Ihara, R., Hayashi, T., Toda, T. Gait improvement after levofloxacin administration in a progressive supranuclear palsy patient. Clinical Parkinsonism & Related Disorders, 3:100080 2020. DOI: 10.1016/j.prdoa.2020.100080
Fukuda, S., Maeda, H., Sakurai, M. Reevaluation of motoneuron morphology: diversity and regularity among motoneurons innervating different arm muscles along a proximal–distal axis. Scientific Reports 10, 13089, 2020. doi:10.1038/s41598-020-69662-z
Yoshida, M., Hayashi, T., Fujii, K., Ishiura, H., Tsuji, S., Sakurai, Y. Selective impairment of On-reading (Chinese-style pronunciation) in alexia with agraphia for kanji due to subcortical hemorrhage in the left posterior middle temporal gyrus, Neurocase, 26(4):220-226, 2020. doi:10.1080/13554794.2020.1788608
Matsukawa, T., Yamamoto, T., Honda, A., Toya, T., Ishiura, H., Mitsui, J., Tanaka, M., Hao, A., Shinohara, A., Ogura, M., Kataoka, K., Seo, S., Kumano, K., Hosoi, M., Narukawa, N., Yasunaga, A., Maki, H., Ichikawa, M., Nannya, Y., Imai, Y., Takahashi, T., Takahashi, Y., Nagasako, Y., Yasaka, K., Koshi Mano K., Kawabe Matsukawa, M., Miyagawa, T., Hamada, M., Sakuishi, K., Hayashi, T., Iwata, A., Terao, Y., Shimizu, J., Goto, J., Mori, M., Kunimatsu, A., Aoki, S., Hayashi, S., Nakamura, F., Arai, S., Monma, K., Ogata, K., Yoshida, T., Abe, O., Inazawa, J., Toda, T., Kurokawa, M., Tsuji, S. Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophy. Brain Communications, 2(1) fcz048, Jan 2020. doi:10.1093/braincomms/fcz048
Kurihara, M., Ishiura, H., Bannai, T., Mitsui, J., Yoshimura, J., Morishita, S., Hayashi, T., Shimizu, J., Toda, T., Tsuji, S. Novel de novo KIF1A mutation in a patient with autism, hyperactivity, epilepsy, sensory disturbance, and spastic paraplegia. Internal Medicine, Dec 2019. doi:10.2169/internalmedicine.3661-19
Kameda, H., Murabe, N., Odagaki, K., Mizukami, H., Ozawa, K., Sakurai, M. Differential innervation within a transverse plane of spinal gray matter by sensorimotor cortices, with special reference to the somatosensory cortices. Journal of Comparative Neurology, 527(8)1401-1415, 2019. doi:10.1002/cne.24626
Odagaki, K., Kameda, H., Hayashi, T., Sakurai, M. Mediolateral and dorsoventral projection patterns of cutaneous afferents within transverse planes of the mouse spinal dorsal horn. Journal of Comparative Neurology, 527(5)972-984, 2019. doi:10.1002/cne.24593
Watanabe, T., Anno, M., Matsubayashi, Y., Nagasako, Y., Sakuishi, K., Fujimoto, Y., Tachibana, N., Taniguchi, Y., Hayashi, T., Oshima, Y., Tsuji, S., Tanaka, S. Hypoglossal nerve palsy as a cause of severe dysphasia along with the oropharyngeal stenosis due to occipito-cervical kyphosis. Case Reports in Orthopedics, vol. 2019, Article ID 7982847, 4 pages, 2019. doi:10.1155/2019/7982847
Uchigami, H., Sato, K., Kubota, A., Hayashi, T., Shimizu, J., Ikemura, M., Toda, T. ‘Localized’ chronic invasive fungal rhinosinusitis without serological abnormalities. Neurology and Clinical Neuroscience, 7(2):96-97, 2019. doi:10.1111/ncn3.12252
Miyano, R., Kurihara, M., Orimo, K., Mano, T., Kaburaki, T., Tanaka, R., Nishijima, H., Ikemura, M., Takahashi, M., Mori, H., Mutoh, T., Hamada, M., Hayashi, T., Toda, T. Severe visual impairment and subclinical encephalitis preceding clinical signs of chondritis in relapsing polychondritis. Neurology and Clinical Neuroscience, 7(2):75-77, 2019. doi:10.1111/ncn3.12243
Katsuse, K., Kurihara, M., Sugiyama, Y., Kodama, S., Takahashi, M., Momose, T., Yumoto, M., Kaneko, K., Takahashi, T., Kubota, A., Hayashi, T., Toda, T. Aphasic status epilepticus preceding tumefactive left hemisphere lesion in anti-MOG antibody associated disease. Multiple Sclerosis and Related Disorders, 27:91-94, 2019. doi:10.1016/j.msard.2018.10.012
Murabe, N., Mori, T., Fukuda, S., Isoo, N., Ohno, T., Mizukami, H., Ozawa, K., Yoshimura, Y., Sakurai, M. Higher primate-like direct corticomotoneuronal connections are transiently formed in a juvenile subprimate mammal. Scientific Reports 8(1): 16536, 2018. doi:10.1038/s41598-018-34961-z
Niido, M., Fukuda, S., Ohno, T., Sakurai, M. Specific distribution of target muscles receiving transient cortico-motoneuronal direct connections in the juvenile rodent: similarity to higher primates. Teikyo medical journal 41(4):137-148, 2018.
Gondo, T., Kurihara, M., Sugiyama, Y., Mano, T., Mori, H., Hayashi T., Tsuji S. Longitudinally extensive vasogenic edema following spinal cord infarction. Neurology and Clinical Neuroscience, 6(5):143-145, 2018. doi.org/10.1111/ncn3.12215
Kodama, S., Mano, T., Kakumoto, T., Ishiura, H., Hagiwara, A., Kamiya, K., Hayashi, T., Tsuji, S. Ketotic hyperglycemia-related seizure with reversible white matter lesion: metabolic implication of its reversibility based on magnetic resonance spectroscopy study. Journal of the Neurological Sciences, 390:20-21, 2018. doi:10.1016/j.jns.2018.04.006
Ishiura, H., Doi, K., Mitsui, J., Yoshimura, J., Matsukawa, MK., Fujiyama, A, Toyoshima, Y., Kakita, A., Takahashi, H., Suzuki, Y., Sugano, S., Qu, W., Ichikawa, K., Yurino, H., Higasa, K., Shibata, S., Mitsue, A., Tanaka, M., Ichikawa, Y., Takahashi, Y., Date, H., Matsukawa, T., Kanda, J., Nakamoto, FK., Higashihara, M., Abe, K., Koike, R., Sasagawa, M., Kurohane, Y., Hasegawa, N., Kanesawa, N., Kondo, T., Tada, M., Takano, H., Saito, Y., Sanpei, K., Onodera, O., Nishizawa, M., Nakamura, M., Sakiyama, Y., Ohtsuka, M., Ueki, A., Kaida, K., Shimizu, J., Hanajima, R., Hayashi, T., Terao, Y., Terada, S., Hamada, M., Shirota, Y., Kubota, A., Ugawa, Y., Koh, K., Takiyama, Y., Ohsawa-Yoshida, N., Ishiura, S., Kira, J., Tamaoka, A., Akiyama, H., Otsuki, T., Sano, A., Ikeda, A., Goto, J., Morishita, S., Tsuji, S. Intronic TTTCA pentanucleotide repeat expansions cause benign adult familial myoclonic epilepsy. Nature Genetics, 50(4):581–590, 2018. doi:10.1038/s41588-018-0067-2 PMID:29507423
Kurihara, M., Ishiura, H., Sasaki T., Otsuka J., Hayashi T., Terao Y., Matsukawa T., Mitsui J., Kaneko J., Nishiyama K., Doi K., Yoshimura J., Morishita S., Shimizu J., Tsuji S. Novel de novo KCND3 mutation in a Japanese patient with intellectual disability, cerebellar ataxia, myoclonus, and dystonia. Cerebellum, 17(2):273-242, 2018. doi: 10.1007/s12311-017-0883-4 PMID:28895081
Kodama, S., Mano, T., Masuzawa, A., Hirata, Y., Nagasako, Y., Mano, KK., Hamada, M., Terao, Y., Hayashi, T., Ono, M., Tsuji, S. Tacrolimus-induced reversible cerebral vasoconstriction syndrome with delayed multi-segmental vasoconstriction. Journal of Stroke and Cerebrovascular Diseases 26(5):e75–e77, 2017. doi:10.1016/j.jstrokecerebrovasdis.2017.03.006 PMID:28342655
Yoshida, M., Hayashi, T., Fujii, K., Kawai, K., Tsuji, S., Iwata, A. Recovered recall memory after decompression of the fornix by surgical removal of pineal tumor. Neurology, 86(8):790-791, 2016. doi:10.1212/WNL.0000000000002394 PMID:26903489
Isoo, N., Ohno, T., Isowaki, M., Fukuda, S., Murabe, N., Mizukami, H., Ozawa, K., Mishina, M., Sakurai, M. The decline in synaptic GluN2B and rise in inhibitory neurotransmission determine the end of a critical period. Scientific Reports 6:34196, 2016. doi:10.1038/srep34196 PMID:27677249
Ogawa, G. Identification of auditory fields responding to synthetic vowels in rat auditory cortex. Teikyo medical journal 39(5):183-198,2016.
Ogawa, G, Nishida, Y., Fukuda, S., Kudoh, M. A rat model for human speech sound discrimination: Discrimination learning of synthetic vowels by rats. Teikyo medical journal 39(3):95-107, 2016.
Maeda, H., Fukuda, S., Kameda, H., Murabe, N., Isoo, N., Mizukami, H., Ozawa, K., Sakurai, M. Corticospinal axons make direct synaptic connections with spinal motoneurons innervating forearm muscles early during postnatal development in the rat. The Journal of Physiology, 594(1):189-205, 2016. doi:10.1113/JP270885 PMID: 26503304
Tanaka, N., Hayashi, T., Tsuji, S., Iwata, A. Abdominal tremor in Parkinson’s disease. Movement Disorders Clinical Practice, 2(1):104-105, 2015. DOI:10.1002/mdc3.12119.
Watanabe, T., Hanajima, R., Shirota, Y., Tsutsumi, R., Shimizu, T., Hayashi, T., Terao, Y., Ugawa, Y., Katsura, M., Kunimatsu, A., Ohtomo, K., Hirose, S., Miyashita, Y., Konishi, S. Effects of rTMS of Pre-Supplementary Motor Area on Fronto Basal Ganglia Network Activity during Stop-Signal Task. Journal of Neuroscience. 35(12):4813-4823, 2015. doi:10.1523/JNEUROSCI.3761-14.2015 PMID:25810512
Shinya, Y., Miyawaki, S., Nakatomi, H., Okano, A., Imai, H., Shin, M., Sato, K., Tsuchida, T., Hayashi, T., Terao, Y., Numakura, S.,j Morikawa, T., Shibahara, J., Kikuta, S., Kondo, K., Tatsuno, K., Mori, H., Kunimatsu, A., Tsuji, S., Saito, N. Recurrent cerebral aneurysm formation and rupture within a short period due to invasive aspergillosis of the nasal sinus; pathological analysis of the catastrophic clinical course. International Journal of Clinical and Experimental Pathology 8(10):13510-13522, 2015. PMID:26722566
Kamiyama, T., Kameda, H., Murabe, N., Fukuda, S., Yoshioka, N., Mizukami, H., Ozawa, K., Sakurai, M. Corticospinal tract development and spinal cord innervation differ between cervical and lumbar targets. Journal of Neuroscience 35:1181-1191, 2015. PMID:25609632
Ishiura, H., Takahashi, Y., Hayashi, T., Saito, K., Furuya, H., Watanabe, M., Murata, M., Suzuki, M., Sugiura, A., Umemura, H., Ueda, N., Goto, J., Tsuji, S. Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses. Journal of Human Genetics, 59(3):163-72, 2014. DOI:10.1038/jhg.2013.139 PMID:24451228
書籍
林 俊宏, 高橋 倫子 (監修) コスタンゾ明解生理学 原著第6版.エルゼビア・ジャパン,東京 2019年9月 (ISBN: 4860342364)