Yuji Okamoto - Publications

Institute of Science and Technology, Austria 

53 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Vandael D, Okamoto Y, Jonas P. Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses. Nature Communications. 12: 2912. PMID 34006874 DOI: 10.1038/s41467-021-23153-5  1
2021 Vandael D, Okamoto Y, Borges-Merjane C, Vargas-Barroso V, Suter BA, Jonas P. Subcellular patch-clamp techniques for single-bouton stimulation and simultaneous pre- and postsynaptic recording at cortical synapses. Nature Protocols. 16: 2947-2967. PMID 33990799 DOI: 10.1038/s41596-021-00526-0  1
2021 Douzono M, Nobuhara Y, Maruta K, Okamoto Y, Sonoda Y, Takashima H. [Inherited Creutzfeldt-Jakob disease with four-octapeptide repeat insertional mutation in the prion gene]. Rinsho Shinkeigaku = Clinical Neurology. PMID 33867415 DOI: 10.5692/clinicalneurol.cn-001558  0.01
2020 Ie Y, Okamoto Y, Inoue T, Seo T, Ohto T, Yamada R, Tada H, Aso Y. Improving Intramolecular Hopping Charge Transport via Periodical Segmentation of π-Conjugation in a Molecule. Journal of the American Chemical Society. PMID 33350820 DOI: 10.1021/jacs.0c10560  0.01
2020 Taniguchi T, Ando M, Okamoto Y, Yoshimura A, Higuchi Y, Hashiguchi A, Shiga K, Hayashida A, Hatano T, Ishiura H, Mitsui J, Hattori N, Mizuno T, Nakagawa M, Tsuji S, et al. Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan. Clinical Genetics. PMID 33179255 DOI: 10.1111/cge.13881  0.01
2020 Okamoto Y, Sumiya M, Nakamura Y, Suzuki Y. Effective silicon production from SiCl source using hydrogen radicals generated and transported at atmospheric pressure. Science and Technology of Advanced Materials. 21: 482-491. PMID 32939173 DOI: 10.1080/14686996.2020.1789438  0.01
2020 Ishihara S, Okamoto Y, Tanabe H, Yoshimura A, Higuchi Y, Yuan JH, Hashiguchi A, Ishiura H, Mitsui J, Suwazono S, Oya Y, Sasaki M, Nakagawa M, Tsuji S, Ohya Y, et al. Clinical features of inherited neuropathy with BSCL2 mutations in Japan. Journal of the Peripheral Nervous System : Jpns. PMID 32108980 DOI: 10.1111/jns.12369  0.01
2019 Sawada J, Katayama T, Tokashiki T, Kikuchi S, Kano K, Takahashi K, Saito T, Adachi Y, Okamoto Y, Yoshimura A, Takashima H, Hasebe N. The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins. Internal Medicine (Tokyo, Japan). PMID 31554751 DOI: 10.2169/internalmedicine.2905-19  0.01
2019 Ie Y, Okamoto Y, Inoue T, Tone S, Seo T, Honda Y, Tanaka S, Lee SK, Ohto T, Yamada R, Tada H, Aso Y. Highly Planar and Completely Insulated Oligothiophenes: Effects of π-Conjugation on Hopping Charge Transport. The Journal of Physical Chemistry Letters. PMID 31132274 DOI: 10.1021/acs.jpclett.9b00747  0.01
2019 Li J, Suda K, Ueoka I, Tanaka R, Yoshida H, Okada Y, Okamoto Y, Hiramatsu Y, Takashima H, Yamaguchi M. Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability. Experimental Cell Research. PMID 30953623 DOI: 10.1016/j.yexcr.2019.03.040  0.01
2018 Yoshimura A, Yuan JH, Hashiguchi A, Ando M, Higuchi Y, Nakamura T, Okamoto Y, Nakagawa M, Takashima H. Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 30257968 DOI: 10.1136/jnnp-2018-318839  0.01
2018 Ohkura A, Negoto T, Aoki T, Noguchi K, Okamoto Y, Komatani H, Kawano T, Mukasa A, Morioka M. Stenotic changes of the posterior cerebral artery are a major contributing factor for cerebral infarction in moyamoya disease. Surgical Neurology International. 9: 105. PMID 29930871 DOI: 10.4103/sni.sni_18_18  0.01
2018 Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, et al. Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy. Brain : a Journal of Neurology. PMID 29718187 DOI: 10.1093/brain/awy104  0.04
2018 Tanabe H, Higuchi Y, Yuan JH, Hashiguchi A, Yoshimura A, Ishihara S, Nozuma S, Okamoto Y, Matsuura E, Ishiura H, Mitsui J, Takashima R, Kokubun N, Maeda K, Asano Y, et al. Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan. Journal of the Peripheral Nervous System : Jpns. PMID 29381233 DOI: 10.1111/jns.12252  0.04
2018 Yuan JH, Hashiguchi A, Okamoto Y, Yoshimura A, Ando M, Shiomi K, Saito K, Takahashi M, Ichinose K, Ohmichi T, Ichikawa K, Tadashi A, Takigawa H, Shibayama H, Takashima H. Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2. Journal of Human Genetics. PMID 29321516 DOI: 10.1038/s10038-017-0388-5  0.01
2017 Ando M, Hashiguchi A, Okamoto Y, Yoshimura A, Hiramatsu Y, Yuan J, Higuchi Y, Mitsui J, Ishiura H, Umemura A, Maruyama K, Matsushige T, Morishita S, Nakagawa M, Tsuji S, et al. Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study. Journal of the Peripheral Nervous System : Jpns. PMID 28660751 DOI: 10.1111/jns.12228  0.01
2017 Kawashima K, Okamoto Y, Annayev O, Toyokura N, Takahashi R, Lippmaa M, Itaka K, Suzuki Y, Matsuki N, Koinuma H. Combinatorial screening of halide perovskite thin films and solar cells by mask-defined IR laser molecular beam epitaxy. Science and Technology of Advanced Materials. 18: 307-315. PMID 28567176 DOI: 10.1080/14686996.2017.1314172  0.01
2017 Hirayanagi K, Okamoto Y, Takai E, Ishizawa K, Makioka K, Fujita Y, Kaneko Y, Tanaka M, Takashima H, Ikeda Y. Bilateral striatal necrosis caused by a founder mitochondrial 14459G>A mutation in two independent Japanese families. Journal of the Neurological Sciences. 378: 177-181. PMID 28566160 DOI: 10.1016/j.jns.2017.05.015  0.01
2017 Yuan JH, Hashiguchi A, Yoshimura A, Yaguchi H, Tsuzaki K, Ikeda A, Wada-Isoe K, Ando M, Nakamura T, Higuchi Y, Hiramatsu Y, Okamoto Y, Takashima H. Clinical diversity caused by novel IGHMBP2 variants. Journal of Human Genetics. PMID 28202949 DOI: 10.1038/jhg.2017.15  0.01
2016 Okamoto Y, Lipstein N, Hua Y, Lin KH, Brose N, Sakaba T, Midorikawa M. Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice. Elife. 5. PMID 27154627 DOI: 10.7554/eLife.14643  1
2016 Higuchi Y, Hashiguchi A, Yuan J, Yoshimura A, Mitsui J, Ishiura H, Tanaka M, Ishihara S, Tanabe H, Nozuma S, Okamoto Y, Matsuura E, Ohkubo R, Inamizu S, Shiraishi W, et al. Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2. Annals of Neurology. PMID 26991897 DOI: 10.1002/ana.24612  1
2015 Hiramatsu Y, Yoshimura M, Saigo R, Arata H, Okamoto Y, Matsuura E, Maruyama H, Takashima H. Toxocara canis myelitis involving the lumbosacral region: a case report. The Journal of Spinal Cord Medicine. 1-15. PMID 26832660 DOI: 10.1080/10790268.2015.1114230  1
2015 Nozuma S, Okamoto Y, Higuchi I, Yuan J, Hashiguchi A, Sakiyama Y, Yoshimura A, Higuchi Y, Takashima H. Clinical and Electron Microscopic Findings in Two Patients with Mitochondrial Myopathy Associated with Episodic Hyper-creatine Kinase-emia. Internal Medicine (Tokyo, Japan). 54: 3209-14. PMID 26666615 DOI: 10.2169/internalmedicine.54.5444  1
2015 Ie Y, Okamoto Y, Tone S, Aso Y. Synthesis, Properties, and π-Dimer Formation of Oligothiophenes Partially Bearing Orthogonally Fused Fluorene Units. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 16688-95. PMID 26407071 DOI: 10.1002/chem.201502606  1
2015 Pehlivan D, Beck CR, Okamoto Y, Harel T, Akdemir ZH, Jhangiani SN, Withers MA, Goksungur MT, Carvalho CM, Czesnik D, Gonzaga-Jauregui C, Wiszniewski W, Muzny DM, Gibbs RA, Rautenstrauss B, et al. The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26378787 DOI: 10.1038/Gim.2015.124  1
2015 Sakiyama Y, Kanda N, Higuchi Y, Yoshimura M, Wakaguri H, Takata Y, Watanabe O, Yuan J, Tashiro Y, Saigo R, Nozuma S, Yoshimura A, Arishima S, Ikeda K, Shinohara K, ... ... Okamoto Y, et al. New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan. Neurology® Neuroimmunology & Neuroinflammation. 2: e143. PMID 26309903 DOI: 10.1212/NXI.0000000000000143  0.01
2015 Gonzaga-Jauregui C, Harel T, Gambin T, Kousi M, Griffin LB, Francescatto L, Ozes B, Karaca E, Jhangiani SN, Bainbridge MN, Lawson KS, Pehlivan D, Okamoto Y, Withers M, Mancias P, et al. Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy. Cell Reports. 12: 1169-83. PMID 26257172 DOI: 10.1016/J.Celrep.2015.07.023  0.01
2014 Hashiguchi A, Higuchi Y, Nomura M, Nakamura T, Arata H, Yuan J, Yoshimura A, Okamoto Y, Matsuura E, Takashima H. Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs. Journal of the Peripheral Nervous System : Jpns. 19: 311-6. PMID 25583183 DOI: 10.1111/jns.12102  1
2014 Komeyama K, Okamoto Y, Takaki K. Cobalt-catalyzed formal [4+2] cycloaddition of α,α'-dichloro-ortho-xylenes with alkynes. Angewandte Chemie (International Ed. in English). 53: 11325-8. PMID 25160750 DOI: 10.1002/anie.201406807  1
2014 Midorikawa M, Okamoto Y, Sakaba T. Developmental changes in Ca2+ channel subtypes regulating endocytosis at the calyx of Held. The Journal of Physiology. 592: 3495-510. PMID 24907302 DOI: 10.1113/jphysiol.2014.273243  1
2014 Okamoto Y, Goksungur MT, Pehlivan D, Beck CR, Gonzaga-Jauregui C, Muzny DM, Atik MM, Carvalho CM, Matur Z, Bayraktar S, Boone PM, Akyuz K, Gibbs RA, Battaloglu E, Parman Y, et al. Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 386-94. PMID 24136616 DOI: 10.1038/Gim.2013.155  1
2013 Okamoto Y, Pehlivan D, Wiszniewski W, Beck CR, Snipes GJ, Lupski JR, Khajavi M. Curcumin facilitates a transitory cellular stress response in Trembler-J mice. Human Molecular Genetics. 22: 4698-705. PMID 23847051 DOI: 10.1093/hmg/ddt318  0.01
2013 Zhao Z, Hu J, Sakiyama Y, Okamoto Y, Higuchi I, Li N, Shen H, Takashima H. DYSF mutation analysis in a group of Chinese patients with dysferlinopathy Clinical Neurology and Neurosurgery. 115: 1234-1237. PMID 23254335 DOI: 10.1016/j.clineuro.2012.11.010  1
2012 Tokunaga S, Hashiguchi A, Yoshimura A, Maeda K, Suzuki T, Haruki H, Nakamura T, Okamoto Y, Takashima H. Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation. Neurogenetics. 13: 359-65. PMID 22847150 DOI: 10.1007/s10048-012-0338-5  1
2012 Miyake H, Kajimoto Y, Murai H, Nomura S, Ono S, Okamoto Y, Sumi Y. Assessment of a quick reference table algorithm for determining initial postoperative pressure settings of programmable pressure valves in patients with idiopathic normal pressure hydrocephalus: SINPHONI subanalysis. Neurosurgery. 71: 722-8; discussion 72. PMID 22653392 DOI: 10.1227/NEU.0b013e318260fef7  0.01
2011 Okamoto Y, Higuchi I, Sakiyama Y, Tokunaga S, Watanabe O, Arimura K, Nakagawa M, Takashima H. A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia. Annals of Neurology. 70: 486-92. PMID 21905081 DOI: 10.1002/ana.22498  1
2011 Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M. Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis. Journal of Neurology. 258: 1998-2008. PMID 21533827 DOI: 10.1007/s00415-011-6056-3  0.01
2011 Sakiyama Y, Okamoto Y, Higuchi I, Inamori Y, Sangatsuda Y, Michizono K, Watanabe O, Hatakeyama H, Goto Y, Arimura K, Takashima H. A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy. Acta Neuropathologica. 121: 775-83. PMID 21424749 DOI: 10.1007/s00401-011-0818-y  0.01
2011 Hayashi T, Nakamura M, Ichiba M, Matsuda M, Kato M, Shiokawa N, Shimo H, Tomiyasu A, Mori S, Tomiyasu Y, Ishizuka T, Inamori Y, Okamoto Y, Umehara F, Arimura K, et al. Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: a case report and phenotypic comparison with a previously reported case. Psychiatry and Clinical Neurosciences. 65: 105-8. PMID 21265945 DOI: 10.1111/j.1440-1819.2010.02169.x  0.01
2009 Hirano R, Takashima H, Okubo R, Okamoto Y, Maki Y, Ishida S, Suehara M, Hokezu Y, Arimura K. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan. Journal of Human Genetics. 54: 377-81. PMID 19444286 DOI: 10.1038/jhg.2009.44  1
2009 Fukushima S, Hirohata M, Okamoto Y, Yamashita S, Ishida S, Shigemori M. Anterior inferior cerebellar artery dissecting aneurysm in a juvenile: case report. Neurologia Medico-Chirurgica. 49: 81-4. PMID 19246870 DOI: 10.2176/nmc.49.81  0.01
2007 Okamoto Y, Higashiyama H, Inoue H, Kanematsu M, Kinoshita M, Asano S. Quantitative image analysis in adipose tissue using an automated image analysis system: differential effects of peroxisome proliferator-activated receptor-alpha and -gamma agonist on white and brown adipose tissue morphology in AKR obese and db/db diabetic mice. Pathology International. 57: 369-77. PMID 17539968 DOI: 10.1111/j.1440-1827.2007.02109.x  0.01
2007 Rong JX, Qiu Y, Hansen MK, Zhu L, Zhang V, Xie M, Okamoto Y, Mattie MD, Higashiyama H, Asano S, Strum JC, Ryan TE. Adipose mitochondrial biogenesis is suppressed in db/db and high-fat diet-fed mice and improved by rosiglitazone. Diabetes. 56: 1751-60. PMID 17456854 DOI: 10.2337/db06-1135  0.01
2007 Okamoto Y, Higashiyama H, Rong JX, McVey MJ, Kinoshita M, Asano S, Hansen MK. Comparison of mitochondrial and macrophage content between subcutaneous and visceral fat in db/db mice. Experimental and Molecular Pathology. 83: 73-83. PMID 17434481 DOI: 10.1016/j.yexmp.2007.02.007  1
2007 Higashiyama H, Billin AN, Okamoto Y, Kinoshita M, Asano S. Expression profiling of peroxisome proliferator-activated receptor-delta (PPAR-delta) in mouse tissues using tissue microarray. Histochemistry and Cell Biology. 127: 485-94. PMID 17333240 DOI: 10.1007/s00418-007-0279-5  0.01
2007 Yoshida T, Tomozawa Y, Arisato T, Okamoto Y, Hirano H, Nakagawa M. The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells. Journal of Human Genetics. 52: 362-9. PMID 17318298 DOI: 10.1007/s10038-007-0124-7  0.01
2007 Miyazaki Y, Tang J, Maeda Y, Nakano M, Wang L, Nolte RT, Sato H, Sugai M, Okamoto Y, Truesdale AT, Hassler DF, Nartey EN, Patrick DR, Ho ML, Ozawa K. Orally active 4-amino-5-diarylurea-furo[2,3-d]pyrimidine derivatives as anti-angiogenic agent inhibiting VEGFR2 and Tie-2. Bioorganic & Medicinal Chemistry Letters. 17: 1773-8. PMID 17276055 DOI: 10.1016/j.bmcl.2006.12.077  0.08
2007 Higashiyama H, Yoshimoto D, Okamoto Y, Kikkawa H, Asano S, Kinoshita M. Receptor-activated Smad localisation in bleomycin-induced pulmonary fibrosis. Journal of Clinical Pathology. 60: 283-9. PMID 16751304 DOI: 10.1136/jcp.2006.037606  1
2006 Okamoto Y, Takashima H, Higuchi I, Matsuyama W, Suehara M, Nishihira Y, Hashiguchi A, Hirano R, Ng AR, Nakagawa M, Izumo S, Osame M, Arimura K. Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene. Neurogenetics. 7: 175-83. PMID 16779558 DOI: 10.1007/s10048-006-0046-0  0.01
2004 Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families. Neurogenetics. 5: 215-21. PMID 15455264 DOI: 10.1007/s10048-004-0194-z  0.01
2003 Kinoshita T, Imaizumi T, Miura Y, Fujimoto H, Ayabe M, Shoji H, Okamoto Y, Takashima H, Osame M, Nakagawa M. A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation. Neuroscience Letters. 350: 169-72. PMID 14550921  0.01
2002 Kitamura S, Kohno Y, Okamoto Y, Takeshita M, Ohta S. Reductive metabolism of an alpha,beta-ketoalkyne, 4-phenyl-3-butyn-2-one, by rat liver preparations. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 30: 414-20. PMID 11901095 DOI: 10.1124/dmd.30.4.414  0.01
2002 Okamoto Y, Mitsuyama H, Jonosono M, Hirata K, Arimura K, Osame M, Nakagawa M. Autosomal dominant palatal myoclonus and spinal cord atrophy. Journal of the Neurological Sciences. 195: 71-6. PMID 11867077  0.01
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