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Atsushi Kobayashi - Publications

Affiliations: 
Tohoku University, Sendai-shi, Miyagi-ken, Japan 
Area:
glycosidase
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31 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
2020 Erdemsurakh O, Purevdorj B, Ochirbat K, Adilbish A, Vanaabaatar B, Aoshima K, Kobayashi A, Kimura T. Pathological and Immunohistochemical Analyses of Naturally Occurring Equine Glanders Using an Anti-BpaB Antibody. Veterinary Pathology. 300985820953422. PMID 32885748 DOI: 10.1177/0300985820953422  0.304
2020 Kaneko MK, Sano M, Takei J, Asano T, Sayama Y, Hosono H, Kobayashi A, Konnai S, Kato Y. Development and Characterization of Anti-Sheep Podoplanin Monoclonal Antibodies PMab-253 and PMab-260. Monoclonal Antibodies in Immunodiagnosis and Immunotherapy. 39: 144-155. PMID 32679010 DOI: 10.1089/Mab.2020.0018  0.304
2020 Hamaguchi T, Sakai K, Kobayashi A, Kitamoto T, Ae R, Nakamura Y, Sanjo N, Arai K, Koide M, Katada F, Harada M, Murai H, Murayama S, Tsukamoto T, Mizusawa H, et al. Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases. Emerging Infectious Diseases. 26: 1140-1146. PMID 32442393 DOI: 10.3201/Eid2606.181969  0.31
2020 Kobayashi A. [Update on Iatrogenic Creutzfeldt-Jakob Disease]. Brain and Nerve. 72: 437-443. PMID 32284468 DOI: 10.11477/Mf.1416201542  0.313
2019 Iwasaki Y, Hiraga K, Ito S, Ando T, Akagi A, Riku Y, Mimuro M, Miyahara H, Kobayashi A, Kitamoto T, Yoshida M. Autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease with spongiform changes of the cerebral cortex. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 31515858 DOI: 10.1111/Neup.12595  0.326
2019 Iwasaki Y, Kato H, Ando T, Akagi A, Mimuro M, Miyahara H, Kobayashi A, Kitamoto T, Yoshida M. Autopsied case of sporadic Creutzfeldt-Jakob disease classified as MM1+2C-type. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 31062411 DOI: 10.1111/Neup.12557  0.326
2019 Kobayashi A, Iwasaki Y, Takao M, Saito Y, Iwaki T, Qi Z, Torimoto R, Shimazaki T, Munesue Y, Isoda N, Sawa H, Aoshima K, Kimura T, Kondo H, Mohri S, et al. A novel combination of prion strain co-occurrence in patients with sporadic Creutzfeldt-Jakob disease. The American Journal of Pathology. PMID 30926338 DOI: 10.1016/J.Ajpath.2019.02.012  0.367
2018 Furukawa F, Sanjo N, Kobayashi A, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T. Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene. Prion. 12: 315-319. PMID 30394185 DOI: 10.1080/19336896.2018.1541689  0.303
2018 Ishizawa K, Mitsufuji T, Shioda K, Kobayashi A, Komori T, Nakazato Y, Kitamoto T, Araki N, Yamamoto T, Sasaki A. An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid. Brain and Behavior. e1117. PMID 30240140 DOI: 10.1002/Brb3.1117  0.302
2018 Kobayashi A, Matsuura Y, Takeuchi A, Yamada M, Miyoshi I, Mohri S, Kitamoto T. A domain responsible for spontaneous conversion of bank vole prion protein. Brain Pathology (Zurich, Switzerland). PMID 30051525 DOI: 10.1111/Bpa.12638  0.327
2018 Ito Y, Sanjo N, Hizume M, Kobayashi A, Ohgami T, Satoh K, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T. Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene. Biochemical and Biophysical Research Communications. PMID 29382530 DOI: 10.1016/J.Bbrc.2018.01.119  0.344
2018 Munesue Y, Shimazaki T, Qi Z, Isoda N, Sawa H, Aoshima K, Kimura T, Mohri S, Kitamoto T, Kobayashi A. Development of a quick bioassay for the evaluation of transmission properties of acquired prion diseases. Neuroscience Letters. PMID 29329906 DOI: 10.1016/J.Neulet.2018.01.014  0.346
2017 Iwasaki Y, Saito Y, Aiba I, Kobayashi A, Mimuro M, Kitamoto T, Yoshida M. An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques. Neuropathology. 37: 241-248. PMID 28568896 DOI: 10.1111/Neup.12350  0.313
2016 Takeuchi A, Kobayashi A, Parchi P, Yamada M, Morita M, Uno S, Kitamoto T. Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 26878132 DOI: 10.1038/Labinvest.2016.27  0.335
2015 Kobayashi A, Parchi P, Yamada M, Mohri S, Kitamoto T. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 26669818 DOI: 10.1111/Neup.12270  0.372
2015 Kobayashi A, Teruya K, Matsuura Y, Shirai T, Nakamura Y, Yamada M, Mizusawa H, Mohri S, Kitamoto T. The influence of PRNP polymorphisms on human prion disease susceptibility: an update. Acta Neuropathologica. PMID 26022925 DOI: 10.1007/S00401-015-1447-7  0.321
2015 Kobayashi A, Matsuura Y, Iwaki T, Iwasaki Y, Yoshida M, Takahashi H, Murayama S, Takao M, Kato S, Yamada M, Mohri S, Kitamoto T. Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties. Brain Pathology (Zurich, Switzerland). PMID 25851836 DOI: 10.1111/Bpa.12264  0.306
2015 Kobayashi A, Parchi P, Yamada M, Brown P, Saverioni D, Matsuura Y, Takeuchi A, Mohri S, Kitamoto T. Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology? Journal of Virology. 89: 3939-46. PMID 25609817 DOI: 10.1128/Jvi.03183-14  0.33
2014 Araki K, Nakano Y, Kobayashi A, Matsudaira T, Sugiura A, Takao M, Kitamoto T, Murayama S, Obi T. Extensive cortical spongiform changes with cerebellar small amyloid plaques: the clinicopathological case of MV2K+C subtype in Creutzfeldt-Jakob disease. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 34: 541-6. PMID 24984899 DOI: 10.1111/Neup.12133  0.328
2014 Kobayashi A, Matsuura Y, Mohri S, Kitamoto T. Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems. Acta Neuropathologica Communications. 2: 32. PMID 24685293 DOI: 10.1186/2051-5960-2-32  0.318
2013 Kobayashi A, Iwasaki Y, Otsuka H, Yamada M, Yoshida M, Matsuura Y, Mohri S, Kitamoto T. Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein. Acta Neuropathologica Communications. 1: 74. PMID 24252157 DOI: 10.1186/2051-5960-1-74  0.358
2013 Takeuchi A, Kobayashi A, Ironside JW, Mohri S, Kitamoto T. Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes. The Journal of Biological Chemistry. 288: 21659-66. PMID 23792955 DOI: 10.1074/Jbc.M113.470328  0.329
2012 Donaldson DS, Kobayashi A, Ohno H, Yagita H, Williams IR, Mabbott NA. M cell-depletion blocks oral prion disease pathogenesis Mucosal Immunology. 5: 216-225. PMID 22294048 DOI: 10.1038/Mi.2011.68  0.306
2011 Kobayashi A, Mizukoshi K, Iwasaki Y, Miyata H, Yoshida Y, Kitamoto T. Co-occurrence of types 1 and 2 PrP(res) in sporadic Creutzfeldt-Jakob disease MM1. The American Journal of Pathology. 178: 1309-15. PMID 21356381 DOI: 10.1016/J.Ajpath.2010.11.069  0.35
2010 Kobayashi A, Sakuma N, Matsuura Y, Mohri S, Aguzzi A, Kitamoto T. Experimental verification of a traceback phenomenon in prion infection. Journal of Virology. 84: 3230-8. PMID 20089646 DOI: 10.1128/Jvi.02387-09  0.332
2009 Kobayashi A, Asano M, Mohri S, Kitamoto T. A traceback phenomenon can reveal the origin of prion infection. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 29: 619-24. PMID 19659941 DOI: 10.1111/J.1440-1789.2008.00973.X  0.343
2009 Hiraga C, Kobayashi A, Kitamoto T. The number of octapeptide repeat affects the expression and conversion of prion protein. Biochemical and Biophysical Research Communications. 382: 715-9. PMID 19318088 DOI: 10.1016/J.Bbrc.2009.03.093  0.324
2009 Hizume M, Kobayashi A, Teruya K, Ohashi H, Ironside JW, Mohri S, Kitamoto T. Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection. The Journal of Biological Chemistry. 284: 3603-9. PMID 19074151 DOI: 10.1074/Jbc.M809254200  0.301
2008 Kobayashi A, Arima K, Ogawa M, Murata M, Fukuda T, Kitamoto T. Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients. Acta Neuropathologica. 116: 561-6. PMID 18751990 DOI: 10.1007/S00401-008-0425-8  0.325
2007 Kobayashi A, Asano M, Mohri S, Kitamoto T. Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain. The Journal of Biological Chemistry. 282: 30022-8. PMID 17709374 DOI: 10.1074/Jbc.M704597200  0.355
2005 Kobayashi A, Satoh S, Ironside JW, Mohri S, Kitamoto T. Type 1 and type 2 human PrPSc have different aggregation sizes in methionine homozygotes with sporadic, iatrogenic and variant Creutzfeldt-Jakob disease. The Journal of General Virology. 86: 237-40. PMID 15604452 DOI: 10.1099/Vir.0.80389-0  0.315
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