Papers - ATARASHI Ryuichiro
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Persistent prion infection disturbs the function of Oct-1, resultingin the down-regulation of murine interferon regulatory factor-3. Reviewed
Homma T, Ishibashi D, Nakagaki T, Fuse T, Sano K, Satoh K, Atarashi R,Nishida N.
Scientific Reports 4 6006 2014.8
Language：English Publishing type：Research paper (scientific journal)
DOI： 10.1038/srep06006.
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Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene. Reviewed
Qina T, Sanjo N*, Hizume M, Higuma M, Tomita M, Atarashi R, Satoh K, Nozaki I, Hamaguchi T, Nakamura Y, Kobayashi A, Kitamoto T, Murayama S, Murai H, Yamada M, Mizusawa H
BMJ Open 4 ( 5 ) e004968 2014.5
Language：English Publishing type：Research paper (scientific journal)
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Increased expression of p62/SQSTM1 in prion diseases and its associationwith pathogenic prion protein. Reviewed
Homma T, Ishibashi D*, Nakagaki T, Satoh K, Sano K, Atarashi R, Nishida N
Scientific reports 4 4504 2014.3
Language：English Publishing type：Research paper (scientific journal)
DOI： 10.1038/srep04504.
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Age-dependent impairment of eyeblink conditioning in prion protein-deficient mice. Reviewed
Kishimoto Y, Hirono M, Atarashi R, Sakaguchi S, Yoshioka T, Katamine S, Kirino Y
PLoS One 8 ( 4 ) e60627 2013.4
Language：English Publishing type：Research paper (scientific journal)
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Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay. Reviewed International coauthorship
Sano K, Satoh K, Atarashi R, Takashima H, Iwasaki Y, Yoshida M, Sanjo N, Murai H, Mizusawa H, Schmitz M, Zerr I, Kim YS, Nishida N
PLoS One 8 ( 1 ) e54915 2013.1
Language：English Publishing type：Research paper (scientific journal)
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Cutting Edge: Brucella abortus exploits a cellular prion protein on intestinal M cells as an invasive receptor. Reviewed
Nakato G, Hase K, Suzuki M, Kimura M, Ato M, Hanazato M, Tobiume M, Horiuchi M, Atarashi R, Nishida N, Watarai M, Imaoka K, Ohno H
Journal of immunology (Baltimore, Md. : 1950) 189 ( 4 ) 1540 - 1544 2012.8
Language：English Publishing type：Research paper (scientific journal)
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Protective role of interferon regulatory factor 3-mediated signaling against prion infection. Reviewed
Ishibashi D, Atarashi R, Fuse T, Nakagaki T, Yamaguchi N, Satoh K, Honda K, Nishida N
Journal of Virology 86 ( 9 ) 4947 - 4955 2012.2
Language：English Publishing type：Research paper (scientific journal)
DOI： 10.1128/JVI.06326-11
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Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement study. Reviewed
Fujita K*, Harada M, Sasaki M, Yuasa T, Sakai K, Hamaguchi T, Sanjo N,Shiga Y, Satoh K, Atarashi R, Shirabe S, Nagata K, Maeda T, Murayama S,Izumi Y, Kaji R, Yamada M, Mizusawa H
BMJ Open 2 ( 1 ) e000649 2012.1
Language：English Publishing type：Research paper (scientific journal)
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High sensitivity of an ELISA kit for detection of the gamma-isoform of 14-3-3 proteins: usefulness in laboratory diagnosis ofhuman prion disease. Reviewed
Matsui Y, Satoh K*, Miyazaki T, Shirabe S, Atarashi R, Mutsukura K, Satoh A, Kataoka Y, Nishida N
BMC Neurology 11 120 2011.10
Language：English Publishing type：Research paper (scientific journal)
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Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors. Reviewed International coauthorship
Kim JI, Cali I, Surewicz K, Kong Q, Raymond GJ, Atarashi R, Race B, Qing L, Gambetti P, Caughey B, Surewicz WK
The Journal of Biological Chemistry 285 ( 19 ) 14083 - 14087 2010.5
Language：English Publishing type：Research paper (scientific journal)
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Distinct structures of scrapie prion protein (PrPSc)-seeded versus spontaneous recombinant prion protein fibrils revealed by hydrogen/deuterium exchange. Reviewed International coauthorship
Smirnovas V, Kim JI, Lu X, Atarashi R, Caughey B, Surewicz WK
The Journal of Biological Chemistry 284 ( 36 ) 24233 - 24234 2009.9
Language：English Publishing type：Research paper (scientific journal)
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Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking. Reviewed International coauthorship
Atarashi R, Wilham JM, Christensen L, Hughson AG, Moore RA, Johnson LM, Onwubiko HA, Priola SA, Caughey B
Nature methods 5 ( 3 ) 211 - 212 2008.3
Language：English Publishing type：Research paper (scientific journal)
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Biological and biochemical characteristics of prion strains conserved in persistently infected cell cultures. Reviewed
Arima K, Nishida N, Sakaguchi S, Shigematsu K, Atarashi R, Yamaguchi N, Yoshikawa D, Yoon J, Watanabe K, Kobayashi N, Mouillet-Richard S, Lehmann S, Katamine S
Journal of virology 79 ( 11 ) 7104 - 7112 2005.6
Language：English Publishing type：Research paper (scientific journal)
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Abnormal activation of glial cells in the brains of prion protein-deficient mice ectopically expressing prion protein-like protein, PrPLP/Dpl. Reviewed
Atarashi R, Sakaguchi S, Shigematsu K, Arima K, Okimura N, Yamaguchi N, Li A, Kopacek J, Katamine S
Molecular Medicine 7 ( 12 ) 803 - 809 2001.12
Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)
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Early appearance but lagged accumulation of detergent-insoluble prion protein in the brains of mice inoculated with a mouse-adapted Creutzfeldt-Jakob disease agent. Reviewed
Nakaoke R, Sakaguchi S, Atarashi R, Nishida N, Arima K, Shigematsu K, Katamine S
Cellular and Molecular Neurobiology 20 ( 6 ) 717 - 730 2000.12
Language：English Publishing type：Research paper (scientific journal)
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Physiological expression of the gene for PrP-like protein, PrPLP/Dpl, by brain endothelial cells and its ectopic expression in neurons PrP-deficient mice ataxic due to Purkinje cell degeneration. Reviewed
Li A, Sakaguchi S, Shigematsu K, Atarashi R, Roy BC, Nakaoke R, Arima K, Okimura N, Kopacek J, Katamine S
The American Journal of Pathology 157 ( 5 ) 1447 - 1452 2000.11
Language：English Publishing type：Research paper (scientific journal)
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Identification of a novel gene encoding a PrP-like protein expressed as chimeric transcripts fused to PrP exon 1/2 in ataxic mouse line with a disrupted PrP gene. Reviewed
Li A, Sakaguchi S, Atarashi R, Roy BC, Nakaoke R, Arima K, Okimura N, Kopacek J, Shigematsu K
Cellular and Molecular Neurobiology 20 ( 5 ) 553 - 567 2000.10
Language：English Publishing type：Research paper (scientific journal)
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Upregulation of the genes encoding lysosomal hydrolases, a perforin-like protein, and peroxidases in the brains of mice affected with an experimental prion disease. Reviewed International coauthorship
Kopacek J, Sakaguchi S, Shigematsu K, Nishida N, Atarashi R, Nakaoke R, Moriuchi R, Niwa M, Katamine S
Journal of Virology 74 ( 1 ) 411 - 417 2000.1
Language：English Publishing type：Research paper (scientific journal)
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A mouse prion protein transgene rescues mice deficient for the prion protein gene from purkinje cell degeneration and demyelination. Reviewed International coauthorship
Nishida N, Tremblay P, Sugimoto T, Shigematsu K, Shirabe S, Petromilli C, Erpel SP., Nakaoke R, Atarashi R, Houtani T, Torchia M, Sakaguchi S, DeArmond SJ, Prusiner SB, Katamine S
Laboratory Investigation 79 ( 6 ) 689 - 697 1999.6
Language：English Publishing type：Research paper (scientific journal)
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Prion protein is necessary for latent learning and long-term memory retention. Reviewed
Nishida N, Katamine S*, Shigematsu K, Nakatani A, Sakamoto N, Hasegawa S, Nakaoke R, Atarashi R, Kataoka Y, Miyamoto T
Cellular and Molecular Neurobiology 17 ( 5 ) 537 - 545 1997.10
Language：English Publishing type：Research paper (scientific journal)