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Yoshihiro Kino, Ph.D. - Publications

Affiliations: 
Laboratory for Structural Neuropathology RIKEN Brain Science Institute, Wakō-shi, Saitama-ken, Japan 
Area:
polyglutamine disorders
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45 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 Satoh JI, Kino Y, Yanaizu M, Ishida T, Saito Y. Reactive astrocytes express Aggregatin () in the brains of Alzheimer's disease and Nasu-Hakola disease. Intractable & Rare Diseases Research. 9: 217-221. PMID 33139980 DOI: 10.5582/Irdr.2020.03080  0.384
2020 Yanaizu M, Washizu C, Nukina N, Satoh JI, Kino Y. CELF2 regulates the species-specific alternative splicing of TREM2. Scientific Reports. 10: 17995. PMID 33093587 DOI: 10.1038/s41598-020-75057-x  0.543
2020 Miyazaki H, Yamanaka T, Oyama F, Kino Y, Kurosawa M, Yamada-Kurosawa M, Yamano R, Shimogori T, Hattori N, Nukina N. FACS array-based cell purification yields a specific transcriptome of striatal medium spiny neurons in a murine Huntington disease model. The Journal of Biological Chemistry. PMID 32499373 DOI: 10.1074/Jbc.Ra120.012983  0.682
2019 Satoh JI, Kino Y, Yanaizu M, Ishida T, Saito Y. Microglia express TMEM119 in the brains of Nasu-Hakola disease. Intractable & Rare Diseases Research. 8: 260-265. PMID 31890453 DOI: 10.5582/Irdr.2019.01123  0.382
2019 Sone J, Mitsuhashi S, Fujita A, Mizuguchi T, Hamanaka K, Mori K, Koike H, Hashiguchi A, Takashima H, Sugiyama H, Kohno Y, Takiyama Y, Maeda K, Doi H, Koyano S, ... ... Kino Y, et al. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease. Nature Genetics. PMID 31332381 DOI: 10.1038/S41588-019-0459-Y  0.324
2018 Satoh JI, Kino Y, Yanaizu M, Ishida T, Saito Y. Microglia express gamma-interferon-inducible lysosomal thiol reductase in the brains of Alzheimer's disease and Nasu-Hakola disease. Intractable & Rare Diseases Research. 7: 251-257. PMID 30560017 DOI: 10.5582/Irdr.2018.01119  0.381
2018 Yanaizu M, Sakai K, Tosaki Y, Kino Y, Satoh JI. Small nuclear RNA-mediated modulation of splicing reveals a therapeutic strategy for a TREM2 mutation and its post-transcriptional regulation. Scientific Reports. 8: 6937. PMID 29720600 DOI: 10.1038/S41598-018-25204-2  0.391
2018 Satoh JI, Kino Y, Yanaizu M, Saito Y. Alzheimer's disease pathology in Nasu-Hakola disease brains. Intractable & Rare Diseases Research. 7: 32-36. PMID 29552443 DOI: 10.5582/Irdr.2017.01088  0.394
2017 Satoh JI, Kino Y, Yanaizu M, Tosaki Y, Sakai K, Ishida T, Saito Y. Microglia express ABI3 in the brains of Alzheimer's disease and Nasu-Hakola disease. Intractable & Rare Diseases Research. 6: 262-268. PMID 29259854 DOI: 10.5582/Irdr.2017.01073  0.372
2017 Satoh JI, Kino Y, Yanaizu M, Tosaki Y, Sakai K, Ishida T, Saito Y. Expression of GPR17, a regulator of oligodendrocyte differentiation and maturation, in Nasu-Hakola disease brains. Intractable & Rare Diseases Research. 6: 50-54. PMID 28357182 DOI: 10.5582/Irdr.2016.01097  0.34
2017 Satoh J, Tosaki Y, Sakai K, Yanaizu M, Kino Y. RNA sequencing data analysis identifies a difference in gene expression profile between microglia and astrocytes after lipopolysaccharide-induced neuroinflammation Clinical and Experimental Neuroimmunology. 8: 60-62. DOI: 10.1111/Cen3.12351  0.335
2017 Miyazaki H, Oyama F, Kino Y, Kurosawa M, Yamada-Kurosawa M, Yamanaka T, Shimogori T, Hattori N, Nukina N. Gene expression profiling of medium spiny neurons in Huntington’s disease model mouse Journal of the Neurological Sciences. 381: 583. DOI: 10.1016/J.Jns.2017.08.1643  0.649
2016 Satoh JI, Kino Y, Yanaizu M, Tosaki Y, Sakai K, Ishida T, Saito Y. Expression of gp91phox and p22phox, catalytic subunits of NADPH oxidase, on microglia in Nasu-Hakola disease brains. Intractable & Rare Diseases Research. 5: 275-279. PMID 27904823 DOI: 10.5582/Irdr.2016.01086  0.347
2016 Satoh JI, Yanaizu M, Tosaki Y, Sakai K, Kino Y. Targeted sequencing approach to identify genetic mutations in Nasu-Hakola disease. Intractable & Rare Diseases Research. 5: 269-274. PMID 27904822 DOI: 10.5582/Irdr.2016.01064  0.302
2016 Kino Y, Washizu C, Kurosawa M, Yamada M, Doi H, Takumi T, Adachi H, Katsuno M, Sobue G, Hicks GG, Hattori N, Shimogori T, Nukina N. FUS/TLS acts as an aggregation-dependent modifier of polyglutamine disease model mice. Scientific Reports. 6: 35236. PMID 27739513 DOI: 10.1038/Srep35236  0.607
2016 Freyermuth F, Rau F, Kokunai Y, Linke T, Sellier C, Nakamori M, Kino Y, Arandel L, Jollet A, Thibault C, Philipps M, Vicaire S, Jost B, Udd B, Day JW, et al. Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy. Nature Communications. 7: 11067. PMID 27063795 DOI: 10.1038/Ncomms11067  0.523
2015 Satoh JI, Kino Y, Asahina N, Takitani M, Miyoshi J, Ishida T, Saito Y. TMEM119 marks a subset of microglia in the human brain. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 26250788 DOI: 10.1111/Neup.12235  0.32
2015 Kitano S, Kino Y, Yamamoto Y, Takitani M, Miyoshi J, Ishida T, Saito Y, Arima K, Satoh J. Bioinformatics Data Mining Approach Suggests Coexpression of AGTPBP1 with an ALS-linked Gene C9orf72. Journal of Central Nervous System Disease. 7: 15-26. PMID 26106267 DOI: 10.4137/JCNSD.S24317  0.315
2015 Kino Y, Washizu C, Kurosawa M, Yamada M, Miyazaki H, Akagi T, Hashikawa T, Doi H, Takumi T, Hicks GG, Hattori N, Shimogori T, Nukina N. FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosis. Acta Neuropathologica Communications. 3: 24. PMID 25907258 DOI: 10.1186/S40478-015-0202-6  0.634
2015 Kurosawa M, Matsumoto G, Kino Y, Okuno M, Kurosawa-Yamada M, Washizu C, Taniguchi H, Nakaso K, Yanagawa T, Warabi E, Shimogori T, Sakurai T, Hattori N, Nukina N. Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington's model mice. Human Molecular Genetics. 24: 1092-105. PMID 25305080 DOI: 10.1093/Hmg/Ddu522  0.649
2015 Kino Y, Washizu C, Kurosawa M, Oma Y, Hattori N, Ishiura S, Nukina N. Nuclear localization of MBNL1: splicing-mediated autoregulation and repression of repeat-derived aberrant proteins. Human Molecular Genetics. 24: 740-56. PMID 25274774 DOI: 10.1093/Hmg/Ddu492  0.58
2014 Satoh J, Asahina N, Kitano S, Kino Y. A Comprehensive Profile of ChIP-Seq-Based PU.1/Spi1 Target Genes in Microglia. Gene Regulation and Systems Biology. 8: 127-39. PMID 25574134 DOI: 10.4137/Grsb.S19711  0.39
2014 Satoh J, Yamamoto Y, Asahina N, Kitano S, Kino Y. RNA-Seq data mining: downregulation of NeuroD6 serves as a possible biomarker for alzheimer's disease brains. Disease Markers. 2014: 123165. PMID 25548427 DOI: 10.1155/2014/123165  0.33
2014 Satoh J, Kino Y, Yamamoto Y, Kawana N, Ishida T, Saito Y, Arima K. PLD3 is accumulated on neuritic plaques in Alzheimer's disease brains. Alzheimer's Research & Therapy. 6: 70. PMID 25478031 DOI: 10.1186/S13195-014-0070-5  0.361
2014 Miyazaki H, Oyama F, Inoue R, Aosaki T, Abe T, Kiyonari H, Kino Y, Kurosawa M, Shimizu J, Ogiwara I, Yamakawa K, Koshimizu Y, Fujiyama F, Kaneko T, Shimizu H, et al. Singular localization of sodium channel β4 subunit in unmyelinated fibres and its role in the striatum. Nature Communications. 5: 5525. PMID 25413837 DOI: 10.1038/Ncomms6525  0.582
2014 Satoh J, Motohashi N, Kino Y, Ishida T, Yagishita S, Jinnai K, Arai N, Nakamagoe K, Tamaoka A, Saito Y, Arima K. LC3, an autophagosome marker, is expressed on oligodendrocytes in Nasu-Hakola disease brains. Orphanet Journal of Rare Diseases. 9: 68. PMID 24886140 DOI: 10.1186/1750-1172-9-68  0.352
2014 Satoh J, Kino Y, Kawana N, Yamamoto Y, Ishida T, Saito Y, Arima K. TMEM106B expression is reduced in Alzheimer's disease brains. Alzheimer's Research & Therapy. 6: 17. PMID 24684749 DOI: 10.1186/Alzrt247  0.381
2014 Asada A, Yamazaki R, Kino Y, Saito T, Kimura T, Miyake M, Hasegawa M, Nukina N, Hisanaga S. Cyclin-dependent kinase 5 phosphorylates and induces the degradation of ataxin-2. Neuroscience Letters. 563: 112-7. PMID 24486837 DOI: 10.1016/J.Neulet.2014.01.046  0.522
2014 Maheshwari M, Bhutani S, Das A, Mukherjee R, Sharma A, Kino Y, Nukina N, Jana NR. Dexamethasone induces heat shock response and slows down disease progression in mouse and fly models of Huntington's disease. Human Molecular Genetics. 23: 2737-51. PMID 24381308 DOI: 10.1093/Hmg/Ddt667  0.674
2011 Koebis M, Ohsawa N, Kino Y, Sasagawa N, Nishino I, Ishiura S. Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. 16: 961-72. PMID 21794030 DOI: 10.1111/J.1365-2443.2011.01542.X  0.379
2011 Kino Y, Washizu C, Aquilanti E, Okuno M, Kurosawa M, Yamada M, Doi H, Nukina N. Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations. Nucleic Acids Research. 39: 2781-98. PMID 21109527 DOI: 10.1093/Nar/Gkq1162  0.548
2010 Bauer PO, Goswami A, Wong HK, Okuno M, Kurosawa M, Yamada M, Miyazaki H, Matsumoto G, Kino Y, Nagai Y, Nukina N. Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein. Nature Biotechnology. 28: 256-63. PMID 20190739 DOI: 10.1038/Nbt.1608  0.703
2009 Doumanis J, Wada K, Kino Y, Moore AW, Nukina N. RNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation. Plos One. 4: e7275. PMID 19789644 DOI: 10.1371/Journal.Pone.0007275  0.567
2009 Kino Y, Washizu C, Oma Y, Onishi H, Nezu Y, Sasagawa N, Nukina N, Ishiura S. MBNL and CELF proteins regulate alternative splicing of the skeletal muscle chloride channel CLCN1. Nucleic Acids Research. 37: 6477-90. PMID 19720736 DOI: 10.1093/Nar/Gkp681  0.557
2009 Bauer PO, Wong HK, Oyama F, Goswami A, Okuno M, Kino Y, Miyazaki H, Nukina N. Inhibition of Rho kinases enhances the degradation of mutant huntingtin. The Journal of Biological Chemistry. 284: 13153-64. PMID 19278999 DOI: 10.1074/Jbc.M809229200  0.63
2009 Sasagawa N, Ohno E, Kino Y, Watanabe Y, Ishiura S. Identification of Caenorhabditis elegans K02H8.1 (CeMBL), a functional ortholog of mammalian MBNL proteins. Journal of Neuroscience Research. 87: 1090-7. PMID 19021294 DOI: 10.1002/Jnr.21942  0.368
2008 Onishi H, Kino Y, Morita T, Futai E, Sasagawa N, Ishiura S. MBNL1 associates with YB-1 in cytoplasmic stress granules. Journal of Neuroscience Research. 86: 1994-2002. PMID 18335541 DOI: 10.1002/Jnr.21655  0.32
2008 Toriumi K, Oma Y, Kino Y, Futai E, Sasagawa N, Ishiura S. Expression of polyalanine stretches induces mitochondrial dysfunction. Journal of Neuroscience Research. 86: 1529-37. PMID 18214990 DOI: 10.1002/Jnr.21619  0.367
2008 Mori D, Sasagawa N, Kino Y, Ishiura S. Quantitative analysis of CUG-BP1 binding to RNA repeats. Journal of Biochemistry. 143: 377-83. PMID 18039683 DOI: 10.1093/Jb/Mvm230  0.337
2007 Oma Y, Kino Y, Toriumi K, Sasagawa N, Ishiura S. Interactions between homopolymeric amino acids (HPAAs). Protein Science : a Publication of the Protein Society. 16: 2195-204. PMID 17766374 DOI: 10.1110/Ps.072955307  0.335
2007 Nezu Y, Kino Y, Sasagawa N, Nishino I, Ishiura S. Expression of MBNL and CELF mRNA transcripts in muscles with myotonic dystrophy. Neuromuscular Disorders : Nmd. 17: 306-12. PMID 17331722 DOI: 10.1016/J.Nmd.2007.01.002  0.38
2005 Oma Y, Kino Y, Sasagawa N, Ishiura S. Comparative analysis of the cytotoxicity of homopolymeric amino acids. Biochimica Et Biophysica Acta. 1748: 174-9. PMID 15769594 DOI: 10.1016/J.Bbapap.2004.12.017  0.315
2004 Oma Y, Kino Y, Sasagawa N, Ishiura S. Intracellular localization of homopolymeric amino acid-containing proteins expressed in mammalian cells. The Journal of Biological Chemistry. 279: 21217-22. PMID 14993218 DOI: 10.1074/Jbc.M309887200  0.385
2004 Kino Y, Mori D, Oma Y, Takeshita Y, Sasagawa N, Ishiura S. Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats. Human Molecular Genetics. 13: 495-507. PMID 14722159 DOI: 10.1093/Hmg/Ddh056  0.355
2003 Sasagawa N, Kino Y, Takeshita Y, Oma Y, Ishiura S. Overexpression of human myotonic dystrophy protein kinase in Schizosaccharomyces pombe induces an abnormal polarized and swollen cell morphology. Journal of Biochemistry. 134: 537-42. PMID 14607980 DOI: 10.1093/Jb/Mvg171  0.332
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