检索结果 - Hiroshi Doi

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  1. 1
    Mother-to-child Transmission of Human T-cell Lymphotropic Virus Type 1

    Mother-to-child Transmission of Human T-cell Lymphotropic Virus Type 1 由 Hiroyuki Moriuchi, Hideaki Masuzaki, Hiroshi Doi, Shigeru Katamine

    出版 2013
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  2. 2
    Mutant Huntingtin reduces HSP70 expression through the sequestration of NF-Y transcription factor

    Mutant Huntingtin reduces HSP70 expression through the sequestration of NF-Y transcription factor 由 Tomoyuki Yamanaka, Haruko Miyazaki, Fumitaka Oyama, Masaru Kurosawa, Chika Washizu, Hiroshi Doi, Nobuyuki Nukina

    出版 2008
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  3. 3
    Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations

    Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations 由 Yoshihiro Kino, Chika Washizu, Elisa Aquilanti, Misako Okuno, Masaru Kurosawa, Mizuki Yamada, Hiroshi Doi, Nobuyuki Nukina

    出版 2010
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  4. 4
    Successful prediction of cardiovascular risk by new non-invasive vascular indexes using suprasystolic cuff oscillometric waveform analysis

    Successful prediction of cardiovascular risk by new non-invasive vascular indexes using suprasystolic cuff oscillometric waveform analysis 由 Rie Sasaki-Nakashima, Tabito Kino, Lin Chen, Hiroshi Doi, Shintaro Minegishi, Kaito Abe, Teruyasu Sugano, Masataka Taguri, Tomoaki Ishigami

    出版 2016
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  5. 5
    Structure of the gene for human transglutaminase 1.

    Structure of the gene for human transglutaminase 1. 由 K Yamanishi, Johji Inazawa, Foo Min Liew, K. Nonomura, Takeshi Ariyama, Hirokazu Yasuno, T. Abe, Hiroshi Doi, J Hirano, Shoji Fukushima

    出版 1992
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  6. 6
    RNA-binding Protein TLS Is a Major Nuclear Aggregate-interacting Protein in Huntingtin Exon 1 with Expanded Polyglutamine-expressing Cells

    RNA-binding Protein TLS Is a Major Nuclear Aggregate-interacting Protein in Huntingtin Exon 1 with Expanded Polyglutamine-expressing Cells 由 Hiroshi Doi, Kazumasa Okamura, Peter Bauer, Yoshiaki Furukawa, Hideaki Shimizu, Masaru Kurosawa, Yoko Machida, Haruko Miyazaki, Kenichi Mitsui, Yoshiyuki Kuroiwa, Nobuyuki Nukina

    出版 2008
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  7. 7
    The threshold of hypothyroidism after radiation therapy for head and neck cancer: a retrospective analysis of 116 cases

    The threshold of hypothyroidism after radiation therapy for head and neck cancer: a retrospective analysis of 116 cases 由 Masayuki Fujiwara, Norihiko Kamikonya, Soichi Odawara, Hitomi Suzuki, Y. Niwa, Yasuhiro Takada, Hiroshi Doi, Tomonori Terada, Nobuhiro Uwa, Kosuke Sagawa, Shozo Hirota

    出版 2015
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  8. 8
    Siponimod inhibits microglial inflammasome activation

    Siponimod inhibits microglial inflammasome activation 由 Hiroyasu Komiya, Hideyuki Takeuchi, Akihiro Ogasawara, Yuki Ogawa, S. Kubota, Shunta Hashiguchi, Keita Takahashi, Misako Kunii, Kenichi Tanaka, Mikiko Tada, Hiroshi Doi, Fumiaki Tanaka

    出版 2025
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  9. 9
    De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen α2 Chain Cause Porencephaly

    De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen α2 Chain Cause Porencephaly 由 Yuriko Yoneda, Kazuhiro Haginoya, Hiroshi Arai, Shigeo Yamaoka, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kenji Yokochi, Hitoshi Osaka, Mitsuhiro Kato, Naomichi Matsumoto, Hirotomo Saitsu

    出版 2011
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  10. 10
    FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosis

    FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosis 由 Yoshihiro Kino, Chika Washizu, Masaru Kurosawa, Mizuki Yamada, Haruko Miyazaki, Takumi Akagi, Tsutomu Hashikawa, Hiroshi Doi, Toru Takumi, Geoffrey G. Hicks, Nobutaka Hattori, Tomomi Shimogori, Nobuyuki Nukina

    出版 2015
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  11. 11
    Runx2 Represses Myocardin-Mediated Differentiation and Facilitates Osteogenic Conversion of Vascular Smooth Muscle Cells

    Runx2 Represses Myocardin-Mediated Differentiation and Facilitates Osteogenic Conversion of Vascular Smooth Muscle Cells 由 Toru Tanaka, Hiroko Sato, Hiroshi Doi, Carolina A. Yoshida, Takehisa Shimizu, Hiroki Matsui, Miki Yamazaki, Hideo Akiyama, Keiko Kawai‐Kowase, Tatsuya Iso, Toshihisa Komori, Masashi Arai, Masahiko Kurabayashi

    出版 2007
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  12. 12
    Clinical Outcome of Nonculprit Plaque Ruptures in Patients With Acute Coronary Syndrome in the PROSPECT Study

    Clinical Outcome of Nonculprit Plaque Ruptures in Patients With Acute Coronary Syndrome in the PROSPECT Study 由 Yong Xie, Gary S. Mintz, Junqing Yang, Hiroshi Doi, Andrés Íñiguez, George Dangas, Patrick W. Serruys, John McPherson, Bertil Wennerblom, Ke Xu, Giora Weisz, Gregg W. Stone, Akiko Maehara

    出版 2014
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  13. 13
    Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features

    Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features 由 Yuriko Yoneda, Hirotomo Saitsu, Mayumi Touyama, Yoshio Makita, Akie Miyamoto, Keisuke Hamada, Naohiro Kurotaki, Hiroaki Tomita, Kiyomi Nishiyama, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kazuhiro Ogata, Kenji Naritomi, Naomichi Matsumoto

    出版 2012
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  14. 14
    MTCL1 plays an essential role in maintaining Purkinje neuron axon initial segment

    MTCL1 plays an essential role in maintaining Purkinje neuron axon initial segment 由 Tomoko Satake, Kazunari Yamashita, Kenji Hayashi, Satoko Miyatake, Miwa Tamura‐Nakano, Hiroshi Doi, Yasuhide Furuta, Go Shioi, Eriko Miura, Yukari H. Takeo, Kunihiro Yoshida, Hiroyuki Yahikozawa, Naomichi Matsumoto, Michisuke Yuzaki, Atsushi Suzuki

    出版 2017
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  15. 15
    Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis

    Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis 由 Mikiko Tada, Hiroshi Doi, Shigeru Koyano, Shun Kubota, Ryoko Fukai, Shunta Hashiguchi, Noriko Hayashi, Yuko Kawamoto, Misako Kunii, Kenichi Tanaka, Keita Takahashi, Yuki Ogawa, Ryo Iwata, Shoji Yamanaka, Hideyuki Takeuchi, Fumiaki Tanaka

    出版 2017
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  16. 16
    Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy

    Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy 由 Hirotomo Saitsu, Hitoshi Osaka, Masayuki Sasaki, Jun‐ichi Takanashi, Keisuke Hamada, Akio Yamashita, Hidehiro Shibayama, Masaaki Shiina, Yukiko Kondo, Kiyomi Nishiyama, Yoshinori Tsurusaki, Noriko Miyake, Hiroshi Doi, Kazuhiro Ogata, Ken Inoue, Naomichi Matsumoto

    出版 2011
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  17. 17
    CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations

    CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations 由 Masashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, Ayami Ozaki, Yasushi Oya, H. Konishi, Akinori Nakamura, Ryu Abe, Hiroshi Takai, Ritsuko Hanajima, Hiroshi Doi, Fumiaki Tanaka, Hisayoshi Nakamura, Ikuya Nonaka, Zhaoxia Wang, Shinichiro Hayashi, S. Noguchi, Ichizo Nishino

    出版 2020
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  18. 18
    Impact of Post-Intervention Minimal Stent Area on 9-Month Follow-Up Patency of Paclitaxel-Eluting Stents

    Impact of Post-Intervention Minimal Stent Area on 9-Month Follow-Up Patency of Paclitaxel-Eluting Stents 由 Hiroshi Doi, Akiko Maehara, Gary S. Mintz, Alan S.L. Yu, Hong Wang, Lazar Mandinov, Jeffrey J. Popma, Stephen G. Ellis, Eberhard Grube, Keith D. Dawkins, Neil J. Weissman, Mark Turco, John A. Ormiston, Gregg W. Stone

    出版 2009
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  19. 19
    Mitochondrial Complex III Deficiency Caused by a Homozygous<i>UQCRC2</i>Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation

    Mitochondrial Complex III Deficiency Caused by a Homozygous<i>UQCRC2</i>Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation 由 Noriko Miyake, Shoji Yano, Chika Sakai, Hideyuki Hatakeyama, Yuichi Matsushima, Masaaki Shiina, Yoriko Watanabe, James Bartley, José E. Abdenur, Raymond Wang, Richard Chang, Yoshinori Tsurusaki, Hiroshi Doi, Mitsuko Nakashima, Hirotomo Saitsu, Kazuhiro Ogata, Yu-ichi Goto, Naomichi Matsumoto

    出版 2012
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  20. 20
    Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation

    Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation 由 Hiroshi Doi, Kunihiro Yoshida, Takao Yasuda, Mitsunori Fukuda, Y. Fukuda, Hiroshi Morita, Shu-ichi Ikeda, Rumiko Kato, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Haruya Sakai, Satoko Miyatake, Masaaki Shiina, Nobuyuki Nukina, Shigeru Koyano, Shoji Tsuji, Yoshiyuki Kuroiwa, Naomichi Matsumoto

    出版 2011
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