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17 results for Furuno,+Masaaki

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ArticlesPeer ReviewedFull Text
C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution
Author / Creator:Kouno, Tsukasa ; Moody, Jonathan ; Kwon, Andrew Tae-Jun ; Shibayama, Youtaro ; Kato, Sachi ; Huang, Yi ; Böttcher, Michael ; Motakis, Efthymios ; Mendez, Mickaël ; Severin, Jessica ; Luginbühl, Joachim ; Abugessaisa, Imad ; Hasegawa, Akira ; Takizawa, Satoshi ; Arakawa, Takahiro ; Furuno, Masaaki ; Ramalingam, Naveen ; West, Jay ; Suzuki, Harukazu ; Kasukawa, Takeya ; Lassmann, Timo ; Hon, Chung-Chau ; Arner, Erik ; Carninci, Piero ; Plessy, Charles ; Shin, Jay W.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2019-01, Vol.10 (1), p.360-360, Article 360
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xcore: an R package for inference of gene expression regulators
Author / Creator:Migdał, Maciej ; Arakawa, Takahiro ; Takizawa, Satoshi ; Furuno, Masaaki ; Suzuki, Harukazu ; Arner, Erik ; Winata, Cecilia Lanny ; Kaczkowski, Bogumił
Publisher:England: BioMed Central Ltd
Journal title:BMC bioinformatics, 2023-01, Vol.24 (1), p.14-14, Article 14
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Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa
Author / Creator:Katagiri, Satoshi ; Akahori, Masakazu ; Sergeev, Yuri ; Yoshitake, Kazutoshi ; Ikeo, Kazuho ; Furuno, Masaaki ; Hayashi, Takaaki ; Kondo, Mineo ; Ueno, Shinji ; Tsunoda, Kazushige ; Shinoda, Kei ; Kuniyoshi, Kazuki ; Tsurusaki, Yohinori ; Matsumoto, Naomichi ; Tsuneoka, Hiroshi ; Iwata, Takeshi
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-09, Vol.9 (9), p.e108721-e108721
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CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability
Author / Creator:Minegishi, Yuriko ; Sheng, XunLun ; Yoshitake, Kazutoshi ; Sergeev, Yuri ; Iejima, Daisuke ; Shibagaki, Yoshio ; Monma, Norikazu ; Ikeo, Kazuho ; Furuno, Masaaki ; Zhuang, Wenjun ; Liu, Yani ; Rong, Weining ; Hattori, Seisuke ; Iwata, Takeshi
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2016-09, Vol.6 (1), p.33742-33742, Article 33742
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Clusters of Internally Primed Transcripts Reveal Novel Long Noncoding RNAs
Author / Creator:Furuno, Masaaki ; Pang, Ken C ; Ninomiya, Noriko ; Fukuda, Shiro ; Frith, Martin C ; Bult, Carol ; Kai, Chikatoshi ; Kawai, Jun ; Carninci, Piero ; Hayashizaki, Yoshihide ; Mattick, John S ; Suzuki, Harukazu
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2006-04, Vol.2 (4), p.e37-e37
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RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa
Author / Creator:Tsuneoka, Hiroshi ; Iwata, Takeshi ; Okada, Tetsuji ; Furuno, Masaaki ; Yoshitake, Kazutoshi ; Nishino, Jo ; Itabashi, Takeshi ; Akahori, Masakazu ; Hayashi, Takaaki ; Katagiri, Satoshi ; Ikeo, Kazuho
Publisher:Cairo, Egypt: Hindawi Limiteds
Journal title:Journal of Ophthalmology, 2014-01, Vol.2014 (1), p.205-214
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A framework for identification of on- and off-target transcriptional responses to drug treatment
Author / Creator:Huang, Yi ; Furuno, Masaaki ; Arakawa, Takahiro ; Takizawa, Satoshi ; de Hoon, Michiel ; Suzuki, Harukazu ; Arner, Erik
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2019-11, Vol.9 (1), p.17603-9, Article 17603
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Discovery of widespread transcription initiation at microsatellites predictable by sequence-based deep neural network
Author / Creator:Grapotte, Mathys ; Saraswat, Manu ; Bessière, Chloé ; Menichelli, Christophe ; Ramilowski, Jordan A. ; Severin, Jessica ; Hayashizaki, Yoshihide ; Itoh, Masayoshi ; Tagami, Michihira ; Murata, Mitsuyoshi ; Kojima-Ishiyama, Miki ; Noma, Shohei ; Noguchi, Shuhei ; Kasukawa, Takeya ; Hasegawa, Akira ; Suzuki, Harukazu ; Nishiyori-Sueki, Hiromi ; Frith, Martin C. ; Chatelain, Clément ; Carninci, Piero ; de Hoon, Michiel J. L. ; Wasserman, Wyeth W. ; Bréhélin, Laurent ; Lecellier, Charles-Henri
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2021-06, Vol.12 (1), p.3297-3297, Article 3297
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Author Correction: Discovery of widespread transcription initiation at microsatellites predictable by sequence-based deep neural network
Author / Creator:Grapotte, Mathys ; Saraswat, Manu ; Bessière, Chloé ; Menichelli, Christophe ; Ramilowski, Jordan A. ; Severin, Jessica ; Hayashizaki, Yoshihide ; Itoh, Masayoshi ; Tagami, Michihira ; Murata, Mitsuyoshi ; Kojima-Ishiyama, Miki ; Noma, Shohei ; Noguchi, Shuhei ; Kasukawa, Takeya ; Hasegawa, Akira ; Suzuki, Harukazu ; Nishiyori-Sueki, Hiromi ; Frith, Martin C. ; Chatelain, Clément ; Carninci, Piero ; de Hoon, Michiel J. L. ; Wasserman, Wyeth W. ; Bréhélin, Laurent ; Lecellier, Charles-Henri
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2022-03, Vol.13 (1), p.1200-1200, Article 1200
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Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutation
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Yoshitake, Kazutoshi ; Abe, Kosuke ; Ikeo, Kazuho ; Furuno, Masaaki ; Tsunoda, Kazushige ; Kusaka, Shunji ; Shimomura, Yoshikazu ; Iwata, Takeshi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Documenta ophthalmologica, 2014-06, Vol.128 (3), p.219-228
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Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs
Author / Creator:Maeda, Norihiro ; Kasukawa, Takeya ; Oyama, Rieko ; Gough, Julian ; Frith, Martin ; Engström, Pär G ; Lenhard, Boris ; Aturaliya, Rajith N ; Batalov, Serge ; Beisel, Kirk W ; Bult, Carol J ; Fletcher, Colin F ; Forrest, Alistair R. R ; Furuno, Masaaki ; Hill, David ; Itoh, Masayoshi ; Kanamori-Katayama, Mutsumi ; Katayama, Shintaro ; Katoh, Masaru ; Kawashima, Tsugumi ; Quackenbush, John ; Ravasi, Timothy ; Ring, Brian Z ; Shibata, Kazuhiro ; Sugiura, Koji ; Takenaka, Yoichi ; Teasdale, Rohan D ; Wells, Christine A ; Zhu, Yunxia ; Kai, Chikatoshi ; Kawai, Jun ; Hume, David A ; Carninci, Piero ; Hayashizaki, Yoshihide
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2006-04, Vol.2 (4), p.e62-e62
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Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Yoshitake, Kazutoshi ; Ikeo, Kazuho ; Furuno, Masaaki ; Tsunoda, Kazushige ; Kusaka, Shunji ; Shimomura, Yoshikazu ; Iwata, Takeshi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Documenta ophthalmologica, 2015-08, Vol.131 (1), p.71-79
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Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy
Author / Creator:Kuniyoshi, Kazuki ; Ikeo, Kazuho ; Sakuramoto, Hiroyuki ; Furuno, Masaaki ; Yoshitake, Kazutoshi ; Hatsukawa, Yoshikazu ; Nakao, Akira ; Tsunoda, Kazushige ; Kusaka, Shunji ; Shimomura, Yoshikazu ; Iwata, Takeshi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Documenta ophthalmologica, 2015-02, Vol.130 (1), p.49-55
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RHO mutations
Author / Creator:Hayashi, Takaaki ; Tsuneoka, Hiroshi ; Akahori, Masakazu ; Yoshitake, Kazutoshi ; Ikeo, Kazuho ; Okada, Tetsuji ; Katagiri, Satoshi ; Nishino, Jo ; Furuno, Masaaki ; Itabashi, Takeshi ; Iwata, Takeshi
Publisher:Hindawi Limited
Journal title:Journal of ophthalmology, 2014-01, p.AA1
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Clusters of internally primed transcripts reveal novel long noncoding RNAs
Author / Creator:Masaaki Furuno ; Ken C Pang ; Noriko Ninomiya ; Shiro Fukuda ; Martin C Frith ; Carol Bult ; Chikatoshi Kai ; Jun Kawai ; Piero Carninci ; Yoshihide Hayashizaki ; John S Mattick ; Harukazu Suzuki
Publisher:Public Library of Science (PLoS)
Journal title:PLoS genetics, 2006-04, Vol.2 (4), p.e37
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Efficient Development of Platform Cell Lines Using CRISPR-Cas9 and Transcriptomics Analysis
Author / Creator:Kwon, Andrew Tae-Jun ; Mohri, Kohta ; Takizawa, Satoshi ; Arakawa, Takahiro ; Takahashi, Maiko ; Kaczkowski, Bogumil ; Furuno, Masaaki ; Suzuki, Harukazu ; Tagami, Shunsuke ; Mukai, Hidefumi ; Arner, Erik
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2020-09
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ArticlesFull Text
C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution
Author / Creator:Kouno, Tsukasa ; Moody, Jonathan ; Kwon, Andrew ; Shibayama, Youtaro ; Kato, Sachi ; Huang, Yi ; Michael B ttcher ; Motakis, Efthymios ; Micka l Mendez ; Severin, Jessica ; Joachim Luginb hl ; Abugessaisa, Imad ; Hasegawa, Akira ; Takizawa, Satoshi ; Arakawa, Takahiro ; Furuno, Masaaki ; Ramalingam, Naveen ; West, Jay ; Suzuki, Harukazu ; Takeya Kasukawa ; Lassmann, Timo ; Chung-Chau, Hon ; Arner, Erik ; Carninci, Piero ; Plessy, Charles ; Shin, Jay W
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2018-06
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C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution

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xcore: an R package for inference of gene expression regulators

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Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa

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CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability

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Clusters of Internally Primed Transcripts Reveal Novel Long Noncoding RNAs

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RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa

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A framework for identification of on- and off-target transcriptional responses to drug treatment

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Discovery of widespread transcription initiation at microsatellites predictable by sequence-based deep neural network

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Author Correction: Discovery of widespread transcription initiation at microsatellites predictable by sequence-based deep neural network

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Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutation

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Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs

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Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations

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Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy

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RHO mutations

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Clusters of internally primed transcripts reveal novel long noncoding RNAs

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Efficient Development of Platform Cell Lines Using CRISPR-Cas9 and Transcriptomics Analysis

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C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution

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