Hideo Matsuda

ORCID: 0000-0002-4701-3779
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About
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Research Areas
  • Genomics and Phylogenetic Studies
  • Bioinformatics and Genomic Networks
  • Gene expression and cancer classification
  • Machine Learning in Bioinformatics
  • RNA and protein synthesis mechanisms
  • Distributed and Parallel Computing Systems
  • Cell Image Analysis Techniques
  • Algorithms and Data Compression
  • Single-cell and spatial transcriptomics
  • Gene Regulatory Network Analysis
  • Microbial Metabolic Engineering and Bioproduction
  • RNA Research and Splicing
  • Genomics and Chromatin Dynamics
  • Scientific Computing and Data Management
  • Molecular Biology Techniques and Applications
  • RNA modifications and cancer
  • Cancer-related molecular mechanisms research
  • Parallel Computing and Optimization Techniques
  • Genetic diversity and population structure
  • Bacterial Genetics and Biotechnology
  • Silicon Carbide Semiconductor Technologies
  • Protein Structure and Dynamics
  • Genetics, Bioinformatics, and Biomedical Research
  • Computational Drug Discovery Methods
  • DNA and Biological Computing

Osaka University
2016-2025

Ube Frontier University
2014

The University of Tokyo
2002-2009

Osaka Health Science University
2002-2006

Toshiba (South Korea)
1998-2005

Polytechnic University
1999-2004

Toshiba (Japan)
2000-2003

Hachinohe National College of Technology
2003

Kobe University
1986-2002

Tokyo Polytechnic University
2002

Piero Carninci Takeya Kasukawa Shintaro Katayama Julian Gough Martin C. Frith and 95 more Norihiro Maeda Rieko Oyama Timothy Ravasi Boris Lenhard Christine A. Wells Rimantas Kodzius Koya Shimokawa Vladimir B. Bajić Steven E. Brenner Serge Batalov Alistair R. R. Forrest Mihaela Zavolan Melissa J. Davis Laurens Wilming Vassilis Aidinis Jonathan Allen Alberto Ambesi‐Impiombato Rolf Apweiler Rajith Aturaliya Timothy L. Bailey Mukul S. Bansal Laura L. Baxter Kirk W. Beisel Tom Bersano Hidemasa Bono Alistair M. Chalk Kuo Ping Chiu Vijayata Choudhary Alan Christoffels D. R. Clutterbuck Mark L. Crowe Emiliano Dalla Brian P. Dalrymple Bernard de Bono Giusy Della Gatta Diego di Bernardo Thomas A. Down Pär G. Engström Michela Fagiolini Geoffrey J. Faulkner Colin Fletcher Tatsuya Fukushima Masaaki Furuno Sugiko Futaki Manuela Gariboldi Patrik Georgii‐Hemming T Gingeras Takashi Gojobori Richard E. Green Stefano Gustincich Matthias Harbers Yoshitaka Hayashi Takao K. Hensch Nobutaka Hirokawa David E. Hill Łukasz Huminiecki Michele Iacono Kazuho Ikeo Atsushi Iwama Takanori Ishikawa Lars Martin Jakt Alexander Kanapin Masaru Katoh Yuka Imamura Kawasawa Janet Kelso Hiroshi Kitamura Hiroaki Kitano George Kollias Sivanand Krishnan Adéle Kruger Sarah Kummerfeld Igor V. Kurochkin Liana F. Lareau Dejan Lazarević Leonard Lipovich Jinfeng Liu Sabino Liuni Sean McWilliam M. Madan Babu Martin Madera Luigi Marchionni Hideo Matsuda Shu‐ichi Matsuzawa Hiroaki Miki Flavio Mignone S. Miyake Ken A. Morris Salim Mottagui‐Tabar Nicola Mulder Norio Nakano Hiromitsu Nakauchi Patrick Ng Roland Nilsson Seiji Nishiguchi Shigemichi Nishikawa

This study describes comprehensive polling of transcription start and termination sites analysis previously unidentified full-length complementary DNAs derived from the mouse genome. We identify 5' 3' boundaries 181,047 transcripts with extensive variation in arising alternative promoter usage, splicing, polyadenylation. There are 16,247 new protein-coding transcripts, including 5154 encoding proteins. Genomic mapping transcriptome reveals transcriptional forests, overlapping on both...

10.1126/science.1112014 article EN Science 2005-09-01

<h3>Importance</h3> Application of deep learning algorithms to whole-slide pathology images can potentially improve diagnostic accuracy and efficiency. <h3>Objective</h3> Assess the performance automated at detecting metastases in hematoxylin eosin–stained tissue sections lymph nodes women with breast cancer compare it pathologists' diagnoses a setting. <h3>Design, Setting, Participants</h3> Researcher challenge competition (CAMELYON16) develop solutions for node (November 2015-November...

10.1001/jama.2017.14585 article EN JAMA 2017-12-12
Yasushi Okazaki Masaaki Furuno Takeya Kasukawa Jun Adachi Hidemasa Bono and 95 more Shinji Kondo Itoshi Nikaido Naoki Osato Rintaro Saito Harukazu Suzuki Itaru Yamanaka Hidenori Kiyosawa Ken Yagi Yuji Tomaru Yuki Hasegawa A Nogami Christian Schönbach Takashi Gojobori Richard M. Baldarelli David P. Hill Carol J. Bult David Hume John Quackenbush Lynn M. Schriml Alexander Kanapin Hideo Matsuda Serge Batalov Kirk W. Beisel Judith A. Blake Dirck Bradt Vladimir Brusić C. Chothia Lori E Corbani Sharon Cousins Emiliano Dalla Tommaso A. Dragani Colin Fletcher Alistair R. R. Forrest Kenneth S. Frazer Terry Gaasterland Manuela Gariboldi Carmela Gissi Adam Godzik Julian Gough Sean M. Grimmond Stefano Gustincich Nobutaka Hirokawa Ian J. Jackson Erich D. Jarvis Akio Kanai Hideya Kawaji Yuka Imamura Kawasawa Rafal M. Kedzierski Benjamin L. King Akihiko Konagaya Igor V. Kurochkin Yong Suk Lee Boris Lenhard Paul Lyons Donna Maglott Lois J. Maltais Luigi Marchionni Louise M. McKenzie Hiromi Miki Takeshi Nagashima Koji Numata Toshihisa Okido William J. Pavan Geo Pertea Graziano Pesole Nikolai Petrovsky Rekha Sukamar Pillai Joan Pontius Qi Dong Sridhar Ramachandran Timothy Ravasi James Reed Deborah J. Reed James F. Reid Brian Z. Ring Martin Ringwald Albin Sandelin C. Schneider Colin A. Semple Mitsutoshi Setou Kiyo Shimada Răzvan Sultana Yasuhiro Takenaka Martin S. Taylor Rohan D. Teasdale Masaru Tomita Roberto Verardo Lukas Wagner Claes Wahlestedt Yan Wang Yuka Watanabe Christine A. Wells Laurens Wilming Anthony Wynshaw‐Boris Masashi Yanagisawa

Only a small proportion of the mouse genome is transcribed into mature messenger RNA transcripts. There an international collaborative effort to identify all full-length mRNA transcripts from mouse, and ensure that each represented in physical collection clones. Here we report manual annotation 60,770 complementary DNA sequences. These are clustered 33,409 'transcriptional units', contributing 90.1% newly established transcriptome database. Of these transcriptional units, 4,258 new...

10.1038/nature01266 article EN public-domain Nature 2002-12-01

We have developed a new tool, called fastDNAml, for constructing phylogenetic trees from DNA sequences. The program can be run on wide variety of computers ranging Unix workstations to massively parallel systems, and is available the Ribosomal Database Project (RDP) by anonymous FTP. Our uses maximum likelihood approach based version 3.3 Felsenstein's dnaml program. Several enhancements, including algorithmic changes, significantly improve performance reduce memory usage, making it feasible...

10.1093/bioinformatics/10.1.41 article EN Bioinformatics 1994-01-01

10.1038/35055500 article EN Nature 2001-02-08
Harukazu Suzuki Alistair R. R. Forrest Erik van Nimwegen Carsten O. Daub Piotr J. Balwierz and 95 more Katharine M. Irvine Timo Lassmann Timothy Ravasi Yuki Hasegawa Michiel de Hoon Shintaro Katayama Kate Schroder Piero Carninci Yasuhiro Tomaru Mutsumi Kanamori-Katayama Atsutaka Kubosaki Altuna Akalin Yoshinari Ando Erik Arner Maki Asada Hiroshi Asahara Timothy L. Bailey Vladimir B. Bajić Denis C. Bauer Anthony G Beckhouse Nicolas Bertin Johan Björkegren Frank Brombacher Erika Bulger Alistair M. Chalk Joe Chiba Nicole Cloonan Adam Dawe Josée Dostie Pär G. Engström Magbubah Essack Geoffrey J. Faulkner J. Lynn Fink David Fredman Ko Fujimori Masaaki Furuno Takashi Gojobori Julian Gough Sean M. Grimmond Mika Gustafsson Megumi Hashimoto Takehiro Hashimoto Mariko Hatakeyama Susanne Heinzel Yoshihide Hayashizaki Oliver Hofmann Michael Hörnquist Łukasz Huminiecki Kazuho Ikeo Naoko Imamoto Satoshi Inoue Yusuke Inoue Ryoko Ishihara Takao Iwayanagi Anders J. Skanderup Mandeep Kaur Hideya Kawaji Markus C. Kerr Ryuichiro Kimura Syuhei Kimura Yasumasa Kimura Hiroaki Kitano Hisashi Koga Toshio Kojima Shinji Kondo T. Konno Anders Krogh Adéle Kruger Ajit Kumar Boris Lenhard Andreas Lennartsson Morten Lindow Marina Lizio Cameron Ross MacPherson Norihiro Maeda Christopher A. Maher Monique Maqungo Jessica C. Mar Nicholas Matigian Hideo Matsuda John S. Mattick Stuart Meier Sei Miyamoto Etsuko Miyamoto‐Sato Kazuhiko Nakabayashi Yutaka Nakachi Mika Nakano Sanne Nygaard Toshitsugu Okayama Yasushi Okazaki Haruka Okuda-Yabukami Valerio Orlando Jun Otomo Mikhail Pachkov Nikolai Petrovsky

10.1038/ng.375 article EN Nature Genetics 2009-04-19
Tadashi Imanishi Takeshi Itoh Yutaka Suzuki Claire O’Donovan Satoshi Fukuchi and 95 more Kanako O. Koyanagi Roberto A. Barrero Takuro Tamura Yumi Yamaguchi‐Kabata Motohiko Tanino Kei Yura Satoru Miyazaki Kazuho Ikeo Keiichi Homma Arek Kasprzyk Tetsuo Nishikawa Mika Hirakawa Jean Thierry‐Mieg Danielle Thierry‐Mieg Jennifer Ashurst Libin Jia Mitsuteru Nakao Michael A. Thomas Nicola Mulder Youla Karavidopoulou Lihua Jin Sangsoo Kim Tomohiro Yasuda Boris Lenhard Éric Eveno Yoshiyuki Suzuki Chisato Yamasaki Jun‐ichi Takeda Craig A. Gough Phillip B. Hilton Yasuyuki Fujii Hiroaki Sakai Susumu Tanaka Clara Amid M. Bellgard Maria de Fátima Bonaldo Hidemasa Bono Susan K. Bromberg Anthony J. Brookes Elspeth A. Bruford Piero Carninci Claude Chelala C Couillault Sandro J. de Souza Marie-Anne Debily Marie‐Dominique Devignes Inna Dubchak Toshinori Endo Anne Estreicher Eduardo Eyras Kaoru Fukami-Kobayashi Gopal Gopinath Esther Graudens Yoonsoo Hahn Michael Han Ze‐Guang Han Kousuke Hanada Hideki Hanaoka Erimi Harada Katsuyuki Hashimoto Ursula Hinz Momoki Hirai Teruyoshi Hishiki Ian Hopkinson Sandrine Imbeaud Hidetoshi Inoko Alexander Kanapin Yayoi Kaneko Takeya Kasukawa Janet Kelso Paul Kersey Reiko Kikuno Kouichi Kimura Bernhard Korn Vladimir Kuryshev Izabela Makałowska Takashi Makino Shuhei Mano Régine Mariage‐Samson Jun Mashima Hideo Matsuda Hans‐Werner Mewes Satoshi Minoshima Keiichi Nagai Hideki Nagasaki Naoki Nagata Rajni Nigam Osamu Ogasawara Osamu Ohara Masafumi Ohtsubo Norihiro Okada Toshihisa Okido Satoshi Oota Motonori Ota Toshio Ota

The human genome sequence defines our inherent biological potential; the realization of biology encoded therein requires knowledge function each gene. Currently, in this area is still limited. Several lines investigation have been used to elucidate structure and genes genome. Even so, gene prediction remains a difficult task, as varieties transcripts may vary great extent. We thus performed an exhaustive integrative characterization 41,118 full-length cDNAs that capture complete functional...

10.1371/journal.pbio.0020162 article EN cc-by PLoS Biology 2004-04-19

Bone homeostasis is regulated by communication between bone-forming mature osteoblasts (mOBs) and bone-resorptive osteoclasts (mOCs). However, the spatial-temporal relationship mode of interaction in vivo remain elusive. Here we show, using an intravital imaging technique, that mOB mOC functions are via direct cell-cell contact these cell types. The mOBs mOCs mainly occupy discrete territories steady state, although detected spatiotemporally limited areas. In addition, a pH-sensing...

10.1038/s41467-017-02541-w article EN cc-by Nature Communications 2018-01-15

Genome reduction by removing dispensable genomic sequences in bacteria is commonly used both fundamental and applied studies to determine the minimal genetic requirements for a living system or develop highly efficient bioreactors. Nevertheless, whether how accumulative loss of disturbs bacterial growth remains unclear. To investigate relationship between genome growth, series Escherichia coli strains carrying genomes reduced stepwise manner were used. Intensive analyses revealed that...

10.1093/dnares/dsw035 article EN cc-by-nc DNA Research 2016-07-03

Abstract Bone morphogenetic protein (BMP)-2 plays a central role in bone-tissue engineering because of its potent bone-induction ability. However, the process BMP-induced bone formation vivo remains poorly elucidated. Here, we aimed to establish method for intravital imaging entire BMP-2-induced ectopic formation. Using multicolor transgenic mice, visualized spatiotemporal induction, including appearance and motility osteoblasts osteoclasts, angiogenesis, collagen-fiber formation,...

10.1038/s41598-020-61825-2 article EN cc-by Scientific Reports 2020-03-16

A general overview of the protein sequence set for mouse transcriptome produced during FANTOM2 sequencing project is presented here. We applied different algorithms to characterize sequences derived from a nonredundant representative (RPS) and variant (VPS) transcriptome. The functional characterization assignment Gene Ontology terms was done by analysis proteome using InterPro. Superfamily database analyses gave detailed structural classification according SCOP provide additional evidence...

10.1101/gr.978703 article EN cc-by-nc Genome Research 2003-06-01

Obesity causes excess fat accumulation in white adipose tissues (WAT) and also other insulin-responsive organs such as the skeletal muscle, increasing risk for insulin resistance, which can lead to obesity-related metabolic disorders. Peroxisome proliferator-activated receptor-α (PPARα) is a master regulator of fatty acid oxidation whose activator known improve hyperlipidemia. However, molecular mechanisms underlying PPARα activator-mediated reduction adiposity improvement disorders are...

10.1074/jbc.m116.767590 article EN cc-by Journal of Biological Chemistry 2017-04-13

In vivo two-photon fluorescence imaging is a powerful modality to monitor cell dynamics in biomedical studies. To detect protein functions living animals real-time, fluorescent probes must show quick response the target function specific tissues. Here, we developed rhodamine-based small-molecule probe called Red-pHocas (red pH-activatable for osteoclast activity sensing) reversibly acidic environments spatiotemporal analysis of proton pumps. The introduction electron-withdrawing N-alkyl...

10.1021/acscentsci.9b00220 article EN publisher-specific-oa ACS Central Science 2019-05-01

Osteoclastic bone resorption and osteoblastic formation/replenishment are closely coupled in metabolism. Anabolic parathyroid hormone (PTH), which is commonly used for treating osteoporosis, shifts the balance from osteoclastic to osteoblastic, although it unclear how these cells coordinately regulated by PTH. Here, we identify a serine protease inhibitor, secretory leukocyte inhibitor (SLPI), as critical mediator that involved PTH-mediated shift phase. Slpi highly upregulated osteoblasts...

10.1038/s41467-021-22402-x article EN cc-by Nature Communications 2021-04-09

PURPOSE: Breast cancer tumors frequently have intratumor heterogeneity. Tumors with high heterogeneity caused therapeutic resistance and human epidermal growth factor receptor 2 (HER2) in response to HER2-targeted therapies. This study aimed investigate whether HER2 levels were clinically related poor prognosis for adjuvant therapies primary breast cancers.&#x0D; METHODS: included patients (n = 251) treated was manifested by the shape of fluorescence situ hybridization amplification (FISH)...

10.20944/preprints202402.1136.v1 preprint EN 2024-02-20

Breast cancer tumors frequently have intratumoral heterogeneity (ITH). Tumors with high ITH cause therapeutic resistance and human epidermal growth factor receptor 2 (HER2) in response to HER2-targeted therapies. This study aimed investigate whether HER2 levels were clinically related a poor prognosis for adjuvant therapy primary breast cancers. included patients (n = 251) treated was manifested by the shape of fluorescence situ hybridization amplification (FISH) distributed histograms gene...

10.3390/cancers16051062 article EN Cancers 2024-03-05

10.1016/s0304-3975(98)00091-7 article EN publisher-specific-oa Theoretical Computer Science 1999-01-01

Femoral condyle geometry was evaluated in 30 normal and varus knees using magnetic resonance imaging. In the sagittal view, distal part of medial deformed knees, but there no significant difference posterior between knees. transverse transepicondylar axis(a reliable rotational landmark) showed approximately 6° external rotation relative to condylar axis The results this study suggest that hypoplasia exists at addition, may be a landmark is internal when total knee arthroplasty performed.

10.1097/00003086-199804000-00022 article EN Clinical Orthopaedics and Related Research 1998-04-01

Both large deletions in genome and heat shock stress would lead to alterations the gene expression profile; however, whether there is any potential linkage between these disturbances transcriptome have not been discovered. Here, relationship genomic environmental contributions was analyzed by comparing transcriptomes of bacterium Escherichia coli (strain MG1655 its extensive deletion derivative, MDS42) grown regular transient conditions.The analysis showed following: (i) a reorganization...

10.1186/1471-2164-14-25 article EN cc-by BMC Genomics 2013-01-16
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