MATSUURA Tohru

J-GLOBAL         Last updated: Dec 17, 2018 at 20:17
 
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Name
MATSUURA Tohru
Affiliation
Nagoya University
Section
Graduate School of Medicine
Job title
Associate Professor

Research Areas

 
 

Academic & Professional Experience

 
1998
   
 
- Postdoctoral Fellow, Neurology, Baylor College of Medicine
 
2000
   
 
- Instructor, Neurology, Baylor College of Medicine
 
2002
   
 
- Assistant Professor, Molecular and Human Genetics, Baylor College of Medicine
 

Awards & Honors

 
2003
Young Investigator Award, National Ataxia Foundation
 

Published Papers

 
Yokose M, Furuya K, Suzuki M, Ozawa T, Kim Y, Miura K, Matsuzono K, Mashiko T, Tada M, Koide R, Shimazaki H, Matsuura T, Fujimoto S
Neuro-ophthalmology (Aeolus Press)   42(5) 309-311   Oct 2018   [Refereed]
Matsuzono K, Arai N, Suzuki M, Kim Y, Ozawa T, Mashiko T, Shimazaki H, Koide R, Matsuura T, Fujimoto S
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association   27(6) e110-e112   Jun 2018   [Refereed]
Mashiko T, Sakashita E, Kasashima K, Tominaga K, Kuroiwa K, Nozaki Y, Matsuura T, Hamamoto T, Endo H
The Journal of biological chemistry   291(29) 14996-15007   Jul 2016   [Refereed]
Chen G, Masuda A, Konishi H, Ohkawara B, Ito M, Kinoshita M, Kiyama H, Matsuura T, Ohno K
Scientific reports   6 25317   Apr 2016   [Refereed]
Imada H, Sakatani T, Sawada M, Matsuura T, Fukushima N, Nakano I
Pathology international   65(10) 549-553   Oct 2015   [Refereed]

Books etc

 
Genetics of Myotonic Dystrophy: Disease Mechanism, Current Management and Therapeutic Development
MATSUURA Tohru (Part:Joint Work, Myotonic Dystrophy)
Springer   Jan 2018   
Spinocerebellar Ataxia Type 10 in: GeneReviews at GeneTests: Medical Genetics Information Resource.
Copyright, University of Washington, Seattle. 1997-2006. Available at http://www.genetests.org.   2006   
非翻訳領域リピート病のRNA病態.
Medical Science Digest   2006   
SCA10の分子遺伝学.
神経研究の進歩   2006   
Spinocerebellar Ataxia Type 10 in: /GeneReviews /at GeneTests: Medical Genetics Information Resource.
Copyright, University of Washington, Seattle. 1997-2004. Available at www.genetests.org <http://www.geneclinics.org/>.   2004   
Spinocerebellar ataxia type 10: a disease caused by a large ATTCT repeat expansion.
Adv Exp Med Biol   2002   
Spinocerebellar Ataxia Type 10: A Disease Caused by a Large ATTCT Repeat Expansion. In: Trinucleotide Expansions and Human Diseases.
Timchenko L ed. Landes Bioscience, Georgetown   2002   
Spinocerebellar Ataxia Type 10 in: /GeneReviews /at GeneTests: Medical Genetics Information Resource.
Copyright, University of Washington, Seattle. 1997-2002. Available at www.genetests.org <http://www.geneclinics.org/>.   2002   
Spinocerebellar ataxia type 10. In: Genetics of Movement Disorders.
Pulst SM ed. Academic Press, San Diego   2001   
SCA10遺伝子の同定―新しいリピート (pentanucleotide repeat) 病.
臨床神経学   2001   

Conference Activities & Talks

 
Pancreatic Cancer in FXTAS Individual: Altered DNA Damage Response?
MATSUURA Tohru
9th International Conference on Unstable Microsatellites & Human Disease   22 Apr 2018   
RNA disease mechanism in DM1 and SCA10 brain [Invited]
MATSUURA Tohru
29 Jul 2015   
Parkinsonism in SCAs [Invited]
MATSUURA Tohru
13th International Parkinson’s Disease Symposium in Takamatsu (iPDST)   21 Feb 2014   
RNA-mediated disease mechanism of spinocerebellar ataxia type 10
MATSUURA Tohru
7th International Conference on Unstable Microsatellites & Human Disease   13 Jun 2012   
RNA-mediated disease mechanism of spinocerebellar ataxia type 10 [Invited]
MATSUURA Tohru
22 May 2010   

Works

 
Research Grants from National Ataxia Foundation, MN, USA ($25,000) “The role of interruptions in SCA10 expansion and disease”
2005 - 2005
Research Grants (Olivopontocerebellar atrophy and related disorders) from NORD ($40,000) “Characterization of the SCA10 ATTCT Expansion and Implications of the Sequence Configurations”
2005 - 2005
Young Investigator Award from National Ataxia Foundation, MN, USA  ($100,000) “RNA disease mechanism in spinocerebellar ataxia type 10”
2003 - 2004
Research Grants (Olivopontocerebellar atrophy and related disorders) from National Organization for Rare Disorders (NORD), CT, USA ($40,000) “Complete survey of SCA10 mutation in multiethnic ataxia patients”
2003 - 2004
Research Grants from National Ataxia Foundation, MN, USA ($30,000) “Search for an expansion mutation of ATTCT/AGAAT repeats in unassigned ataxia patients”
2002 - 2002

Patents

 
DNA TEST FOR SCA-10
USPTO#6,885,497