Nakashima Mitsuko

J-GLOBAL         Last updated: Oct 7, 2018 at 23:05
 

Research Areas

 
 

Academic & Professional Experience

 
Apr 2017
 - 
Today
Associate professor, Department of Biochemistry, Hamamatsu University School of Medicine
 
Apr 2012
 - 
Mar 2017
Yokohama City University School of Medicine Medical Course Human Genetics
 
Sep 2008
 - 
Mar 2012
Human Genome Center, Institute of Medical Science, the University of Tokyo
 

Education

 
Apr 2004
 - 
Mar 2008
Medical and dental sciences, Graduate School of Biomedical Sciences, Nagasaki University
 
Apr 1995
 - 
Mar 2001
School of Medicine, Nagasaki University
 

Published Papers

 
Tsuchida N, Hamada K, Shiina M, Kato M, Kobayashi Y, Tohyama J, Kimura K, Hoshino K, Ganesan V, Teik KW, Nakashima M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Saitsu H, Ogata K, Miyatake S, Matsumoto N
Clinical genetics      Oct 2018   [Refereed]
Takeguchi R, Haginoya K, Uchiyama Y, Fujita A, Nagura M, Takeshita E, Inui T, Okubo Y, Sato R, Miyabayashi T, Togashi N, Saito T, Nakagawa E, Sugai K, Nakashima M, Saitsu H, Matsumoto N, Sasaki M
Brain & development   40(8) 728-732   Sep 2018   [Refereed]
Hamada N, Ogaya S, Nakashima M, Nishijo T, Sugawara Y, Iwamoto I, Ito H, Maki Y, Shirai K, Baba S, Maruyama K, Saitsu H, Kato M, Matsumoto N, Momiyama T, Nagata KI
Brain : a journal of neurology      Sep 2018   [Refereed]
Hamanaka K, Miyatake S, Zerem A, Lev D, Blumkin L, Yokochi K, Fujita A, Imagawa E, Iwama K, Nakashima M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Saitsu H, van der Knaap MS, Lerman-Sagie T, Matsumoto N
Journal of human genetics      Sep 2018   [Refereed]
Belal H, Nakashima M, Matsumoto H, Yokochi K, Taniguchi-Ikeda M, Aoto K, Amin MB, Maruyama A, Nagase H, Mizuguchi T, Miyatake S, Miyake N, Iijima K, Nonoyama S, Matsumoto N, Saitsu H
Human mutation   39(8) 1070-1075   Aug 2018   [Refereed]
Daida A, Hamano SI, Ikemoto S, Matsuura R, Nakashima M, Matsumoto N, Kato M
Epileptic disorders : international epilepsy journal with videotape   20(4) 313-318   Aug 2018   [Refereed]
Miyatake S, Kato M, Sawaishi Y, Saito T, Nakashima M, Mizuguchi T, Mitsuhashi S, Takata A, Miyake N, Saitsu H, Matsumoto N
Annals of neurology   84(1) 159-161   Jul 2018   [Refereed]
Uchiyama Y, Yanagisawa K, Kunishima S, Shiina M, Ogawa Y, Nakashima M, Hirato J, Imagawa E, Fujita A, Hamanaka K, Miyatake S, Mitsuhashi S, Takata A, Miyake N, Ogata K, Handa H, Matsumoto N, Mizuguchi T
Clinical genetics      Jul 2018   [Refereed]
Suzuki-Muromoto S, Wakusawa K, Miyabayashi T, Sato R, Okubo Y, Endo W, Inui T, Togashi N, Kato A, Oba H, Nakashima M, Saitsu H, Matsumoto N, Haginoya K
Journal of human genetics   63(6) 749-753   Jun 2018   [Refereed]
Nakajima J, Oana S, Sakaguchi T, Nakashima M, Numabe H, Kawashima H, Matsumoto N, Miyake N
Journal of human genetics   63(4) 529-532   Apr 2018   [Refereed]

Misc

 
Nakashima M, Kouga T, Lourenço CM, Shiina M, Goto T, Tsurusaki Y, Miyatake S, Miyake N, Saitsu H, Ogata K, Osaka H, Matsumoto N
Epilepsia      Nov 2015   [Refereed]
Nakashima M, Saitsu H, Takei N, Tohyama J, Kato M, Kitaura H, Shiina M, Shirozu H, Masuda H, Watanabe K, Ohba C, Tsurusaki Y, Miyake N, Zheng Y, Sato T, Takebayashi H, Ogata K, Kameyama S, Kakita A, Matsumoto N
Annals of neurology   78(3) 375-386   Sep 2015   [Refereed]
Nakashima M, Miyajima M, Sugano H, Iimura Y, Kato M, Tsurusaki Y, Miyake N, Saitsu H, Arai H, Matsumoto N
Journal of human genetics   59(12) 691-693   Dec 2014   [Refereed]
Nakashima M, Kashii H, Murakami Y, Kato M, Tsurusaki Y, Miyake N, Kubota M, Kinoshita T, Saitsu H, Matsumoto N
Neurogenetics   15(3) 193-200   Aug 2014   [Refereed]
Nakashima M, Takano K, Osaka H, Aida N, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N
Journal of human genetics   59(8) 471-474   Aug 2014   [Refereed]
中島 光子, 松本 直通
細胞   45(3) 128-131   Mar 2013
【ケロイド・瘢痕を知る】 ゲノムワイド関連解析を用いた日本人ケロイド疾患感受性領域の同定
中島 光子, 前佛 均
Aesthetic Dermatology   22(2) 79-89   Jun 2012
ケロイドの形成には創傷治癒の遷延や機械的刺激などの外的要因に加え、かねてより遺伝素因との関連が強く疑われてきた。そこでわれわれはゲノムワイド関連解析(GWAS)によりケロイド疾患感受性領域の検索を行い、3領域4座位がケロイドと強い関連を示すことを明らかにした。3領域のうち2領域において既知の遺伝子(FOXL2、PRR23B、NEDD4)が存在しており、いずれの遺伝子もこれまでケロイドとの関連が報告されていない新規候補遺伝子であった。今回同定された遺伝子多型(SNP)が遺伝子の発現量やタンパ...
Nakashima M, Chung S, Takahashi A, Kamatani N, Kawaguchi T, Tsunoda T, Hosono N, Kubo M, Nakamura Y, Zembutsu H
Nature genetics   42(9) 768-771   Sep 2010   [Refereed]
Nakashima M, Tsuda M, Kinoshita A, Kishino T, Kondo S, Shimokawa O, Niikawa N, Yoshiura K
Clinical chemistry   54(10) 1746-1748   Oct 2008   [Refereed]
Nakashima M, Nakano M, Hirano A, Kishino T, Kondoh S, Miwa N, Niikawa N, Yoshiura K
Journal of human genetics   53(1) 34-41   2008   [Refereed]

Conference Activities & Talks

 
WDR45 mutations in three male patients with West syndrome
Nakashima Mitsuko
66th Annual Meeting of The American Society of Human Genetics   Oct 2016   
De novo DNM1 mutations in two cases of epileptic encephalopathy
Nakashima Mitsuko
13th International Congress of Human Genetics   Apr 2016   
Somatic mutations in the MTOR gene cause focal cortical dysplasia type IIb
Nakashima Mitsuko
65th Annual Meeting of The American Society of Human Genetics   9 Oct 2015   
Novel compound heterozygous PIGT mutations caused multiple congenital anomalies-hypotonia-seizures syndrome
Nakashima Mitsuko
64th Annual Meeting of The American Society of Human Genetics   Oct 2014   
A genome-wide association study for keloid disease and involvement of FOXL2 in keloid formation
Nakashima Mitsuko
Nov 2011   

Association Memberships