INOUE Ken

J-GLOBAL         Last updated: Oct 7, 2018 at 17:48
 
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Name
INOUE Ken
Affiliation
National Center of Neurology and Psychiatry
Section
National Institute of Neuroscience,Ncnp
Job title
Head
Degree
Ph.D.(Yokohama City University(Japan)), M.D.(Yokohama City University(Japan))

Research Areas

 
 

Academic & Professional Experience

 
1992
 - 
1993
Post doc. Univ. California, San Diego
 
 
   
 
Dept. Pharmacology
 
1997
 - 
2002
Post doc. Baylor College of Medicine,
 
 
   
 
Dept. Molecular and Human Genetics
 
2002
 - 
2004
Assistant Professor. Baylor College of Medicine,
 

Education

 
 
 - 
1994
psychiatry, Graduate School, Division of Medicine, Yokohama City University
 
 
   
 
Medicine, School of Medicine, Yokohama City University
 

Published Papers

 
Akutsu Y, Shirai K, Takei A, Goto Y, Aoyama T, Watanabe A, Imamura M, Enokizono T, Ohto T, Hori T, Suzuki K, Hayashi M, Masumoto K, Inoue K
American journal of medical genetics. Part A   176(5) 1195-1199   May 2018   [Refereed]
Kubo KI, Deguchi K, Nagai T, Ito Y, Yoshida K, Endo T, Benner S, Shan W, Kitazawa A, Aramaki M, Ishii K, Shin M, Matsunaga Y, Hayashi K, Kakeyama M, Tohyama C, Tanaka KF, Tanaka K, Takashima S, Nakayama M, Itoh M, Hirata Y, Antalffy B, Armstrong DD, Yamada K, Inoue K, Nakajima K
JCI insight   2(10)    May 2017   [Refereed]
Gotoh L, Inoue K, Helman G, Mora S, Maski K, Soul JS, Bloom M, Evans SH, Goto YI, Caldovic L, Hobson GM, Vanderver A
Molecular genetics and metabolism   119(3) 293   Nov 2016   [Refereed]
Shimojima K, Maruyama K, Kikuchi M, Imai A, Inoue K, Yamamoto T
Intractable & rare diseases research   5(3) 214-217   Aug 2016   [Refereed]

Misc

 
Inoue K, Khajavi M, Ohyama T, Hirabayashi S, Wilson J, Reggin JD, Mancias P, Butler IJ, Wilkinson MF, Wegner M, Lupski JR. Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations
Nat Genet   36: 361-369    2004
Inoue K, Shilo K, Boerkoel, CF, Crowe C, Sawady J, Lupski JR, Agamanolis DP. Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg-Hirschsprung disease: phenotypes linked by SOX10 mutation
Ann Neurol   52: 836-842    2002
Inoue K, Osaka H, Thurston VC, Clarke J, Yoneyama A, Rosenbarker L, Bird TD, Hodes ME, Shaffer LG, Lupski JR. Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in ・・・
Am J Hum Genet   71: 838-852    2002
Inoue K, Osaka H, Thurston VC, Clarke J, Yoneyama A, Rosenbarker L, Bird TD, Hodes ME, Shaffer LG, Lupski JR. Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotype...
Inoue K, Tanaka H, Scaglia F, Araki A, Kashork CD, Shaffer LG, Lupski JR. Compensating for CNS dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvement
Ann Neurol   50: 747-754    2001
Inoue K, Lupski JR. Molecular mechanisms for genomic disorders
Annual Review Genomics and Human Genetics   50: 747-754    2001

Books etc

 
Inoue K, Lupski JR. Mendelian, Non-mendelian, multigenetic and complex traits. In: Rosenberg RN, Prusiner SB, DiMauro S, Barchi RL, Nestler EJ, eds. The Molecular Basis of Neurological and Psychiatric Disease. Third edition.
Butter Heinemann. Philadelphia, PA.   

Works

 
Molecular Genetics of Pelizaeus-Merzbacher disease
2004 - 2010
Human Inherited diseases caused by SOX10 mutations
2004 - 2010

Research Grants & Projects

 
Physiological roles of non-sense mediated mRNA decay
The Other Research Programs
Project Year: 2004 - 2009
Molecular genetics of Pelizaeus Merzbacher disease
The Other Research Programs
Project Year: 1995 - 2010
Human inherited diseases caused by SOX10 mutations
Contract Research
Project Year: 1998 - 2010