IWAKI Akiko 岩城明子

Researcher Number	30253454
Other IDs
Affiliation (based on the past Project Information) *help	2011: 九州大学, 生体防御医学研究所, 講師 2007 – 2011: Kyushu University, Medical Institute of bioregulation, Assistant Professor 2001 – 2006: 九州大学, 生体防御医学研究所, 助手 1994 – 2000: 九州大学, 遺伝情報実験施設, 助手
Review Section/Research Field	Principal Investigator Human genetics / Molecular biology / Nerve anatomy/Neuropathology Except Principal Investigator Human genetics / Human genetics / Psychiatric science
Keywords	Principal Investigator PLP / ゲノム / neurological disorder / genome / gene / 遺伝学 / 神経科学 / 脳神経疾患 / 遺伝子 / Stress … More / Crystallin / Heat shock protein / クリスタン / ストレス蛋白質 / ストレス / クリスタリン / 熱ショック蛋白質 / myelin / dysmyelination / プロテオリピド蛋白質 / ミエリン形成不全症 / ミエリン / ミエリン形成不全 / ゲノム医科学 / 細胞接着因子 / 自閉症 / 遺伝子改変マウス … More Except Principal Investigator 関連解析 / HbE / AAV / 連鎖不平衡 / ノックアウトマウス / 多型 / knockout mouse / phencyclidine / linkage disequilibrium / polymorphism / glutamate receptor / association study / affected sib-pair analysis / schizophrenia / 精神分裂病(統合失調症) / 覚醒剤 / フェンシクリジン / グルタミン酸受容体 / 罹患同胞対解析 / 統合失調症(精神分裂病) / splicing / antisense / insulator / thalassemia / globin gene / gene therapy / 転写 / 赤芽球 / アンセンチ / スプライシング / アンチセンス / インスレータ / サラセミア / グロビン遺伝子 / 遺伝子治療 / 連鎖不均衡 / グルタミン酸伝達系 / 遺伝統計学 / 脳神経疾患 / PCP / 精神疾患 / 発現解析 / ハプロタイプ / 行動解析 / 遺伝子改変マウス / グルタミン酸 / ゲノム / 統合失調症 / 多因子病 / ディファレンシャルディスプレイ / CCK / SNP / amphiphysin / c-fos / Zebrin band / メタンフェタミン / 小脳 / 精神分裂病 Less

Molecular analysis of the CNTN4 knockout micePrincipal Investigator
- Principal Investigator
  
  IWAKI Akiko
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Kyushu University
Multidimensional approaches to molecular basis of schizophrenia
- Principal Investigator
  
  FUKUMAKI Yasuyuki
- Project Period (FY)
  2006 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Human genetics
- Research Institution
  Kyushu University
Molecular basis of leukodystrophy caused by a dosage-sensitive genePrincipal Investigator
- Principal Investigator
  
  IWAKI Akiko
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Kyushu University
Molecular analysis of schizophrenia by the integrated approach
- Principal Investigator
  
  FUKUMAKI Yasuyuki
- Project Period (FY)
  2002 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Human genetics
- Research Institution
  KYUSHU UNIVERSITY
精神分裂病の分子病因に関する小脳モジュール構造解析からのアプローチ
- Principal Investigator
  
  FUKUMAKI Yasuyuki
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Psychiatric science
- Research Institution
  Kyushu University
Expression of the HSPB2 and αB-crystallin genes located in a head-to-head mannerPrincipal Investigator
- Principal Investigator
  
  IWAKI Akiko
- Project Period (FY)
  1998 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Molecular biology
- Research Institution
  KYUSHU UNIVERSITY
Basic spproaches for gene therapy of hemoglobinopathy
- Principal Investigator
  
  FUKUMAKI Yasuyuki
- Project Period (FY)
  1996 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  KYUSHU UNIVERSITY
Molecular Pathology of the dysmyelinating diseases and generation of the model animalsPrincipal Investigator
- Principal Investigator
  
  IWAKI Akiko
- Project Period (FY)
  1994 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Nerve anatomy/Neuropathology
- Research Institution
  Kyushu University

All 2012 2011 2010 2009 2008 2007 2006 2005 Other

All Journal Article Presentation

[Journal Article] Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion2012
- Author(s)
  Torisu, Iwaki, et al
- Journal Title
  
  Brain Dev
  
  Volume: (In press) Issue: 10 Pages: 852-856
- DOI
  10.1016/j.braindev.2012.02.006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359, KAKENHI-PROJECT-21790995, KAKENHI-PROJECT-23591503, KAKENHI-PROJECT-24791068
[Journal Article] Partial SPAST and DPY30 deletions in a Japanese spastic paraplegia type 4 family2011
- Author(s)
  Miura S, Shibata H, Kida H, Noda K, Toyama T, Iwasaki N, Iwaki A, Ayabe M, Aizawa H, Taniwaki T, Fukumaki Y
- Journal Title
  
  Neurogenetics
  
  Volume: 12 Pages: 25-31
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Journal Article] An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene2011
- Author(s)
  Suzuki SO, Iwaki T, Arakawa K, Furuya H, Fujii N, Iwaki A
- Journal Title
  
  Acta Neuropathol
  
  Volume: 122 Pages: 775-781
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Journal Article] An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions2011
- Author(s)
  Matsuoka T, Fujii N, Kondo A, Iwaki A, Hokonohara T, Honda H, Sasaki K, Suzuki SO, Iwaki T
- Journal Title
  
  Neuropathology
  
  Volume: 31 Pages: 71-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Journal Article] Comprehensive behavioural study of GluR4 knockout mice : implication in cognitive function2010
- Author(s)
  Sagata N, Iwaki A, Aramaki T, Takao K, Kura S, Tsuzuki T, Kawakami R, Ito I, Kitamura T, Sugiyama H, Miyakawa T, Fukumaki Y
- Journal Title
  
  Genes Brain Behav
  
  Volume: 9 Pages: 899-909
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Journal Article] FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion2010
- Author(s)
  Suzuki N, Aoki M, Warita H, Kato M, Mizuno H, Shimakura N, Akiyama T, Furuya H, Hokonohara T, Iwaki A, Togashi S, Konno H, Itoyama Y
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 252-4
- NAID
  10030734667
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Journal Article] Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation2010
- Author(s)
  Tateishi T, Hokonohara T, Yamasaki R, Miura S, Kikuchi H, Iwaki A, Tashiro H, Furuya H, Nagara Y, Ohyagi Y, Nukina N, Iwaki T, Fukumaki Y, Kira JI
- Journal Title
  
  Acta Neuropathol
  
  Volume: 119 Pages: 355-364
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Journal Article] Heterozygous deletion of ITPR1,but not SUMF1 in spinocerebellar ataxia type162008
- Author(s)
  Iwaki A, et. al.
- Journal Title
  
  J.Med.Genet 45
  
  Pages: 32-35
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17590287
[Journal Article] Heterozygous deletion of ITPR1, but not SUMF1in spinocerebellar ataxia type 162008
- Author(s)
  Iwaki, A., et al.
- Journal Title
  
  J. Med. Genet. 45
  
  Pages: 32-35
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18209012
[Journal Article] Heterozygous deletion of ITPR1, but not SUMF1 in spinocerebellar ataxia type 16.2008
- Author(s)
  Iwaki, A., Kawano, Y., Miura, S., Shibata, H., Matsuse, D., Li, W., Furuya, H., Ohyagi, Y., Taniwaki, T., Kira, J., Fukumaki, Y
- Journal Title
  
  J. Med. Genet 45
  
  Pages: 32-35
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Journal Article] Heterozygous deletion of ITPR1,but not SUMF1 in spinocerebellar ataxia type 162008
- Author(s)
  Iwaki A., et. al.
- Journal Title
  
  J. Med. Genet 45
  
  Pages: 32-35
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17590287
[Journal Article] Heterozygous deletion of ITPR1, but not SUMF1 in spinocerebellar ataxia type16.2008
- Author(s)
  Iwaki, A., et. al.
- Journal Title
  
  J.Med.Genet. 45
  
  Pages: 32-35
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18209012
[Journal Article] Heterozygous deletion of ITPR1, but not SUMF1 in spinocerebellar ataxia type 162008
- Author(s)
  Iwaki A., Kawano Y., Miura S., Shibata H., Matsuse D., Li W., Furuya H., Ohyagi Y., Taniwaki T., Kira J. and Fukumaki Y.
- Journal Title
  
  J. Med. Genet. 45
  
  Pages: 32-35
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18209012
[Journal Article] A novel expression system for artificial miRNA containing no endogenous miRNA precursor sequences2007
- Author(s)
  Shibata, A., Iwaki, A., Fukumaki, Y
- Journal Title
  
  J. RNAi Gene Silencing 3
  
  Pages: 237-247
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Journal Article] A novel expression system for artificial miRNA containing no endogenous miRNA precursor sequences2007
- Author(s)
  Shibata, A., Iwaki, A. and Fukumaki, Y.
- Journal Title
  
  J.RNAi Gene Silencing 3
  
  Pages: 237-247
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18209012
[Journal Article] Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion
- Author(s)
  Torisu H, Iwaki A, Takeshita K, Hiwatashi A, Sanefuji M, Fukumaki Y, Hara T
- Journal Title
  
  Brain Dev
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590359
[Presentation] Generation and behavioral analysis of GluR4 knockout mice2011
- Author(s)
  Iwaki A, Sagata N, Aramaki T, Takao K, Miyakawa T, Kawakami R, Ito I, Kitamura T, Sugiyama H, Kura S, Tsuzuki T, Fukumaki Y
- Organizer
  The 56th Annual Meeting of Japan Society of Human Genetics
- Year and Date
  2011-11-09
- Data Source
  KAKENHI-PROJECT-21590359
[Presentation] Molecular mechanisms of behavioral abnormalities of knockout mice of Grm3.2011
- Author(s)
  Fujioka R, Nii T, Iwaki A, Kitaichi, K, Ito I, Shibata A, Nomura M, Hattori S, Takao K, Miyakawa T and Fukumaki Y.
- Organizer
  The 34th Annual Meeting of the Molecular Biology Society of Japan
- Year and Date
  2011-12-14
- Data Source
  KAKENHI-PROJECT-21590359
[Presentation] Comprehensive behavioral analysis of mGluR3 knockout mice2010
- Author(s)
  Nii T, Fujioka R, Iwaki A, Hattori S, Takao K, Shibata A, Nomura M, Miyakawa T and Fukumaki Y.
- Organizer
  The 33 rd Annual Meeting of the Molecular Biology Society of Japan
- Year and Date
  2010-12-08
- Data Source
  KAKENHI-PROJECT-21590359
[Presentation] Adult-onset spastic paraplegia type 2 with a novel mutation in exon 7 of PLP1An autopsy case2009
- Author(s)
  Iwaki A, Suzuki SO, Arakawa K, Furuya H, Fujii N, Fukumaki Y, and Iwaki T.
- Organizer
  59th Annual Meeting of the American Society of Human Genetics
- Year and Date
  2009-10-21
- Data Source
  KAKENHI-PROJECT-21590359
[Presentation] Generation and analysis of schizophrenia susceptibility candidate gene Grm3 KO mice.2009
- Author(s)
  Nii T, Iwaki A, Sasaki T, Shibata A, Fukuyoshi Y, Sagata N, Nomura M, Fukumaki Y
- Organizer
  The 32nd Annual Meeting of the Molecular Biology Society of Japan
- Year and Date
  2009-12-12
- Data Source
  KAKENHI-PROJECT-21590359
[Presentation] 人工miRNAを用いた遺伝子発現制御系の開発2007
- Author(s)
  金子沙世, 柴田篤志, 岩城明子, 野村政壽, 服巻保幸
- Organizer
  第30回日本分子生物学会年会・第80回日本生化学会大会合同大会
- Place of Presentation
  神戸
- Year and Date
  2007-12-14
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Gene silencing mediated by artificial miRNAs2007
- Author(s)
  Sayo, Kaneko, Atsushi, Shibata, Akiko, Iwaki, Yasuyuki, Fukumaki
- Organizer
  The 30th Annual Meeting of the Molecular Biology Society of Japan
- Place of Presentation
  Yokohama
- Year and Date
  2007-12-14
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Methylation state of the PLP1 promoter in Pelizaeus-Merzbacher disease2006
- Author(s)
  Naoki, Matsumoto, Yasuyuki, Fukumaki, Akiko, Iwaki
- Organizer
  MBSJ Forum 2006
- Place of Presentation
  Nagoya
- Year and Date
  2006-12-08
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Pelizaeus-Merzbacher disease caused by PLP1 duplication2006
- Author(s)
  Kenji, Kurosawa, Hitoshi, Osaka, Kaori, Masuko, Akiko, Iwaki, Hiroko, Iwamoto, Sumio, Yamashita
- Organizer
  The 48th Meeting of the Japanese Society of Child Neurology
- Place of Presentation
  Tokyo
- Year and Date
  2006-06-02
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Pelizaeus-Merzbacher disease caused by PLP1 deletion(PLP null syndrome)2005
- Author(s)
  Hiroyuki, Torisu, Ryutaro, Kira, Yasunari, Sakai, Masashi, Sanefuji, Yoshimi, Takemoto, Toshiro, Hara, Kenzo, Takeshita, Akiko, Iwaki
- Organizer
  The 47th Meeting of the Japanese Society of Child Neurology
- Place of Presentation
  Kumamoto
- Year and Date
  2005-05-20
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Pelizaeus-Merzbacher病の遺伝子解析:PLP欠損を招く新たな機構2005
- Author(s)
  岩城明子, 他7名
- Organizer
  第28回日本分子生物学会年会
- Place of Presentation
  福岡
- Year and Date
  2005-12-08
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Gene silencing using an artificial pri-miRNA expression system2005
- Author(s)
  Atsushi, Shibata, Akiko, Iwaki, Yasuyuki, Fukumaki
- Organizer
  The 28th Annual Meeting of the Molecular Biology Society of Japan
- Place of Presentation
  Fukuoka
- Year and Date
  2005-12-09
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287
[Presentation] Two different PLP1 abnormalities result in PLP null syndorome2005
- Author(s)
  Akiko, Iwaki, Naoki, Matsumoto, Akiko, Ochi, Hiroyuki, Torisu, Ryutaro, Kira, Toshiro, Hara, Kenzo, Takeshita, Yasuyuki, Fukumaki
- Organizer
  The 28th Annual Meeting of the Molecular Biology Society of Japan
- Place of Presentation
  Fukuoka
- Year and Date
  2005-12-08
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590287

1. FUKUMAKI Yasuyuki (90128083)

# of Collaborated Projects: 4 results

# of Collaborated Products: 2 results

IWAKI Akiko 岩城 明子

Research Projects

Research Products

Co-Researchers

Molecular analysis of the CNTN4 knockout micePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Multidimensional approaches to molecular basis of schizophrenia

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular basis of leukodystrophy caused by a dosage-sensitive genePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular analysis of schizophrenia by the integrated approach

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

精神分裂病の分子病因に関する小脳モジュール構造解析からのアプローチ

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Expression of the HSPB2 and αB-crystallin genes located in a head-to-head mannerPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Basic spproaches for gene therapy of hemoglobinopathy

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular Pathology of the dysmyelinating diseases and generation of the model animalsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion2012

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Partial SPAST and DPY30 deletions in a Japanese spastic paraplegia type 4 family2011

Author(s)

Journal Title

Data Source

[Journal Article] An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene2011

Author(s)

Journal Title

Data Source

[Journal Article] An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions2011

Author(s)

Journal Title

Data Source

[Journal Article] Comprehensive behavioural study of GluR4 knockout mice : implication in cognitive function2010

Author(s)

Journal Title

Data Source

[Journal Article] FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion2010

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation2010

Author(s)

IWAKI Akiko 岩城明子