Methyl CpG-binding protein 2 (a mutation of which causes rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains

Author

ITOH, Masayuki¹ ; IDE, Shuhei¹ ; TANABE, Yuzo⁸ ; GOTO, Yu-Ichi¹ ; TAKASHIMA, Sachio² ; KUDO, Shinichi³ ; NOMURA, Yoshiko⁴ ; SEGAWA, Masaya⁴ ; KUBOTA, Takeo⁵ ; MORI, Hideo⁶ ; TANAKA, Shigeki⁷ ; HORIE, Hiroshi⁸
[1] Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan
[2] Yanagawa Institute for Developmental Disabilities, International University of Health and Welfare, Fukuoka, Japan
[3] Department of Biological Science, Hokkaido Institute of Public Health, Sapporo, Japan
[4] Segawa Neurological Clinic for Children, Tokyo, Japan
[5] Department of Epigenetic Medicine, University of Yamanashi, Yamanashi, Japan
[6] Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan
[7] Department of Neurology, Juntendo University Urayasu Hospital, Chiba, Japan
[8] Chiba Children's Hospital, Chiba, Japan

Source

Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 2, pp 117-123, 7 p ; ref : 31 ref

CODEN

JNENAD

ISSN

0022-3069

Scientific domain

Neurology

Publisher

Lippincott Williams & Wilkins, Hagerstown, MD

Publication country

United States

Document type

Article

Language

English

Author keyword

Insulin-like growth factor binding protein 3 Methyl CpG-binding protein 2 Rett syndrome

Keyword (fr)

Animal Homme Mutation Protéine liaison IGFBP Protéine liaison Rett syndrome Souris Système nerveux pathologie Encéphale pathologie Maladie dégénérative Maladie héréditaire Mammalia Rodentia Système nerveux central pathologie Vertebrata

Keyword (en)

Animal Human Mutation Insulin like growth factor binding protein Binding protein Rett syndrome Mouse Nervous system diseases Cerebral disorder Degenerative disease Genetic disease Mammalia Rodentia Central nervous system disease Vertebrata

Keyword (es)

Animal Hombre Mutación Proteína enlace IGFBP Proteína enlace Rett síndrome Ratón Sistema nervioso patología Encéfalo patología Enfermedad degenerativa Enfermedad hereditaria Mammalia Rodentia Sistema nervosio central patología Vertebrata

Classification

Pascal

002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17C Vascular diseases and vascular malformations of the nervous system

Pascal

002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17D Malformations of the nervous system

Discipline

Neurology

Origin

Inist-CNRS

Database

PASCAL

INIST identifier

18525427

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS