Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism
- Author
- MAKINO, Satoshi1 2 ; KAJI, Ryuji1 ; LEE, Lillian V5 ; OGASAWARA, Kazumasa6 ; TOOYAMA, Ikuo7 ; AKATSU, Hiroyasu8 ; NISHIMURA, Masataka1 ; TAMIYA, Gen1 2 ; ANDO, Satoshi1 2 ; TOMIZAWA, Maiko2 ; YASUNO, Katsuhito2 ; GOTO, Satoshi3 ; MATSUMOTO, Shinnichi1 ; TABUENA, Ma. Daisy4 ; MARANON, Elma4 ; DANTES, Marita5
[1] Department of Neurology and Neuroscience, University of Tokushima Graduate School of Medicine, Tokushima, Japan
[2] Department of Molecular Life Science, Tokai University School of Medicine, Kanagawa, Japan
[3] Department of Neurosurgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan
[4] Department of Internal Medicine, Section of Neurology, West Visayas State University Medical Center, Jaro, Iloilo, Panay, Philippines
[5] Department of Health, Philippine Children's Medical Center, Quezon City, Philippines
[6] Department of Pathology, Shiga University of Medical Science, Otsu, Japan
[7] Molecular Neuroscience Research Center, Shiga University of Medical Science, Otsu, Japan
[8] Choju Medical Institute, Fukushimura Hospital, Toyohashi, Japan - Source
American journal of human genetics. 2007, Vol 80, Num 3, pp 393-406, 14 p ; ref : 30 ref
- Publisher
- University of Chicago Press, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Association Caractère lié au sexe Chromosome X Dystonie Expression génique Génétique Homme Maladie héréditaire Neurone Parkinsonisme Encéphale pathologie Extrapyramidal syndrome Mouvement involontaire Muscle strié pathologie Système nerveux central pathologie Système nerveux pathologie Trouble neurologique
- Keyword (en)
- Association Sex linked character X-Chromosome Dystonia Gene expression Genetics Human Genetic disease Neuron Parkinsonism Cerebral disorder Extrapyramidal syndrome Involuntary movement Striated muscle disease Central nervous system disease Nervous system diseases Neurological disorder
- Keyword (es)
- Asociación Carácter ligado al sexo Cromosoma X Distonía Expresión genética Genética Hombre Enfermedad hereditaria Neurona Parkinson síndrome Encéfalo patología Extrapiramidal síndrome Movimiento involuntario Músculo estriado patología Sistema nervosio central patología Sistema nervioso patología Trastorno neurológico
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A04 Molecular and cellular biology
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A01 Nervous system as a whole
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Medical genetics Molecular and cell biology Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18565396
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
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DOI
10.1086/512129 
https://dx.doi.org/10.1086/512129
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