Disruption of actin-binding domain-containing dystonin protein causes dystonia musculorum in mice

European Journal of Neuroscience

Volumn 40, Issue 10, 2014, Pages 3458-3471

  Horie, Masao ^a   Watanabe, Keisuke ^a   Bepari, Asim K ^a   Nashimoto, Jun ichiro ^a   Araki, Kimi ^b   Sano, Hiromi ^c   Chiken, Satomi ^c   Nambu, Atsushi ^c   Ono, Katsuhiko ^d   Ikenaka, Kazuhiro ^c   Kakita, Akiyoshi ^e   Yamamura, Ken ichi ^b   Takebayashi, Hirohide ^a,f  

^a NIIGATA UNIVERSITY GRADUATE SCHOOL OF MEDICAL AND DENTAL SCIENCES   (Japan)

^b KUMAMOTO UNIVERSITY   (Japan)

^c NATIONAL INSTITUTE FOR PHYSIOLOGICAL SCIENCES   (Japan)

^d KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^e NIIGATA UNIVERSITY   (Japan)

^f JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Autonomic neuropathy; Dystonia; Gene trap mutant; Hereditary sensory; Neurodegeneration

Indexed keywords

BULLOUS PEMPHIGOID ANTIGEN 1; DYSTONIN LACZ FUSION PROTEIN; HYBRID PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; CYTOSKELETON PROTEIN; DST PROTEIN, MOUSE; ISOPROTEIN; NERVE PROTEIN;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN NERVE CELL; CELL ACTIVITY; CENTRAL NERVOUS SYSTEM; CONTROLLED STUDY; DST GENE; DYSTONIA; EMBRYO; FEMALE; GENE; GENETIC CODE; LOSS OF FUNCTION MUTATION; MALE; MOUSE; NERVE DEGENERATION; NONHUMAN; PERIPHERAL NERVOUS SYSTEM; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; ANIMAL; BRAIN; C57BL MOUSE; DISEASE MODEL; DYSTONIC DISORDER; GENETICS; METABOLISM; PATHOLOGY; PATHOPHYSIOLOGY; SKELETAL MUSCLE; SPINAL CORD; SPINAL GANGLION; TRANSGENIC MOUSE; TRIGEMINAL NERVE;

ANIMALS; BRAIN; CARRIER PROTEINS; CYTOSKELETAL PROTEINS; DISEASE MODELS, ANIMAL; DYSTONIC DISORDERS; FEMALE; GANGLIA, SPINAL; MALE; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; MUSCLE, SKELETAL; NERVE TISSUE PROTEINS; PHENOTYPE; PROTEIN ISOFORMS; SPINAL CORD; TRIGEMINAL NERVE;

EID: 84916894733     PISSN: 0953816X     EISSN: 14609568     Source Type: Journal    
DOI: 10.1111/ejn.12711     Document Type: Article

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