Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the Dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI

Human Molecular Genetics

Volumn 23, Issue 10, 2014, Pages 2694-2710

  Ferrier, Andrew ^a,c   Sato, Tadasu ^a,b   De Repentigny, Yves ^a   Gibeault, Sabrina ^a   Bhanot, Kunal ^a   O'Meara, Ryan W ^a,c   Lynch Godrei, Anisha ^a,c   Kornfeld, Samantha F ^a,c   Young, Kevin G ^e   Kothary, Rashmi ^a,c,d  

^a OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

^b TOHOKU UNIVERSITY   (Japan)

^c UNIVERSITY OF OTTAWA   (Canada)

^d UNIVERSITY OF OTTAWA   (Canada)

^e NATIONAL RESEARCH COUNCIL CANADA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BULLOUS PEMPHIGOID ANTIGEN 1; DYSTONIN A1; DYSTONIN A2; DYSTONIN A3; PRION PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; CYTOSKELETON PROTEIN; DST PROTEIN, MOUSE; NERVE PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUTOPHAGY; CELL POPULATION; CELL SURVIVAL; CELL VIABILITY; CONTRACTURE; CONTROLLED STUDY; DEATH; DISORIENTATION; DYSAUTONOMIA; DYSTONIA; GOLGI COMPLEX; HEREDITARY SENSORY AUTONOMIC NEUROPATHY VI; HISTOPATHOLOGY; HOMOZYGOSITY; LIFESPAN; LIMB DISEASE; MICROTUBULE; MOUSE; NERVE CELL DEGENERATION; NERVE FIBER; NERVE FIBER DEGENERATION; NEUROMUSCULAR SYNAPSE; NEUROPATHY; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIMARY CULTURE; PRIORITY JOURNAL; PROMOTER REGION; PROPRIOCEPTION; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SENSORY NERVE CELL; SPINAL GANGLION; ANIMAL; C57BL MOUSE; CELL CULTURE; DISEASE MODEL; GENETICS; HUMAN; INTRACELLULAR MEMBRANE; METABOLISM; MUSCLE SPINDLE; MYELINATED NERVE; PATHOLOGY; TORSION DYSTONIA; TRANSGENE; TRANSGENIC MOUSE;

ANIMALS; CARRIER PROTEINS; CELLS, CULTURED; CYTOSKELETAL PROTEINS; DISEASE MODELS, ANIMAL; DYSTONIA MUSCULORUM DEFORMANS; GANGLIA, SPINAL; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; INTRACELLULAR MEMBRANES; MICE, INBRED C57BL; MICE, TRANSGENIC; MICROTUBULES; MUSCLE SPINDLES; NERVE FIBERS, MYELINATED; NERVE TISSUE PROTEINS; NEUROMUSCULAR JUNCTION; PHENOTYPE; PROPRIOCEPTION; SENSORY RECEPTOR CELLS; TRANSGENES;

EID: 84898776266     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt663     Document Type: Article

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