Glycine receptor channels in spinal motoneurons are abnormal in a transgenic mouse model of amyotrophic lateral sclerosis

Journal of Neuroscience

Volumn 31, Issue 8, 2011, Pages 2815-2827

  Chang, Qing ^a   Martin, Lee J ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; ENHANCED GREEN FLUORESCENT PROTEIN; GLYCINE RECEPTOR; MESSENGER RNA;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL CELL; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; EMBRYO; FEMALE; GABAERGIC SYSTEM; IMMUNOCYTOCHEMISTRY; MALE; MOUSE; NONHUMAN; PATCH CLAMP; POSTSYNAPTIC DENSITY; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION; SPINAL CORD MOTONEURON; STOMACH PARESIS; TRANSGENIC MOUSE; WHOLE CELL;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; CELLS, CULTURED; DISEASE MODELS, ANIMAL; DOWN-REGULATION; FEMALE; HUMANS; MALE; MICE; MICE, TRANSGENIC; MOTOR NEURONS; NEURAL INHIBITION; RECEPTORS, GLYCINE; SPINAL CORD; SUPEROXIDE DISMUTASE;

EID: 79951991424     PISSN: 02706474     EISSN: 15292401     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.2475-10.2011     Document Type: Article

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