Molecular phenotyping of the mouse ky mutant reveals UCP1 upregulation at the neuromuscular junctions of dystrophic soleus muscle

Neuromuscular Disorders

Volumn 14, Issue 3, 2004, Pages 217-228

  Blanco, G ^a   Pritchard, C ^a   Underhill, P ^a   Breeds, S ^a   Townsend, K M F ^a   Greenfield, A ^a   Brown, Steve D M ^a  

^a MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

Author keywords

Kyphoscoliosis; Microarrays; Muscular dystrophy; Uncoupling proteins

Indexed keywords

CHOLINERGIC RECEPTOR; UNCOUPLING PROTEIN 1;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DNA MICROARRAY; EXTENSOR DIGITORUM LONGUS MUSCLE; GENE EXPRESSION; IMMUNOFLUORESCENCE; MOLECULAR DYNAMICS; MOUSE; MUSCULAR DYSTROPHY; NEUROMUSCULAR SYNAPSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RNA ANALYSIS; SARCOLEMMA; SOLEUS MUSCLE; UNINDEXED SEQUENCE; UPREGULATION; VALIDATION PROCESS;

EID: 1242293854     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2003.09.008     Document Type: Article

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