Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic component

Human Molecular Genetics

Volumn 18, Issue 7, 2009, Pages 1353-1367

  Kudryashova, Elena ^a   Wu, Jun ^a   Havton, Leif A ^a   Spencer, Melissa J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MUSCLE PROTEIN; MYOSIN; TRIPARTITE MOTIF PROTEIN 32; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; ELECTRON MICROSCOPY; GENE FREQUENCY; GENE MUTATION; GENETIC IDENTIFICATION; GENETIC VARIABILITY; LIMB GIRDLE MUSCULAR DYSTROPHY; LIMB GIRDLE MUSCULAR DYSTROPHY TYPE 2H; MOUSE; MYOPATHY; NERVOUS TISSUE; NEUROFILAMENT; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SARCOPLASMIC RETICULUM; SKELETAL MUSCLE;

ANIMALS; AXONS; BRAIN; GENE DELETION; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MUSCLE, SKELETAL; MUSCULAR DISEASES; MYELIN SHEATH; MYOSIN HEAVY CHAINS; NEUROFILAMENT PROTEINS; NEUROGENESIS; PROTEIN ISOFORMS; UBIQUITIN-PROTEIN LIGASES;

MURINAE; MUS;

EID: 63149150621     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddp036     Document Type: Article

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