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Volumn 19, Issue 11, 2010, Pages 2191-2207

Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL NUCLEUS INCLUSION BODY; CONTROLLED STUDY; DISEASE COURSE; DISEASE MARKER; DISEASE SEVERITY; GENETIC DISORDER; GENETIC REGULATION; MOLECULAR BIOLOGY; MOUSE; MUSCLE ATROPHY; MUSCLE STRENGTH; NONHUMAN; OCULOPHARYNGEAL MUSCULAR DYSTROPHY; PHENOTYPE; PRIORITY JOURNAL; SKELETAL MUSCLE; SOLEUS MUSCLE; TRANSCRIPTOMICS; ANALYSIS OF VARIANCE; ANIMAL; BIOLOGICAL MODEL; COMPLICATION; FAST MUSCLE FIBER; GENE EXPRESSION PROFILING; GENETICS; GLYCOLYSIS; IMMUNOHISTOCHEMISTRY; METABOLISM; MUSCLE CONTRACTION; MUSCULAR ATROPHY; PATHOLOGY; PHYSIOLOGY; PRINCIPAL COMPONENT ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TRANSGENIC MOUSE; WESTERN BLOTTING;

EID: 77953586729     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddq098     Document Type: Article
Times cited : (70)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.