Muscle function and running activity in mouse models of hereditary muscle dystrophy: Impact of double knockout for dystrophin and the transcription factor MyoD

Muscle and Nerve

Volumn 45, Issue 4, 2012, Pages 544-551

  Mangner, Norman ^a   Adams, Volker ^a   Sandri, Marcus ^a   Hoellriegel, Robert ^a   Hambrecht, Rainer ^b   Schuler, Gerhard ^a   Gielen, Stephan ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b Hospital Links der Weser   (Germany)

Author keywords

Dystrophin; Exercise; Force analysis; Muscle injury; MyoD

Indexed keywords

DYSTROPHIN; MYOD PROTEIN; MYOD1 MYOGENIC DIFFERENTIATION PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EXERCISE; FEMALE; GENOTYPE; MALE; MOUSE; MUSCLE FUNCTION; MUSCULAR DYSTROPHY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RUNNING; SEDENTARY LIFESTYLE; SOLEUS MUSCLE; ANATOMY; ANIMAL; C57BL MOUSE; DISEASE COURSE; GENETICS; MOUSE MUTANT; MUSCLE CONTRACTION; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; SKELETAL MUSCLE; X CHROMOSOME LINKED MUSCULAR DYSTROPHIC MOUSE;

ANATOMY, CROSS-SECTIONAL; ANIMALS; DISEASE PROGRESSION; DYSTROPHIN; FEMALE; GENOTYPE; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED MDX; MICE, KNOCKOUT; MUSCLE CONTRACTION; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; MYOD PROTEIN; PHENOTYPE; RUNNING;

EID: 84860328245     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.22318     Document Type: Article

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