A hypoplastic model of skeletal muscle development displaying reduced foetal myoblast cell numbers, increased oxidative myofibres and improved specific tension capacity

Developmental Biology

Volumn 343, Issue 1-2, 2010, Pages 51-62

  Otto, Anthony ^a   Macharia, Raymond ^b   Matsakas, Antonios ^a   Valasek, Petr ^a   Mankoo, Baljinder S ^c   Patel, Ketan ^a  

^a UNIVERSITY OF READING   (United Kingdom)

^b ROYAL VETERINARY COLLEGE   (United Kingdom)

^c KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

Embryogenesis; Hypertrophy; Meox; Muscle; Myogenesis; Skeletal

Indexed keywords

HOMEODOMAIN PROTEIN; MUTANT PROTEIN; PROTEIN MEOX2; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL COUNT; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EMBRYO; FETUS; FETUS CELL; GENE DELETION; GENE LOSS; HYPOPLASIA; MALE; MOUSE; MUSCLE DEVELOPMENT; MUSCLE FIBRIL; MUSCLE MASS; MUSCLE TONE; MYOBLAST; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SKELETAL MUSCLE; WILD TYPE;

ANIMALIA; MUS;

EID: 77953703347     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2010.04.014     Document Type: Article

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