Laminin-α2 but not -α1-mediated adhesion of human (Duchenne) and murine (mdx) dystrophic myotubes is seriously defective

FEBS Letters

Volumn 408, Issue 3, 1997, Pages 341-344

  Angoli, Damiano ^a   Corona, Paola ^a   Baresi, Rita ^b   Mora, Marina ^b   Wanke, Enzo ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

Dystroglycan; Duchenne dystrophy; Laminin; mdx myotube; Merosin

Indexed keywords

DYSTROPHIN; GLYCAN; CYTOSKELETON PROTEIN; DAG1 PROTEIN, HUMAN; DYSTROGLYCAN; LAMININ; LAMININ A; LAMININ ALPHA2; LAMININ RECEPTOR; MEMBRANE PROTEIN;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CELL ADHESION; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; DYSTROPHY; EXTRACELLULAR MATRIX; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; MOUSE; MYOTUBE; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ASSAY; ANIMAL; ANIMAL MUSCULAR DYSTROPHY; CELL CULTURE; GENETICS; MECHANICAL STRESS; MUSCLE CELL; MUSCULAR DYSTROPHY; PATHOPHYSIOLOGY; PHYSIOLOGY; REFERENCE VALUE; SKELETAL MUSCLE; X CHROMOSOME; X CHROMOSOME LINKED MUSCULAR DYSTROPHIC MOUSE;

ANIMALS; CELL ADHESION; CELLS, CULTURED; CYTOSKELETAL PROTEINS; DYSTROGLYCANS; EXTRACELLULAR MATRIX; HUMANS; LAMININ; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED MDX; MUSCLE FIBERS; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; MUSCULAR DYSTROPHY, ANIMAL; RECEPTORS, LAMININ; REFERENCE VALUES; STRESS, MECHANICAL; X CHROMOSOME;

EID: 0031586947     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(97)00460-2     Document Type: Article

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