Specific Absence of the α1 Subunit of the Dihydropyridine Receptor in Mice with Muscular Dysgenesis

This publication has 31 references indexed in Scilit:

• Calcium currents in embryonic and neonatal mammalian skeletal muscle.
  The Journal of general physiology, 1988
• Conserved organization of the human and murine T-cell receptor β-gene families
  Nature, 1988
• Excitation-contraction uncoupling in the developing skeletal muscle of the muscular dysgenesis mouse embryo
  Biochimie, 1987
• Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscle
  Nature, 1987
• Abnormal transverse tubule system and abnormal amount of receptors for Ca2+ channel inhibitors of the dihydropyridine family in skeletal muscle from mice with embryonic muscular dysgenesis
  Developmental Biology, 1985
• Appearance of contractile activity in muscular dysgenesis () mouse myotubes during coculture with normal spinal cord cells
  Developmental Biology, 1982
• Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
  Proceedings of the National Academy of Sciences, 1979
• Voltage Dependent Charge Movement in Skeletal Muscle: a Possible Step in Excitation–Contraction Coupling
  Nature, 1973
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970
• Lethal Genes and Analysis of Differentiation
  Science, 1963