A Tropomyosin-2 Mutation Suppresses a Troponin I Myopathy in<i>Drosophila</i>
Benyoussef Naïmi(University of York), John C. Sparrow(University of York), Alberto Ferrús(Consejo Superior de Investigaciones Científicas), Inmaculada Canal(Instituto Cajal), Andrew Harrison(University of York), Upendra Nongthomba(University of York), Mark Cummins(University of York), Samantha Clark(University of York)
Cited by 41
Related Papers
Monoclonal antibodies against the Drosophila nervous system.
|Proceedings of the National Academy of Sciences|1982|534
Shaker encodes a family of putative potassium channel proteins in the nervous system of Drosophila.
|The EMBO Journal|1988|445
Mutations and polymorphisms of the skeletal muscle α-actin gene (<i>ACTA1</i>)
|Human Mutation|2009|246
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)
|Neuromuscular Disorders|2003|215
Abnormal action potentials associated with the <i>Shaker</i> complex locus of <i>Drosophila</i>
|Proceedings of the National Academy of Sciences|1981|179