Items where Author is "Meissner, Gerhard"

2009

Ghassemi, Farshid and Vukcevic, Mirko and Xu, Le and Zhou, Haiyan and Meissner, Gerhard and Muntoni, Francesco and Jungbluth, Heinz and Zorzato, Francesco and Treves, Susan. (2009) A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity. Cell Calcium, 45 (2). pp. 192-197.

2007

Lyfenko, Alla D. and Ducreux, Sylvie and Wang, Ying and Xu, Le and Zorzato, Francesco and Ferreiro, Ana and Meissner, Gerhard and Treves, Susan and Dirksen, Robert T.. (2007) Two central core disease (CCD) deletions in the C-terminal region of RYR1 alter muscle excitation-contraction (EC) coupling by distinct mechanisms. Human Mutation, 28 (1). pp. 61-68.

2006

Zhou, Haiyan and Yamaguchi, Naohiro and Xu, Le and Wang, Ying and Sewry, Caroline and Jungbluth, Heinz and Zorzato, Francesco and Bertini, Enrico and Muntoni, Francesco and Meissner, Gerhard and Treves, Susan. (2006) Characterization of recessive RYR1 mutations in core myopathies. Human Molecular Genetics, 15 (18). pp. 2791-2803.

2003

Zorzato, Francesco and Yamaguchi, Naohiro and Xu, Le and Meissner, Gerhard and Müller, Clemens R. and Pouliquin, Pierre and Muntoni, Francesco and Sewry, Caroline and Girard, Thierry and Treves, Susan. (2003) Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor. Human Molecular Genetics, 12 (4). pp. 379-388.