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Items where Author is "Zhou, Haiyan"

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Jump to: 2016 | 2015 | 2009 | 2007 | 2006
Number of items: 7.

2016

Lopez, Rubén J. and Byrne, Susan and Vukcevic, Mirko and Sekulic-Jablanovic, Marijana and Xu, Lifen and Brink, Marijke and Alamelu, Jay and Voermans, Nicol and Snoeck, Marc and Clement, Emma and Muntoni, Francesco and Zhou, Haiyan and Radunovic, Aleksandar and Mohammed, Shehla and Wraige, Elizabeth and Zorzato, Francesco and Treves, Susan and Jungbluth, Heinz. (2016) An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities. Science Signaling, 9 (435). ra68.

2015

Rokach, Ori and Sekulic-Jablanovic, Marijana and Voermans, Nicol and Wilmshurst, Jo and Pillay, Komala and Heytens, Luc and Zhou, Haiyan and Muntoni, Francesco and Gautel, Mathias and Nevo, Yoram and Mitrani-Rosenbaum, Stella and Attali, Ruben and Finotti, Alessia and Gambari, Roberto and Mosca, Barbara and Jungbluth, Heinz and Zorzato, Francesco and Treves, Susan. (2015) Epigenetic changes as a common trigger of muscle weakness in congenital myopathies. Human Molecular Genetics, 24 (16). pp. 4636-4647.

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

Jungbluth, Heinz and Zhou, Haiyan and Sewry, Caroline A. and Robb, Stephanie and Treves, Susan and Bitoun, Marc and Guicheney, Pascale and Buj-Bello, Anna and Bönnemann, Carsten and Muntoni, Francesco. (2007) Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders , 17 (4). pp. 338-345.

Zorzato, Francesco and Jungbluth, Heinz and Zhou, Haiyan and Muntoni, Francesco and Treves, Susan. (2007) Functional effects of mutations identified in patients with multiminicore disease. IUBMB Life, 59 (1). pp. 14-20.

Zhou, Haiyan and Jungbluth, Heinz and Sewry, Caroline A. and Feng, Lucy and Bertini, Enrico and Bushby, Kate and Straub, Volker and Roper, Helen and Rose, Michael R. and Brockington, Martin and Kinali, Maria and Manzur, Adnan and Robb, Stephanie and Appleton, Richard and Messina, Sonia and D'Amico, Adele and Quinlivan, Ros and Swash, Michael and Müller, Clemens R. and Brown, Susan and Treves, Susan and Muntoni, Francesco. (2007) Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies. Brain, 130 (8). pp. 2024-2036.

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.

This list was generated on Thu Sep 16 12:35:41 2021 CEST.