siRNA-mediated Allele-specific Silencing of a COL6A3 Mutation in a Cellular Model of Dominant Ullrich Muscular Dystrophy

Por Bolduc, Véronique, Zou, Yaqun, Ko, Dayoung, Bönnemann, Carsten G
Publicado em 2014

No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans

Por Bolduc, Véronique, Chagnon, Pierre, Provost, Sylvie, Dubé, Marie-Pierre, Belisle, Claude, Gingras, Marianne, Mollica, Luigina, Busque, Lambert
Publicado em 2007

Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies

Por Bolduc, Véronique, Marlow, Gareth, Boycott, Kym M., Saleki, Khalil, Inoue, Hiroshi, Kroon, Johan, Itakura, Mitsuo, Robitaille, Yves, Parent, Lucie, Baas, Frank, Mizuta, Kuniko, Kamata, Nobuyuki, Richard, Isabelle, Linssen, Wim H.J.P., Mahjneh, Ibrahim, de Visser, Marianne, Bashir, Rumaisa, Brais, Bernard
Publicado em 2010

Mosaicism for dominant collagen VI mutations as a cause for intra-familial phenotypic variability

Por Donkervoort, Sandra, Hu, Ying, Stojkovic, Tanya, Voermans, Nicol, Foley, A. Reghan, Leach, Meganne E, Dastgir, Jahannaz, Bolduc, Veronique, Cullup, Thomas, de Becdelièvre, Alix, Yang, Lin, Su, Hai, Meilleur, Katherine, Schindler, Alice B., Kamsteeg, Erik-Jan, Richard, Pascale, Butterfield, Russell, Winder, Thomas L., Crawford, Thomas, Weiss, Robert B., Muntoni, Francesco, Allamand, Valérie, Bönnemann, Carsten G.
Publicado no Hum Mutat (2015)