Drieke Vandamme
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Drieke Vandamme has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Bruno Constantin
Institut de Physiologie et Biologie Cellulaire, UMR CNRS/Université de Poitiers 6187, Pôle Biologie Santé, 86022 Poitiers cedex, France
1 shared publication - Christophe Ampe
Ghent University
1 shared publication - Davina Tondeleir
Department of Biochemistry, Faculty of Medicine and Health Sciences, Ghent University, A. Baertsoenkaai 3, Gent, Belgium
1 shared publication - Davy Waterschoot
Department of Medical Protein Research, VIB, B-9000 Ghent, Belgium
1 shared publication - Ellen Lambert
Department of Plant Production, Faculty of Bioscience Engineering, UGent, Coupure associations 653, Gent, Belgium
1 shared publication - Heidi Rommelaere
Ablynx N.V., Ghent, Belgium
1 shared publication
Latest Publications
- Open Access
- 1 January 2009
- Published by Springer Nature in BMC Research Notes
- Vol. 2 (1) , 40
Phenotypes induced by NM causing α-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes
Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with α-skeletal muscle actin mutations. We previously showed that actin mutations can cause four different biochemical phenotypes and that expression of NM associated actin mutants in fibroblasts, myoblasts and myotubes induces a range of cellular defects.
- 1 January 2009
- Published by Springer Nature in BMC Research Notes
- Vol. 2 (1) , 40
Open AccessPhenotypes induced by NM causing α-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes
Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with α-skeletal muscle actin mutations. We previously showed that actin mutations can cause four different biochemical phenotypes and that expression of NM associated actin mutants in fibroblasts, myoblasts and myotubes induces a range of cellular defects.