Showing results (1-10 of 35) with videos related to
Sort By:
Pageof 4
Materials Science & Engineering. C, Materials for Biological Applications|August 6, 2013
Alignment of muscle precursor cells on the vertical edges of thick carbon nanotube filmsIan Holt, Ingo Gestmann, Andrew C WrightNeuromuscular Disorders : NMD|May 16, 2006
Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium compositionIan Holt, Thi Man Nguyen, Manfred Wehnert, et al.Neuromuscular Disorders : NMD|June 12, 2020
Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophyEmily C Storey, Ian Holt, Glenn E Morris, et al.Neuromuscular Disorders : NMD|November 25, 2011
A rapid immunohistochemical test to distinguish congenital myotonic dystrophy from X-linked myotubular myopathyCaroline A Sewry, Ros C M Quinlivan, Waney Squier, et al.Neuromuscular Disorders : NMD|March 30, 2024
Proteomic characterization of human LMNA-related congenital muscular dystrophy muscle cellsEmily C Storey, Ian Holt, Sharon Brown, et al.Human Mutation|February 11, 2011
Characterization of MSH2 variants by endogenous gene modification in mouse embryonic stem cellsEva A L Wielders, Rob J Dekker, Ian Holt, et al.Cytoskeleton (Hoboken, N.J.)|June 17, 2014
Nesprin-1 and nesprin-2 regulate endothelial cell shape and migrationSamantha J King, Karolin Nowak, Narendra Suryavanshi, et al.Plos Genetics|May 14, 2009
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic miceStéphanie Tomé, Ian Holt, Winfried Edelmann, et al.Journal of Cell Science|June 5, 2003
Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivoIan Holt, Cecilia Ostlund, Colin L Stewart, et al.Brain Structure & Function|June 18, 2016
Monoclonal antibody Py recognizes neurofilament heavy chain and is a selective marker for large diameter neurons in the brainHeidi R Fuller, Lucia Marani, Ian Holt, et al.Pageof 4