Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Biljana Ilkovski

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Advances in Experimental Medicine and Biology|February 3, 2009
Investigations into the pathobiology of thin-filament myopathiesBiljana Ilkovski
Neuromuscular Disorders : NMD|November 18, 2005
Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathyBiljana Ilkovski, Sophie Clement, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindredDavid O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Journal of Neuropathology and Experimental Neurology|April 27, 2010
In vitro analysis of rod composition and actin dynamics in inherited myopathiesAurélie Vandebrouck, Ana Domazetovska, Nancy Mokbel, et al.
Annals of Neurology|March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportionNigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
Brain : a Journal of Neurology|October 12, 2007
Mechanisms underlying intranuclear rod formationAna Domazetovska, Biljana Ilkovski, Sandra T Cooper, et al.
Human Molecular Genetics|June 17, 2004
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoformsBiljana Ilkovski, Kristen J Nowak, Ana Domazetovska, et al.
Journal of Neuropathology and Experimental Neurology|August 22, 2008
Disease severity and thin filament regulation in M9R TPM3 nemaline myopathyBiljana Ilkovski, Nancy Mokbel, Raymond A Lewis, et al.
Cell Motility and the Cytoskeleton|October 31, 2007
Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscleNicole Vlahovich, Galina Schevzov, Visalini Nair-Shaliker, et al.
Annals of Neurology|August 21, 2007
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weaknessAna Domazetovska, Biljana Ilkovski, Vikash Kumar, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|February 3, 2009
Investigations into the pathobiology of thin-filament myopathiesBiljana Ilkovski
Neuromuscular Disorders : NMD|November 18, 2005
Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathyBiljana Ilkovski, Sophie Clement, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindredDavid O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Journal of Neuropathology and Experimental Neurology|April 27, 2010
In vitro analysis of rod composition and actin dynamics in inherited myopathiesAurélie Vandebrouck, Ana Domazetovska, Nancy Mokbel, et al.
Annals of Neurology|March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportionNigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
Brain : a Journal of Neurology|October 12, 2007
Mechanisms underlying intranuclear rod formationAna Domazetovska, Biljana Ilkovski, Sandra T Cooper, et al.
Human Molecular Genetics|June 17, 2004
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoformsBiljana Ilkovski, Kristen J Nowak, Ana Domazetovska, et al.
Journal of Neuropathology and Experimental Neurology|August 22, 2008
Disease severity and thin filament regulation in M9R TPM3 nemaline myopathyBiljana Ilkovski, Nancy Mokbel, Raymond A Lewis, et al.
Cell Motility and the Cytoskeleton|October 31, 2007
Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscleNicole Vlahovich, Galina Schevzov, Visalini Nair-Shaliker, et al.
Annals of Neurology|August 21, 2007
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weaknessAna Domazetovska, Biljana Ilkovski, Vikash Kumar, et al.
Pageof 2