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The New England Journal of Medicine|February 25, 2011
Perilipin deficiency and autosomal dominant partial lipodystrophySheetal Gandotra, Caroline Le Dour, William Bottomley, et al.Nature Communications|December 22, 2022
Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutationsCaroline Le Dour, Maria Chatzifrangkeskou, Coline Macquart, et al.Cell Reports|August 25, 2021
The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathiesNicolas Vignier, Maria Chatzifrangkeskou, Luca Pinton, et al.Journal of Cellular and Molecular Medicine|February 18, 2009
The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stressValerie L R M Verstraeten, Sandrine Caputo, Maurice A M van Steensel, et al.Pageof 2