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Histochemistry and Cell Biology|August 25, 2012
Cytoplasmic localization of PML particles in laminopathiesF Houben, W H De Vos, I P C Krapels, et al.Human Molecular Genetics|August 12, 2011
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathiesWinnok H De Vos, Frederik Houben, Miriam Kamps, et al.Human Molecular Genetics|July 11, 2006
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulationValerie L R M Verstraeten, Jos L V Broers, Maurice A M van Steensel, 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 4