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European Journal of Cell Biology|October 13, 2005
Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophyIsabell Motsch, Manuja Kaluarachchi, Lindsay J Emerson, et al.
Nature Communications|March 31, 2016
Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelopePetra Mikolcevic, Michitaka Isoda, Hiroki Shibuya, et al.
Molecular and Cellular Biology|May 2, 2006
SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeletonFarhana Haque, David J Lloyd, Dawn T Smallwood, et al.
Journal of Human Genetics|June 24, 2011
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spotCharlotte A Brown, Juergen Scharner, Kevin Felice, et al.
Plos Genetics|September 12, 2014
Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organizationPeter Meinke, Elisabetta Mattioli, Farhana Haque, et al.
Journal of Cell Science|January 27, 2005
Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscleQiuping Zhang, Cassandra D Ragnauth, Jeremy N Skepper, et al.
Human Molecular Genetics|March 29, 2013
Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2αTatiana V Cohen, Viola F Gnocchi, Jonathan E Cohen, et al.
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