LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies

(2011) Winnok H. De Vos et al.   HUMAN MOLECULAR GENETICS

The nucleoporin Nup88 is interacting with nuclear lamin A

(2011) Yvonne C. Lussi et al.   MOLECULAR BIOLOGY OF THE CELL

Distinct association of the nuclear pore protein Nup153 with A- and B-type lamins

(2011) Teiba Al-Haboubi et al.   Nucleus

The role of Drosophila Lamin C in muscle function and gene expression

(2010) G. Dialynas et al.   DEVELOPMENT

Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations

(2010) Juergen Scharner et al.   HUMAN MUTATION

Hereditary muscular dystrophies and the heart

(2010) M.C.E. Hermans et al.   NEUROMUSCULAR DISORDERS

A Comparative Study of Drosophila and Human A-Type Lamins

(2009) Sandra R. Schulze et al.   PLoS One

Sensory mechanisms controlling the timing of larval developmental and behavioral transitions require the Drosophila DEG/ENaC subunit, Pickpocket1

(2008) Joshua A. Ainsley et al.   DEVELOPMENTAL BIOLOGY

Adult stem cell maintenance and tissue regeneration in the ageing context: the role for A-type lamins as intrinsic modulators of ageing in adult stem cells and their niches

(2008) Vanja Pekovic et al.   JOURNAL OF ANATOMY