<p>Our model is based on the actin cortical network at the cell surface of erythrocytes, except that lamin filaments also anchor to emerin-based junctional complexes. Spectrin heterodimers bind short actin filaments at the erythrocyte membrane; we therefore speculate that nuclear isoforms of αII-spectrin (J. M. H. and K. L. W., unpublished data) act similarly. Direct binding of emerin and αII-spectrin has not yet been tested. Nuclear isoforms of protein 4.1, which are essential for nuclear assembly (<a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.0020231#pbio-0020231-Krauss1" target="_blank">Krauss et al. 2002</a>), have the potential to cross-link short actin filaments and spectrin filaments at the inner membrane ...
Emerin is a type II inner nuclear membrane (INM) protein of unknown function. Emerin function is lik...
The nuclear envelope (NE) comprises two membranes (inner and outer) with embedded nuclear pore compl...
More than 100 genetic mutations causing X-linked Emery–Dreifuss muscular dystrophy have been identif...
X-linked Emery-Dreifuss muscular dystrophy is caused by loss of emerin, a LEM-domain protein of the ...
The type II inner nuclear membrane protein emerin is a component of the LINC complex that connects t...
β-dystroglycan (β-DG) assembles with lamins A/C and B1 and emerin at the nuclear envelope (NE) to ma...
The actin cortex is a thin network coupled to the plasma membrane of cells, responsible for e.g., ce...
In this review we discuss some of the proteins for which a role in linking actin to the fibroblast p...
Physical interactions between lamins and emerin were investigated by co-immunoprecipitation of in vi...
AbstractNesprin-1α is a spectrin repeat (SR)-containing, transmembrane protein of the inner nuclear ...
Structural protein 4.1, which has crucial interactions within the spectin-actin lattice of the human...
International audienceHuman emerin is an inner nuclear membrane protein involved in the response of ...
The nuclear envelope (NE) plays a fundamental role in the cell by separating nuclear from cytoplasmi...
Emerin is a type II inner nuclear membrane (INM) protein of unknown function. Emerin function is lik...
Emerin is a nuclear envelope protein whose biological function remains to be elucidated. Mutations o...
Emerin is a type II inner nuclear membrane (INM) protein of unknown function. Emerin function is lik...
The nuclear envelope (NE) comprises two membranes (inner and outer) with embedded nuclear pore compl...
More than 100 genetic mutations causing X-linked Emery–Dreifuss muscular dystrophy have been identif...
X-linked Emery-Dreifuss muscular dystrophy is caused by loss of emerin, a LEM-domain protein of the ...
The type II inner nuclear membrane protein emerin is a component of the LINC complex that connects t...
β-dystroglycan (β-DG) assembles with lamins A/C and B1 and emerin at the nuclear envelope (NE) to ma...
The actin cortex is a thin network coupled to the plasma membrane of cells, responsible for e.g., ce...
In this review we discuss some of the proteins for which a role in linking actin to the fibroblast p...
Physical interactions between lamins and emerin were investigated by co-immunoprecipitation of in vi...
AbstractNesprin-1α is a spectrin repeat (SR)-containing, transmembrane protein of the inner nuclear ...
Structural protein 4.1, which has crucial interactions within the spectin-actin lattice of the human...
International audienceHuman emerin is an inner nuclear membrane protein involved in the response of ...
The nuclear envelope (NE) plays a fundamental role in the cell by separating nuclear from cytoplasmi...
Emerin is a type II inner nuclear membrane (INM) protein of unknown function. Emerin function is lik...
Emerin is a nuclear envelope protein whose biological function remains to be elucidated. Mutations o...
Emerin is a type II inner nuclear membrane (INM) protein of unknown function. Emerin function is lik...
The nuclear envelope (NE) comprises two membranes (inner and outer) with embedded nuclear pore compl...
More than 100 genetic mutations causing X-linked Emery–Dreifuss muscular dystrophy have been identif...