Results 161 to 170 of about 4,236 (177)
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BAF is required for emerin assembly into the reforming nuclear envelope

Journal of Cell Science, 2001
Mutations in emerin cause the X-linked recessive form of Emery-Dreifuss muscular dystrophy (EDMD). Emerin localizes at the inner membrane of the nuclear envelope (NE) during interphase, and diffuses into the ER when the NE disassembles during mitosis. We analyzed the recruitment of wildtype and mutant GFP-tagged emerin proteins during nuclear envelope ...
T, Haraguchi   +7 more
openaire   +2 more sources

Intracellular trafficking of emerin, the Emery-Dreifuss muscular dystrophy protein

Journal of Cell Science, 1999
ABSTRACT Emerin is an integral protein of the inner nuclear membrane that is mutated or not expressed in patients with Emery-Dreifuss muscular dystrophy. Confocal immunofluorescence microscopy studies of the intracellular targeting of truncated forms of emerin, some of which are found in patients with Emery-Dreifuss muscular dystrophy ...
C, Ostlund   +4 more
openaire   +2 more sources

Emerin and inherited disease

2004
(cont.) nucleus and at the nuclear surface.
openaire   +1 more source

SSCP analysis of the emerin gene

Neuromuscular Disorders, 1996
Luisa Politano, Vincenzo Nigro
openaire   +1 more source

Atrioventricular block in dilated cardiomyopathy and mutation in emerin gene

Medicina Clínica (English Edition), 2023
Néstor, Báez-Ferrer   +2 more
openaire   +2 more sources

Emerin

2008
openaire   +1 more source

Identification of an Emerin–β-Catenin Complex in the Heart Important for Intercalated Disc Architecture and β-Catenin Localisation

Cellular and Molecular Life Sciences, 2010
Elisabeth Ehler   +2 more
exaly  

Multiple and Surprising New Functions for Emerin, a Nuclear Membrane Protein

Current Opinion in Cell Biology, 2004
Katherine L Wilson
exaly  

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