Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype
about
A visual screen of a GFP-fusion library identifies a new type of nuclear envelope membrane proteinMammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processesLoss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophyThe nuclear envelope LEM-domain protein emerinBuilding a nuclear envelope at the end of mitosis: coordinating membrane reorganization, nuclear pore complex assembly, and chromatin de-condensationThe endonuclease Ankle1 requires its LEM and GIY-YIG motifs for DNA cleavage in vivoAbnormal nuclear shape and impaired mechanotransduction in emerin-deficient cellsThe Inner Nuclear Membrane Protein Nemp1 Is a New Type of RanGTP-Binding Protein in EukaryotesAn in vitro nuclear disassembly system reveals a role for the RanGTPase system and microtubule-dependent steps in nuclear envelope breakdown.Further characterisation of the molecular signature of quiescent and activated mouse muscle satellite cells.New role for EMD (emerin), a key inner nuclear membrane protein, as an enhancer of autophagosome formation in the C16-ceramide autophagy pathwayBarrier-to-autointegration factor phosphorylation on Ser-4 regulates emerin binding to lamin A in vitro and emerin localization in vivo.LINC complexes in health and disease.SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeletonAbnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophyEmerin in health and disease.Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type laminsMechanical properties of the cell nucleus and the effect of emerin deficiency.Sumoylated protein tyrosine phosphatase 1B localizes to the inner nuclear membrane and regulates the tyrosine phosphorylation of emerinEmerin is hyperphosphorylated and redistributed in herpes simplex virus type 1-infected cells in a manner dependent on both UL34 and US3.Nuclear lamins in the brain - new insights into function and regulation.Muscular Dystrophy Mutations Impair the Nuclear Envelope Emerin Self-assembly PropertiesSignificance of host cell kinases in herpes simplex virus type 1 egress and lamin-associated protein disassembly from the nuclear lamina.Incorporation of the nuclear pore basket protein nup153 into nuclear pore structures is dependent upon lamina assembly: evidence from cell-free extracts of Xenopus eggs.Herpes simplex virus infection induces phosphorylation and delocalization of emerin, a key inner nuclear membrane protein.Tyrosine phosphorylation of nuclear-membrane protein emerin by Src, Abl and other kinases.
P2860
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P2860
Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@ast
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@en
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@nl
type
label
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@ast
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@en
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@nl
prefLabel
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@ast
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@en
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@nl
P2093
P1476
Aberrant intracellular targeti ...... s muscular dystrophy phenotype
@en
P2093
J Kendrick-Jones
P304
P407
P478
111 ( Pt 6)
P577
1998-03-01T00:00:00Z