Results 21 to 30 of about 3,007 (176)

The role of SYNE1/2 variants as a potential predisposition factor for the onset of endometriosis [PDF]

open access: yesFrontiers in Immunology
Endometriosis (EM) is a chronic, inflammatory gynaecological disorder defined by the presence of endometrial-like tissue outside the uterine cavity, most frequently affecting the ovaries, peritoneum, and uterosacral ligaments.
Aurora Santin   +19 more
doaj   +2 more sources

Mouse models of nesprin-related diseases [PDF]

open access: yesBiochemical Society Transactions, 2018
Nesprins (nuclear envelope spectrin repeat proteins) are a family of multi-isomeric scaffolding proteins. Nesprins form the LInker of Nucleoskeleton-and-Cytoskeleton (LINC) complex with SUN (Sad1p/UNC84) domain-containing proteins at the nuclear envelope,
Derek T. Warren   +9 more
core   +5 more sources

Apoptosis-induced translocation of nesprin-2 from the nuclear envelope to mitochondria is associated with mitochondrial dysfunction

open access: yesNucleus
Accumulating evidence suggests that the nuclear envelope (NE) is not just a target, but also a mediator of apoptosis. We showed recently that the NE protein nesprin-2 has pro-apoptotic activity, which involves its subcellular redistribution and Bcl-2 ...
Cecilia Östlund   +2 more
exaly   +3 more sources

Targeted ablation of nesprin 1 and nesprin 2 from murine myocardium results in cardiomyopathy, altered nuclear morphology and inhibition of the biomechanical gene response.

open access: yesPLoS Genetics, 2014
Recent interest has focused on the importance of the nucleus and associated nucleoskeleton in regulating changes in cardiac gene expression in response to biomechanical load.
Indroneal Banerjee   +11 more
doaj   +5 more sources

Elevated SUN1 promotes migratory cell polarity defects through mechanically coupling microtubules to the nuclear lamina [PDF]

open access: yesCommunications Biology
In migratory fibroblasts, front-rear polarity is defined by the centrosome positioned anterior to a rearward nucleus. To achieve this polarity, actin cables couple to nuclear membrane proteins nesprin-2G and SUN2 and drive the nucleus backward.
Yutao Li   +7 more
doaj   +2 more sources

Detection of Diverse and High Molecular Weight Nesprin-1 and Nesprin-2 Isoforms Using Western Blotting

open access: yes, 2016
Heavily utilized in cell and molecular biology, western blotting is considered a crucial technique for the detection and quantification of proteins within complex mixtures. In particular, the detection of members of the nesprin (nuclear envelope spectrin
Iakowos Karakesisoglou   +3 more
core   +3 more sources

Tension-sensitive LINC-RhoA signaling prevents chromatin bridge breakage in cytokinesis [PDF]

open access: yesThe EMBO Journal
In the presence of chromatin bridges in cytokinesis, human cells retain actin-rich structures (actin patches) at the base of the intercellular canal to prevent chromosome breakage.
Sofia Balafouti   +3 more
doaj   +2 more sources

Vimentin molecular linkages with nesprin-3 enhance nuclear deformations by cell geometric constraints [PDF]

open access: yesScientific Reports
The nucleus is the organelle of the cell responsible for controlling protein expression, which has a direct effect on cellular biological functions. Here we show that the cytoskeletal protein vimentin plays an important role in increasing the amount of ...
Maxx Swoger   +9 more
doaj   +2 more sources

Nesprin proteins: bridging nuclear envelope dynamics to muscular dysfunction

open access: yesCell Communication and Signaling
This review presents a comprehensive exploration of the pivotal role played by the Linker of Nucleoskeleton and Cytoskeleton (LINC) complex, with a particular focus on Nesprin proteins, in cellular mechanics and the pathogenesis of muscular diseases ...
Zhou Zi-yi   +4 more
doaj   +3 more sources

Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton. [PDF]

open access: yes, 2009
Meckel-Gruber syndrome (MKS) is a severe autosomal recessively inherited disorder caused by mutations in genes that encode components of the primary cilium and basal body.
HR Dawe (21822902)   +7 more
core   +6 more sources

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