Results 41 to 50 of about 21,470 (214)

Protein interactions at the higher plant nuclear envelope: evidence for a Linker of Nucleoskeleton and Cytoskeleton complex.

open access: yesFrontiers in Plant Science, 2014
Following the description of SAD1/UNC84 (SUN) domain proteins in higher plants, evidence has rapidly increased that plants contain a functional Linker of Nucleoskeleton and Cytoskeleton (LINC) complex bridging the nuclear envelope (NE).
David Edgar Evans   +3 more
doaj   +1 more source

The Role of the LINC Complex in Sperm Development and Function. [PDF]

open access: yesInt J Mol Sci, 2020
The LINC (LInker of Nucleoskeleton and Cytoskeleton) complex is localized within the nuclear envelope and consists of SUN (Sad1/UNc84 homology domain-containing) proteins located in the inner nuclear membrane and KASH (Klarsicht/Anc1/Syne1 homology domain-containing) proteins located in the outer nuclear membrane, hence linking nuclear with cytoplasmic
Kmonickova V   +3 more
europepmc   +4 more sources

The miR-223 host non-coding transcript linc-223 induces IRF4 expression in acute myeloid leukemia by acting as a competing endogenous RNA [PDF]

open access: yes, 2016
Alterations in genetic programs required for terminal myeloid differentiation and aberrant proliferation characterize acute myeloid leukemia (AML) cells.
Bozzoni, Irene   +8 more
core   +2 more sources

Molecular models of LINC complex assembly at the nuclear envelope [PDF]

open access: yesJournal of Cell Science, 2021
ABSTRACT Large protein complexes assemble at the nuclear envelope to transmit mechanical signals between the cytoskeleton and nucleoskeleton. These protein complexes are known as the linkers of the nucleoskeleton and cytoskeleton complexes (LINC complexes) and are formed by the interaction of SUN and KASH domain proteins in the nuclear ...
Zeinab Jahed   +4 more
openaire   +2 more sources

Pushing the (nuclear) envelope into meiosis. [PDF]

open access: yes, 2013
A recent study shows that a short isoform of a mammalian nuclear lamin is important for homologous chromosome interactions during meiotic prophase in ...
Dernburg, Abby F
core   +1 more source

Cell Mechanosensitivity Is Enabled by the LINC Nuclear Complex [PDF]

open access: yesCurrent Molecular Biology Reports, 2016
Mechanoresponses in mesenchymal stem cells (MSCs) guide both differentiation and function. In this review, we focus on advances in0 our understanding of how the cytoplasmic cytoskeleton, nuclear envelope and nucleoskeleton, which are connected via LINC (Linker of Nucleoskeleton and Cytoskeleton) complexes, are emerging as an integrated dynamic ...
Gunes, Uzer   +2 more
openaire   +2 more sources

The LINC Between Mechanical Forces and Chromatin

open access: yesFrontiers in Physiology, 2021
The heart continually senses and responds to mechanical stimuli that balance cardiac structure and activity. Tensile forces, compressive forces, and shear stress are sensed by the different cardiac cell types and converted into signals instructing proper
Olga Lityagina   +2 more
doaj   +1 more source

Increasing the talk-time of mobile radios with efficient linear transmitter architectures [PDF]

open access: yes, 2000
In order to meet the linearity specification of standards such as GSM EDGE and TETRA the power amplifier (PA) linearisation methods in common usage today result in low DC to RF efficiency (e.g. Cartesian loop and adaptive predistortion).
Beach, MA   +3 more
core   +2 more sources

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization. [PDF]

open access: yesPLoS Genetics, 2014
Proteins of the nuclear envelope (NE) are associated with a range of inherited disorders, most commonly involving muscular dystrophy and cardiomyopathy, as exemplified by Emery-Dreifuss muscular dystrophy (EDMD).
Peter Meinke   +10 more
doaj   +1 more source

LINC complex alterations in DMD and EDMD/CMT fibroblasts [PDF]

open access: yesEuropean Journal of Cell Biology, 2012
Emery-Dreifuss muscular dystrophy (EDMD) is a late onset-disease characterized by skeletal muscle wasting and heart defects with associated risk of sudden death. The autosomal dominant form of the disease is caused by mutations in the LMNA gene encoding LaminA and C, the X-linked form results from mutations in the gene encoding the inner nuclear ...
Taranum, Surayya   +8 more
openaire   +2 more sources

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