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Targeted knockdown of the integrin focal adhesion complex components beta-integrin, PINCH (zeige LIMS1 ELISA Kits), and integrin-linked kinase caused formation of multinucleate epidermal cells within the Drosophila larval epidermis.
PINCH (zeige LIMS1 ELISA Kits) and ILK have an independent capacity to localize at muscle attachment sites in vivo.
ILK functions as an essential hub in the assembly of its partner proteins at sites of integrin adhesion.
We conclude that ILK is critical for maintaining the collecting duct epithelium and renal function and is a key intermediate for periostin (zeige POSTN ELISA Kits) activation of signaling pathways involved in cyst growth and fibrosis in PKD (zeige PRKD1 ELISA Kits).
Ilk and ELMO2 (zeige ELMO2 ELISA Kits) modulate recycling endosomes in keratinocytes undergoing intercellular adhesion mediated through cell-cell contacts, including E-cadherin (zeige CDH1 ELISA Kits)-based adherens junctions.
Ilk regulates cellular mechanics facilitating the motility in 3D extracellular matrices.
It was concluded that ILK depletion modifies the transcription of GLUT4 (zeige SLC2A4 ELISA Kits), which results in reduced peripheral insulin (zeige INS ELISA Kits) sensitivity and glucose uptake, suggesting ILK as a molecular target and a prognostic biomarker of insulin (zeige INS ELISA Kits) resistance.
results demonstrate that TGF-beta1 (zeige TGFB1 ELISA Kits)-induced autophagy links beta-catenin (zeige CTNNB1 ELISA Kits) and Smad (zeige SMAD1 ELISA Kits) signaling to promote epithelial-mesenchymal transition in C1.1 cells through a novel pY654-beta-catenin (zeige CTNNB1 ELISA Kits)/p-Smad2 (zeige SMAD2 ELISA Kits)/ILK pathway.
ILK deletion impaired the developmental profile, proliferation, and differentiation of oligodendrocyte precursor cells.
Our results define ILK as a key mechanotransducer in modulating breast cancer stem-like cells development in response to tissue mechanics and oxygen tension.
iNOS (zeige NOS2 ELISA Kits)-derived NO plays a crucial role during atherosclerosis by regulating the endocytic-lysosomal degradation of ILK in endothelial cells.
Hepatic ILK deletion has no effect on insulin (zeige INS ELISA Kits) action in lean mice but sensitizes the liver to insulin (zeige INS ELISA Kits) during the challenge of high fat feeding. This effect corresponds to changes in the expression and activation of key insulin (zeige INS ELISA Kits) signaling pathways as well as a greater capacity for hepatic mitochondrial glucose oxidation.
this study has identified a new role for Parvin (zeige PARVA ELISA Kits) and alphaPix (zeige ARHGEF6 ELISA Kits) downstream of the integrin-ILK signaling axis for mammary epithelial cell differentiation.
Heart failure in recessive embryonic lethal zebrafish mutant main squeeze (msq) mutants is due to a mutation in the integrin-linked kinase (ilk) gene.
The lost-contact mutant on chromosome 10 encodes a nonsense mutation (Y319X) associated with defective cardiomyocytes & endothelial cells that leads to severe myocardial dysfunction. There is epistatic regulation between laminin-alpha4, integrin, & Ilk.
Data show that integrin-linked kinase is an essential component downstream of laminin and integrin alpha7, providing strengthening of skeletal muscle fibre adhesion with the extracellular matrix.
Emodin inhibits the migration and invasion abilities of human endometrial stromal cells by by facilitating the mesenchymal-epithelial transition through targeting integrin-linked kinase.
KRAS-E2F1-ILK-hnRNPA1 regulatory loop enables pancreatic cancer cells to promote oncogenic KRAS signaling and to interact with the tumor microenvironment to promote aggressive phenotypes.
Data indicate a regulatory role for tetraspanin 8 (Tspan8 (zeige TSPAN8 ELISA Kits)) in melanoma progression by modulating cell-matrix interactions through beta1 integrin - integrin-linked kinase (ILK) axis and establish Tspan8 (zeige TSPAN8 ELISA Kits) as a negative regulator of ILK activity.
Overexpression of ILK therefore promoted the proliferation of SHG44 human glioma cells, reduced apoptosis and reduced sensitivity to TMZ via decreasing the activity of caspase3.
Using in vitro studies, we demonstrated that ILK and PI3K (zeige PIK3CA ELISA Kits)/AKT (zeige AKT1 ELISA Kits) inhibitors suppressed the contraction of fibroblast-populated collagen lattices, inhibited fibroblast migration, and interrupted the effect of TGF-beta1 (zeige TGFB1 ELISA Kits) on promoting alpha smooth muscle actin (zeige ACTG2 ELISA Kits) (alpha-SMA (zeige SMN1 ELISA Kits)) expression in fibroblasts.
During human endometrial decidualization, ILK is essential for morphologic transformation of endometrial stromal cells through organization of the actin cytoskeleton.
These data suggest a novel link between Tiam1 and RhoG/ILK /ELMO2 pathway as upstream effectors of the Rac1-mediated phagocytic process in trabecular meshwork cells.
Integrin-linked kinase (ILK, MGC129022) is an important regulator of the endothelial phenotype and vascular network formation by directing the assembly and/or maturation of alpha5beta1-competent matrix-forming adhesions.
Rac1 only partially restores the spreading defects of integrin linked kinasse (ILK)-depleted cells, suggesting that an additional ILK-dependent signal is required for cell spreading.
Profilin (zeige PFN1 ELISA Kits)-dependent dissociation of G-actin (zeige ACTB ELISA Kits)-Tbeta4 complexes simultaneously liberates actin for filament assembly and facilitates Tbeta4 binding to integrin-linked kinase (ILK) in the lamellipodia.
Transduction of extracellular matrix signals through integrins influences intracellular and extracellular functions, and appears to require interaction of integrin cytoplasmic domains with cellular proteins. Integrin-linked kinase (ILK), interacts with the cytoplasmic domain of beta-1 integrin. This gene encodes a serine/threonine protein kinase with 4 ankyrin-like repeats, which associates with the cytoplasmic domain of beta integrins and acts as a proximal receptor kinase regulating integrin-mediated signal transduction. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene.
, Integrin-linked kinase
, integrin linked kinase
, integrin-linked protein kinase
, integrin-linked kinase
, Integrin-linked protein kinase
, integrin binding protein kinase
, main squeeze
, beta-integrin-linked kinase
, 59 kDa serine/threonine-protein kinase
, integrin-linked kinase-2