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The exosomes-containing miR-7-5p is a crucial mediator of bystander autophagy.
we confirmed that the RASSF2-PAR-4 axis was mainly responsible for miR-7 functions in CAFs using bioinformatics methods. Overexpression of miR-7 in CAFs led to down-regulation of RASSF2, which dramatically decreased the secretion of PAR-4 from CAFs and then enhanced the proliferation and migration of the co-cultured cancer cells.
The miR-7 can inhibit the activation of ERK/MAPK (show MAPK1 Proteins) signaling pathway by down-regulating FAK (show PTK2 Proteins) expression, thereby suppressing the proliferation, migration and invasion of NSCLC cells. The miR-7 and its target gene FAK (show PTK2 Proteins) may be novel targets for the diagnosis and treatment of NSCLC.
Serum miR-7 was significantly elevated in the T2DM patients [(401.0+/-34.37) fmol/L, P<0.001] and in the T2DMC patients [(501.4+/-81.69) fmol/L, P<0.001] when compared with the controls [(175.7+/-16.59) fmol/L].
LILRB1 is used for immune evasion by Plasmodium falciparum by associating with RIFINs.
Data indicate the MHC class I-LILRB1 signaling axis as an important regulator of the effector function of innate immune cells.
RT-PCR analysis of serum samples confirmed that miR-7-5p and miR (show MLXIP Proteins)-26b-5p were upregulated in the serum of left ventricular hypertrophy hypertensive patients compared with healthy subjects. Our findings suggest that these miRNAs may play a role in the pathogenesis of hypertensive left ventricular hypertrophy and may represent novel biomarkers for this disease.
LILRB1 ligation during the differentiation of monocytes to dendritic cells in vitro results in increased ABIN1 (show TNIP1 Proteins) expression. ABIN1 (show TNIP1 Proteins) mediates the effects of LILRB1 ligation-induced inhibitory effects on immune responses.
the results support that a regulated assembly of these noncanonical HLA-I conformers during the immune response may enhance the avidity of their interaction with LILRB1.
miR7 negatively regulates PAK1 (show PAK1 Proteins) protein expression but has no effect on PAK1 (show PAK1 Proteins) mRNA expression. Knockdown of PAK1 (show PAK1 Proteins) expression markedly suppressed thyroid cancer cell proliferation, migration and invasion.
This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene.
CD85 antigen-like family member J
, Ig-like transcript 2
, leukocyte immunoglobulin-like receptor subfamily B member 1
, leukocyte immunoglobulin-like receptor subfamily B member 1 soluble isoform
, monocyte/macrophage immunoglobulin-like receptor 7