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Taken together, these results provide new insights into the mechanism of action of LCoR (zeige Lcor Proteine) and RIP140 and highlight their strong interplay for the control of gene expression and cell proliferation in breast cancer cells.
Study found low expression level of RIP140 in tumor-associated macrophages (TAM (zeige CCNA1 Proteine)) of hepatocellular carcinoma (HCC (zeige FAM126A Proteine)) tissues and demonstrated that RIP140 expression in plays a role in the growth of hepatoma cells.
results indicated that there was a significant association between migraine and gene-gene interaction among the CYP19A1 (zeige CYP19A1 Proteine), FSHR (zeige FSHR Proteine), ESR1 (zeige ESR1 Proteine) and NRIP1.
Data indicate that nuclear receptor interacting protein 1 (NRIP1) is elevated in tumors compared to cancer adjacent normal tissue.
NOP14 (zeige Nop14 Proteine) suppresses breast cancer progression by inhibiting NRIP1/Wnt (zeige WNT2 Proteine)/beta-catenin (zeige CTNNB1 Proteine) pathway.
NRIP1 contributes to the mitochondrial dysfunction observed in DS. Furthermore, they suggest that the NRIP1-PGC-1alpha axe might represent a potential therapeutic target for restoring altered mitochondrial function in DS.
RIP140 gene has been shown to be involved in the regulation of energy expenditure, in mammary gland development and intestinal homeostasis as well as in behavior and cognition
Downregulation of RIP140 promoted the tumorigenicity of HCC (zeige FAM126A Proteine) cells in vitro.
Data suggest that vitamin D receptor (zeige VDR Proteine) target genes (NRIP1; DUSP10 (zeige DUSP10 Proteine), dual specificity phosphatase 10 (zeige DUSP10 Proteine); THBD (zeige THBD Proteine), thrombomodulin (zeige THBD Proteine); TRAK1 (zeige TRAK1 Proteine), trafficking protein kinesin binding 1 (zeige TRAK1 Proteine)) can be used as markers for individual's response to vitamin D3 supplements.
RIP140 negatively regulated the macrophage expression of ATP-binding cassette transporters A1 and G1.
It is able to modulate the transcription of certain genes involved in AD pathology, such as b-APP (zeige APP Proteine) cleaving enzyme (BACE1 (zeige BACE Proteine)) and GSK3. Consequently, we found that RIP140 overexpression reduced the generation of Ab in a neuroblastoma (zeige ARHGEF16 Proteine) cell line by decreasing the transcription of b-APP (zeige APP Proteine) cleaving enzyme via a PPARge dependent mechanism.
These data indicate that dominant NRIP1 mutations can cause kidney and urinary tract by interference with retinoic acid transcriptional signaling, shedding light on the well documented association between abnormal vitamin A levels and renal malformations in humans, and suggest a possible gene-environment pathomechanism in this disease
RIP140 has a unique role in the acute effect of beta-3 adrenergic receptor (zeige ADRB3 Proteine) activation.
depletion of receptor-interacting protein 140 could significantly alleviate the inhibitory effects of estrogen on osteoclasts formation and bone resorption activity.
RIP140 protects LSD1 (zeige KDM1A Proteine)'s catalytic domain and antagonizes its Jade-2 (zeige PHF15 Proteine)-mediated ubiquitination and degradation.
Nuclear receptor interacting protein 140 (RIP140) is an identified nuclear receptor corepressor that has been shown to suppress mitochondrial biogenesis in skeletal muscle.
Data show that 7,12-dimethylbenzanthracene (DMBA)-induced carcinogenesis is suppressed in nuclear receptor interacting protein 1 (Nrip1) knockout mice.
RIP140 plays an important role in maintaining brain cholesterol homeostasis through, partially, regulating cholesterol metabolism in, and mobilization from, astrocyte.
RIP140 translocation to the cytoplasm is an early response to ER stress and provides protection against neuronal death.
Study revealed an emotional regulatory function of macrophage-derived RIP140 in the VMH, and secondary dysregulation of NPY (zeige NPY Proteine) within hypothalamic astrocyte population, which might be associated with the observed behavioral phenotype of MPhiRIPKD mice.
Nuclear receptor interacting protein 1 (NRIP1) is a nuclear protein that specifically interacts with the hormone-dependent activation domain AF2 of nuclear receptors. Also known as RIP140, this protein modulates transcriptional activity of the estrogen receptor.
nuclear receptor interacting protein 1
, nuclear receptor-interacting protein 1-like
, nuclear factor RIP140
, nuclear receptor-interacting protein 1
, receptor interacting protein 140
, receptor-interacting protein 140