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results indicated that there was a significant association between migraine and gene-gene interaction among the CYP19A1 (show CYP19A1 ELISA Kits), FSHR (show FSHR ELISA Kits), ESR1 (show ESR1 ELISA Kits) and NRIP1.
Data indicate that nuclear receptor interacting protein 1 (NRIP1) is elevated in tumors compared to cancer adjacent normal tissue.
NOP14 (show Nop14 ELISA Kits) suppresses breast cancer progression by inhibiting NRIP1/Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) pathway.
NRIP1 contributes to the mitochondrial dysfunction observed in DS. Furthermore, they suggest that the NRIP1-PGC-1alpha (show PPARGC1A ELISA Kits) 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 (show FAM126A ELISA Kits) cells in vitro.
Data suggest that vitamin D receptor target genes (NRIP1; DUSP10, dual specificity phosphatase 10; THBD, thrombomodulin; TRAK1, trafficking protein kinesin binding 1) 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.
The associations of rs2616984 in CSMD1 gene, putative associations of rs3131296 in NOTCH4 (show NOTCH4 ELISA Kits) gene, and associations of rs2229741 of NRIP1 gene with Alzheimer's disease have been found in a Russian population.
data suggest that RIP140 plays an important role in ERalpha (show ESR1 ELISA Kits)-mediated transcriptional regulation in breast cancer and response to tamoxifen treatment
RIP140 protects LSD1's catalytic domain and antagonizes its Jade-2-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 (show NPY ELISA Kits) within hypothalamic astrocyte population, which might be associated with the observed behavioral phenotype of MPhiRIPKD mice.
RIP140 knockdown in macrophages led to significant white adipose tissue browning, improved systemic insulin (show INS ELISA Kits) sensitivity, particularly under high fat diet feeding, and an altered adipose tissue macrophage profile.
RIP140 blocks the BRITE program in white adipose tissue.
RIP140 stimulated APC (show APC ELISA Kits) transcription and inhibited beta-catenin (show CTNNB1 ELISA Kits) activation and target gene expression.
RIP140 regulates mammary gland development by promoting the generation of key mitogenic signals.
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