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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Nuclear receptor interacting protein 1

RIP140, receptor interacting protein 140, Receptor-Interacting Protein, NRIP1
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. [provided by RefSeq, Jul 2008] (from NCBI)
Top mentioned proteins: CAN, ACID, V1a, RIP3, Histone
Papers on RIP140
Evaluation of RIP1K and RIP3K expressions in the malignant and benign breast tumors.
Atri et al., Tehrān, Iran. In Tumour Biol, Feb 2016
UNASSIGNED: Receptor-interacting protein kinase 1 (RIP1K) and RIP3K belong to RIPK family, which regulate cell survival and cell death.
[Comparison of efficiency and cytotoxicity of different transfection reagents in transfecting RIP140-siRNA into Kupffer cells].
Liu et al., Chongqing, China. In Nan Fang Yi Ke Da Xue Xue Bao, Jan 2016
OBJECTIVE: To compare the efficiency and cytotoxicity of different transfection reagents used in transfection of RIP140-siRNA into Kupffer cells to optimize the transfection conditions.
Differential role of RIP1 in Smac mimetic-mediated chemosensitization of neuroblastoma cells.
Fulda et al., Frankfurt am Main, Germany. In Oncotarget, Jan 2016
Mechanistic studies reveal that Receptor-interacting protein (RIP)1 is required for DOX/BV6-, but not for VCR/BV6-induced apoptosis, since transient or stable knockdown of RIP1 or the pharmacological RIP1 inhibitor necrostatin-1 significantly reduce apoptosis.
Cordycepin Suppresses Thymic Stromal Lymphopoietin Expression via Blocking Caspase-1 and Receptor-Interacting Protein 2 Signaling Pathways in Mast Cells.
Jeong et al., In Biol Pharm Bull, Dec 2015
Cordycepin also significantly reduced the phosphorylation of receptor-interacting protein 2 and inhibitory kappa B (IκB) kinase β.
Suppressing Receptor-Interacting Protein 140: a New Sight for Salidroside to Treat Cerebral Ischemia.
Yan et al., Nanjing, China. In Mol Neurobiol, Dec 2015
We also built the stable receptor-interacting protein 140 (RIP140)-overexpressing SH-SY5Y cells.
The emerging role of the transcriptional coregulator RIP140 in solid tumors.
Cavaillès et al., Montpellier, France. In Biochim Biophys Acta, Aug 2015
RIP140 is a transcriptional coregulator (also known as NRIP1) which plays very important physiological roles by finely tuning the activity of a large number of transcription factors.
The serine threonine kinase RIP3: lost and found.
Kim et al., Aurora, United States. In Bmb Rep, Jun 2015
Receptor-interacting protein kinase-3 (RIP3, or RIPK3) is an essential protein in the "programmed", or "regulated" necrosis cell death pathway that is activated in response to death receptor ligands and other types of cellular stress.
Manipulation of apoptosis and necroptosis signaling by herpesviruses.
Mocarski et al., Atlanta, United States. In Med Microbiol Immunol, Jun 2015
Receptor-interacting protein kinase (RIP)3 (also called RIPK3) mediates necrotic death by phosphorylating an executioner protein, MLKL, leading to plasma membrane leakage.
Expression and role of RIP140/NRIP1 in chronic lymphocytic leukemia.
Cavaillès et al., Montpellier, France. In J Hematol Oncol, 2014
RIP140 is a transcriptional coregulator, (also known as NRIP1), which finely tunes the activity of various transcription factors and plays very important physiological roles.
Necroptosis, in vivo detection in experimental disease models.
Vandenabeele et al., Gent, Belgium. In Semin Cell Dev Biol, 2014
Initially, Receptor-Interacting Protein Kinase 1 (RIPK1) and RIPK3 kinase activity were uniquely associated with induction of necroptosis, however recent evidence suggests pleiotropic functions in cell death, inflammation and survival, obscuring a clear picture.
RIPK1 blocks early postnatal lethality mediated by caspase-8 and RIPK3.
Green et al., Memphis, United States. In Cell, 2014
Receptor-interacting protein kinase (RIPK)-1 is involved in RIPK3-dependent and -independent signaling pathways leading to cell death and/or inflammation.
Activity of protein kinase RIPK3 determines whether cells die by necroptosis or apoptosis.
Dixit et al., San Francisco, United States. In Science, 2014
Receptor-interacting protein kinase 1 (RIPK1) and RIPK3 trigger pro-inflammatory cell death termed "necroptosis."
Regulation of RIP1 kinase signalling at the crossroads of inflammation and cell death.
Yuan et al., Boston, United States. In Nat Rev Mol Cell Biol, 2013
Receptor-interacting protein 1 (RIP1) kinase has emerged as a key upstream regulator that controls inflammatory signalling as well as the activation of multiple cell death pathways, including apoptosis and necroptosis.
Phosphorylation of Dishevelled by protein kinase RIPK4 regulates Wnt signaling.
Dixit et al., San Francisco, United States. In Science, 2013
Receptor-interacting protein kinase 4 (RIPK4) is required for epidermal differentiation and is mutated in Bartsocas-Papas syndrome.
Genetic coregulation of age of female sexual maturation and lifespan through circulating IGF1 among inbred mouse strains.
Paigen et al., Bar Harbor, United States. In Proc Natl Acad Sci U S A, 2012
IGF1 may coregulate female sexual maturation and longevity; wild-derived strains carry specific alleles that delay sexual maturation; and Nrip1 is involved in regulating sexual maturation and may affect longevity by regulating IGF1 level.
NF-κB-mediated degradation of the coactivator RIP140 regulates inflammatory responses and contributes to endotoxin tolerance.
Wei et al., Minneapolis, United States. In Nat Immunol, 2012
Our results identify RelA as an adaptor with which the E3 ligase SCF fine tunes NF-kappaB target genes by targeting the coactivator RIP140
A possible 5'-NRIP1/UHRF1-3' fusion gene detected by array CGH analysis in a Ph+ ALL patient.
Lee et al., Oklahoma City, United States. In Cancer Genet, 2011
The fusion of NRIP1 with UHRF1 involved in the unbalanced translocation between chromosomes 19 and 21 in a patient with an ALL-positive for a t(9;22) translocation.
Absence of RIP140 reveals a pathway regulating glut4-dependent glucose uptake in oxidative skeletal muscle through UCP1-mediated activation of AMPK.
Parker et al., London, United Kingdom. In Plos One, 2011
Findings reinforce the participation of RIP140 in the maintenance of energy homeostasis by acting as an inhibitor of energy production.
[Effects of receptor interacting protein 140 on the biological activity of glia cells].
Guo et al., Beijing, China. In Zhonghua Yi Xue Za Zhi, 2011
RIP140 effectively inhibits the proliferation and facilitates the apoptosis of microglioma cells.
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