Isolation of proteins that interact specifically with the retinoid X receptor: two novel orphan receptors
about
SMRTe, a silencing mediator for retinoid and thyroid hormone receptors-extended isoform that is more related to the nuclear receptor corepressorA new family of nuclear receptor coregulators that integrate nuclear receptor signaling through CREB-binding proteinDefinition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesisActivation of the orphan receptor RIP14 by retinoidsGRIP1, a novel mouse protein that serves as a transcriptional coactivator in yeast for the hormone binding domains of steroid receptorsPeroxisome proliferator-activated receptor-gamma coactivator 1alpha (PGC-1alpha) regulates triglyceride metabolism by activation of the nuclear receptor FXRMolecular mechanisms involved in farnesol-induced apoptosisIdentification of E-box factor TFE3 as a functional partner for the E2F3 transcription factorHepatic cholesterol metabolism and resistance to dietary cholesterol in LXRbeta-deficient micePlant sterols as anticancer nutrients: evidence for their role in breast cancerFXR signaling in the enterohepatic systemRole of farnesoid X receptor and bile acids in alcoholic liver diseaseFarnesoid X receptor: a master regulator of hepatic triglyceride and glucose homeostasisHeterodimeric interaction between retinoid X receptor alpha and orphan nuclear receptor OR1 reveals dimerization-induced activation as a novel mechanism of nuclear receptor activationPoly(ADP-ribose) polymerase 1 promotes oxidative-stress-induced liver cell death via suppressing farnesoid X receptor α.Deletion of mouse FXR gene disturbs multiple neurotransmitter systems and alters neurobehaviorNSAIDs Ibuprofen, Indometacin, and Diclofenac do not interact with Farnesoid X Receptor.Coordinated Actions of FXR and LXR in Metabolism: From Pathogenesis to Pharmacological Targets for Type 2 DiabetesIdentification of novel pathways that control farnesoid X receptor-mediated hypocholesterolemia.Transcriptional silencing is defined by isoform- and heterodimer-specific interactions between nuclear hormone receptors and corepressorsUrinary metabolomics in Fxr-null mice reveals activated adaptive metabolic pathways upon bile acid challengeSterol upregulation of human CETP expression in vitro and in transgenic mice by an LXR elementRegulation of thyroid hormone activation via the liver X-receptor/retinoid X-receptor pathway.A structural model of the constitutive androstane receptor defines novel interactions that mediate ligand-independent activityDeciphering the nuclear bile acid receptor FXR paradigm.Regulation of FXR transcriptional activity in health and disease: Emerging roles of FXR cofactors and post-translational modificationsTissue-specific function of farnesoid X receptor in liver and intestineFarnesoid X receptor, overexpressed in pancreatic cancer with lymph node metastasis promotes cell migration and invasion.Targeting of N-CoR and histone deacetylase 3 by the oncoprotein v-erbA yields a chromatin infrastructure-dependent transcriptional repression pathwayBile acid-activated nuclear receptor FXR suppresses apolipoprotein A-I transcription via a negative FXR response element.Studies in mice, hamsters, and rats demonstrate that repression of hepatic apoA-I expression by taurocholic acid in mice is not mediated by the farnesoid-X-receptorThe bile acid membrane receptor TGR5: a valuable metabolic target.Nuclear receptors in renal diseaseNuclear receptors in nonalcoholic Fatty liver diseaseGenome-wide profiling of liver X receptor, retinoid X receptor, and peroxisome proliferator-activated receptor α in mouse liver reveals extensive sharing of binding sitesDirect modulation of simian virus 40 late gene expression by thyroid hormone and its receptor.Structural Basis for Small Molecule NDB (N-Benzyl-N-(3-(tert-butyl)-4-hydroxyphenyl)-2,6-dichloro-4-(dimethylamino) Benzamide) as a Selective Antagonist of Farnesoid X Receptor α (FXRα) in Stabilizing the Homodimerization of the Receptor.FXR and liver carcinogenesisYeast hormone response element assays detect and characterize GRIP1 coactivator-dependent activation of transcription by thyroid and retinoid nuclear receptorsAn Intestinal Microbiota-Farnesoid X Receptor Axis Modulates Metabolic Disease.
P2860
Q22009109-6483CC90-E186-4ECB-B4B6-53B4FF57F1B8Q22254332-BBB7C6CF-3A9B-46CB-AEE5-D78DF64FC112Q24305561-2FE26ED3-2729-4993-A57D-3EB20E1528AEQ24317351-187F8E8F-8FD1-4BF3-9B53-6EB5B893CDFAQ24600501-1E45C9B4-6A62-48BC-A548-3ECCCA5B92A1Q24623871-F3BDAB62-FEB4-4362-8EF3-362B472A2F67Q24655100-286035EE-24FC-4307-9FF2-515A2392F8C5Q24673143-A6B1E781-A456-4624-B41A-1BA6E1A04AE2Q24681140-77322F89-5528-4E32-8F16-E2BBBC366543Q26861053-6E9055F6-3714-4386-98CF-B7AE04CB908AQ27014753-3FC25CC8-D526-4530-BC9A-A5F2F0CA3E54Q28086898-F94B29BD-6379-4605-AEB9-B9BE2CDB9854Q28253815-9693BFF3-004B-4A5D-B4FC-8A1EF7785BA7Q28569572-13E19F5B-033F-46AC-8A7C-23AEE6C1BB7FQ30557596-F2705BE2-792C-4234-9AF9-BDD32DB0CC14Q30633123-E9F0C129-E491-44A0-9CF0-A507C16B04E5Q30666362-78DBA097-62DA-423E-A607-2E5A3BE5E557Q33608251-AE254DB2-E28F-4D7D-AE7C-25489C5C7A42Q33661459-2ACE1234-C899-40B6-A0C5-8DCDDE015161Q33780043-FD6B9905-412B-4979-9FF2-2C6ACFCF2917Q33784497-BB4683ED-4948-44D8-A327-4D7134362B5CQ33939047-8686F934-01CC-4E20-837E-AFFB256DD158Q34100137-BF877A78-7B6C-4F4E-932A-3730A008A2FCQ34283520-09CB1CC1-8F5A-4914-A9FA-51E4979FD064Q34626518-B76CC915-C233-4C15-B0E0-AA0392437236Q34694229-DD92841C-8E62-49EC-BC32-BABAF98936BAQ34714107-A9990883-CAA5-4C51-8165-483A476B1CE6Q34727267-FC0D92B3-B511-4D49-9C18-79D25B471755Q34732688-06021F54-5FE1-4A7A-B821-C1FE69AB7BFDQ34790389-6AC66C74-6C27-4E01-BF73-9C53246FCA60Q34955918-C4A3BFCA-75C7-425C-BB0A-85D713AEB508Q35082232-45C4CEAF-46DB-46DA-ABBA-3844FB2248C3Q35120702-A9BDBE2A-6FCF-42B5-97B3-BA44470DE557Q35609154-D39453E9-E52B-4B48-B1B7-33EC537C8431Q35739204-2EB985E8-E7BA-479E-AA40-B1BBA20C4040Q35875001-26C65D8F-E398-4730-9540-84182108B87EQ35925879-C79CFED6-6FB2-4592-84CC-80EE68950B1FQ36063712-3BDB2841-0F05-45C7-B3D4-7249127AE243Q36104499-2E018234-E938-43AF-8CA3-772894E0813DQ36136449-F2E9B734-4BDB-40C9-BF4C-B4F103A9B992
P2860
Isolation of proteins that interact specifically with the retinoid X receptor: two novel orphan receptors
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Isolation of proteins that int ...... or: two novel orphan receptors
@ast
Isolation of proteins that int ...... or: two novel orphan receptors
@en
Isolation of proteins that int ...... or: two novel orphan receptors
@nl
type
label
Isolation of proteins that int ...... or: two novel orphan receptors
@ast
Isolation of proteins that int ...... or: two novel orphan receptors
@en
Isolation of proteins that int ...... or: two novel orphan receptors
@nl
prefLabel
Isolation of proteins that int ...... or: two novel orphan receptors
@ast
Isolation of proteins that int ...... or: two novel orphan receptors
@en
Isolation of proteins that int ...... or: two novel orphan receptors
@nl
P2093
P921
P356
P1476
Isolation of proteins that int ...... or: two novel orphan receptors
@en
P2093
P356
10.1210/MEND.9.1.7760852
P407
P577
1995-01-01T00:00:00Z