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Adiponectin (show ADIPOQ Proteins) and adiponectin (show ADIPOQ Proteins) receptor genes are coexpressed during zebrafish embryogenesis and regulated by food deprivation
Decreased expression of ADIPOR1 is associated with polycystic ovary syndrome.
sequence- and structure-based computational tools were employed in this study to functionally and structurally characterize the coding Nonsynonymous Single Nucleotide Polymorphisms of ADIPOR1 gene listed in the single nucleotide polymorphisms database.
PCR results showed expression of adiponectin (show ADIPOQ Proteins), AdipoR1, AdipoR2 (show ADIPOR2 Proteins), follicle-stimulating hormone receptor (FSHR (show FSHR Proteins)), and luteinizing hormone receptor (LHR (show LHCGR Proteins)) in granulosa cells (GCs (show GCLC Proteins)). After controlling body mass index (BMI) values, qRT-PCR demonstrated a decreased expression of adiponectin (show ADIPOQ Proteins) system in GCs (show GCLC Proteins) of polycystic ovary syndromepatients compared to those in controls
ADPOR1 variants, rs3737884*G and rs7514221*C, may be shared risk factors associated with CAD, T2D, and T2D with CAD in a population of northeast China.
Expression of AdipoR1 gene receptor was increased in endometriotic stromal cells.
miR (show MLXIP Proteins)-323 may increase VEGF-A (show VEGFA Proteins)-mediated cancer vascularization in PC cells through AdipoR1 suppression.
We did not find any significant associations with ADIPOR1 gene variants and fasting plasma triglycerides in HIV-infected patients.
In conclusion, neutrophil AdipoRs (AdipoR1, AdipoR2 (show ADIPOR2 Proteins)) upregulation was associated with early stages of vascular injury, hypertension severity, and low serum levels of adiponectin (show ADIPOQ Proteins)
The ADIPOR1 rs1342387(G/A) polymorphism, but not rs12733285(C/T) or rs7539542(C/G), may be associated with cancer risk, especially risk of colorectal cancer in Asians.
Results demonstrate that the non-conserved N-terminal trunks dictate the cell-surface expression and temporal signaling profiles of AdipoR1 and AdipoR2 (show ADIPOR2 Proteins).
This study demonstrated the presence of adiponectin (show ADIPOQ Proteins) and its receptors in the uteri, conceptuses, and trophoblasts of pregnant pigs and that the local adiponectin (show ADIPOQ Proteins) system is dependent on the stage of pregnancy.
Data suggest AdipoR1/adiponectin (show ADIPOQ Proteins) signaling up-regulates gene expression of hepatocyte enzymes involved in fatty acid metabolism and protects hepatocyte from nonesterified fatty acids by activating phosphatidylinositol 3-kinase (PI3K/AKT (show AKT1 Proteins)) signaling.
study demonstrated that adiponectin (show ADIPOQ Proteins) and adiponectin (show ADIPOQ Proteins) receptors 1 and 2 messenger RNAs and proteins are present in the porcine hypothalamus and that their expression levels are determined by the pig's endocrine status related to the oestrous cycle
This study demonstrated the presence of adiponectin (show ADIPOQ Proteins), AdipoR1 and AdipoR2 (show ADIPOR2 Proteins) genes and proteins in the porcine uterus and the effect of the stage of the oestrous cycle on the expression of the adiponectin (show ADIPOQ Proteins) system.
Data indicate that AdipoR1 and AdipoR2 (show ADIPOR2 Proteins) mRNAs and proteins are present in the porcine pituitary and that adiponectin (show ADIPOQ Proteins) receptors expression is dependent on endocrine status of the animals.
Results showed a high polymorphism of the ADIPOR1 and a complexity in its transcription level in longissimus dorsi from five pig breeds: Duroc, Polish Large White, Polish Landrace, Pietrain and Pulawska.
The cloning and characterization of adiponectin (show ADIPOQ Proteins), ADIPOR1, and ADIPOR2 (show ADIPOR2 Proteins) are reported.
FISH localization of 4 BAC clones harbouring potential candidate genes for fatness traits: DGAT1 (show DGAT1 Proteins) (SSC4p15), PPARA (show PPARA Proteins) (SSC5p15), ADIPOR1 (SSC10p13) and CREB (show CREB1 Proteins) (SSC15q24)
Insulin (show INS Proteins) regulates the expression of adiponectin (show ADIPOQ Proteins) and adiponectin (show ADIPOQ Proteins) receptors in porcine adipocytes.
Low level expression of adiponectin (show ADIPOQ Proteins) mRNA was found in all areas of bovine mammary gland tissues examined. AdipoR1 and AdipoR2 (show ADIPOR2 Proteins) mRNAs were also detected in mammary tissues and their expression was particularly prominent in the parenchyma and cistern.
The physiologic status of the ovary has significant effects on the natural expression patterns of adiponectin (show ADIPOQ Proteins) and its receptors in follicular and luteal cells of bovine ovary.
High salt is an important suppressor of cardioprotective APN (show ANPEP Proteins) and AdipoR1 in cardiac myocytes.
AdipoR1, not AdipoR2 (show ADIPOR2 Proteins), was first identified as a receptor of CTRP6 during the process of mitotic clonal expansion. Collectively, we suggest that CTRP6 mediates the ectopic lipogenesis through AdipoR1/Erk (show EPHB2 Proteins)/PPARgamma (show PPARG Proteins) signaling pathway in myoblasts.
The results demonstrated a dynamic dysfunction of APN (show ANPEP Proteins)/AdipoR1 axis accompanying progression of diabetes mellitus in mice with cerebral ischemia.
physiologic adiponectin (show ADIPOQ Proteins) levels enhance the vasorelaxative response to acetylcholine by inducing nitric oxide production through AdipoR1/Cav-1 (show CAV1 Proteins) mediated signaling.
AdipoR1 is expressed on adipose tissue-resident Tregs, mainly Helios (show ZNFN1A2 Proteins)(+) Tregs, and this expression is dependent on weight and fat accumulation. This data proposes a new mechanism through which weight gain might alter immunoregulation.
Adiponectin (show ADIPOQ Proteins) directly acts on murine dermal gammadelta-T cells to suppress IL-17 (show IL17A Proteins) synthesis via AdipoR1.
At high glucose concentrations in vitro, AdipoR1 regulated the survival of neural stem cells through the p53 (show TP53 Proteins)/p21 pathway and the proliferation- and differentiation-related factors of neural stem cells via TLX (show NR2E1 Proteins).
Electroacupuncture induces protective effects against cerebral ischemia through AdipoR1-mediated phosphorylation of GSK-3Beta.
lack of AdipoR1 impairs myocardial mitochondrial function and coupling, suggesting that impaired AdipoR1 signaling may contribute to mitochondrial dysfunction and mitochondrial uncoupling in Type 2 diabetic hearts.
AdipoR1 overexpression in retinal pigment epithelium cells enhances docosahexaenoic acid uptake, whereas AdipoR1 silencing has the opposite effect.
This gene encodes a protein which acts as a receptor for adiponectin, a hormone secreted by adipocytes which regulates fatty acid catabolism and glucose levels. Binding of adiponectin to the encoded protein results in activation of an AMP-activated kinase signaling pathway which affects levels of fatty acid oxidation and insulin sensitivity. A pseudogene of this gene is located on chromosome 14.
adiponectin receptor 1
, adiponectin receptor type I
, adiponectin receptor protein 1-like
, adiponectin receptor protein 1
, progestin and adipoQ receptor family member I