Browse our anti-Resistin (RETN) Antibodies

Rhesus Monkey Resistin (RETN) interaction partners

1. The effects of exogenous human kisspeptin-10 (KP10) were studied on three important adipokines, namely, adiponectin, leptin, and resistin in a set of four chair-restraint habituated intact adult male rhesus monkeys.

Human Resistin (RETN) interaction partners

1. High plasma resistin associates with severe acute kidney injury in Puumala hantavirus infection.

2. Adiponectin but not resistin levels were associated with intensity of liver dysfunction and worse prognosis in patients with alcoholic liver disease, suggesting a potential as a prognostic biomarker.

3. In patients with peripheral arterial disease, higher levels of resistin were associated with impaired endothelial function and an increased rate of adverse cardiac events.

4. Overexpression of resistin in chondrosarcoma cells significantly enhanced VEGF-C production and lymphangiogenesis.

5. Results provide evidence that Visfatin and resistin regulate the expression levels of some miRNA involved in osteoarthritis pathogenesis and exert catabolic functions in chondrocytes via the NF-kappaB pathway.

6. Higher circulating resistin correlated with node-negative patients and longer DFS independent of Body mass index and estrogen receptor status in women with Early-onset breast cancer

7. Resistin 420G > C and 62G > A gene polymorphisms play a role in Endometrial Cancer (EC) development. Multivariate regression analysis revealed that the presence of 420G + allele increased the EC risk 1.99 fold while the presence of 62A + allele was shown to decrease the risk of EC.

8. Resistin can be released by degranulating neutrophils and blunts neutrophil plaque infiltration by modulating their migration towards known atherosclerotic mediators.

9. This study is the first to examine the risk factors associated with RETN single nucleotide polymorphisms in Oral squamous cell carcinoma progression and development in Taiwan.

10. providing evidence for a causal role of resistin in shaping the risk of mortality in diabetic patients.

11. The data revealed no correlation between the Resistin rs3745367 polymorphism and cancer risk.

12. serum level higher among infants with severe sepsis and among those who needed mechanical ventilation

13. in patients with coronary artery disease and without acute myocardial infarction leptin may represent a potential mechanism of adverse cardiac remodeling. Resistin and TNF-alpha might not be involved in ventricular remodeling in these patients.

14. The results of this study indicated that resistin gene polymorphisms might affect the genetic predisposition of rheumatoid arthritis in Chinese population.

15. It was demonstrated that high resistin expression was predominantly observed in lung adenocarcinoma tissues. It is associated with a more malignant clinicopathological status and poorer survival. Resistin could promote A549 and H1975 tumor cell proliferation, migration and invasion while inhibit their apoptosis in vitro.

16. A multi-cytokine resistin pathway is operational in humans, and it plays a substantial role in cardiovascular events in high-risk individuals.

17. An increase in resistin concentration expressed also as resistin/BMI, and resistin/adiponectin ratios, observed in children with cystic fibrosis may suggests that this adipokine is involved in the inflammatory process underlying the disease and is related to worse spirometric parameters describing airways obstruction.

18. n T2 mice, the mRNA expression of Retn showed a moderate up-regulation (fold change=8.32; p=0.0019) in the adipose tissues. Iapp expression was also significantly up-regulated (fold change=9.78; p=0.012). Moreover, a 6.36-fold up-regulation for Drd5 was observed in the adipose tissues of T2 mice

19. RETN and CAP1 polymorphisms and gene expression may be potential biomarkers for breast cancer risk

20. resistin induced MUC5AC and MUC5B expression via activation of different signaling pathways in human airway epithelial cells.

Mouse (Murine) Resistin (RETN) interaction partners

1. Resistin inhibited the activation of CREB, resulting in suppression of PGC-1alpha. Importantly, overexpressing PGC-1alpha can rescue the inhibitory effects of resistin on fatty acid beta oxidation.

2. Resistin-associated VSMC dysfunction and intimal hyperplasia are related to PKCepsilon-dependent Nox activation and ROS generation

3. Resistin may enhance inflammation by cross-talking with TLR4/NF-kappaB signaling during the development of coronary arteritis in mice

4. OLI is a physiological repressor of systemic resistin release whereas FFA upregulate resistin release in vitro from adipocytes.

5. Resistin possibly acts via an intracrine pathway as an intracellular sensor, regulating the adipocyte insulin sensitivity.

6. In 3T3-L1 adipocytes, catechin and quercetin attenuated TNF-alpha-induced elevated protein carbonyls, increased proinflammatory cytokine expression (MCP-1, resistin), and decreased adiponectin.

7. Mouse Resistin has regulative effects on murine bone marrow hematopoiesis.

8. murine resistin is increased in the lungs of wild-type mice following acute ozone exposure but does not promote ozone-induced lung pathology.

9. Inhibition of miR-696 restored the triglycerides content by up to 80%, which suggests that, in C2C12 cells, resistin at least partially increases the deposition of lipids through miR-696.

10. Antiresistin RNA oligo ameliorated metabolic abnormalities and histopathology of nonalcoholic fatty liver disease through attenuating proinflammatory cytokines

11. Resistin regulates PAI-1 expression in 3T3-L1 adipocytes via Akt phosphorylation.

12. Oxidized-LDL promotes the expression and secretion of visfatin and resistin through its activation of endoplasmic reticulum stress.

13. ET type-A receptor, ERK1/2, JNKs, AKT, and JAK2, but not ET type-B receptor or p38, are necessary for the ET-1 stimulation of resistin gene expression

14. resistin is a negative regulator of SIRT1 in both human hepatoma cell line HepG2 and mouse hepatocytes.

15. Both resistin gene expression and its secretion from the epididymal adipose tissue were decreased in db/db obese mice, while the insulin-sensitizing drug rosiglitazone increased resistin production.

16. lipid content was significantly decreased in 3T3-L1 cells transfected with anti-resistin small interfering RNA (siRNA) after adipocyte differentiation

17. The effect between resistin and adiponectin on the proliferation of vascular smooth muscle cells (VSMCs), was investigated.

18. The current study was initiated to determine whether resistin has additional roles in glucose-dependent insulinotropic polypeptide -regulated adipocyte functions.

19. significant changes in fasting-induced adipose factor (FIAF), resistin (Rstn), long-form leptin receptor (LepRb) and suppressor of cytokine-3 (SOCS3) gene expression following chronic SCI and with advanced age

20. results identify resistin as a potential inhibitory ligand for the receptor ROR1 and demonstrate, for the first time, that ROR1 plays an important role in adipogenesis and glucose homeostasis in 3T3-L1 cellsand glucose homeostasis in 3T3-L1 cells.

Pig (Porcine) Resistin (RETN) interaction partners

1. The data suggest that there is local cooperation between resistin and PPARgamma expression in the porcine ovary. Resistin significantly increased the expression of PPARgamma, whereas PPARgamma decreased resistin expression; thus, PPARgamma is a new key regulator of resistin expression and function.

2. The expression, immunolocalization and concentration of resistin in different sized ovarian follicles, was investigated.