44 results on '"Kang, Sona"'
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2. TET3 plays a critical role in white adipose development and diet-induced remodeling
3. The glucocorticoid receptor represses, whereas C/EBPβ can enhance or repress CYP26A1 transcription
4. AIFM2 is required for high-intensity aerobic exercise by promoting glucose utilization
5. AIFM2 is required for high-intensity aerobic exercise by promoting glucose utilization
6. AIFM2 is Required for High-Intensity Aerobic Exercise by Promoting Glucose Utilization
7. Epigenetic regulation of inflammatory factors in adipose tissue
8. JMJD8 is a Novel Molecular Nexus Between Adipocyte-Intrinsic Inflammation and Insulin Resistance
9. JMJD8 Is a Novel Molecular Nexus Between Adipocyte-Intrinsic Inflammation and Insulin Resistance
10. JMJD8 is a Novel Molecular Nexus Between Adipocyte-Intrinsic Inflammation and Insulin Resistance
11. Adipocyte-Specific Transgenic and Knockout Models
12. A necessary role of DNMT3A in endurance exercise by suppressing ALDH1L1‐mediated oxidative stress
13. Adipose Tissue Malfunction Drives Metabolic Dysfunction in Alström Syndrome
14. The role of striated muscle Pik3r1 in glucose and protein metabolism following chronic glucocorticoid exposure
15. Insulin-sensitizing effects of vitamin D repletion mediated by adipocyte vitamin D receptor: Studies in humans and mice
16. TET1 is a beige adipocyte-selective epigenetic suppressor of thermogenesis
17. 4261 Insulin Sensitizing Effects of Vitamin D Mediated through Reduced Adipose Tissue Inflammation and Fibrosis: Evidence from a Human Randomized Trial and Mice Studies
18. Skeletal muscle DNMT3A plays a necessary role in endurance exercise by regulating oxidative capacity of red muscles
19. The Role of the Gut Microbiome in Energy Balance With a Focus on the Gut-Adipose Tissue Axis
20. The role of DNA methylation in thermogenic adipose biology
21. Functional Implications of DNA Methylation in Adipose Biology
22. TET2 facilitates PPARγ agonist–mediated gene regulation and insulin sensitization in adipocytes
23. DNMT3a and TET2 in adipocyte insulin sensitivity
24. Insulin Sensitizing Effects of Vitamin D Mediated through Reduced Adipose Tissue Inflammation and Fibrosis
25. Dnmt3a is an epigenetic mediator of adipose insulin resistance
26. Author response: Dnmt3a is an epigenetic mediator of adipose insulin resistance
27. Exploration of Underlying Mechanism of Anti-adipogenic Activity of Sulfuretin
28. IRF3 promotes adipose inflammation and insulin resistance and represses browning
29. Nuclear Mechanisms of Insulin Resistance
30. MicroRNA-181b Improves Glucose Homeostasis and Insulin Sensitivity by Regulating Endothelial Function in White Adipose Tissue
31. Identification of nuclear hormone receptor pathways causing insulin resistance by transcriptional and epigenomic analysis
32. IRF4 Is a Key Thermogenic Transcriptional Partner of PGC-1α
33. Early B-cell Factor-1 (EBF1) Is a Key Regulator of Metabolic and Inflammatory Signaling Pathways in Mature Adipocytes
34. Arterial territory-specific phosphorylated retinoblastoma protein species and CDK2 promote differences in the vascular smooth muscle cell response to mitogens
35. Interferon Regulatory Factor 4 Regulates Obesity-Induced Inflammation Through Regulation of Adipose Tissue Macrophage Polarization
36. Regulation of Early Adipose Commitment by Zfp521
37. Mammalian Stem Cells Reprogramming in Response to Terahertz Radiation
38. Inhibitor of DNA Binding 2 Is a Small Molecule-Inducible Modulator of Peroxisome Proliferator-Activated Receptor-γ Expression and Adipocyte Differentiation
39. Phosphorylation of CCAAT/Enhancer-binding Protein α Regulates GLUT4 Expression and Glucose Transport in Adipocytes
40. Wnt Signaling Stimulates Osteoblastogenesis of Mesenchymal Precursors by Suppressing CCAAT/Enhancer-binding Protein α and Peroxisome Proliferator-activated Receptor γ
41. Wnt10b Inhibits Obesity in ob/ob and Agouti Mice
42. Role of wnts in prostate cancer bone metastases
43. Effects of Wnt Signaling on Brown Adipocyte Differentiation and Metabolism Mediated by PGC-1α
44. Wnt10b Inhibits Development of White and Brown Adipose Tissues
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