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251 results on '"β-arrestins"'

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1. MC4R Variants Modulate α-MSH and Setmelanotide Induced Cellular Signaling at Multiple Levels.

2. The complex nature of CXCR4 mutations in WHIM syndrome

3. β-arrestin1 regulates astrocytic reactivity via Drp1-dependent mitochondrial fission: implications in postoperative delirium

4. β-arrestin1 regulates astrocytic reactivity via Drp1-dependent mitochondrial fission: implications in postoperative delirium.

5. Endo‐lysosomal sorting of G‐protein‐coupled receptors by ubiquitin: Diverse pathways for G‐protein‐coupled receptor destruction and beyond

6. The reduced serum concentrations of β-arrestin-1 and β-arrestin-2 in pregnancies complicated with gestational diabetes mellitus.

7. Corrigendum: Biased signaling of protease-activated receptors.

8. Intracellular VHHs to monitor and modulate GPCR signaling.

9. Deciphering the signaling mechanisms of β‐arrestin1 and β‐arrestin2 in regulation of cancer cell cycle and metastasis.

10. β2 -Adrenoceptor agonist profiling reveals biased signalling phenotypes for the β2 -adrenoceptor with possible implications for the treatment of asthma.

12. MC4R Variants Modulate α-MSH and Setmelanotide Induced Cellular Signaling at Multiple Levels.

13. Intracellular VHHs to monitor and modulate GPCR signaling

14. Determining the Effects of Differential Expression of GRKs and β-arrestins on CLR-RAMP Agonist Bias.

15. The Atypical Chemerin Receptor GPR1 Displays Different Modes of Interaction with β-Arrestins in Humans and Mice with Important Consequences on Subcellular Localization and Trafficking.

16. Determining the Effects of Differential Expression of GRKs and β-arrestins on CLR-RAMP Agonist Bias

17. Structural snapshot of a β-arrestin-biased receptor.

18. β-Arrestins as Important Regulators of Glucose and Energy Homeostasis.

19. The complex nature of CXCR4 mutations in WHIM syndrome.

20. Metabolic Functions of G Protein-Coupled Receptors and β-Arrestin-Mediated Signaling Pathways in the Pathophysiology of Type 2 Diabetes and Obesity

21. Metabolic Functions of G Protein-Coupled Receptors and β-Arrestin-Mediated Signaling Pathways in the Pathophysiology of Type 2 Diabetes and Obesity.

22. Noncanonical Activity of Endocannabinoids and Their Receptors in Central and Peripheral Synapses.

23. Mécanismes d'action et rôles multiples des β-arrestines dans la biologie des récepteurs couplés aux protéines G.

24. Chapter Twenty-Two Endosomal Signaling by Protease-Activated Receptors

25. Endosomal signaling by protease-activated receptors.

26. Biochemical insights into structure and function of arrestins.

27. The Atypical Chemerin Receptor GPR1 Displays Different Modes of Interaction with β-Arrestins in Humans and Mice with Important Consequences on Subcellular Localization and Trafficking

28. Key Metabolic Functions of β-Arrestins: Studies with Novel Mouse Models.

29. The Two β-Arrestins Regulate Distinct Metabolic Processes: Studies with Novel Mutant Mouse Models

30. Exploring GPCR‐arrestin interfaces with genetically encoded crosslinkers.

31. Key phosphorylation sites in GPCRs orchestrate the contribution of β‐Arrestin 1 in ERK1/2 activation.

32. Emerging Insights into the Structure and Function of Complement C5a Receptors.

33. β-arrestin expression in corticotroph tumor cells is modulated by glucocorticoids.

35. GRKs and β-Arrestins: 'Gatekeepers' of Mitochondrial Function in the Failing Heart

36. Differential Involvement of ACKR3 C-Tail in β-Arrestin Recruitment, Trafficking and Internalization

37. GRKs and β-Arrestins: "Gatekeepers" of Mitochondrial Function in the Failing Heart.

38. TRPV1 Activation Promotes β-arrestin2 Interaction with the Ribosomal Biogenesis Machinery in the Nucleolus: Implications for p53 Regulation and Neurite Outgrowth

39. Nitric Oxide and S-Nitrosylation in Cardiac Regulation: G Protein-Coupled Receptor Kinase-2 and β-Arrestins as Targets

40. The Phosphorylation of CCR6 on Distinct Ser/Thr Residues in the Carboxyl Terminus Differentially Regulates Biological Function

41. Label-free cell signaling pathway deconvolution of angiotensin type 1 receptor reveals time-resolved G-protein activity and distinct AngII and AngIIIIV responses.

42. Emerging Paradigm of Intracellular Targeting of G Protein-Coupled Receptors.

43. Molecular evidence and clinical importance of β‐arrestins expression in patients with acromegaly.

44. Cyclopeptide Dmt-[D-Lys-p-CF3-Phe-Phe-Asp]NH2, a novel G protein-biased agonist of the mu opioid receptor.

45. Novel Structural Insights into GPCR–β-Arrestin Interaction and Signaling.

46. Somatostatin Receptor Type 2 (SSTR2) Internalization and Intracellular Trafficking in Pituitary GH-Secreting Adenomas: Role of Scaffold Proteins and Implications for Pharmacological Resistance.

47. β-arrestin signalling and bias in hormone-responsive GPCRs.

48. β-Arrestin-biased AT1R stimulation promotes extracellular matrix synthesis in renal fibrosis.

49. β-arrestins negatively control human adrenomedullin type 1-receptor internalization.

50. Identification of human somatostatin receptor 2 domains involved in internalization and signaling in QGP-1 pancreatic neuroendocrine tumor cell line.

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