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Manuela Pfeiffer

Researcher at Otto-von-Guericke University Magdeburg

Publications -  8
Citations -  1698

Manuela Pfeiffer is an academic researcher from Otto-von-Guericke University Magdeburg. The author has contributed to research in topics: Receptor & Internalization. The author has an hindex of 8, co-authored 8 publications receiving 1654 citations.

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Journal ArticleDOI

A Dual Role for the SDF-1/CXCR4 Chemokine Receptor System in Adult Brain: Isoform-Selective Regulation of SDF-1 Expression Modulates CXCR4-Dependent Neuronal Plasticity and Cerebral Leukocyte Recruitment after Focal Ischemia

TL;DR: The cellular expression of SDF-1 isoforms and CXCR4 in the brain of mice receiving systemic lipopolysaccharide (LPS) or permanent focal cerebral ischemia is examined to find the isoform-specific regulation of S DF-1 expression modulates neurotransmission and cerebral infiltration via distinct CX CR4-dependent pathways.
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Homo- and Heterodimerization of Somatostatin Receptor Subtypes INACTIVATION OF sst3 RECEPTOR FUNCTION BY HETERODIMERIZATION WITH sst2A

TL;DR: In this article, the sst2A-sst3 heterodimer exhibited high affinity binding to somatostatin-14 and the Sst2-selective ligand L-779, 976 but not to the Sost3-selectively ligand l-796,778.
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Heterodimerization of Somatostatin and Opioid Receptors Cross-modulates Phosphorylation, Internalization, and Desensitization

TL;DR: Dimmerization of the sst2A somatostatin receptor and the μ-opioid receptor, members of closely related G protein-coupled receptor families, is examined to provide direct evidence for heterodimerization of sst 2A and MOR1 in human embryonic kidney 293 cells.
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Morphine induces terminal μ‐opioid receptor desensitization by sustained phosphorylation of serine‐375

TL;DR: It is shown that morphine promotes terminal MOR desensitization by inducing a persistent modification of Ser375, which is a selective phosphorylation of the carboxy‐terminal residue 375.
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Differential β-Arrestin Trafficking and Endosomal Sorting of Somatostatin Receptor Subtypes

TL;DR: It is shown that somatostatin receptors profoundly differ in patterns of β-arrestin mobilization and endosomal sorting, which may provide important clues about the regulation of receptor responsiveness during long-term administration of som atostatin analogs.