Zobrazeno 1 - 10
of 189
pro vyhledávání: '"Kyeong-Man Kim"'
Publikováno v:
Cellular & Molecular Biology Letters, Vol 29, Iss 1, Pp 1-23 (2024)
Abstract Transactivation of epidermal growth factor receptors (EGFR) provides intricate control over multiple regulatory cellular processes that merge the diversity of G protein-coupled receptors (GPCRs) with the robust signaling capacities of recept
Externí odkaz:
https://doaj.org/article/c809f781c35341f786a27114164239b3
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-20 (2023)
Abstract Background Desensitization of G protein–coupled receptors (GPCRs) refers to a rapid attenuation of responsiveness that occurs with repeated or continuous exposure to agonists. GRK-mediated phosphorylation and subsequent binding with arrest
Externí odkaz:
https://doaj.org/article/821709d2f9954b0ab3725ffa08df6c5d
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2023)
The mouse hippocampal neuronal cell line HT22 is frequently used as an in vitro model to investigate the role of hippocampal cholinergic neurons in cognitive functions. HT22 cells are derived from hippocampal neuronal HT4 cells. However, whether thes
Externí odkaz:
https://doaj.org/article/4c24426573094b1a98e9fe8d2f6c54bc
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e68351 (2013)
Beta-arrestins (β-arrestin1 and β-arrestin2) are known as cytosolic proteins that mediate desensitization and internalization of activated G protein-coupled receptors. In addition to these functions, β-arrestins have been found to work as adaptor
Externí odkaz:
https://doaj.org/article/5940f0f370e64881b0d3dd21a3ac20f1
Publikováno v:
Biochemical and Biophysical Research Communications. 628:40-48
Publikováno v:
Biomolecules & Therapeutics. 31:176-182
Among 14 subtypes of serotonin receptors (5-HTRs), 5-HT
Autor:
Dooti, Kundu, Anlin, Zhu, Eunae, Kim, Suresh, Paudel, Choon-Gon, Jang, Yong Sup, Lee, Kyeong-Man, Kim
Publikováno v:
Biomolecules & Therapeutics. 31:108-115
Numerous psychotropic and addictive substances possess structural features similar to those of β-phenethylamine (β-PEA). In this study, we selected 29 β-PEA derivatives and determined their structure-activity relationship (SAR) to their ability to
Publikováno v:
British Journal of Pharmacology. 178:3498-3516
Background and purpose α4β2 nicotinic acetylcholine receptor (nAChR), a subtype of the ligand-gated ion channel, is abundantly expressed in the brain and implicated in several neurological disorders. The endocytosis of nAChR plays important roles i
Autor:
Srijan Acharya, Seung Hoon Cheon, Anlin Zhu, Kyeong-Man Kim, Eunae Kim, Suresh Paudel, Xiao Min
Publikováno v:
Biomolecules & Therapeutics
In this study, we determined the effect of 24 different synthetic 4-benzylpiperidine carboxamides on the reuptake of serotonin, norepinephrine, and dopamine (DA), and characterized their structure–activity relationship. The compounds with a two-car
Autor:
Kyeong-Man Kim
Publikováno v:
International Journal of Molecular Sciences. 24:6742
Dopamine receptors are classified into five subtypes, with D2R and D3R playing a crucial role in regulating mood, motivation, reward, and movement. Whereas D2R are distributed widely across the brain, including regions responsible for motor functions