Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Johanna Jyrkkärinne"'
Autor:
Jenni Küblbeck, Toni Rönkkö, Björn Windshügel, Wolfgang Sippl, Paavo Honkakoski, Maija Lahtela-Kakkonen, Antti Poso, Anu J. Tervo, Johanna Jyrkkärinne
Publikováno v:
Journal of Medicinal Chemistry. 51:7181-7192
The human constitutive androstane receptor (CAR, NR1I3) is an important regulator of xenobiotic metabolism and other physiological processes. So far, only few CAR agonists are known and no explicit mechanism has been proposed for their action. Thus,
Autor:
Wolfgang Sippl, Björn Windshügel, Jenni Küblbeck, Johanna Jyrkkärinne, Paavo Honkakoski, Miia Turpeinen, Antti Poso
Publikováno v:
Biochemical Pharmacology. 76:1288-1297
The constitutive androstane receptor (CAR; NR1I3) is a nuclear receptor responsible for the recognition of potentially toxic endo- and exogenous compounds whose elimination from the body is accelerated by the CAR-mediated inducible expression of meta
Autor:
Björn Windshügel, Paavo Honkakoski, Wolfgang Sippl, Johanna Jyrkkärinne, Jenni Vanamo, Antti Poso
Publikováno v:
Journal of Molecular Graphics and Modelling. 25:644-657
The constitutive androstane receptor (CAR) possesses an intrinsic basal activity whose structural basis has been analysed during the last decade. Recently, we published a homology model of the CAR ligand binding domain (LBD) based on the X-ray struct
Publikováno v:
Journal of Molecular Modeling. 11:69-79
The constitutive androstane receptor (CAR) belongs to the superfamily of nuclear-hormone receptors that function as ligand-activated transcription factors. CAR plays an essential role in the metabolism of xenobiotics and shows—in contrast to relate
Publikováno v:
Drug metabolism and drug interactions. 28(2)
The constitutive androstane receptor (CAR; NR1I3) has emerged as one of the main drug- and xenobiotic-sensitive transcriptional regulators. It has a major effect on the expression of several oxidative and conjugative enzymes and transporters, and hen
Autor:
Tuomo Laitinen, Antti Poso, Paavo Honkakoski, Juha Pulkkinen, Reino Laatikainen, Jenni Küblbeck, Johanna Jyrkkärinne
Publikováno v:
Journal of chemical information and modeling. 52(2)
Constitutive androstane receptor (CAR), along with pregnane x receptor (PXR), is an important metabolic sensor in the hepatocytes. Like all other nuclear receptors (NRs), CAR works in concert with coregulator proteins, coactivators, and corepressors
Autor:
Björn Windshügel, Ferdinand Molnár, Tapio Nevalainen, Jayendra Z. Patel, Paavo Honkakoski, Johanna Jyrkkärinne, Tuomo Laitinen, Jenni Küblbeck, Tiina Kuningas, Antti Poso, Wolfgang Sippl
Publikováno v:
Molecular pharmaceutics. 8(6)
The human constitutive androstane receptor (CAR, NR1I3) is one of the key regulators of xenobiotic and endobiotic metabolism. The unique properties of human CAR, such as the high constitutive activity and the complexity of signaling, as well as the l
Autor:
Ferdinand Molnár, Timo Rousu, Paavo Honkakoski, Tobias Abel, Ari Tolonen, Timo Korjamo, Tanja Kortelainen, Johanna Jyrkkärinne, Tuomo Laitinen, Jouko Uusitalo, Jenni Küblbeck
Publikováno v:
Biochemical pharmacology. 82(12)
The so-called human xenosensors, constitutive androstane receptor (hCAR), pregnane X receptor (hPXR) and aryl hydrocarbon receptor (hAhR), participate in drug metabolism and transport as well as in several endogenous processes by regulating the expre
Autor:
Johanna Jyrkkärinne, Björn Windshügel, Wolfgang Sippl, Markku Ylisirniö, Mikael Peräkylä, Paavo Honkakoski, Janne Mäkinen, Antti Poso
Publikováno v:
The Journal of biological chemistry. 280(7)
The human constitutive androstane receptor (CAR, NR1I3) is an important ligand-activated regulator of oxidative and conjugative enzymes and transport proteins. Because of the lack of a crystal structure of the ligand-binding domain (LBD), wide specie
Autor:
Paavo Honkakoski, Mika Reinisalo, Johanna Jyrkkärinne, Olavi Pelkonen, Hinfan Chung, Kaisa Niemi, Janne Mäkinen, Pirkko Viitala
mCAR (mouse constitutive androstane receptor; NR1I3) controls the expression of cytochrome P450 as well as other enzymes involved in drug and steroid metabolism. The high basal activity of mCAR can be modulated by inhibitory steroids related to andro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6b6ac4eb38749a87297b34ab8b33766
https://europepmc.org/articles/PMC1223782/
https://europepmc.org/articles/PMC1223782/