SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Kozielewicz P) "

Sökning: WFRF:(Kozielewicz P)

  • Resultat 1-10 av 24
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  •  
2.
  • Alexander, Stephen P. H., et al. (författare)
  • The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors
  • 2023
  • Ingår i: BRITISH JOURNAL OF PHARMACOLOGY. - : British pharmacological society. - 0007-1188 .- 1476-5381. ; 180
  • Tidskriftsartikel (refereegranskat)abstract
    • The Concise Guide to PHARMACOLOGY 2023/24 is the sixth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of approximately 1800 drug targets, and about 6000 interactions with about 3900 ligands. There is an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes almost 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at . G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2023, and supersedes data presented in the 2021/22, 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.
  •  
3.
  • Christopoulos, Arthur, et al. (författare)
  • THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: G protein-coupled receptors.
  • 2021
  • Ingår i: British journal of pharmacology. - : Wiley. - 1476-5381 .- 0007-1188. ; 178 Suppl 1
  • Forskningsöversikt (refereegranskat)abstract
    • The Concise Guide to PHARMACOLOGY 2021/22 is the fifth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of nearly 1900 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes over 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.15538. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2021, and supersedes data presented in the 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.
  •  
4.
  •  
5.
  • Kozielewicz, P, et al. (författare)
  • Overexpression of Orphan Receptor GPR61 Increases cAMP Levels upon Forskolin Stimulation in HEK293 Cells: in vitro and in silico Validation of 5-(Nonyloxy)Tryptamine as a Low-Affinity Inverse Agonist
  • 2019
  • Ingår i: Pharmacology. - : S. Karger AG. - 1423-0313 .- 0031-7012. ; 104:5-6, s. 377-382
  • Tidskriftsartikel (refereegranskat)abstract
    • GPR61 is an orphan receptor that belongs to Class A of G-protein-coupled receptors. It has been reported that GPR61 has a constitutive activity and couples to Gα<sub>s</sub>. In the present study, we characterized GPR61 function and ligand binding by experimental and molecular docking studies. We demonstrated that heterologous expression of GPR61 in HEK293 cells enhanced the cAMP synthesis response to forskolin, whereas the basal cAMP synthesis was unaffected. 5-(Nonyloxy)tryptamine inhibited forskolin-stimulated cAMP production in GPR61-expressing HEK293 cells. These studies highlight that the intrinsic activity of this receptor is only measurable following its synergy with Gα<sub>s</sub>.
  •  
6.
  •  
7.
  • Sajkowska-Kozielewicz, JJ, et al. (författare)
  • Geissospermiculatine, a New Alkaloid from Geissospermum reticulatum Bark
  • 2021
  • Ingår i: Molecules (Basel, Switzerland). - : MDPI AG. - 1420-3049. ; 26:1
  • Tidskriftsartikel (refereegranskat)abstract
    • A new alkaloid, geissospermiculatine was characterized in Geissospermum reticulatum A. H. Gentry bark (Apocynaceae). Here, following a simplified isolation protocol, the structure of the alkaloid was elucidated through GC-MS, LC-MS/MS, 1D, and 2D NMR (COSY, ROESY, HSQC, HMBC, 1H-15N HMBC). Cytotoxic properties were evaluated in vitro on malignant THP-1 cells, and the results demonstrated that the cytotoxicity of the alkaloid (30  μg/mL) was comparable with staurosporine (10  μM). Additionally, the toxicity was tested on zebrafish (Danio rerio) embryos in vivo by monitoring their development (0–72 h); toxicity was not evident at 30  μg/mL.
  •  
8.
  •  
9.
  •  
10.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 24
Typ av publikation
tidskriftsartikel (21)
konferensbidrag (2)
forskningsöversikt (1)
Typ av innehåll
refereegranskat (19)
övrigt vetenskapligt/konstnärligt (5)
Författare/redaktör
Petersen, J. (2)
Schulz, Stefan (2)
Kukkonen, Jyrki P. (2)
Christopoulos, Arthu ... (2)
Davenport, Anthony P ... (2)
Kelly, Eamonn (2)
visa fler...
Peters, John A. (2)
Veale, Emma L. (2)
Armstrong, Jane F. (2)
Faccenda, Elena (2)
Harding, Simon D. (2)
Davies, Jamie A. (2)
Abbracchio, Maria Pi ... (2)
Alexander, Wayne (2)
Al-hosaini, Khaled (2)
Barnes, Nicholas M. (2)
Bathgate, Ross (2)
Beaulieu, Jean-Marti ... (2)
Bernstein, Kenneth E ... (2)
Bettler, Bernhard (2)
Birdsall, Nigel J. M ... (2)
Blaho, Victoria (2)
Boulay, Francois (2)
Bousquet, Corinne (2)
Burnstock, Geoffrey (2)
Calo, Girolamo (2)
Castano, Justo P. (2)
Catt, Kevin J. (2)
Ceruti, Stefania (2)
Chazot, Paul (2)
Chiang, Nan (2)
Chini, Bice (2)
Chun, Jerold (2)
Cianciulli, Antonia (2)
Civelli, Olivier (2)
Clapp, Lucie H. (2)
Couture, Rejean (2)
Csaba, Zsolt (2)
Dahlgren, Claes, 194 ... (2)
Dent, Gordon (2)
Douglas, Steven D. (2)
Dournaud, Pascal (2)
Eguchi, Satoru (2)
Escher, Emanuel (2)
Filardo, Edward J. (2)
Fong, Tung (2)
Fumagalli, Marta (2)
Gainetdinov, Raul R. (2)
Gerard, Craig (2)
Gershengorn, Marvin (2)
visa färre...
Lärosäte
Karolinska Institutet (24)
Göteborgs universitet (2)
Uppsala universitet (2)
Språk
Engelska (24)
Forskningsämne (UKÄ/SCB)
Medicin och hälsovetenskap (2)
Naturvetenskap (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy