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  • ...hydrochloride. It is a [[sympathomimetic]] agent with marked [[Adrenergic receptor|alpha adrenergic]] activity. It is a [[vasoconstrictor]] with a rapid acti [[pt:Nafazolina]]
    3 KB (391 words) - 13:14, 20 September 2010
  • ...line in the management of epistaxis. Ann Otol Rhinol Laryngol, 1995. 104(9 Pt 1): p. 704-6.</ref> and eye redness due to minor irritation (marketed as [[ ...pression due to stimulation of central alpha-2 receptors and [[imidazoline receptor]]s, much like [[clonidine]].
    6 KB (713 words) - 13:15, 20 September 2010
  • ...ction there. The cytokine factors then bind with [[endothelium|endothelial receptor]]s on vessel walls, or interact with local [[microglial cell]]s. When these ...ein]] (LBP) binds to LPS. The LBP–LPS complex then binds to the [[CD14]] receptor of a nearby [[macrophage]]. This binding results in the synthesis and relea
    27 KB (3,703 words) - 20:20, 20 September 2010
  • ...519 |doi=10.1097/00043426-200306000-00002 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=1077-4114&volum ...[[Complement Receptor 3|Macrophage-1 antigen]] ([[CD18]]) [[cell receptor|receptor]] on immune cells.<ref name=pmid15084502>{{cite pmid|15084502}} (review)</r
    94 KB (13,321 words) - 21:32, 20 September 2010
  • ...the NMDA receptor, lead exposure decreased the amount of the gene for the receptor in part of the brain.<ref>{{cite web |url=http://www.jhsph.edu/publichealth ...434739}}</ref><ref name="pmid8035397">{{cite journal |author=Lin JL, Huang PT |title=Body lead stores and urate excretion in men with chronic renal disea
    90 KB (13,109 words) - 21:36, 20 September 2010
  • ...driving force for the binding of drugs to their [[receptor (biochemistry)|receptor]] targets.<ref name="Eisenberg">{{cite journal |author=Eisenberg D, McLachl [[pt:Coeficiente de partição]]
    27 KB (3,780 words) - 20:16, 21 September 2010
  • ...g to Le Châtelier's principle thereby explaining the diverse phenomena of receptor activation and desensitization.<ref name="Bio-balance">{{cite web|url=http: [[pt:Princípio de Le Châtelier]]
    12 KB (1,797 words) - 20:16, 21 September 2010
  • ...ule, including any [[protein]], is phosphorylation. Many [[enzyme]]s and [[Receptor (proteomics)|receptors]] are switched "on" or "off" by phosphorylation. Pho ...ly into the cytoplasm. It can be recognised by the [[inositol triphosphate receptor]] (IP3R). IP3 contributes to the activation of [[protein kinase C]] (PKC).<
    63 KB (9,050 words) - 21:26, 21 September 2010
  • ...[angiotensin II receptor antagonist]]s, which directly block [[Angiotensin receptor|angiotensin II AT<sub>1</sub> receptors]]. ...ol|DAG]] → activation of [[Inositol triphosphate receptor|IP<sub>3</sub> receptor]] in [[sarcoplasmic reticulum|SR]] → ↑intracellular Ca<sup>2+</sup>
    14 KB (1,818 words) - 21:27, 21 September 2010
  • !Receptor <BR> (↑ = opens. ↓ = closes) <ref name=boron/> <br> <font size=1> On [[ ...[[acetylcholine]] || ↑[[Muscarinic acetylcholine receptor M2|muscarinic receptor M<sub>2</sub>]]
    11 KB (1,498 words) - 21:28, 21 September 2010
  • !Receptor <br/> (↑ = opens. ↓ = closes) <ref name=boron/> <br> <font size=1> On [ |rowspan=2| [[nitric oxide]] || ↑[[NO receptor]] on smooth muscle || ↑[[cyclic GMP|cGMP]] --> ↑[[protein kinase g|PKG]
    13 KB (1,665 words) - 21:28, 21 September 2010
  • ...enin-Angiotensin System: Emphasis on Blockade of the Angiotensin II Type-1 Receptor ...(ARBs) can be used to prevent angiotensin II from acting on [[angiotensin receptor]]s.
    11 KB (1,520 words) - 12:30, 28 January 2012
  • ...tp://www.nature.com/bjp/journal/v143/n4/full/0705974a.html "Selective GABA-receptor actions of amobarbital on thalamic neurons."] ''British Journal of Pharmaco ...t (military)|frontline]].<ref>[http://www.pbs.org/wgbh/amex/bulge/filmmore/pt.html Use of sodium amytal during WWII]</ref>
    9 KB (1,128 words) - 22:04, 21 September 2010
  • ...month= November | year= 1975 | pages= 530&ndash;4 | volume= 18 | issue= (5 Pt 1) | pmid=1102231 | accessdate= 2008-02-22}}</ref><ref name="Phillips">{{ci ...ref> and there may be other modes of action such as through [[histamine H3 receptor]]s<ref name="Girard">{{cite journal | author= Girard P, Pansart Y, Coppé M
    9 KB (1,159 words) - 22:06, 21 September 2010
  • ...ervous]] and [[immune system]]s of animals and that activate [[cannabinoid receptor]]s , and 3. '''synthetic cannabinoids''', a structurally diverse class of m {{Main|Cannabinoid receptor}}
    49 KB (6,487 words) - 22:06, 21 September 2010
  • ...brain: isolation, structure elucidation, and interactions with the opiate receptor |journal=Proc Natl Acad Sci USA |volume=73 |issue=7 |pages=2515–9 |year=1 ...for the κ<sub>1</sub> opioid receptors. μ opioid receptors are the main receptor through which [[morphine]] acts. Classically, μ opioid receptors are presy
    18 KB (2,467 words) - 22:06, 21 September 2010
  • ...elieve minor throat irritation. Menthol also acts as a weak [[kappa Opioid receptor]] [[agonist]]. [[pt:Mentol]]
    15 KB (2,008 words) - 22:07, 21 September 2010
  • ...ub>1</sub>]] and [[CB2 receptor|CB<sub>2</sub>]] [[receptor_(biochemistry)|receptor]]s, with lower [[affinity_(pharmacology)|affinity]] in comparison to [[THC] [[pt:Canabinol]]
    3 KB (352 words) - 22:07, 21 September 2010
  • | url = http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0271-0749&volum ...affinity for [[Cannabinoid_receptor#CB1|CB<sub>1</sub>]] and [[Cannabinoid receptor#CB2|CB<sub>2</sub>]] receptors but acts as an indirect antagonist of cannab
    17 KB (2,198 words) - 22:07, 21 September 2010
  • ...|CB<sub>1</sub>]] receptor, which is the most abundant [[G protein-coupled receptor]] in the [[brain]]. ...inoid receptor]] antagonist [[rimonabant]] (SR141716A) as well as [[opioid receptor]] antagonists (opioid blockers) [[naloxone]] and [[naloxonazine]].<ref name
    50 KB (6,686 words) - 22:09, 21 September 2010

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