 Receptors, Drug
"Receptors, Drug" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Proteins that bind specific drugs with high affinity and trigger intracellular changes influencing the behavior of cells. Drug receptors are generally thought to be receptors for some endogenous substance not otherwise specified.
| Descriptor ID |
D011955
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| MeSH Number(s) |
D12.776.827
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Receptors, Drug".
Below are MeSH descriptors whose meaning is more specific than "Receptors, Drug".
This graph shows the total number of publications written about "Receptors, Drug" by people in this website by year, and whether "Receptors, Drug" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 | | 2001 | 1 | 0 | 1 | | 2002 | 0 | 1 | 1 | | 2004 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2009 | 0 | 2 | 2 | | 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Receptors, Drug" by people in Profiles.
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Krueger JN, Wilmot JH, Teratani-Ota Y, Puhger KR, Nemes SE, Crestani AP, Lafreniere MM, Wiltgen BJ. Amnesia for context fear is caused by widespread disruption of hippocampal activity. Neurobiol Learn Mem. 2020 11; 175:107295.
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Tamura Y, Tanabe K, Kitagawa W, Uchida S, Schreiner GF, Johnson RJ, Nakagawa T. Nicorandil, a K(atp) channel opener, alleviates chronic renal injury by targeting podocytes and macrophages. Am J Physiol Renal Physiol. 2012 Aug 01; 303(3):F339-49.
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Edwards AG, Rees ML, Gioscia RA, Zachman DK, Lynch JM, Browder JC, Chicco AJ, Moore RL. PKC-permitted elevation of sarcolemmal KATP concentration may explain female-specific resistance to myocardial infarction. J Physiol. 2009 Dec 01; 587(Pt 23):5723-37.
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Vijayaraghavan S. Glial-neuronal interactions--implications for plasticity and drug addiction. AAPS J. 2009 Mar; 11(1):123-32.
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Florez JC, Jablonski KA, Kahn SE, Franks PW, Dabelea D, Hamman RF, Knowler WC, Nathan DM, Altshuler D. Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program. Diabetes. 2007 Feb; 56(2):531-6.
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Moreau C, Gally F, Jacquet-Bouix H, Vivaudou M. The size of a single residue of the sulfonylurea receptor dictates the effectiveness of K ATP channel openers. Mol Pharmacol. 2005 Apr; 67(4):1026-33.
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Mironova GD, Negoda AE, Marinov BS, Paucek P, Costa AD, Grigoriev SM, Skarga YY, Garlid KD. Functional distinctions between the mitochondrial ATP-dependent K+ channel (mitoKATP) and its inward rectifier subunit (mitoKIR). J Biol Chem. 2004 Jul 30; 279(31):32562-8.
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Lin W, Ogura T, Kinnamon SC. Acid-activated cation currents in rat vallate taste receptor cells. J Neurophysiol. 2002 Jul; 88(1):133-41.
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Abdallah JG, Schrier RW, Edelstein C, Jennings SD, Wyse B, Ellison DH. Loop diuretic infusion increases thiazide-sensitive Na(+)/Cl(-)-cotransporter abundance: role of aldosterone. J Am Soc Nephrol. 2001 Jul; 12(7):1335-1341.
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Saseen JJ, Carter BL. Dual calcium-channel blocker therapy in the treatment of hypertension. Ann Pharmacother. 1996 Jul-Aug; 30(7-8):802-10.
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