About: Michael Spedding

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Michael Spedding (en) Michael Spedding (es) Michael Spedding (nl) Michael Spedding (sl) Michael Spedding (ast)
skos:prefLabel	Michael Spedding (en) Michael Spedding (es) Michael Spedding (nl) Michael Spedding (sl) Michael Spedding (ast)
name	Michael Spedding (en) Michael Spedding (es) Michael Spedding (nl) Michael Spedding (sl) Michael Spedding (ast)
given name	wds:Q42388779-CDBDDFED-E301-45FE-82CF-9DF4D655D57A
given name	Michael
instance of	wds:Q42388779-3068874D-F169-4B11-99B7-9047C836059F
instance of	Homo sapiens
Loop ID	wds:Q42388779-E821DB5C-5461-4E36-9038-92246B8E94DF
Loop ID	444912
occupation	wds:Q42388779-D1C9D57D-5DCA-46BB-98E7-85F4F418F1A6
employer	wds:Q42388779-3721297A-B646-44FF-95B4-C83B394A732A wds:Q42388779-54EBAF66-B9FC-41A9-A4F4-03814FEFEB15 wds:Q42388779-9D941611-A3EC-4126-A37A-744FE1DD4420 wds:Q42388779-B0FB494C-45DF-4B0F-9C93-A47240A5FC19
sex or gender	wds:Q42388779-EAF739EC-42B9-4C77-A4A3-EEE47CCB87DA
ISNI	wds:Q42388779-D59847C6-2F9E-46A0-BCA9-0448C4739FF0
VIAF ID	wds:Q42388779-A59CA45B-4F6F-4F83-9FB7-409D1C255EFE
Library of Congress authority ID	wds:Q42388779-45A21606-77C6-48EF-85AD-6AEB689E2EB6
DBLP author ID	wds:Q42388779-D8844DBE-4B51-4069-AAC9-8A119D57870A
IdRef ID	wds:Q42388779-26177924-6af4-4f3c-962e-7d6471e0ef50
WorldCat Identities ID (superseded)	wds:Q42388779-B99FEA55-466F-44AA-BB60-F0642D5CDBFB
VIAF ID	http://viaf.org/viaf/311780795
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2014153562
DBLP author ID	https://dblp.org/pid/31/7244.rdf
IdRef ID	http://www.idref.fr/224002252/id
occupation	researcher
employer	University of Sunderland Sunderland Royal Hospital Institut de Recherches Servier
sex or gender	male
ISNI	0000000459547131
VIAF ID	311780795
Library of Congress authority ID	no2014153562
DBLP author ID	31/7244
IdRef ID	224002252
WorldCat Identities ID (superseded)	lccn-no2014153562
ORCID iD	wds:Q42388779-031A497A-31BF-483E-B791-EBA1D3A62972
ORCID iD	https://orcid.org/0000-0002-1248-8221
ORCID iD	0000-0002-1248-8221
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42388779
is author of	Positive allosteric modulators of AMPA receptors are neuroprotective against lesions induced by an NMDA agonist in neonatal mouse brain Antidepressants reverse the attenuation of the neurotrophic MEK/MAPK cascade in frontal cortex by elevated platform stress; reversal of effects on LTP is associated with GluA1 phosphorylation Tianeptine potentiates AMPA receptors by activating CaMKII and PKA via the p38, p42/44 MAPK and JNK pathways IUPHAR-DB: the IUPHAR database of G protein-coupled receptors and ion channels International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology IUPHAR-DB: new receptors and tools for easy searching and visualization of pharmacological data IUPHAR-DB: updated database content and new features A functional correlate for the dihydropyridine binding site in rat brain. Cognitive dysfunction in psychiatric disorders: characteristics, causes and the quest for improved therapy A nomenclature for ligand-gated ion channels A proposal for an updated neuropsychopharmacological nomenclature Functional correlates of dopamine D3 receptor activation in the rat in vivo and their modulation by the selective antagonist, (+)-S 14297: II. Both D2 and "silent" D3 autoreceptors control synthesis and release in mesolimbic, mesocortical and nigros International Union of Pharmacology. XLVI. G protein-coupled receptor list. Overview of nomenclature of nuclear receptors The Concise Guide to PHARMACOLOGY 2013/14: ligand-gated ion channels. The Concise Guide to PHARMACOLOGY 2013/14: nuclear hormone receptors The Concise Guide to PHARMACOLOGY 2013/14: enzymes. International Union of Basic and Clinical Pharmacology. LXVII. Recommendations for the recognition and nomenclature of G protein-coupled receptor heteromultimers. Alpha 2-adrenoceptor subtypes and imidazoline-like binding sites in the rat brain The IUPHAR/BPS Guide to PHARMACOLOGY: an expert-driven knowledgebase of drug targets and their ligands Inhibition of the constitutive activity of human 5-HT1A receptors by the inverse agonist, spiperone but not the neutral antagonist, WAY 100,635 Design, synthesis and pharmacological evaluation of new series of naphthalenic analogues as melatoninergic (MT1/MT2) and serotoninergic 5-HT2C dual ligands (I). Functional interactions of calcium-antagonists in K+-depolarized smooth muscle International Union of Pharmacology. LVI. Ghrelin receptor nomenclature, distribution, and function S 14297, a novel selective ligand at cloned human dopamine D3 receptors, blocks 7-OH-DPAT-induced hypothermia in rats The Concise Guide to PHARMACOLOGY 2013/14: G protein-coupled receptors Classification of calcium channels and the sites of action of drugs modifying channel function Factors modifying the tissue selectivity of calcium-antagonists. 2,3-benzodiazepine-type AMPA receptor antagonists and their neuroprotective effects. Modulation of sexual behaviour in the rat by a potent and selective alpha 2-adrenoceptor antagonist, delequamine (RS-15385-197). BDNF increases rat brain mitochondrial respiratory coupling at complex I, but not complex II

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