About: Joshua Rokach

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

Canadian biochemist

Attributes	Values
rdf:type	Item
description	bithcheimiceoir Ceanadach (ga) kanadischer Biochemiker (de) عالم كيمياء حيوية كندي (ar) Canadian biochemist (en) bioquímicu canadianu (ast) biochimiste canadien (fr)
rdfs:label	Joshua Rokach (en) Joshua Rokach (ca) Joshua Rokach (es) Joshua Rokach (fr) Joshua Rokach (ga) Joshua Rokach (nl) Joshua Rokach (sl) Joshua Rokach (sq) Joshua Rokach (ast)
skos:prefLabel	Joshua Rokach (en) Joshua Rokach (ca) Joshua Rokach (es) Joshua Rokach (fr) Joshua Rokach (ga) Joshua Rokach (nl) Joshua Rokach (sl) Joshua Rokach (sq) Joshua Rokach (ast)
name	Joshua Rokach (en) Joshua Rokach (ca) Joshua Rokach (es) Joshua Rokach (fr) Joshua Rokach (ga) Joshua Rokach (nl) Joshua Rokach (sl) Joshua Rokach (sq) Joshua Rokach (ast)
given name	wds:Q28878223-9B544A96-189F-4D3E-A848-DCFD3C67C233
given name	Joshua
instance of	wds:Q28878223-2e35fc64-40ca-1855-e12c-9c1b18660e50
instance of	Homo sapiens
award received	wds:Q28878223-563306c9-46e9-a959-1c45-8c505a16e0dc
award received	Acfas Urgel-Archambeault Award
occupation	wds:Q28878223-78288fe8-40a9-3b98-8216-d11f95e281ee
sex or gender	wds:Q28878223-dd447758-472c-1bf4-c880-0e02aa878e36
VIAF ID	wds:Q28878223-fff5c30c-47bc-6461-0a99-09114726a6c7
Library of Congress authority ID	wds:Q28878223-715B1FA7-2A7F-4293-B189-73C72819CF4F
IdRef ID	wds:Q28878223-BA8D3DAE-723A-4A37-A98D-86A79689FAF7
country of citizenship	wds:Q28878223-9f931d76-4416-3482-6774-29837b1be7e6
SHARE Catalogue author ID	wds:Q28878223-8ACA9B3C-C2A1-460D-81C0-85FDAA09F346
family name	wds:Q28878223-b5821bdd-49b3-76e2-9584-3daf6d7910ef
WorldCat Identities ID (superseded)	wds:Q28878223-9B79309B-D63A-46B3-A8CE-B6F0B48B61F3
VIAF ID	http://viaf.org/viaf/31072088
Library of Congress authority ID	http://id.loc.gov/authorities/names/n87947767
IdRef ID	http://www.idref.fr/242969283/id
occupation	biochemist
sex or gender	male
VIAF ID	31072088
Library of Congress authority ID	n87947767
IdRef ID	242969283
country of citizenship	Malawi
SHARE Catalogue author ID	91268
family name	Rokach
WorldCat Identities ID (superseded)	lccn-n87947767
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28878223
is author of	Biochemistry, biology and chemistry of the 5-lipoxygenase product 5-oxo-ETE Enhanced formation of 5-oxo-6,8,11,14-eicosatetraenoic acid by cancer cells in response to oxidative stress, docosahexaenoic acid and neutrophil-derived 5-hydroxy-6,8,11,14-eicosatetraenoic acid 5-oxo-6,8,11,14-eicosatetraenoic acid induces the infiltration of granulocytes into human skin Airway epithelial cells synthesize the lipid mediator 5-oxo-ETE in response to oxidative stress Regulation of 5-hydroxyeicosanoid dehydrogenase activity in monocytic cells 5-oxo-ETE is a major oxidative stress-induced arachidonate metabolite in B lymphocytes Interactions between 5-oxo-ETE and chemokines in stimulating eosinophils Biosynthesis, biological effects, and receptors of hydroxyeicosatetraenoic acids (HETEs) and oxoeicosatetraenoic acids (oxo-ETEs) derived from arachidonic acid An efficient approach to the synthesis of LTB4 and ω-substituted LTB4 metabolites 12-Oxo-LTB4, a Key Pivotal Intermediate in LTB4 Metabolism Effects of prostaglandin D2, 15-deoxy-Delta12,14-prostaglandin J2, and selective DP1 and DP2 receptor agonists on pulmonary infiltration of eosinophils in Brown Norway rats Structure-activity relationship study of β-oxidation resistant indole-based 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) receptor antagonists. Total Synthesis of a Potent Proinflammatory 5-Oxo-ETE and Its 6,7-Dihydro Biotransformation Product Total synthesis of proinflammatory dihydro-12-KETE metabolites Human neutrophils convert the sebum-derived polyunsaturated fatty acid Sebaleic acid to a potent granulocyte chemoattractant A convenient strategy for the synthesis of β,γ-unsaturated aldehydes and acids. A construction of skipped dienes A photoaffinity probe for 5-hydroxyeicosanoid dehydrogenase suitable for radioiodination The synthesis of a 5-HETE photoaffinity ligand Quantification of lipid mediator metabolites in human urine from asthma patients by electrospray ionization mass spectrometry: controlling matrix effects. The design and synthesis of a 5-HETE affinity chromatography ligand for 5-hydroxyeicosanoid dehydrogenase In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys. The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor High-Pressure Liquid Chromatography of Oxo-Eicosanoids Derived from Arachidonic Acid Metabolism and pharmacokinetics of a potent N-acylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) in rats and monkeys. A new synthetic approach for 4(S)-hydroxycyclopent-2-enone: a precursor to prostanoid synthesis Synthesis of 12-KETE and its 8,9-trans-isomer Reductive Deprotection of Silyl Groups with Wilkinson's Catalyst/Catechol Borane A new method for the preparation of olefins from vicinal diols The Total Synthesis of Tritiated and Deuterated 5-Oxo-ETE, a Novel Inflammatory Mediator The Total Synthesis of 5-Oxo-12(S)-hydroxy-6(E),8(Z),10(E),14(Z)-eicosatetraenoic Acid and Its 8,9-trans-Isomer and Their Identification in Human Platelets Stereoselective synthesis of two highly potent 5-oxo-ETE receptor antagonists Targeting the OXE receptor as a potential novel therapy for asthma Silyl group deprotection by Pd/C/H2. A facile and selective method An efficient preparation of stereospecific β-hydroxy nitriles Intramolecular sulfur-assisted NaBH4 reduction of esters synthesis of 5-oxo-ETE and 5-oxo-12-HETE Inhibition of allergen-induced dermal eosinophilia by an oxoeicosanoid receptor antagonist in non-human primates Corrigendum to "In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys" [Biochem. Pharmacol. 138 (2017) 107-118]
is author of	wds:Q28250633-3199BB49-8538-4505-99B3-8BDF0A933904

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