Results 161 to 170 of about 3,781 (209)

Summary of Reivision of Law Concerning Protectin of Radiation Hazard

Journal of the Atomic Energy Society of Japan / Atomic Energy Society of Japan, 1960
openaire   +2 more sources

Correction for Gobbetti et al., Protectin D1n-3 DPA and resolvin D5n-3 DPA are effectors of intestinal protection. [PDF]

Proc Natl Acad Sci U S A
europepmc   +1 more source

Docosahexaenoic Acid and Its Metabolites Protect against Ozone-induced Pulmonary Inflammation. [PDF]

Am J Respir Cell Mol Biol
Yaeger MJ, Ngatikaura T, Zecchino N, Lovins HB, Schott E, Cochran SJ, Hutton G, Ray JL, Saunders B, Leuenberger LA, Kilburg-Basnyat B, Virk R, Van Duinen R, Mo X, Armstrong M, McFadden MI, Fenton JI, Reisdorph N, Forero A, Ballinger MN, Tighe RM, Shaikh SR, Gowdy KM.   +22 more
europepmc   +1 more source

Intestinal flora composition and fecal metabolic phenotype in elderly patients with sleep disorders combined with type 2 diabetes. [PDF]

Aging Med (Milton)
Yin Z, Xie H, Liu F, Kong X, Chen W, Gong Y, Ge W.   +6 more
europepmc   +1 more source

Specialized Pro-Resolving Mediators as Emerging Players in Cardioprotection: From Inflammation Resolution to Therapeutic Potential. [PDF]

Acta Physiol (Oxf)
De Bartolo A, Romeo N, Angelone T, Rocca C.   +3 more
europepmc   +1 more source

Synthetic Studies Towards Analogs Of Protectin D1

, 2016
openaire   +1 more source

Confusion between protectin D1 (PD1) and its isomer protectin DX (PDX). An overview on the dihydroxy-docosatrienes described to date

Biochimie, 2014
There is currently a growing interest in docosahexaenoic acid (DHA) oxygenated metabolites. Among them, protectin D1 (PD1), an endogenous dihydroxylated and non-cyclic docosatriene made through lipoxygenation and hydrolysis of an epoxide intermediate, shows appealing biological effects.
Laurence Balas, Michel Guichardant, Thierry Durand   +2 more
exaly   +6 more sources

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Total synthesis of the antiinflammatory and proresolving protectin D1

Tetrahedron Letters, 2011
Stereoselective total synthesis of protectin D1 was completed through construction of the Z,E,E-triene structure by using the Suzuki coupling between the vinyl borane (C13–C22) and the vinyl iodide (C1–C12). The Z-enyne, the acetylene precursor of the vinyl borane was synthesized from optically active γ-TMS allylic alcohol in a straightforward way.
Narihito Ogawa, Yuichi Kobayashi
exaly   +2 more sources