FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W3012784865> ?p ?o ?g. }

• W3012784865 endingPage "597" @default.
• W3012784865 startingPage "595" @default.
• W3012784865 abstract "Long-chain fatty acid (LCFA) transport is fundamental to human pathophysiology, and its impairment has been implicated in cardiovascular disease, cancer, and obesity-linked diabetes (1Kris-Etherton P.M. AHA Science Advisory. Monounsaturated fatty acids and risk of cardiovascular disease. American Heart Association. Nutrition Committee.Circulation. 1999; 100: 1253-1258Crossref PubMed Scopus (280) Google Scholar, 2Simopoulos A.P. Essential fatty acids in health and chronic disease.Am. J. Clin. Nutr. 1999; 70: 560S-569SCrossref PubMed Scopus (1273) Google Scholar, 3Wilk J.B. Tsai M.Y. Hanson N.Q. Gaziano J.M. Djousse L. Plasma and dietary omega-3 fatty acids, fish intake, and heart failure risk in the Physicians' Health Study.Am. J. Clin. Nutr. 2012; 96: 882-888Crossref PubMed Scopus (32) Google Scholar, 4Palomer X. Pizarro-Delgado J. Barroso E. Vazquez-Carrera M. Palmitic and oleic acid: the yin and yang of fatty acids in type 2 diabetes mellitus.Trends Endocrinol. Metab. 2018; 29: 178-190Abstract Full Text Full Text PDF PubMed Scopus (161) Google Scholar). Physiologically, LCFAs are an energy source, precursors to regulatory molecules, and components of complex lipids such as triacylglycerols (TAGs), phospholipids, and cholesteryl esters, which occur in plasma lipoproteins and living cells. Most physiological LCFAs contain 16 or 18 carbons with up to three double bonds (5Abdelmagid S.A. Clarke S.E. Nielsen D.E. Badawi A. El-Sohemy A. Mutch D.M. Ma D.W. Comprehensive profiling of plasma fatty acid concentrations in young healthy Canadian adults.PLoS One. 2015; 10: e0116195Crossref PubMed Scopus (141) Google Scholar, 6Pownall, H. J., A. S., Reynaud, E., Harper, S., Choi, K., Rohrbach, Q., Pao, R. S., Reeves, and A. M., Gotto, . Effects of 12 weeks of dietary fish oil, polyunsaturated fat, monounsaturated fat, and saturated fat on plasma lipoprotein structure and composition. Omega-3 Fatty Acids in Nutrition, Vascular Biology, and Medicine. 1994:263. American Heart Association, Dallas, TX.Google Scholar) and associate with lipid surfaces at diffusion-controlled rates with kon ~109 M−1sec−1. They spontaneously transfer as monomers between lipid surfaces and albumin at rates that increase with decreasing chain length with a t1/2 of ~5–200 msec (7Massey J.B. Bick D.H. Pownall H.J. Spontaneous transfer of monoacyl amphiphiles between lipid and protein surfaces.Biophys. J. 1997; 72: 1732-1743Abstract Full Text PDF PubMed Scopus (71) Google Scholar). Lipoprotein turnover occurs with t1/2 ~3 to 5 days so that LCFA transfer is comparatively rapid. Given that the destinations of plasma LCFAs are cells in plasma-perfused tissues, mechanisms by which the LCFAs enter cells are relevant to both normal human physiology and pathophysiology. The plasma membrane comprises a polarity gradient that is hydrocarbon-like at the midmost and polar near leaflet edges (Fig. 1). How LCFAs transfer between lipid surfaces separated by an aqueous phase is largely uncontroversial; LCFAs enter cells by diffusion to and insertion into the outer leaflet, translocation to the inner leaflet, and desorption into the cytoplasm. LCFA desorption occurs by the longitudinal movement of the carboxylate group, followed by the acyl chain. According to the principle of microscopic reversibility, the mechanisms for insertion (kon) and desorption (koff) are the same (8Lewis G.N. A new principle of equilibrium.Proc. Natl. Acad. Sci. USA. 1925; 11: 179-183Crossref PubMed Google Scholar), so that the reverse process (kon), occurs by LCFA insertion into a membrane leaflet acyl chain first, followed by desorption of the anionic, charged form (9Kamp F. Hamilton J.A. pH gradients across phospholipid membranes caused by fast flip-flop of un-ionized fatty acids.Proc. Natl. Acad. Sci. USA. 1992; 89: 11367-11370Crossref PubMed Scopus (249) Google Scholar). However, the debate over the middle step—LCFA translocation from the outer to the inner leaflet (ktr)—continues. The ongoing search for the LCFA translocation mechanisms was influenced by a precedent: glucose transport! Because it has many hydroxyl groups, glucose is insoluble in hydrocarbons and does not spontaneously translocate across the plasma membrane. Rather, its transporter, glucose transporter type 4 (GLUT4), carries glucose into cells, an important process in both adipose tissue and muscle (10James D.E. Brown R. Navarro J. Pilch P.F. Insulin-regulatable tissues express a unique insulin-sensitive glucose transport protein.Nature. 1988; 333: 183-185Crossref PubMed Scopus (440) Google Scholar). This analogy and the assumption that LCFAs are anionic (pKa ~5) have provoked a search for LCFA translocators. One of these, FA transport protein (FATP) was discovered by expression cloning, which identified proteins associated with the uptake and retention of a fluorescent FA (11Schaffer J.E. Lodish H.F. Expression cloning and characterization of a novel adipocyte long fatty acid transport protein.Cell. 1994; 79: 427-436Abstract Full Text PDF PubMed Scopus (724) Google Scholar). Hypothetically, this approach reveals all proteins with activities that convert LCFA to a form that is retained by the cell. Ultimately, FATP was identified as an acyl-CoA synthetase (12Coe N.R. Smith A.J. Frohnert B.I. Watkins P.A. Bernlohr D.A. The fatty acid transport protein (FATP1) is a very long chain acyl-CoA synthetase.J. Biol. Chem. 1999; 274: 36300-36304Abstract Full Text Full Text PDF PubMed Scopus (194) Google Scholar) that converts LCFA to its CoA analog, which does not pass through the plasma membrane because of the high polarity (13Wolkowicz P.E. Pownall H.J. McMillin-Wood J.B. (I-pyrenebutyryl)carnitine and 1-pyrenebutyryl coenzyme A: fluorescent probes for lipid metabolite studies in artificial and natural membranes.Biochemistry. 1982; 21: 2990-2996Crossref PubMed Scopus (16) Google Scholar). CD36, also known as FAT or scavenger receptor class B member 3 (SCARB3), has also been reported to be an LCFA translocator. CD36 is localized to the plasma membrane outer leaflet, and the mechanism by which it transfers LCFA to the inner leaflet adjacent to the cytoplasm is unknown. Several carefully conducted studies have reported that CD36 enhances cellular LCFA uptake (14Abumrad N.A. el-Maghrabi M.R. Amri E.Z. Lopez E. Grimaldi P.A. Cloning of a rat adipocyte membrane protein implicated in binding or transport of long-chain fatty acids that is induced during preadipocyte differentiation. Homology with human CD36.J. Biol. Chem. 1993; 268: 17665-17668Abstract Full Text PDF PubMed Google Scholar, 15Luiken J.J. Glatz J.F. Bonen A. Fatty acid transport proteins facilitate fatty acid uptake in skeletal muscle.Can. J. Appl. Physiol. 2000; 25: 333-352Crossref PubMed Scopus (35) Google Scholar, 16Glatz J.F. Vork M.M. Cistola D.P. van der Vusse G.J. Cytoplasmic fatty acid binding protein: significance for intracellular transport of fatty acids and putative role on signal transduction pathways.Prostaglandins Leukot. Essent. Fatty Acids. 1993; 48: 33-41Abstract Full Text PDF PubMed Scopus (98) Google Scholar), without providing a molecular mechanism. Subsequent studies have compared LCFA uptake by control HEK cells (17Xu S. Jay A. Brunaldi K. Huang N. Hamilton J.A. CD36 enhances fatty acid uptake by increasing the rate of intracellular esterification but not transport across the plasma membrane.Biochemistry. 2013; 52: 7254-7261Crossref PubMed Scopus (69) Google Scholar), in which LCFA metabolism is slower than LCFA translocation, with that of CD36-transfected HEK cells, and found identical rates of LCFA binding and translocation. However, they also revealed diversion of LCFA to TAG synthesis in CD36-expressing cells. This process supports a cellular LCFA concentration gradient of low intracellular and high extracellular LCFA concentration. In a broader context, this gradient could also be maintained by LCFA activation, incorporation into complex lipids, or β-oxidation; in other words, metabolism. In this issue of the Journal of Lipid Research, Jay et al. tested three well-rationalized two-step models of cellular LCFA uptake. Two of these involved protein-based LCFA translocators; in the third, translocation occured solely via a transverse diffusion mechanism sometimes called flip-flop. The authors followed the movement of a natural LCFA (oleic acid) according to its binding to the cell membrane outer leaflet and its translocation to the inner leaflet. The authors monitored these processes by using dual fluorescence probes—acrylodan-labeled intestinal fatty acid-binding protein (ADIFAB) and 2‘,7‘-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), a pH sensor—that respond to each of these steps, respectively. Each of the aforementioned three models has a predicted distinctive profile for ADIFAB and BCECF kinetics. Only the diffusion model gave near-parallel kinetics in adipocytes, which contain putative LCFA transporters, and in protein-free phospholipid vesicles. In control adipocytes, a decline in ADIFAB fluorescence paralleled the growth of BCECF fluorescence, indicating the concurrent disappearance of LCFA in the outer leaflet and external media and its appearance on the inner leaflet, respectively. According to the same fluorescence probes, LCFA uptake differed only slightly at 4°C and 37°C, whereas recovery of the intracellular pH was slower at the lower temperature, a finding consistent with the predicted slowing of intracellular LCFA metabolism at a reduced temperature. The authors complemented these analyses with tests of numerous inhibitors of cellular LCFA transport, and a similar but variable effect was observed with putative inhibitors of LCFA translocation, suggesting, but not proving, that reduced LCFA entry into the cell is due to inhibited metabolism. The LCFA uptake by protein-free vesicles was not affected, suggesting that the metabolic machinery of cells, and not uptake itself, is impaired by the inhibitors. The authors' other experiments focused on the chemistry of several inhibitors of LCFA translocation, notably sulfosuccinimidyl oleate (SSO), reported to highly specifically and competitively inhibit CD36-mediated LCFA transport (18Harmon C.M. Abumrad N.A. Binding of sulfosuccinimidyl fatty acids to adipocyte membrane proteins: isolation and amino-terminal sequence of an 88-kD protein implicated in transport of long-chain fatty acids.J. Membr. Biol. 1993; 133: 43-49Crossref PubMed Scopus (162) Google Scholar). Previous studies with this molecule led to the original postulate that CD36 translocates LCFA. The experiments by Jay and colleagues revealed that SSO modified CD36 as expected; unexpectedly, however, SSO also modified numerous other proteins. The authors speculate that this occurs via SSO reaction with the ∊-amino groups of lysine residues. Two other observations favor the hypothesis that the inhibitors suppress intracellular metabolism. First, all putative LCFA translocation inhibitors reduce the formation of intracellular TAG, the most likely product of LCFA-loaded adipocytes. Second, SSO reacts with many other cellular proteins in addition to CD36. Given the observed nonspecificity of SSO, some of these are likely involved in glycerolipid synthesis. Importantly, overexpression of either glycerol phosphate acyltransferase or lysoglycerol phosphate acyltransferase, enzymes that catalyze key steps in the synthesis of glycerolipids, including TAG, potentiates cellular LCFA uptake (19Ruan H. Pownall H.J. Overexpression of 1-acyl-glycerol-3-phosphate acyltransferase-alpha enhances lipid storage in cellular models of adipose tissue and skeletal muscle.Diabetes. 2001; 50: 233-240Crossref PubMed Scopus (49) Google Scholar, 20Igal R.A. Wang S. Gonzalez-Baro M. Coleman R.A. Mitochondrial glycerol phosphate acyltransferase directs the incorporation of exogenous fatty acids into triacylglycerol.J. Biol. Chem. 2001; 276: 42205-42212Abstract Full Text Full Text PDF PubMed Scopus (79) Google Scholar). At phospholipid interfaces, the pKa of LCFA is ~7 (21Doody M.C. Pownall H.J. Kao Y.J. Smith L.C. Mechanism and kinetics of transfer of a fluorescent fatty acid between single-walled phosphatidylcholine vesicles.Biochemistry. 1980; 19: 108-116Crossref PubMed Scopus (151) Google Scholar), meaning that half of it is in the protonated and uncharged form. Given that the major physicochemical barrier to LCFA translocation is the hydrocarbon interior of the lipid bilayer, it is intuitively satisfying that the diffusion model behaves according to the solubility of protonated LCFA in hydrocarbons (22Calvo B.C. Collado I. Cepeda E.A. Solubilities of palmitic acid in pure solvents and its mixtures.J. Chem. Eng. Data. 2009; 54: 64-68Crossref Scopus (21) Google Scholar, 23Smith R. Tanford C. Hydrophobicity of long chain n-alkyl carboxylic acids, as measured by their distribution between heptane and aqueous solutions.Proc. Natl. Acad. Sci. USA. 1973; 70: 289-293Crossref PubMed Google Scholar) (22Calvo B.C. Collado I. Cepeda E.A. Solubilities of palmitic acid in pure solvents and its mixtures.J. Chem. Eng. Data. 2009; 54: 64-68Crossref Scopus (21) Google Scholar, 23Smith R. Tanford C. Hydrophobicity of long chain n-alkyl carboxylic acids, as measured by their distribution between heptane and aqueous solutions.Proc. Natl. Acad. Sci. USA. 1973; 70: 289-293Crossref PubMed Google Scholar). In studies of cellular LCFA transport, there has been an ongoing debate between the “diffusionists” and the “translocationists” (14Abumrad N.A. el-Maghrabi M.R. Amri E.Z. Lopez E. Grimaldi P.A. Cloning of a rat adipocyte membrane protein implicated in binding or transport of long-chain fatty acids that is induced during preadipocyte differentiation. Homology with human CD36.J. Biol. Chem. 1993; 268: 17665-17668Abstract Full Text PDF PubMed Google Scholar, 15Luiken J.J. Glatz J.F. Bonen A. Fatty acid transport proteins facilitate fatty acid uptake in skeletal muscle.Can. J. Appl. Physiol. 2000; 25: 333-352Crossref PubMed Scopus (35) Google Scholar, 16Glatz J.F. Vork M.M. Cistola D.P. van der Vusse G.J. Cytoplasmic fatty acid binding protein: significance for intracellular transport of fatty acids and putative role on signal transduction pathways.Prostaglandins Leukot. Essent. Fatty Acids. 1993; 48: 33-41Abstract Full Text PDF PubMed Scopus (98) Google Scholar, 17Xu S. Jay A. Brunaldi K. Huang N. Hamilton J.A. CD36 enhances fatty acid uptake by increasing the rate of intracellular esterification but not transport across the plasma membrane.Biochemistry. 2013; 52: 7254-7261Crossref PubMed Scopus (69) Google Scholar, 18Harmon C.M. Abumrad N.A. Binding of sulfosuccinimidyl fatty acids to adipocyte membrane proteins: isolation and amino-terminal sequence of an 88-kD protein implicated in transport of long-chain fatty acids.J. Membr. Biol. 1993; 133: 43-49Crossref PubMed Scopus (162) Google Scholar, 19Ruan H. Pownall H.J. Overexpression of 1-acyl-glycerol-3-phosphate acyltransferase-alpha enhances lipid storage in cellular models of adipose tissue and skeletal muscle.Diabetes. 2001; 50: 233-240Crossref PubMed Scopus (49) Google Scholar, 20Igal R.A. Wang S. Gonzalez-Baro M. Coleman R.A. Mitochondrial glycerol phosphate acyltransferase directs the incorporation of exogenous fatty acids into triacylglycerol.J. Biol. Chem. 2001; 276: 42205-42212Abstract Full Text Full Text PDF PubMed Scopus (79) Google Scholar, 21Doody M.C. Pownall H.J. Kao Y.J. Smith L.C. Mechanism and kinetics of transfer of a fluorescent fatty acid between single-walled phosphatidylcholine vesicles.Biochemistry. 1980; 19: 108-116Crossref PubMed Scopus (151) Google Scholar, 22Calvo B.C. Collado I. Cepeda E.A. Solubilities of palmitic acid in pure solvents and its mixtures.J. Chem. Eng. Data. 2009; 54: 64-68Crossref Scopus (21) Google Scholar, 23Smith R. Tanford C. Hydrophobicity of long chain n-alkyl carboxylic acids, as measured by their distribution between heptane and aqueous solutions.Proc. Natl. Acad. Sci. USA. 1973; 70: 289-293Crossref PubMed Google Scholar, 24Pownall H. Moore K. Commentary on fatty acid wars: the diffusionists versus the translocatists.Arterioscler. Thromb. Vasc. Biol. 2014; 34: e8-e9Crossref PubMed Scopus (12) Google Scholar, 25Bonen A. Chabowski A. Luiken J.J. Glatz J.F. Is membrane transport of FFA mediated by lipid, protein, or both? Mechanisms and regulation of protein-mediated cellular fatty acid uptake: molecular, biochemical, and physiological evidence.Physiology (Bethesda). 2007; 22: 15-29Crossref PubMed Scopus (183) Google Scholar, 26Glatz J.F.C. Luiken J. Dynamic role of the transmembrane glycoprotein CD36 (SR-B2) in cellular fatty acid uptake and utilization.J. Lipid Res. 2018; 59: 1084-1093Abstract Full Text Full Text PDF PubMed Scopus (87) Google Scholar, 27Hamilton J.A. New insights into the roles of proteins and lipids in membrane transport of fatty acids.Prostaglandins Leukot. Essent. Fatty Acids. 2007; 77: 355-361Abstract Full Text Full Text PDF PubMed Scopus (86) Google Scholar) because mechanisms guide therapeutic strategies. Physiologically, uncontrolled LCFA movement into and out of cells would be expected to impair the cellular response to changing energy demands. Whereas a regulated translocator could be the needed controller, an alternative mechanism, which is supported by the Jay et al. paper, is that this can also be achieved by regulating the balance between intracellular TAG synthesis versus hydrolysis, which transfer LCFAs into or liberate LCFAs from fat droplets, respectively. The findings of this article do not prove that there are no FA translocators, but rather provide compelling support for a model of metabolism-driven translocation by diffusion. Impaired FA uptake by adipose tissue and the resulting excess of plasma LCFA are mechanistically linked to impaired glucose disposal, a hallmark of type 2 diabetes (28McGarry J.D. What if Minkowski had been ageusic? An alternative angle on diabetes.Science. 1992; 258: 766-770Crossref PubMed Scopus (559) Google Scholar). Proposals for therapeutic approaches that address this impairment differ between translocationists and diffusionists—translocationists would target the putative LCFA transporters. In the context of this paper, however, the diffusionists would target intracellular metabolism that consumes LCFA, notably, by oxidation, TAG synthesis (19Ruan H. Pownall H.J. Overexpression of 1-acyl-glycerol-3-phosphate acyltransferase-alpha enhances lipid storage in cellular models of adipose tissue and skeletal muscle.Diabetes. 2001; 50: 233-240Crossref PubMed Scopus (49) Google Scholar, 20Igal R.A. Wang S. Gonzalez-Baro M. Coleman R.A. Mitochondrial glycerol phosphate acyltransferase directs the incorporation of exogenous fatty acids into triacylglycerol.J. Biol. Chem. 2001; 276: 42205-42212Abstract Full Text Full Text PDF PubMed Scopus (79) Google Scholar), and possibly the regulatory role of CD36. The paper by Jay and colleagues provides a compelling context for the development of these much-needed therapeutic approaches favored by the diffusionists." @default.
• W3012784865 created "2020-03-27" @default.
• W3012784865 creator A5089801293 @default.
• W3012784865 date "2020-05-01" @default.
• W3012784865 modified "2023-10-18" @default.
• W3012784865 title "Commentary on SSO and other putative inhibitors of FA transport across membranes by CD36 disrupt intracellular metabolism, but do not affect fatty acid translocation" @default.
• W3012784865 cites W1512516272 @default.
• W3012784865 cites W1976177239 @default.
• W3012784865 cites W2003978380 @default.
• W3012784865 cites W2006248254 @default.
• W3012784865 cites W2013859761 @default.
• W3012784865 cites W2036344921 @default.
• W3012784865 cites W2046933775 @default.
• W3012784865 cites W2062387478 @default.
• W3012784865 cites W2063253820 @default.
• W3012784865 cites W2065173009 @default.
• W3012784865 cites W2078637473 @default.
• W3012784865 cites W2086151415 @default.
• W3012784865 cites W2087813533 @default.
• W3012784865 cites W2091191922 @default.
• W3012784865 cites W2091525442 @default.
• W3012784865 cites W2094091679 @default.
• W3012784865 cites W2094840146 @default.
• W3012784865 cites W2096043242 @default.
• W3012784865 cites W2104625557 @default.
• W3012784865 cites W2106716523 @default.
• W3012784865 cites W2115380377 @default.
• W3012784865 cites W2135241587 @default.
• W3012784865 cites W2140871520 @default.
• W3012784865 cites W2316741386 @default.
• W3012784865 cites W2781259227 @default.
• W3012784865 cites W2796174912 @default.
• W3012784865 doi "https://doi.org/10.1194/jlr.c120000745" @default.
• W3012784865 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7193970" @default.
• W3012784865 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32198211" @default.
• W3012784865 hasPublicationYear "2020" @default.
• W3012784865 type Work @default.
• W3012784865 sameAs 3012784865 @default.
• W3012784865 citedByCount "5" @default.
• W3012784865 countsByYear W30127848652020 @default.
• W3012784865 countsByYear W30127848652022 @default.
• W3012784865 crossrefType "journal-article" @default.
• W3012784865 hasAuthorship W3012784865A5089801293 @default.
• W3012784865 hasBestOaLocation W30127848651 @default.
• W3012784865 hasConcept C104317684 @default.
• W3012784865 hasConcept C138626823 @default.
• W3012784865 hasConcept C15744967 @default.
• W3012784865 hasConcept C185592680 @default.
• W3012784865 hasConcept C2776035688 @default.
• W3012784865 hasConcept C2776991927 @default.
• W3012784865 hasConcept C2779828298 @default.
• W3012784865 hasConcept C41625074 @default.
• W3012784865 hasConcept C46312422 @default.
• W3012784865 hasConcept C543025807 @default.
• W3012784865 hasConcept C55493867 @default.
• W3012784865 hasConcept C62231903 @default.
• W3012784865 hasConcept C79879829 @default.
• W3012784865 hasConcept C86803240 @default.
• W3012784865 hasConcept C95444343 @default.
• W3012784865 hasConceptScore W3012784865C104317684 @default.
• W3012784865 hasConceptScore W3012784865C138626823 @default.
• W3012784865 hasConceptScore W3012784865C15744967 @default.
• W3012784865 hasConceptScore W3012784865C185592680 @default.
• W3012784865 hasConceptScore W3012784865C2776035688 @default.
• W3012784865 hasConceptScore W3012784865C2776991927 @default.
• W3012784865 hasConceptScore W3012784865C2779828298 @default.
• W3012784865 hasConceptScore W3012784865C41625074 @default.
• W3012784865 hasConceptScore W3012784865C46312422 @default.
• W3012784865 hasConceptScore W3012784865C543025807 @default.
• W3012784865 hasConceptScore W3012784865C55493867 @default.
• W3012784865 hasConceptScore W3012784865C62231903 @default.
• W3012784865 hasConceptScore W3012784865C79879829 @default.
• W3012784865 hasConceptScore W3012784865C86803240 @default.
• W3012784865 hasConceptScore W3012784865C95444343 @default.
• W3012784865 hasIssue "5" @default.
• W3012784865 hasLocation W30127848651 @default.
• W3012784865 hasLocation W30127848652 @default.
• W3012784865 hasLocation W30127848653 @default.
• W3012784865 hasOpenAccess W3012784865 @default.
• W3012784865 hasPrimaryLocation W30127848651 @default.
• W3012784865 hasRelatedWork W148081301 @default.
• W3012784865 hasRelatedWork W19804102 @default.
• W3012784865 hasRelatedWork W2023240488 @default.
• W3012784865 hasRelatedWork W2062846377 @default.
• W3012784865 hasRelatedWork W2082877035 @default.
• W3012784865 hasRelatedWork W2170639418 @default.
• W3012784865 hasRelatedWork W2564650850 @default.
• W3012784865 hasRelatedWork W2908238761 @default.
• W3012784865 hasRelatedWork W3128550852 @default.
• W3012784865 hasRelatedWork W4288453896 @default.
• W3012784865 hasVolume "61" @default.
• W3012784865 isParatext "false" @default.
• W3012784865 isRetracted "false" @default.
• W3012784865 magId "3012784865" @default.
• W3012784865 workType "article" @default.