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Gotowe bibliografie tematyczne / DOPA

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Gotowa bibliografia na temat „DOPA”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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Artykuły w czasopismach na temat "DOPA"

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Eldrup, Ebbe, and Erik A. Richter. "DOPA, dopamine, and DOPAC concentrations in the rat gastrointestinal tract decrease during fasting." American Journal of Physiology-Endocrinology and Metabolism 279, no. 4 (2000): E815—E822. http://dx.doi.org/10.1152/ajpendo.2000.279.4.e815.

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The aim of the present study was to test the hypothesis that 3,4-dihydroxyphenylalanine (DOPA) and dopamine (DA) in the gastrointestinal tract are to a large extent of exogenous origin and derived from food. Tissue concentrations of norepinephrine (NE), epinephrine (Epi), DA, DOPA, and 3,4-dihydroxyphenylacetic acid (DOPAC), as measured by reverse-phase HPLC with electrochemical detection, were studied in fed and 4-day-fasted Wistar rats as well as in sympathectomized and adrenodemedullated rats. Sympathectomy and adrenal demedullectomy decreased tissue concentrations of NE and Epi, respective

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Eldrup, Ebbe, Svend Erik Møller, JAN Andreasen, and Niels Juel Christensen. "Effects of Ordinary Meals on Plasma Concentrations of 3,4-Dihydroxyphenylalanine, Dopamine Sulphate and 3,4-Dihydroxyphenylacetic Acid." Clinical Science 92, no. 4 (1997): 423–30. http://dx.doi.org/10.1042/cs0920423.

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1. Plasma concentrations of 3,4-dihydroxyphenylalanine (DOPA), dopamine sulphate (DA-S), and 3,4-dihydroxyphenylacetic acid (DOPAC) in humans have been claimed to be indexes of sympathetic nervous activity, but the source and significance of plasma DOPA, DOPAC and DA-S have not been completely elucidated. 2. The effects of ordinary meals on plasma concentrations of total dopamine, mainly DA-S, DOPAC and DOPA were studied in seven healthy subjects. Venous blood was collected every hour for 25 h, while subjects were either fasting or received three meals at 9.00 hours, 13.00 hours and 18.00 hour

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Okada, Maki, Ryuji Nakao, Rie Hosoi та ін. "Microdialysis with Radiometric Monitoring of L-[β-11C]DOPA to Assess Dopaminergic Metabolism: Effect of Inhibitors of L-Amino Acid Decarboxylase, Monoamine Oxidase, and Catechol-O-Methyltransferase on Rat Striatal Dialysate". Journal of Cerebral Blood Flow & Metabolism 31, № 1 (2010): 124–31. http://dx.doi.org/10.1038/jcbfm.2010.58.

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The catecholamine, dopamine (DA), is synthesized from 3,4-dihydroxy-L-phenylalanine (L-DOPA) by aromatic L-amino acid decarboxylase (AADC). Dopamine metabolism is regulated by monoamine oxidase (MAO) and catechol- O-methyltransferase (COMT). To measure dopaminergic metabolism, we used microdialysis with radiometric detection to monitor L-[β-11C]DOPA metabolites in the extracellular space of the rat striatum. We also evaluated the effects of AADC, MAO, and COMT inhibitors on metabolite profiles. The major early species measured after administration of L-[β-11C]DOPA were [11C]3,4-dihydroxyphenyl

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Soares-da-Silva, P., M. Pestana, and M. H. Fernandes. "Involvement of tubular sodium in the formation of dopamine in the human renal cortex." Journal of the American Society of Nephrology 3, no. 9 (1993): 1591–99. http://dx.doi.org/10.1681/asn.v391591.

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This study has examined the influence of sodium (0, 20, 40, 80, 120, and 160 mM) and ouabain (100, 500, and 1,000 microM), an inhibitor of the enzyme Na(+)-K+ ATPase, on the synthesis of dopamine in slices of human renal cortex loaded with exogenous L-dihydroxyphenylalanine (L-DOPA). The deamination of newly formed dopamine into 3,4-dihydroxyphenylacetic acid (DOPAC) was also examined. The formation of dopamine and its deamination to DOPAC in slices and homogenates of human renal cortex closely depended on the concentration of L-DOPA added to the medium; in homogenates of renal cortex, the pro

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Buu, N. T., and C. Lussier. "Origin of dopamine in the rat adrenal cortex." American Journal of Physiology-Renal Physiology 258, no. 2 (1990): F287—F291. http://dx.doi.org/10.1152/ajprenal.1990.258.2.f287.

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The hypothesis that dopamine (DA) is involved in the control of aldosterone secretion is given some support by the finding of DA in the adrenal cortex of several species, but the source of this DA is not known. This study showed that the administration of L-dopa to intact rats or medullectomized rats caused a significant DA increase in the adrenal cortex. The DA increase in the cortex was more pronounced than in the medulla, coincident with higher L-dopa uptake by the cortical tissue. Tyrosine administration raised DA levels only in the medulla. Sympathectomy of the rat by 6-hydroxydopamine tr

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Armando, I., S. Nowicki, J. Aguirre, and M. Barontini. "A decreased tubular uptake of dopa results in defective renal dopamine production in aged rats." American Journal of Physiology-Renal Physiology 268, no. 6 (1995): F1087—F1092. http://dx.doi.org/10.1152/ajprenal.1995.268.6.f1087.

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A major proportion of urinary dopamine derives from the renal decarboxylation of circulating dopa. This study evaluates the effects of aging on renal production of dopamine using 3- and 12-mo-old male Wistar rats. Urinary excretion of Na+, norepinephrine (NE), 3,4-dihydroxyphenylglycol, and dopa were similar in the two groups. Urinary dopamine and 3,4-dihydroxyphenylacetic acid (DOPAC) were lower in older animals (dopamine, 20 +/- 6 vs. 47 +/- 7 nmol/24 h, P < 0.001; DOPAC, 142 +/- 36 vs. 304 +/- 56 nmol/24 h, P < 0.03). Urinary 3-O-methyldopa (OM-dopa) was higher in 12-mo-old rats (6.2

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Lavoie, Mark P., Meg Palmatier, Frank T. Gentile, et al. "Two PC 12 Pheochromocytoma Lines Sealed in Hollow Fiber-Based Capsules Tonically Release L-Dopa In Vitro." Cell Transplantation 2, no. 2 (1993): 163–73. http://dx.doi.org/10.1177/096368979300200209.

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Two PC12 cell-derived lines have been studied following encapsulation into polymer-based hollow fibers with respect to secreted catecholamines and their metabolites. Cellular encapsulation provides a chronic microperfusion environment within which basally secreted PC12 products can be readily measured. Encapsulated PC12 cells grown and held under the conditions specified in this report basally release amounts exceeding their total cellular stores of the dopamine precursor L-DOPA and the electrochemically active dopamine metabolites DOPAC and HVA during 45-min static incubations. Under these sa

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Dutton, J., L. G. Copeland, J. R. Playfer, and N. B. Roberts. "Measuring L-dopa in plasma and urine to monitor therapy of elderly patients with Parkinson disease treated with L-dopa and a dopa decarboxylase inhibitor." Clinical Chemistry 39, no. 4 (1993): 629–34. http://dx.doi.org/10.1093/clinchem/39.4.629.

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Abstract We have established a method for measuring L-dopa in plasma and urine, including the metabolites dopamine and L-dopac, using separation by ion-pair reversed-phase HPLC and quantification with an electrochemical detector. The assay was applied to the therapeutic monitoring of elderly patients with established Parkinson disease being treated with L-dopa plus a dopa decarboxylase inhibitor. Plasma L-dopa was evaluated in relation to dosage and postdose sampling time in 71 outpatients with Parkinson disease. L-Dopa concentrations were greatest in the patients taking the highest dosages pr

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Eisenhofer, G., D. S. Goldstein, R. Stull, et al. "Simultaneous liquid-chromatographic determination of 3,4-dihydroxyphenylglycol, catecholamines, and 3,4-dihydroxyphenylalanine in plasma, and their responses to inhibition of monoamine oxidase." Clinical Chemistry 32, no. 11 (1986): 2030–33. http://dx.doi.org/10.1093/clinchem/32.11.2030.

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Abstract This is a reversed-phase liquid-chromatographic method, with electrochemical detection, for simultaneously measuring, in plasma, the concentrations of the catecholamine precursor dihydroxyphenylalanine (DOPA); the endogenous catecholamines norepinephrine, epinephrine, and dopamine; and the deaminated catecholamine metabolites dihydroxyphenylacetic acid (DOPAC) and dihydroxyphenylglycol (DHPG). We used this method to assess effects of monoamine oxidase (EC 1.4.3.4) inhibition in humans. Plasma DHPG concentrations as determined by the present method (mean 826, SEM 61 ng/L) were similar

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Lorenc-Koci, Elżbieta, Kinga Kamińska, Tomasz Lenda, and Jolanta Konieczny. "The Effect of Chronic Treatment with the Inhibitor of Phosphodiesterase 5 (PDE5), Sildenafil, in Combination with L-DOPA on Asymmetric Behavior and Monoamine Catabolism in the Striatum and Substantia Nigra of Unilaterally 6-OHDA-Lesioned Rats." Molecules 29, no. 18 (2024): 4318. http://dx.doi.org/10.3390/molecules29184318.

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The use of phosphodiesterase inhibitors in the treatment of Parkinson’s disease is currently widely discussed. The study aimed to investigate the impact of acute and chronic treatment with the phosphodiesterase 5 inhibitor, sildenafil, at low and moderate doses of 2 mg/kg and 6 mg/kg, and L-DOPA (12.5 mg/kg), alone or in combination, on asymmetric behavior and dopamine (DA) and serotonin metabolism in the striatum and substantia nigra of unilaterally 6-OHDA-lesioned rats. Acute administration of sildenafil at both tested doses jointly with L-DOPA significantly increased the number of contralat

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Rozprawy doktorskie na temat "DOPA"

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Khan, Ghulam Ahmed. "Enzymatic synthesis of L-DOPA esters." Thesis, University of Reading, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333598.

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Branden, Stansley. "L-dopa and the Serotonergic System." University of Toledo Health Science Campus / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=mco1429543879.

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Wiese, Claudia Anette Elisabeth. "Metabolismus fluorierter DOPA-Isomere in aggregierenden Hirnzellkulturen /." [S.l.] : [s.n.], 1991. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=9542.

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Nelson, Michelle Amy. "Protein bound 3,4 dihydroxyphenyalanine as a signal for enhanced antioxidant defences /." full text via ADT, 2008. http://erl.canberra.edu.au/public/adt-AUC20081209.125208/index.html.

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Moheimen, Jamil. "Striatal neuropeptides associated with L- DOPA-induced dyskinesia." Thesis, Uppsala universitet, Institutionen för farmaceutisk biovetenskap, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-209915.

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Abstract Striatal neuropeptides associated with L-DOPA-induced dyskinesia 2012-02-14 <img src="file:///page2image2248" /> Parkinson's disease (PD) is the most common neurodegenerative disease, with approximately 6 million sufferers in the world. The patients are usually diagnosed between the ages 50-70 years and as the disease progress more symptoms may occur. The cause of the disease is unknown, but the characteristic of PD is that it is a selective degeneration of dopaminergic neurons in the substantia nigra, which leads to an absence of dopamine release in striatum. This affects the motor s

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DIMOV, MICHEL. "Melanomes malins et 5-s-cysteinyl- dopa urinaire." Strasbourg 1, 1991. http://www.theses.fr/1991STR15033.

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Tison, François. "La L-Dopa endogène : aspects neurochimiques, physiologiques et étude anatomofonctionnelle par immunohistochimie dans le cerveau de rat." Bordeaux 2, 1990. http://www.theses.fr/1990BOR23037.

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Nelson, Michelle Amy, and n/a. "Protein Bound 3,4-Dihydroxyphenylalanine as a Signal for Enhanced Antioxidant Defences." University of Canberra. n/a, 2008. http://erl.canberra.edu.au./public/adt-AUC20081209.125208.

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Protein-bound 3,4-dihydroxyphenylalanine (PB-DOPA), a long-lived, redox-active product of protein oxidation, is capable of functioning as both a pro- and anti-oxidant. A number of in vitro and in vivo studies have demonstrated a toxic, non-toxic or even beneficial effect of free DOPA, however little investigation has examined the physiological activity of PB-DOPA. Furthermore, as free DOPA is currently the major treatment available for Parkinson?s disease, most studies have focused on the effect of DOPA within neurological cells or tissues, although the presence of PB-DOPA in other locations,

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Nevalainen, Nina, Martin Lundblad, Greg A. Gerhardt, and Ingrid Strömberg. "Striatal Glutamate Release in L-DOPA-Induced Dyskinetic Animals." Umeå universitet, Institutionen för strålningsvetenskaper, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-67595.

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L-DOPA-induced dyskinesia is a common side effect developed after chronic treatment with 3,4-dihydroxyphenyl-L-alanine (L-DOPA) in Parkinson's disease. The biological mechanisms behind this side effect are not fully comprehended although involvement of dopaminergic, serotonergic, and glutamatergic systems has been suggested. The present study utilizes in vivo amperometry to investigate the impact from unilateral 6-hydroxydopamine lesions and L-DOPA (4 mg/kg, including benserazide 15 mg/kg) -induced dyskinetic behavior on striatal basal extracellular glutamate concentration and potassium-evoked

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Cabral, Kibedi. "Towards optimisation of L-DOPA synthesis in Mucuna pruriens." Thesis, Cardiff University, 2014. http://orca.cf.ac.uk/70680/.

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This study examines the potential for increasing natural L-DOPA drug biosynthesis in Mucuna pruriens by silencing or “knocking down” expression of putative DOPA/tyrosine decarboxylase (Mp-ty/ddc) in situ. Mp-ty/ddc codes for DOPA/tyrosine decarboxylase (Mp-TY/DDC) which converts L-DOPA to dopamine in plants. The hypothesis of the work was that silencing the Mp-ty/ddc gene would result in accumulation of L-DOPA in the plant tissues. This work involved isolation and characterisation of 1.73 kb putative full-length ORF of Mp-ty/ddc. The gene showed 74% homology with TY/DDC protein alignments of o

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Książki na temat "DOPA"

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Riederer, Peter, and Helga Umek, eds. L-Dopa-Substitution der Parkinson-Krankheit. Springer Vienna, 1985. http://dx.doi.org/10.1007/978-3-7091-8822-4.

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1934-, Misu Yoshimi, and Goshima Yoshio, eds. Neurobiology of DOPA as a neurotransmitter. CRC/Taylor & Francis, 2006.

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Koch, E. Pathogenic problems of phenolase enzymatic oxidation of catecholamines and dopa in humans. Elsevier, 1988.

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Pialis, Peter. The production of L-dopa from mushroom tyrosinase immobilized on nyulon 6,6. National Library of Canada, 1996.

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Phǣnngān, Thailand Krom Kānpokkhrō̜ng Kō̜ng Wichākān læ. Facts about DOPA: Alleviation of suffering and promotion of the people's well-being. Kōng Wichākān læ Phǣnngān, Krom Kānpokkhrō̜ng, 2006.

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1933-, Fahn Stanley, ed. Parlodel® (bromocriptine mesylate) in the early management of Parkinson's disease: Excerpts from Recent developments in Parkinson's disease, volume 2. Macmillan Healthcare Information, 1987.

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Wong, Clara Lai Fong. Effect of L-DOPA on dopamine synthesis and tyrosine hydroxylase concentration in young adult nigrostriatal neurons. National Library of Canada = Bibliothèque nationale du Canada, 1991.

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Sacks, Oliver W. Przebudzenia. Wydawnictwo Zysk i S-ka, 2011.

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Sacks, Oliver W. Awakenings: Das Buch zum Film = Zeit des Erwachens. Rowohlt, 1995.

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Sacks, Oliver W. Awakenings. Vintage Books, 2002.

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Części książek na temat "DOPA"

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Maxwell, Robert A., and Shohreh B. Eckhardt. "l-Dopa." In Drug Discovery. Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0469-5_14.

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Fischer, Gabriele, Annemarie Unger, W. Wolfgang Fleischhacker, et al. "l-Dopa." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_955.

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Colzi, A., G. Zürcher, R. Kettler, M. Da Prada, and E. Schneider. "L-Dopa." In Neuro-Psychopharmaka. Springer Vienna, 1992. http://dx.doi.org/10.1007/978-3-7091-3330-9_3.

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Calabria, Ferdinando, and Orazio Schillaci. "18F-DOPA." In Radiopharmaceuticals. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-27779-6_2.

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Calabria, Ferdinando, Mario Leporace, and Orazio Schillaci. "18F-DOPA." In Radiopharmaceuticals. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-54196-4_2.

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Furukawa, Yoshiaki, Mark Guttman, Shinichiro Nakamura, and Stephen J. Kish. "Dopa-Responsive Dystonia." In Movement Disorder Emergencies. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-60761-835-5_24.

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Brouwers, Adrienne H., Klaas P. Koopmans, Rudi A. J. O. Dierckx, and Philip H. Elsinga. "Dopa PET-CT." In PET-CT Beyond FDG A Quick Guide to Image Interpretation. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-93909-2_10.

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States, Lisa J., and Klaus Mohnike. "18F-DOPA PET." In Congenital Hyperinsulinism. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-02961-6_7.

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Furukawa, Yoshiaki, Mark Guttman, and Stephen J. Kish. "Dopa-Responsive Dystonia." In Movement Disorder Emergencies. Humana Press, 2005. http://dx.doi.org/10.1385/1-59259-902-8:209.

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Metze, Dieter, Tam Nguyen, Birgit Haack, et al. "Dopa-responsive Dystonia." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_510.

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Streszczenia konferencji na temat "DOPA"

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Hansen, Douglas C., and Stephen C. Dexter. "A Novel Biopolymer and Its Application as an Anticorrosive for Stainless Steel Alloys in Seawater." In CORROSION 1993. NACE International, 1993. https://doi.org/10.5006/c1993-93491.

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Abstract The adhesive protein of the common blue mussel, Mytilus edulis(L) is a novel biopolymer in that it contains a catechol, L,3,4-dihydroxy-phenylalanine (L-Dopa) in its primary sequence. Adsorption of this protein onto S30403 stainless steel coupons imparts a significant resistance to corrosion when the test coupons are immersed in 3% NaCl and with an applied potential up to +350 mV (SCE). Comparison with other proteins and polymers such as serum albumin (BSA), a low molecular weight catechol (DHBA), and poly-L-lysine indicates that none are as effective as the mussel protein at inhibiti

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Millet, Cecile, Guillaume Néel, Florian Thébault, and Pierre Mauger. "Compatibility of Dope Free Solution with Dense CO2 Streams." In CONFERENCE 2024. AMPP, 2024. https://doi.org/10.5006/c2024-20930.

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Abstract In the framework of the injection of anthropogenic CO2 for supporting energy transition, more and more wells will be used for injecting dense CO2 streams. Dope free solutions for premium OCTG connections to replace both storage and running thread compounds are beneficial for saving time (lower running time), for environmental considerations (no discharge of dope) as well as improving running performances. However, they have never been qualified in dense CO2 stream environments containing brines, while dense CO2 is known to be a good solvent toward polymers. A test protocol has been de

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Francois-Heude, Alexandre, and Cécile Millet. "Electrodeposited Zinc Based Plating on Premium OCTG Connections as an Alternative to Storage and Running Dope: Corrosion Performance Evaluation." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-13274.

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Abstract The use of dry coating on Premium OCTG connections to replace both storage and running compounds presents numerous benefits for end-users. As well as improving running performances, it keeps the well clean by preventing the discharge of dope to the environment and into the well bore and it reduces the operational costs by the elimination of storage dope, cleaning and running dope re-application. The solution that has been developed combines: (i) an electrodeposited zinc-based metal plating, which provides anti galling properties and protects the steel from corrosion in storage conditi

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Hashem, Ihab, Jian Wang, and Jan F. M. Van Impe. "Optimizing Individual-based Modelling: A Grid-based Approach to Computationally Efficient Microbial Simulations." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.102831.

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Individual-based modeling (IbM) has emerged as a powerful approach for studying microbial populations, offering a bottom-up framework to simulate cellular behaviors and their interactions. Unlike continuum-based models, IbM explicitly captures the heterogeneity and emergent dynamics of microbial communities, making it invaluable for studying spatially structured phenomena such as nutrient competition, biofilm formation, and colony interactions. However, IbM faces significant computational challenges, particularly in resolving spatial overlaps during simulations of large microbial populations.

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Wang, Lixian, Aria Moaven, Sara Shafiei Alavijeh, and Zhiping Jiang. "Study on Pump and Signal-Induced Polarization Dependent Gain in Bismuth-Doped Fiber for E/S Band Amplification." In Optical Fiber Communication Conference. Optica Publishing Group, 2025. https://doi.org/10.1364/ofc.2025.tu3e.2.

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Signal and pump-induced polarization dependent gains (PDGs) in germanosilicate bismuth-dope fiber are examined separately. PDG’s wavelength dependency, its relation to the gain compression as well as the influence of the BAC subtypes are discussed.

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Farah, Pedro Felisberto Nogueira Viana, Felipe dos Santos Souza, Felipe Oliveira Costa, Mariana Bastos Rodrigues dos Santos, and Yasmim Evelyn Lisboa Barbosa. "L-dopa: main drug induced dyskinesia." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.111.

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Introduction: 3,4-dihydroxy-L-phenylalanine (L-dopa) is the gold standard drug for the treatment of Parkinson’s disease (PD). This disease causes degeneration of dopaminergic cells, L-dopa supplies the lack of dopamine, being effective in its treatment. The average time for the onset of this hyperkinetic disorder is usually 6.5 years and the young age at the beginning of the disease. This pathology may present with chorea, dystonia, myoclonus and stereotypes. Diskinesia-inducing L-dopa (LID) remains one of the most challenging unmet needs in the treatment of PD and other neurodegenerative dise

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Sacha E, Gandhi, Nodehi Anahita, Lawton Michael A, et al. "Dopa responsiveness in Parkinson’s disease." In ABN 2024 annual meeting abstracts. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/jnnp-2024-abn.20.

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Alshehri, Ali, Hani Alshahrani, Abdulrahman Alzahrani, et al. "DOPA: Detecting Open Ports in Android OS." In 2018 IEEE Conference on Communications and Network Security (CNS). IEEE, 2018. http://dx.doi.org/10.1109/cns.2018.8433207.

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Black, Kvar C., Zhongqiang Liu, and Phillip B. Messersmith. "DOPA-Mediated Self-Assembled Biocompatible Plasmonic Nanocrystals." In Frontiers in Optics. OSA, 2007. http://dx.doi.org/10.1364/fio.2007.jsua41.

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Gratz, M., S. Hofmann, C. Kuhn, S. Mahner, U. Jeschke, and A. Vattai. "Verminderte Expression der L-DOPA Decarboxylase im Abortgeschehen." In Jahrestagung der Österreichischen Gesellschaft für Gynäkologie und Geburtshilfe (OEGGG) gemeinsam mit der Bayerischen Gesellschaft für Geburtshilfe und Frauenheilkunde e.V (BGGF). Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1602266.

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Raporty organizacyjne na temat "DOPA"

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Halley, Charlotte. The Gut-Brain Axis: Assessment of EcNL-DOPA in mice and dogs. Iowa State University, 2020. http://dx.doi.org/10.31274/cc-20240624-1441.

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Pina-Burón, María Rosa. Doña Mencía. Institut Català d’Arqueologia Clàssica, 2022. http://dx.doi.org/10.51417/figlinae_018.

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Ficha del yacimiento Doña Mencía ubicado a Écija (Sevilla) incluida en el proyecto "Figlinae Hispanae (FIGHISP). Catálogo en red de las alfarerías hispanorromanas y estudio de la comercialización de sus productos".

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Pina-Burón, María Rosa. Tesorillo de Doña Mencía. Institut Català d’Arqueologia Clàssica, 2022. http://dx.doi.org/10.51417/figlinae_032.

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Ficha del yacimiento Tesorillo de Doña Mencía ubicado a Écija (Sevilla) incluida en el proyecto "Figlinae Hispanae (FIGHISP). Catálogo en red de las alfarerías hispanorromanas y estudio de la comercialización de sus productos".

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León, Carlos. Digital Operational Resilience Act (DORA). FNA, 2023. http://dx.doi.org/10.69701/deff9232.

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One of the key lessons of the 2007-2008 global financial crisis is the importance of financial market infrastructures (FMIs) as a pillar of financial stability. Before, the role of financial market infrastructures, namely the provision of trading, clearing, settling, recording, and compressing services for transactions between financial institutions (FIs) was often taken for granted. This was reflected in FMIs having often been referred to as the financial system’s plumbing, including by the Federal Reserve’s 14th chairman (Bernanke, 2011)—a clear reference to the critical yet concealed import

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Jara, Alejandro. Services, Anti-dumping and Other "New Issues" in the WTO Negotiations and Their Relevance for the FTAA. Inter-American Development Bank, 2002. http://dx.doi.org/10.18235/0012240.

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In the semester following the Doha Ministerial, WTO Members were able to set up the essential elements of the Work Program decided by Ministers at Doha (November 2001), including the negotiations mandated in the declaration.

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Seager, William R. Geologic Map of the Dona Ana 7.5-Minute Quadrangle and Adjacent Areas, Dona Ana County, New Mexico. New Mexico Bureau of Geology and Mineral Resources, 2018. http://dx.doi.org/10.58799/of-gm-267.

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Amiti, Mary, and John Romalis. Will the Doha Round Lead to Preference Erosion? National Bureau of Economic Research, 2007. http://dx.doi.org/10.3386/w12971.

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Defraigne, Pierre. CANCUN: Un Hito en el Camino hacia la Conclusión de la RONDA DE DOHA. Inter-American Development Bank, 2003. http://dx.doi.org/10.18235/0007419.

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El porqué de la agenda de dsarrollo de la Ronda de Doha fortalecimiento del sistema de comercio multilateral contra el unilateralismo redacción de los Tratados de Comercio Regionales [RTA] Respaldo de la dinámica de la liberación del comercio y el establecimiento de normas (crecimiento mundial y políticas locales efectivas) La Agenda de Desarrollo de la Ronda de Doha es parte de una agenda global (Monterrey - Joburg ¿ regiones más desarrolladas [MDR¿s]) en busca de coherencia entre: convergencia norte-sur sustentabilidad

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Research Institute (IFPRI), International Food Policy. Assessing the potential cost of a failed Doha Round. International Food Policy Research Institute, 2017. http://dx.doi.org/10.2499/9780896292499_06.

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Hertel, Thomas, Roman Keeney, Maros Ivanic, and Alan Winters. Why Isn’t the Doha Development Agenda More Poverty Friendly? GTAP Working Paper, 2007. http://dx.doi.org/10.21642/gtap.wp37.

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The breakdown of the WTO negotiations under the Doha Development Agenda has inspired critics to highlight the lack of effort on the part of rich countries to reform their agricultural policies. In this paper, we focus instead the poverty impacts of developing country tariff cuts – particularly those in agriculture. We argue that the Doha Development Agenda is fundamentally less poverty-friendly than it could be -- in large part due to the absence of tariff cuts on staple food products in developing countries. Such cuts would give the poor access to food at world prices, thereby reducing the co

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