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Institution

University of Córdoba (Spain)

EducationCordova, Spain
About: University of Córdoba (Spain) is a education organization based out in Cordova, Spain. It is known for research contribution in the topics: Population & Catalysis. The organization has 12006 authors who have published 22998 publications receiving 537842 citations. The organization is also known as: University of Córdoba (Spain) & Universidad de Córdoba.


Papers
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Journal ArticleDOI
TL;DR: In this article, the effects of including a running coupling constant in high-density QCD evolution were studied and the effect of running coupling on the gluon distribution at large transverse momentum was analyzed.
Abstract: We study the effects of including a running coupling constant in high-density QCD evolution. For fixed coupling constant, QCD evolution preserves the initial dependence of the saturation momentum Q s on the nuclear size A and results in an exponential dependence on rapidity Y, Q s 2(Y) = Q s 2(Y 0 ) exp[ᾱ s d(Y - Y 0 )]. For the running coupling case, we rederive analytical estimates for the A and Y dependences of the saturation scale and test them numerically. The A dependence of Q s vanishes ∞ 1/√Y for large A and Y. The Y dependence is reduced to Q s 2(Y) ∞ exp(Δ′ √Y + X), where we find numerically Δ′ ≃ 3.2. We study the behavior of the gluon distribution at large transverse momentum, characterizing it by an anomalous dimension 1 - γ, which we define in a fixed region of small dipole sizes. In contrast to previous analytical work, we find a marked difference between the fixed coupling (γ ≃ 0.65) and running coupling (γ ∼ 0.85) results. Our numerical findings show that both a scaling function depending only on the variable rQ s and the perturbative double-leading-logarithmic expression provide equally good descriptions of the numerical solutions for very small r values below the so-called scaling window. © 2005 The American Physical Society.

134 citations

Journal ArticleDOI
TL;DR: A review on the current knowledge of SARS-CoV-2 accessory proteins is summarized updating new research that could be critical in understanding SARSCoV2 interaction with the host.
Abstract: There are still many unanswered questions concerning viral SARS-CoV-2 pathogenesis in COVID-19. Accessory proteins in SARS-CoV-2 consist of eleven viral proteins whose roles during infection are still not completely understood. Here, a review on the current knowledge of SARS-CoV-2 accessory proteins is summarized updating new research that could be critical in understanding SARS-CoV-2 interaction with the host. Some accessory proteins such as ORF3b, ORF6, ORF7a and ORF8 have been shown to be important IFN-I antagonists inducing an impairment in the host immune response. In addition, ORF3a is involved in apoptosis whereas others like ORF9b and ORF9c interact with cellular organelles leading to suppression of the antiviral response in infected cells. However, possible roles of ORF7b and ORF10 are still awaiting to be described. Also, ORF3d has been reassigned. Relevant information on the knowns and the unknowns in these proteins is analyzed, which could be crucial for further understanding of SARS-CoV-2 pathogenesis and to design strategies counteracting their actions evading immune responses in COVID-19.

134 citations

Journal ArticleDOI
TL;DR: Molecular, genetic and biochemical approaches to the study of eukaryotic nitrate/nitrite transporters allow an initial understanding of this step, which is much more complex and structured than previously suspected.
Abstract: Nitrate transport is the key step controlling the amount of nitrate incorporated by the cells and subsequent of storage, reduction or export. Molecular, genetic and biochemical approaches to the study of eukaryotic nitrate/nitrite transporters allow an initial understanding of this step, which is much more complex and structured than previously suspected. At the plasma membrane level, two gene families, Nrt1 and Nrt2, account for high- and low-affinity nitrate transporters. Functionality of NRT1 from Arabidopsis and NRT2 proteins from Aspergillus and Chlamydomonas has been demonstrated. However, redundancy of these systems makes it difficult to assign particular physiological roles to each. Data on genes involved in the regulation of nitrate transport and reduction are still scarce. Information on nitrite transporters to the chloroplast is biased by the belief that in vivo nitrous acid diffuses freely to this organellum. The recent progress on these aspects is discussed in this review.

134 citations

Journal ArticleDOI
TL;DR: The results are discussed on the basis of a possible control of root elongation by ASC via its action on peroxidases that are involved in the regulation of cell-wall extensibility.
Abstract: Elongation of onion (Allium cepa L.) roots was highly stimulated by ascorbate (ASC) and its natural precursor I-galactone-[gamma]-lactone (GL). When incubation media were supplemented with lycorine (Lyc), an inhibitor of the ASC biosynthesis, root growth was negligible even in the presence of ASC or GL. ASC completely inhibited in vitro guaiacol peroxidase activities that were isolated from both the apoplast and the cell wall. However, ferulic-acid-dependent peroxidase from the cell wall was partially inhibited by ASC, whereas ferulic acid peroxidase activity from the apoplastic fluid was completely inhibited by ASC as long as ASC was present in the assay medium. ASC content in cells was increased by preincubations with ASC or GL, whereas Lyc reduced it. On the other hand, ASC or GL treatments decreased both apoplast and cell-wall-bound peroxidase activities, whereas Lyc had a slight stimulating effect. These results are discussed on the basis of a possible control of root elongation by ASC via its action on peroxidases that are involved in the regulation of cell-wall extensibility.

134 citations

Journal ArticleDOI
TL;DR: A synoptic and balanced account of the consensus knowledge and recent findings in the field of kisspeptin physiology is provided, which it is predicted will be crucial in shaping the progress of the understanding of the roles played by this family of neuropeptides in reproductive biology.
Abstract: Kisspeptins, a family of neuropeptides encoded by the Kiss1 gene that are mainly expressed in discrete neuronal populations of the hypothalamus, have recently emerged as essential upstream regulatory elements of GnRH (gonadotropin-releasing hormone) neurons and, thereby, potent elicitors of gonadotropin secretion. Indeed, kisspeptins are now recognized as important regulators of key aspects of the maturation and function of the reproductive axis, including the sexual differentiation of the brain, the timing of puberty, the adult regulation of gonadotropin secretion by gonadal hormones, and the control of fertility by metabolic and environmental (e.g., photoperiod) cues. Appreciation of these fundamental biological features has led to the contention that kisspeptins are indispensable elements of the reproductive brain whose relevance goes beyond their crucial physiological roles and may pose potential pathophysiological and therapeutic interest. In spite of such a consensus, recent developments in the field have helped to expand, and somewhat challenged, our current understanding of the neuroendocrine and molecular mechanisms whereby some of the effects of kisspeptins are conducted. This review aims to provide a synoptic and balanced account of the consensus knowledge and recent findings in the field of kisspeptin physiology, which we predict will be crucial in shaping the progress of our understanding of the roles played by this family of neuropeptides in reproductive biology.

134 citations


Authors

Showing all 12089 results

NameH-indexPapersCitations
Jose M. Ordovas123102470978
Liang Cheng116177965520
Pedro W. Crous11580951925
Munther A. Khamashta10962350205
Luis Serrano10545242515
Raymond Vanholder10384140861
Carlos Dieguez10154536404
David G. Bostwick9940331638
Leon V. Kochian9526631301
Abhay Ashtekar9436637508
Néstor Armesto9336926848
Manuel Hidalgo9253841330
Rafael de Cabo9131735020
Harald Mischak9044527472
Manuel Tena-Sempere8735123100
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202333
2022133
20211,640
20201,619
20191,517
20181,348