Analysis of electroencephalograms in Alzheimer's disease patients with multiscale entropy

The aim of this study was to analyse the electroencephalogram (EEG) background activity of Alzheimer’s disease (AD) patients using the Multiscale Entropy (MSE). The MSE is a recently developed method that quantifies the regularity of a signal on different time scales. These time scales are inspected by means of several coarse-grained sequences formed from the analysed signals. We recorded the EEGs from 19 scalp electrodes in 11 AD patients and 11 age-matched controls and estimated the MSE profile for each epoch of the EEG recordings. The shape of the MSE profiles reveals the EEG complexity, and it suggests that the EEG contains information in deeper scales than the smallest one. Moreover, the results showed that the EEG background activity is less complex in AD patients than control subjects. We found significant difference

Nefroblastoma espinal en un Rottweiler

El nefroblastoma espinal es una neoplasia infrecuente en el perro. Se diagnostica en animales jóvenes, afectando, casi exclusivamente, al segmento medular T10 -L2. En este trabajo, e describen los signos clínicos, resultados de las pruebas complementarias y los hallazgos histopatológicos de un perro con un nefroblastoma espinal.

Reply to "Comment on 'Analysis of electroencephalograms in Alzheimer's disease patients with multiscale entropy'"

We appreciate the interest of Dr Tang in our article. Certainly, our previous results should be taken with caution due to the small database size. Nevertheless, it must be noted that this limitation was clearly recognized in our article. Furthermore, our hypothesis is completely justified from the current state of the art in the analysis of electroencephalogram (EEG) signals from Alzheimer's disease (AD) patients. We evaluated whether the multiscale entropy (MSE) analysis of the EEG background activity was useful to distinguish AD patients and controls. We do believe that further discussions about risk factors or related clinicophysiological protein aspects are clearly beyond the scope of our article. For the sake of completeness, we now detail some results that complement our previous analysis. They suggest that the MSE analysis can provide relevant information about the dynamics of AD patients' EEG data. Thus, we must reaffirm our conclusions, although we again acknowledge that further studies are needed

Interstrand DNA covalent binding of two dinuclear Ru(ii) complexes. Influence of the extra ring of the bridging ligand on the DNA interaction and cytotoxic activity

In this work, we report experimental and computational evidences for the intercalation into the DNA base pairs of the free quinones Quinizarin (Q), Naphthazain (N) and the interstrad covalent binding of their p-cymene di-Ruthenium(II) complexes (Cl2Ru2X, with X = N, Q bridging ligands). The intercalation extent for the N complex was larger than for Q, in good agreement with higher relative contour length and melting temperature for the same CX/CDNA ratio and with the computacional mean stacking distances between the ligand and the nearest base-pair (3.34Å and 3.19Å) for N and Q, respectively. However, the apparent binding constant of Q/DNA, two orders higher than that of N/DNA, denotes that the thermal stability of X/DNA complex is more related to the degree of intercalation than to the binding constants magnitude. Cl2Ru2X complexes undergo aquation, forming the aqua-derivatives [(H2O)2Ru2X]2+. These can further bind covalently to DNA via interstrand crosslinking, through both Ru centres and two N7 sites of consecutive Guanines, to give (DNA1,2)Ru2X complexes, by a mechanism similar to that of cisplatin. To the best of our knowledge, this type of interaction with dinuclear Ru(II) complexes has not been reported hitherto. The experimental and computational results reveal that the number of rings of the aromatic moiety and the covalent binding to DNA play a key role in the behaviour of the quinones and their Ru(II) derivatives. The cytotoxicity of the ligands and the corresponding Ru(II) complexes was evaluated in the MCF-7, A2780, A2780cis tumour cells and in the healthy cell line MRC-5. The cytotoxic activity was notable for the N compound and negligible for Q. The IC50 values and the resistance (RF) and selectivity (SF) factors show that the Cl2Ru2N complex is the most promising among the four studied anticancer drugs

Development of an antibody-based capture enzyme-linked immunosorbent assay for detecting echinostoma caproni (trematoda) in experimentally infected rats: kinetics of coproantigen excretion

The present study reports on the development of a coproantigen capture enzyme-linked immunosorbent assay (ELISA) for detecting Echinostoma caproni in experimentally infected rats. The capture ELISA was based on polyclonal rabbit antibodies that recognize excretory–secretory (ES) antigens. The detection limit of pure ES was 3 ng/ml in sample buffer and 60 ng/ml in fecal samples. The test was evaluated using a follow-up of 10 rats experimentally infected with 100 metacercariae of E. caproni, and the results were compared with those of other diagnostic methods such as parasitological examination and antibody titers determined by indirect ELISA. Coproantigens were detected in all the infected rats from the first day postinfection (DPI). The period of maximal coproantigen excretion was between 7 and 21 DPI. The values remained positive until 49–56 DPI, coinciding with the disappearance of the eggs in the stool samples of the infected rats. The kinetics of coproantigen detection were correlated with those of egg output. The present assay provides an alternative tool for the diagnosis of the echinostome infections. The proposed capture ELISA makes possible an earlier diagnosis than that provided by parasitological examination and indirect ELISA and also allows for the differentiation of past and current infections. Our results show that this assay can also be used to monitor the course of echinostome infections.Toledo Navarro, Rafael, [email protected] ; Espert Fernandez, Ana M., [email protected] ; Marcilla Diaz, Antonio, [email protected] ; Esteban Sanchis, Jose Guillermo, [email protected]

Spectroscopy of proton-unbound nuclei by tracking their decay products in-flight: One- and two-proton decays of 15F, 16Ne, and 19Na

14 páginas, 23 figuras, 1 tabla.-- et al.A powerful method of investigating proton-unbound nuclear states by tracking their decay products in flight is discussed in detail. To verify the method, four known levels in 15F, 16Ne, and 19Na were investigated by measuring the angular correlations between protons and the respective heavy-ion fragments stemming from the precursor decays in flight. The parent nuclei of interest were produced in nuclear reactions of one-neutron removal from 17Ne and 20Mg projectiles at energies of 410–450 A MeV. The trajectories of the respective decay products, 14O + p + p and 18Ne + p + p, were measured by applying a tracking technique with microstrip detectors. These data were used to reconstruct the angular correlations of the fragments, which provided information on energies and widths of the parent states. In addition for reproducing properties of known states, evidence for hitherto unknown excited states in 15F and 16Ne was found. This tracking technique has an advantage in studies of exotic nuclei beyond the proton drip line measuring the resonance energies and widths with a high precision although by using low-intensity beams and very thick targets.This work has been supported by Contract EURONS Nos. EC-I3 and FPA2006-13807-C02-01, FPA2007-63074 (MEC, Spain), the INTAS Grant No. 03-54-6545. L.V.G. is supported by FAIR-Russia Research Center grant, Russian Foundation for Basic Research viaGrant Nos. RFBR 08-02-00892 and 08-02-00089-a, and Russian Ministry of Industry and Science Grant No. NSh-7235.2010.2. N.K.T. acknowledges support from the UK Grant No. STFC ST/F012012/1, E.L. is supported by the LOEWE program of the State of Hessen (Helmholtz International Center for FAIR), Germany.Peer Reviewe

General disease resistance loci against biotrophic pathogens in wheat

Dissertação de Mestrado Integrado em Arquitectura, apresentada ao Departamento de Arquitectura da Faculdade de Ciências e Tecnologia da Universidade de Coimbra, sob a orientação do Prof. Doutor Walter Rossa.Um ano depois de a UNESCO inscrever a “Universidade de Coimbra - Alta e Sofia” na lista do Património Mundial da Humanidade e face ao desafio académico de Coimbra Capital Europeia da Cultura em 2027, este trabalho tem como objectivo analisar e perceber como se alterou a imagem urbana da cidade e de que maneira o branding que proponho para a mesma vai clarificar essa imagem, de forma a criar uma linguagem coerente e clara, que traga valor para Coimbra. O trabalho divide-se em quatro partes. A primeira exibe a importância do branding para as cidades, entendendo que este conceito é fundamental para que Coimbra construa uma visão de futuro, com uma melhoria no espaço público e com uma linguagem coerente entre a Universidade a tudo o que a dinamiza. A segunda parte, analisa a evolução da imagem e do sistema urbano do espaço que escolhi como exemplo de trabalho, a antiga Quinta de Santa Cruz, onde foi criado o “boulevard” da cidade, a Avenida Sá da Bandeira e a Praça da República. Na terceira parte, vou analisar criticamente estes dois espaços de maneira a perceber como alterar a imagem suja que a cidade tem hoje, clarificando-a e sabendo que esta zona tem tudo para ser o verdadeiro centro cosmopolita de Coimbra. Por último, associo a esse exemplo um de outra natureza, mas com ele coerente no compto geral do processo, a criação de um logótipo que vai qualificar a cidade e que vai estar presente na mudança do sistema urbano, ajudando a clarificar a imagem da cidade.One year later that UNESCO aggregated “Universidade de Coimbra - Alta e Sofia” at the list of World Heritage Site and the academic challenge of Coimbra European Capital of Culture in 2027, this work aims to analyze and understand how changed the image of urban city , and that way, how the branding that i’ll propose for the city, will clarify this image in order to create a coherent and clear language that bring value to Coimbra. The work is divided into four parts. A first that displays the importance of branding for cities, and how these concept is fundamental to Coimbra build a vision of future, with an improvement in public space and with identical language between the University and everything that surrounds it. The second part examines the evolution of the urban system and the image of the space that i found as an example to work, the old Quinta de Santa Cruz, where the “boulevard” of the city with the Avenue Sá da Bandeira and Republic Square was created. In the third part i will analyze and criticize these two spaces so that you can understand how to clean the soiled image that the city transpires today, in order to make clear that this space has everything to be the true cosmopolitan center of Coimbra. Finally i will associate this example to other of a diferent nature, but coherent in the overall process, the creation of a logo that will qualify the city and that will be present in the changing of urban system helping to clarify the city’s image

β -delayed three-proton decay of 31 Ar

The β decay of Ar31, produced by fragmentation of an Ar36 beam at 880 MeV/nucleon, was investigated. Identified ions of Ar31 were stopped in a gaseous time projection chamber with optical readout allowing us to record decay events with emission of protons. In addition to β-delayed emission of one and two protons we clearly observed the β-delayed three-proton branch. The branching ratio for this channel in Ar31 is found to be 0.07±0.02%

Characterization of the First Conotoxin from Conus ateralbus, a Vermivorous Cone Snail from the Cabo Verde Archipelago

Conus ateralbus is a cone snail endemic to the west side of the island of Sal, in the Cabo Verde Archipelago off West Africa. We describe the isolation and characterization of the first bioactive peptide from the venom of this species. This 30AA venom peptide is named conotoxin AtVIA (δ-conotoxin-like). An excitatory activity was manifested by the peptide on a majority of mouse lumbar dorsal root ganglion neurons. An analog of AtVIA with conservative changes on three amino acid residues at the C-terminal region was synthesized and this analog produced an identical effect on the mouse neurons. AtVIA has homology with δ-conotoxins from other worm-hunters, which include conserved sequence elements that are shared with δ-conotoxins from fish-hunting Conus. In contrast, there is no comparable sequence similarity with δ-conotoxins from the venoms of molluscivorous Conus species. A rationale for the potential presence of δ-conotoxins, that are potent in vertebrate systems in two different lineages of worm-hunting cone snails, is discussed.This work was supported by grants to BMO from the National Institute of General Medical Science, GM 48677 and GM103362. Partial funding was obtained through a PhD grant to JLBN (SFRH/BD/51477/2011) from the European Regional Development Fund (ERDF) through the COMPETE—Operational Competitiveness Program and from national funds through FCT—Foundation for Science and Technology—under the project FCT Project UID/Multi/04423/ and by the project H2020 RISE project EMERTOX—Emergent Marine Toxins in the North Atlantic and Mediterranean: New Approaches to Assess their Occurrence and Future Scenarios in the Framework of Global Environmental Changes—Grant Agreement No. 778069. The sample collection in Cabo Verde was supported by Fundação Calouste Gulbenkian