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Institution

University of Madeira

EducationFunchal, Portugal
About: University of Madeira is a education organization based out in Funchal, Portugal. It is known for research contribution in the topics: Population & Dendrimer. The organization has 1014 authors who have published 2759 publications receiving 59457 citations.


Papers
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Journal ArticleDOI
TL;DR: The lattice equation for one-soliton and multisoliton dynamics governed by the lattice equations is proposed reduction by means of the inverse scattering technique.
Abstract: We discuss different aspects of one-soliton and multisoliton dynamics governed by the lattice equation i\ensuremath{\psi}${\mathrm{\ifmmode \dot{}\else \.{}\fi{}}}_{\mathit{n}}$+(${\mathrm{\ensuremath{\psi}}}_{\mathit{n}\mathrm{\ensuremath{-}}1}$+${\mathrm{\ensuremath{\psi}}}_{\mathit{n}+1}$)(1+\ensuremath{\Vert}${\mathrm{\ensuremath{\psi}}}_{\mathit{n}}$${\mathrm{\ensuremath{\Vert}}}^{2}$)-2\ensuremath{\gamma}(t)n ${\mathrm{\ensuremath{\psi}}}_{\mathit{n}}$=0. We propose reduction of this equation, drastically simplifying its treatment by means of the inverse scattering technique.

64 citations

Journal ArticleDOI
TL;DR: Improvements in haptic channels could lead to even more immersive experiences in high-definition 3D displays and multichannel audio systems.
Abstract: Viewer expectations for rich, immersive interaction with multimedia are driving new technologies- such as high-definition 3D displays and multichannel audio systems-to greater levels of sophistication. While researchers continue to study ways to develop new capabilities for visual and audio sensory channels, improvements in haptic channels could lead to even more immersive experiences.

64 citations

Journal ArticleDOI
TL;DR: The predominance and high diversity of haplogroup E3a*-M2 suggests a demographic expansion in the equatorial western fringe, possibly supported by a local agricultural center.
Abstract: The geographic and ethnolinguistic differentiation of many African Y-chromosomal lineages provides an opportunity to evaluate human migration episodes and admixture processes, in a pan-continental context The analysis of the paternal genetic structure of Equatorial West Africans carried out to date leaves their origins and relationships unclear, and raises questions about the existence of major demographic phenomena analogous to the large-scale Bantu expansions To address this, we have analysed the variation of 31 binary and 11 microsatellite markers on the non-recombining portion of the Y chromosome in Guinea-Bissau samples of diverse ethnic affiliations, some not studied before The Guinea-Bissau Y chromosome pool is characterized by low haplogroup diversity (D = 0470, sd 0033), with the predominant haplogroup E3a*-M2 shared among the ethnic clusters and reaching a maximum of 822% in the Mandenka people The Felupe-Djola and Papel groups exhibit the highest diversity of lineages and harbor the deep-rooting haplogroups A-M91, E2-M75 and E3*-PN2, typical of Sahel's more central and eastern areas Their genetic distinction from other groups is statistically significant (P = 001) though not attributable to linguistic, geographic or religious criteria Non sub-Saharan influences were associated with the presence of haplogroup R1b-P25 and particular lineages of E3b1-M78 The predominance and high diversity of haplogroup E3a*-M2 suggests a demographic expansion in the equatorial western fringe, possibly supported by a local agricultural center The paternal pool of the Mandenka and Balanta displays evidence of a particularly marked population growth among the Guineans, possibly reflecting the demographic effects of the agriculturalist lifestyle and their putative relationship to the people that introduced early cultivation practices into West Africa The paternal background of the Felupe-Djola and Papel ethnic groups suggests a better conserved ancestral pool deriving from East Africa, from where they have supposedly migrated in recent times Despite the overall homogeneity in a multiethnic sample, which contrasts with their social structure, minor clusters suggest the imprints of multiple peoples at different timescales: traces of ancestral inhabitants in haplogroups A-M91 and B-M60, today typical of hunter-gatherers; North African influence in E3b1-M78 Y chromosomes, probably due to trans-Saharan contacts; and R1b-P25 lineages reflecting European admixture via the North Atlantic slave trade

64 citations

Journal ArticleDOI
TL;DR: The data reveals that the formed Au DENPs-β-CD carrier enables efficiently delivery of siRNA to glioma cells, has good cytocompatibility once complexed with the siRNA, and enables enhanced gene silencing to inhibit the expression of Bcl-2 and VEGF proteins.
Abstract: We describe a safe and highly effective non-viral vector system based on β-cyclodextrin (β-CD)-modified dendrimer-entrapped gold nanoparticles (Au DENPs) for improved delivery small interfering RNA (siRNA) to glioblastoma cells. In our approach, we utilized amine-terminated generation 5 poly(amidoamine) dendrimers partially grafted with β-CD as a nanoreactor to entrap Au NPs. The acquired β-CD-modified Au DENPs (Au DENPs-β-CD) were complexed with two different types of therapeutic siRNA (B-cell lymphoma/leukemia-2 (Bcl-2) siRNA and vascular endothelial growth factor (VEGF) siRNA). The siRNA compression ability of the Au DENPs-β-CD was evaluated by various methods. The cytocompatibility of the vector/siRNA polyplexes was assessed by viability assay of cells. The siRNA transfection capability of the formed Au DENPs-β-CD vector was evaluated by flow cytometric assay of the cellular uptake of the polyplexes and Western blot assays of the Bcl-2 and VEGF protein expression. Our data reveals that the formed Au DENPs-β-CD carrier enables efficiently delivery of siRNA to glioma cells, has good cytocompatibility once complexed with the siRNA, and enables enhanced gene silencing to inhibit the expression of Bcl-2 and VEGF proteins. The developed Au DENPs-β-CD vector may be used for efficient siRNA delivery to different biosystems for therapeutic purposes.

64 citations

Journal ArticleDOI
TL;DR: The results show that both groups improved in motor function over time, but the Reh@Task group displayed significantly higher between-group outcomes in the arm subpart of the Fugl-Meyer Assessment Test, which is supportive of the viability of VR tools that combine motor and cognitive training, such as the ReH@Task.
Abstract: Stroke is one of the most common causes of acquired disability, leaving numerous adults with cognitive and motor impairments, and affecting patients' capability to live independently. Virtual Reality (VR) based methods for stroke rehabilitation have mainly focused on motor rehabilitation but there is increasing interest toward the integration of cognitive training for providing more effective solutions. Here we investigate the feasibility for stroke recovery of a virtual cognitive-motor task, the Reh@Task, which combines adapted arm reaching, and attention and memory training. 24 participants in the chronic stage of stroke, with cognitive and motor deficits, were allocated to one of two groups (VR, Control). Both groups were enrolled in conventional occupational therapy, which mostly involves motor training. Additionally, the VR group underwent training with the Reh@Task and the control group performed time-matched conventional occupational therapy. Motor and cognitive competences were assessed at baseline, end of treatment (1 month) and at a 1-month follow-up through the Montreal Cognitive Assessment, Single Letter Cancelation, Digit Cancelation, Bells Test, Fugl-Meyer Assessment Test, Chedoke Arm and Hand Activity Inventory, Modified Ashworth Scale, and Barthel Index. Our results show that both groups improved in motor function over time, but the Reh@Task group displayed significantly higher between-group outcomes in the arm subpart of the Fugl-Meyer Assessment Test. Improvements in cognitive function were significant and similar in both groups. Overall, these results are supportive of the viability of VR tools that combine motor and cognitive training, such as the Reh@Task. Trial Registration: This trial was not registered because it is a small clinical study that addresses the feasibility of a prototype device.

64 citations


Authors

Showing all 1027 results

NameH-indexPapersCitations
Dirk Helbing10164256810
Xiangyang Shi7947022028
Jodi Forlizzi6723717292
Armando J. D. Silvestre6438114739
John W. Clark6070713999
José Luís da Silva5923511972
Carmen S. R. Freire5823910307
Jose Luis Santos544029004
Vladimir V. Konotop5342611073
A. R. Bishop5155111946
Manfred Kaufmann4626620172
José D. Santos452205875
Vassilis Kostakos452707015
Pedro L. Granja441325969
Stéphane Cordier433716802
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20239
202223
2021212
2020233
2019212
2018186