7,194 research outputs found

    Proteinopathy, oxidative stress and mitochondrial dysfunction: cross talk in alzheimer’s disease and parkinson’s disease

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    Alzheimer's disease and Parkinson's disease are two common neurodegenerative diseases of the elderly people that have devastating effects in terms of morbidity and mortality. The predominant form of the disease in either case is sporadic with uncertain etiology. The clinical features of Parkinson's disease are primarily motor deficits, while the patients of Alzheimer's disease present with dementia and cognitive impairment. Though neuronal death is a common element in both the disorders, the postmortem histopathology of the brain is very characteristic in each case and different from each other. In terms of molecular pathogenesis, however, both the diseases have a significant commonality, and proteinopathy (abnormal accumulation of misfolded proteins), mitochondrial dysfunction and oxidative stress are the cardinal features in either case. These three damage mechanisms work in concert, reinforcing each other to drive the pathology in the aging brain for both the diseases; very interestingly, the nature of interactions among these three damage mechanisms is very similar in both the diseases, and this review attempts to highlight these aspects. In the case of Alzheimer's disease, the peptide amyloid beta (A beta) is responsible for the proteinopathy, while alpha-synuclein plays a similar role in Parkinson's disease. The expression levels of these two proteins and their aggregation processes are modulated by reactive oxygen radicals and transition metal ions in a similar manner. In turn, these proteins - as oligomers or in aggregated forms - cause mitochondrial impairment by apparently following similar mechanisms. Understanding the common nature of these interactions may, therefore, help us to identify putative neuroprotective strategies that would be beneficial in both the clinical conditions

    Soliton Lattice and Single Soliton Solutions of the Associated Lam\'e and Lam\'e Potentials

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    We obtain the exact nontopological soliton lattice solutions of the Associated Lam\'e equation in different parameter regimes and compute the corresponding energy for each of these solutions. We show that in specific limits these solutions give rise to nontopological (pulse-like) single solitons, as well as to different types of topological (kink-like) single soliton solutions of the Associated Lam\'e equation. Following Manton, we also compute, as an illustration, the asymptotic interaction energy between these soliton solutions in one particular case. Finally, in specific limits, we deduce the soliton lattices, as well as the topological single soliton solutions of the Lam\'e equation, and also the sine-Gordon soliton solution.Comment: 23 pages, 5 figures. Submitted to J. Math. Phy

    Differential gene expression profile of retinoblastoma compared to normal retina.

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    PURPOSE: The retinoblastoma gene (RB1) is a tumor suppressor gene that was first discovered in a rare ocular pediatric tumor called retinoblastoma (RB). The RB1 gene is essential for normal progression through the cell cycle and exerts part of its function through the family of transcription factors (E2F) and many other intermediaries. In the absence of normal RB1, genomic instability and chromosomal aberrations accumulate, leading to tumor initiation, progression, and ultimately metastasis. The purpose of this report was to identify the molecular pathways that are deregulated in retinoblastoma. METHODS: We compared gene expression signatures of matched normal retinal tissue and retinoblastoma (RB) tumor tissue from six individuals, using microarray analysis followed by statistical and bioinformatic analyses. RESULTS: We identified 1,116 genes with increased expression and 837 with decreased expression in RB tumor tissue compared to matched normal retinal tissue. Functional categories of the cognate genes with the greatest statistical support were cell cycle (309 genes), cell death (437 genes), DNA replication, recombination and repair (270 genes), cellular growth and proliferation (464 genes), and cellular assembly and organization (110 genes). The list included differentially expressed retinal cone-cell-specific markers. These data indicated the predominance of cone cells in RB and support the idea that the latter group of cells may be the cells of origin for RB. CONCLUSIONS: The genes differentially expressed in RB as compared to normal retina belong mainly to DNA damage-response pathways, including, but not limited to, breast cancer associated genes (BRCA1, BRCA2), ataxia telangiectasia mutated gene (ATM), ataxia telangiectasia and Rad3 related gene(ATR), E2F, checkpoint kinase 1 (CHK1) genes. In addition, novel pathways, such as aryl hydrocarbon receptor (AHR) signaling, polo-like kinase and mitosis, purine metabolism pathways were involved. The molecules AHR, CHK1, and polo-like kinases are of particular interest because there are several currently available drugs that target these molecules. Further studies are needed to determine if targeting these pathways in RB will have therapeutic value. It is also important to evaluate the relative importance of these pathways in different cells that make up the normal retina

    The Role of Non-ferrous Metals and Alloys in Electrical Engineering Industries in Particular Relation to Cable Industries

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    Copper, Copper-cadmium and aluminium are available in the form of wire bars and their governing material speci-fication are IS.191, IS.2665 and IS.2067 respectively. The cast weight of the normal wire bars in about 120 kg for copper and copper-cadmium and 35 kg for aluminium

    Intrinsic Curie temperature bistability in ferromagnetic semiconductor resonant tunneling diodes

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    We predict bistability in the Curie temperature-voltage characteristic of double barrier resonant-tunneling structures with dilute ferromagnetic semiconductor quantum wells. Our conclusions are based on simulations of electrostatics and ballistic quantum transport combined with a mean-field theory description of ferromagnetism in dilute magnetic semiconductors.Comment: 10 pages, 3 figures, submitted to Phys. Rev. B; typo removed in revised version - spurious eq.12 immediately after eq.1

    Laser spot welding of laser textured steel to aluminium

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    Laser welding of dissimilar metals (steel and aluminium) was investigated with the aim to increase the maximum tensile shear load of the Fe-Al joints. The increase was achieved by texturing the surface of steel prior to the laser spot welding process which was performed in a lap-joint configuration with the steel positioned on top of the aluminium and with a texture faced down to the aluminium surface. This configuration enabled an increase of the bonding area of the joints, because the molten aluminium filled in the gaps of the texture, without the need of increasing the process energy which typically leads to the growth of the intermetallic compounds. Different textures (containing hexagonally arranged craters, parallel lines, grid and spiral patterns) were tested with different laser welding parameters. The Fe-Al joints obtained with the textured steel were found to have up to 25% higher maximum tensile-shear load than the joints obtained with the untextured steel

    Shape-invariant quantum Hamiltonian with position-dependent effective mass through second order supersymmetry

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    Second order supersymmetric approach is taken to the system describing motion of a quantum particle in a potential endowed with position-dependent effective mass. It is shown that the intertwining relations between second order partner Hamiltonians may be exploited to obtain a simple shape-invariant condition. Indeed a novel relation between potential and mass functions is derived, which leads to a class of exactly solvable model. As an illustration of our procedure, two examples are given for which one obtains whole spectra algebraically. Both shape-invariant potentials exhibit harmonic-oscillator-like or singular-oscillator-like spectra depending on the values of the shape-invariant parameter.Comment: 16 pages, 5 figs; Present e-mail of AG: [email protected]
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