645 research outputs found

    La ciència i la humanitat en el segle vint-i-u

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    A world without war: Is it desirable? Is it feasible?

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    Discovery of the Cobalt Isotopes

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    Twenty-six cobalt isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.Comment: to be published in Atomic Data and Nuclear Data Table

    Creutzfeldt-Jakob Disease and Alzheimer’s Disease: Does Overlap of Mechanism Mean Overlap of Treatment Methods?

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    Alzheimer’s disease is a neurodegenerative disorder that is the 6th leading cause of death in the United States. More than 5.5 million People over the age of 65 are currently diagnosed with Alzheimer’s disease with predictions of 13.8 million to be diagnosed by the year 2050 (Sultana, et al., 2013) (Hebert, Weuve, Scherr, & Evans, 2013). With few treatments available, scientists are desperately looking for a solution to this growing epidemic. Creutzfeldt-Jakob disease is also a neurodegenerative disorder, but with a far less prevalence of only 4.6 persons per million per year. It was discovered that Alzheimer’s and Creutzfeldt-Jakob disease share many pathophysiological mechanisms with each other. Being that both of these illnesses are currently incurable, a thorough critical analysis of mechanisms and potential treatments were preformed to ascertain if knowledge in one disorder can help find a cure for the other. With the strong relationship between these two disorders, it was found that many treatments intended for one illness had positive results for the other (some with slight modifications). The discovery of this correlation improved scientist’s knowledge of the pathological mechanism of these ailments along with finding new and creative ways for treatment. Experiments geared towards the relationship between Alzheimer’s and Creutzfeldt-Jakob disease has brought researchers closer to finding a cure for several neurodegenerative disorders

    Advanced Fluorescence Microscopy Techniques-FRAP, FLIP, FLAP, FRET and FLIM

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    Fluorescence microscopy provides an efficient and unique approach to study fixed and living cells because of its versatility, specificity, and high sensitivity. Fluorescence microscopes can both detect the fluorescence emitted from labeled molecules in biological samples as images or photometric data from which intensities and emission spectra can be deduced. By exploiting the characteristics of fluorescence, various techniques have been developed that enable the visualization and analysis of complex dynamic events in cells, organelles, and sub-organelle components within the biological specimen. The techniques described here are fluorescence recovery after photobleaching (FRAP), the related fluorescence loss in photobleaching (FLIP), fluorescence localization after photobleaching (FLAP), Forster or fluorescence resonance energy transfer (FRET) and the different ways how to measure FRET, such as acceptor bleaching, sensitized emission, polarization anisotropy, and fluorescence lifetime imaging microscopy (FLIM). First, a brief introduction into the mechanisms underlying fluorescence as a physical phenomenon and fluorescence, confocal, and multiphoton microscopy is given. Subsequently, these advanced microscopy techniques are introduced in more detail, with a description of how these techniques are performed, what needs to be considered, and what practical advantages they can bring to cell biological research
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