11 research outputs found

    Phase measurement of GEM 2 paste at 95 °C

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    <p>Phase measurement of GEM 2 paste at 95 °C</p

    AC Impedance and DC resistance LabVIEW program during cure

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    AC Impedance and DC resistance LabVIEW program during cur

    DC resistance of silver prints

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    DC resistance of silver print

    Phase measurement of GEM 1 paste at 95 °C

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    <p>Phase measurement of GEM 1 paste at 95 °C </p

    The AC Impedance measurement at 1 MHz for Paste E structures cured at different temperature for 40 minutes

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    <p>The AC Impedance measurement at 1 MHz for Paste E structures cured at different temperature for 40 minutes</p

    Impedance measurement of conductive film

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    Impedance measurement of Paste E at 95 °C<div><br></div

    DC resistance and AC Impedance measurement of GEM 1 at 95 °C

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    DC resistance and AC Impedance measurement of GEM 1 at 95 °C <div><br><div><br></div></div

    Labview program DC resistance measurement during mechanical bending of conductive film

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    Labview program DC resistance measurement during mechanical bending of conductive film<div><br></div

    Single cell RNA sequencing of human microglia uncovers a subset associated with Alzheimer’s disease

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    © 2020, The Author(s). The extent of microglial heterogeneity in humans remains a central yet poorly explored question in light of the development of therapies targeting this cell type. Here, we investigate the population structure of live microglia purified from human cerebral cortex samples obtained at autopsy and during neurosurgical procedures. Using single cell RNA sequencing, we find that some subsets are enriched for disease-related genes and RNA signatures. We confirm the presence of four of these microglial subpopulations histologically and illustrate the utility of our data by characterizing further microglial cluster 7, enriched for genes depleted in the cortex of individuals with Alzheimer’s disease (AD). Histologically, these cluster 7 microglia are reduced in frequency in AD tissue, and we validate this observation in an independent set of single nucleus data. Thus, our live human microglia identify a range of subtypes, and we prioritize one of these as being altered in AD
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