793 research outputs found

    Alien Registration- Dunn, William B. (Presque Isle, Aroostook County)

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    https://digitalmaine.com/alien_docs/33811/thumbnail.jp

    Inverse opal ceria–zirconia: architectural engineering for heterogeneous catalysis

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    The application of inverse opal structured materials is extended to the ceria–zirconia (Ce_(0.5)Zr_(0.5)O_2) system and the significance of material architecture on heterogeneous catalysis, specifically, chemical oxidation, is examined

    The quantitative effect of a flexible fuselage on the symmetric torsional modes of the wings of a large airplane

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    This thesis document was issued under the authority of another institution, not NPS. At the time it was written, a copy was added to the NPS Library collection for reasons not now known. It has been included in the digital archive for its historical value to NPS. Not believed to be a CIVINS (Civilian Institutions) title.http://www.archive.org/details/quantitativeeffe00fureU.S. Navy (U.S.N.) authors

    Retzian-(La), a new mineral from Sterling Hill, Sussex County, New Jersey

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    ABSTRACT. Retzian-(La), ideally, Mn2La(As04)(OH)4, is a new rare-earth analogue of retzian and retzian-(Nd). It was found associated with willemite, calcite, and frank-!inite, in the Sterling Hill Mine, Ogdensburg, Sussex County, New Jersey, USA. Retzian- (La) is orthorhombic, space group Pban, with a = 5.670(7), b = 12.01(1), and c = 4.869 I Nearly 1983 some euhedral reddish-brown crystals were found in the Sterling Hill Mine and called to the attention of the authors by John Kolic, a miner at Sterling Hill. Examination by X-ray powder diffraction techniques indicated that the crystals were in the retzian family of minerals, and a preliminary microprobe scan indicated that they were La-rich and thus a new mineral, the Laanalogue of retzian, Mn2Ce(As04)(OH)4' and retzian-(Nd), Mn2Nd(As04)(OH)

    Article Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling

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    SUMMARY Oligodendrocyte precursors (OPs) continue to proliferate and generate myelinating oligodendrocytes (OLs) well into adulthood. It is not known whether adult-born OLs ensheath previously unmyelinated axons or remodel existing myelin. We quantified OP division and OL production in different regions of the adult mouse CNS including the 4-month-old optic nerve, in which practically all axons are already myelinated. Even there, all OPs were dividing and generating new OLs and myelin at a rate higher than can be explained by first-time myelination of naked axons. We conclude that adult-born OLs in the optic nerve are engaged in myelin remodeling, either replacing OLs that die in service or intercalating among existing myelin sheaths. The latter would predict that average internode length should decrease with age. Consistent with that, we found that adult-born OLs elaborated much shorter but many more internodes than OLs generated during early postnatal life

    Modulation of SOCS protein expression influences the interferon responsiveness of human melanoma cells

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    <p>Abstract</p> <p>Background</p> <p>Endogenously produced interferons can regulate the growth of melanoma cells and are administered exogenously as therapeutic agents to patients with advanced cancer. We investigated the role of negative regulators of interferon signaling known as suppressors of cytokine signaling (SOCS) in mediating interferon-resistance in human melanoma cells.</p> <p>Methods</p> <p>Basal and interferon-alpha (IFN-α) or interferon-gamma (IFN-γ)-induced expression of SOCS1 and SOCS3 proteins was evaluated by immunoblot analysis in a panel of n = 10 metastatic human melanoma cell lines, in human embryonic melanocytes (HEM), and radial or vertical growth phase melanoma cells. Over-expression of SOCS1 and SOCS3 proteins in melanoma cells was achieved using the PINCO retroviral vector, while siRNA were used to inhibit SOCS1 and SOCS3 expression. Tyr<sup>701</sup>-phosphorylated STAT1 (P-STAT1) was measured by intracellular flow cytometry and IFN-stimulated gene expression was measured by Real Time PCR.</p> <p>Results</p> <p>SOCS1 and SOCS3 proteins were expressed at basal levels in melanocytes and in all melanoma cell lines examined. Expression of the SOCS1 and SOCS3 proteins was also enhanced following stimulation of a subset of cell lines with IFN-α or IFN-γ. Over-expression of SOCS proteins in melanoma cell lines led to significant inhibition of Tyr<sup>701</sup>-phosphorylated STAT1 (P-STAT1) and gene expression following stimulation with IFN-α (IFIT2, OAS-1, ISG-15) or IFN-γ (IRF1). Conversely, siRNA inhibition of SOCS1 and SOCS3 expression in melanoma cells enhanced their responsiveness to interferon stimulation.</p> <p>Conclusions</p> <p>These data demonstrate that SOCS proteins are expressed in human melanoma cell lines and their modulation can influence the responsiveness of melanoma cells to IFN-α and IFN-γ.</p
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