323 research outputs found

    Graduate Recital: Theodore Parge, Percussion; July 26, 1977

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    Centennial East Recital HallTuesday EveningJuly 26, 19778:00 p.m

    Senior Recital: Theodore Parge, Percussion; December 11, 1975

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    CVA Art Gallery IThursday EveningDecember 11, 19758:15 p.m

    Music Educators National Conference, March 19, 1977

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    Music Educators National ConferenceSaturday EveningMarch 19, 197

    Student Recital: Jose R. Alicea, Percussion; Ted Parge, Percussion; Pam Mosier, Accompanist; January 22, 1975

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    Centennial East Recital HallWednesday EveningJanuary 22, 19758:15 p.m

    Senior Recital: Theodore Parge, Percussion; Pam Mosier, Piano; Judith Ross, Flute; December 4, 1975

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    CVA Art Gallery IThursday EveningDecember 4, 19758:15 p.m

    Nanofabrication of spin-transfer torque devices by a PMMA mask one step process: GMR versus single layer devices

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    We present a method to prepare magnetic spin torque devices of low specific resistance in a one step lithography process. The quality of the pillar devices is demonstrated for a standard magnetic double layer device. For single layer devices, we found hysteretic switching and a more complex dynamical excitation pattern in higher fields. A simple model to explain the resistance spikes is presented.Comment: 22 pages, 6 figures, submitted to J. Appl. Phy

    Cadherin-dependent cell aggregation is affected by decapeptide derived from rat extracellular super-oxide dismutase

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    AbstractA synthetic HAV-containing decapeptide homologous to the amino acid sequence 44R-Q53 in rat extracellular superoxide dismutase B affects cadherin-dependent cell aggregation. Cell lines, some of them transfected, expressing different types of cadherins were tested using in vitro cell aggregation and cell dissociation assays. A concentration-dependent inhibition of aggregation by the EC-SOD-derived HAV-containing peptide was detected only in N-cadherin expressing cells. These results suggest the localisation and possible protective role of EC-SOD B for cells expressing N-cadherin

    Purification and crystallization of human Cu/Zn superoxide dismutase recombinantly produced in the protozoan Leishmania tarentolae

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    The rapid and inexpensive production of high-quality eukaryotic proteins in recombinant form still remains a challenge in structural biology. Here, a protein-expression system based on the protozoan Leishmania tarentolae was used to produce human Cu/Zn superoxide dismutase (SOD1) in recombinant form. Sequential integration of the SOD1 expression cassettes was demonstrated to lead to a linear increase in expression levels to up to 30 mg per litre. Chromatographic purification resulted in 90% pure recombinant protein, with a final yield of 6.5 mg per litre of culture. The protein was crystallized and the structures of two new crystal forms were determined. These results demonstrate the suitability of the L. tarentolae expression system for structural research
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