Search Results - "Priola, A"

The PINK1/Parkin pathway of mitophagy exerts a protective effect during prion disease by Ward, Anne, Jessop, Forrest, Faris, Robert, Hollister, Jason, Shoup, Daniel, Race, Brent, Bosio, Catharine M, Priola, Suzette A

“…The PINK1/Parkin pathway of mitophagy has been implicated in the pathogenesis of Parkinson's disease. In prion diseases, a transmissible neurodegenerative…”
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Lack of the immune adaptor molecule SARM1 accelerates disease in prion infected mice and is associated with increased mitochondrial respiration and decreased expression of NRF2 by Ward, Anne, Jessop, Forrest, Faris, Robert, Shoup, Daniel, Bosio, Catharine M, Peterson, Karin E, Priola, Suzette A

“…Prion diseases are a group of fatal, transmissible neurodegenerative diseases of mammals. In the brain, axonal loss and neuronal death are prominent in prion…”
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Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein by Caughey, Byron, Atarashi, Ryuichiro, Moore, Roger A, Sim, Valerie L, Hughson, Andrew G, Dorward, David W, Onwubiko, Henry A, Priola, Suzette A

“…The scrapie prion protein isoform, PrPSc, is a prion-associated marker that seeds the conformational conversion and polymerization of normal protease-sensitive…”
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Imaging of thymus in myasthenia gravis: From thymic hyperplasia to thymic tumor by Priola, A.M, Priola, S.M

“…Myasthenia gravis (MG) is an autoimmune disorder often associated with thymic abnormalities. At onset, thymic lymphoid hyperplasia (TLH) and thymoma can be…”
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Cellular prion protein is present in mitochondria of healthy mice by Faris, Robert, Moore, Roger A., Ward, Anne, Race, Brent, Dorward, David W., Hollister, Jason R., Fischer, Elizabeth R., Priola, Suzette A.

“…Cellular prion protein (PrP C ) is a mammalian glycoprotein which is usually found anchored to the plasma membrane via a glycophosphatidylinositol (GPI)…”
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A Specific Population of Abnormal Prion Protein Aggregates Is Preferentially Taken Up by Cells and Disaggregated in a Strain-Dependent Manner by Choi, Young Pyo, Priola, Suzette A

“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Preparation and characterization of hybrid nanocomposite coatings by photopolymerization and sol–gel process by Amerio, E., Sangermano, M., Malucelli, G., Priola, A., Voit, B.

“…Organic–inorganic nanocomposite hybrid coatings were prepared through a dual-cure process involving cationic photopolymerization of epoxy groups and subsequent…”
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Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity by Wang, Fei, Wang, Xinhe, Orrú, Christina D, Groveman, Bradley R, Surewicz, Krystyna, Abskharon, Romany, Imamura, Morikazu, Yokoyama, Takashi, Kim, Yong-Sun, Vander Stel, Kayla J, Sinniah, Kumar, Priola, Suzette A, Surewicz, Witold K, Caughey, Byron, Ma, Jiyan

“…Prions, characterized by self-propagating protease-resistant prion protein (PrP) conformations, are agents causing prion disease. Recent studies generated…”
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PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection by Marshall, Karen E, Hughson, Andrew, Vascellari, Sarah, Priola, Suzette A, Sakudo, Akikazu, Onodera, Takashi, Baron, Gerald S

“…Glycosylphosphatidylinositol (GPI) anchoring of the prion protein (PrP ) influences PrP misfolding into the disease-associated isoform, PrP , as well as prion…”
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Prion strains depend on different endocytic routes for productive infection by Fehlinger, Andrea, Wolf, Hanna, Hossinger, André, Duernberger, Yvonne, Pleschka, Catharina, Riemschoss, Katrin, Liu, Shu, Bester, Romina, Paulsen, Lydia, Priola, Suzette A., Groschup, Martin H., Schätzl, Hermann M., Vorberg, Ina M.

“…Prions are unconventional agents composed of misfolded prion protein that cause fatal neurodegenerative diseases in mammals. Prion strains induce specific…”
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Porphyrin and Phthalocyanine Antiscrapie Compounds by Priola, Suzette A., Raines, Anne, Caughey, Winslow S.

“…The transmissible spongiform encephalopathies (TSEs) are fatal, neurodegenerative diseases for which no effective treatments are available. The likelihood that…”
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Susceptibility of Common Fibroblast Cell Lines to Transmissible Spongiform Encephalopathy Agents by Vorberg, Ina, Raines, Anne, Story, Brian, Priola, Suzette A.

“…The risk of contamination of tissue culture cells with transmissible spongiform encephalopathy (TSE) agents as a result of the use of animal products as medium…”
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Altered distribution, aggregation, and protease resistance of cellular prion protein following intracranial inoculation by Ward, Anne, Hollister, Jason R, Choi, Young Pyo, Race, Brent, Williams, Katie, Shoup, Daniel W, Moore, Roger A, Priola, Suzette A

“…Prion protein (PrPC) is a protease-sensitive and soluble cell surface glycoprotein expressed in almost all mammalian cell types. PrPSc, a protease-resistant…”
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Susceptibilities of nonhuman primates to chronic wasting disease by Race, Brent, Meade-White, Kimberly D, Miller, Michae W, Barbian, Kent D, Rubenstein, Richard, LaFauci, Giuseppe, Cervenakova, Larisa, Favara, Cynthia, Gardner, Donald, Long, Dan, Parnell, Michael, Striebel, James, Priola, Suzette A, Ward, Anne, Williams, Elizabeth S, Race, Richard, Chesebro, Bruce

“…Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy, or prion disease, that affects deer, elk, and moose. Human susceptibility to CWD…”
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Cells Expressing Anchorless Prion Protein Are Resistant to Scrapie Infection by MCNALLY, Kristin L, WARD, Anne E, PRIOLA, Suzette A

“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Rabbits are not resistant to prion infection by Chianini, Francesca, Fernández-Borges, Natalia, Vidal, Enric, Gibbard, Louise, Pintado, Belén, de Castro, Jorge, Priola, Suzette A, Hamilton, Scott, Eaton, Samantha L, Finlayson, Jeanie, Pang, Yvonne, Steele, Philip, Reid, Hugh W, Dagleish, Mark P, Castilla, Joaquín

“…The ability of prions to infect some species and not others is determined by the transmission barrier. This unexplained phenomenon has led to the belief that…”
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Recombinant prion protein refolded with lipid and RNA has the biochemical hallmarks of a prion but lacks in vivo infectivity by Timmes, Andrew G, Moore, Roger A, Fischer, Elizabeth R, Priola, Suzette A

“…During prion infection, the normal, protease-sensitive conformation of prion protein (PrP(C)) is converted via seeded polymerization to an abnormal, infectious…”
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Proteomics Analysis of Amyloid and Nonamyloid Prion Disease Phenotypes Reveals Both Common and Divergent Mechanisms of Neuropathogenesis by Moore, Roger A, Sturdevant, Dan E, Chesebro, Bruce, Priola, Suzette A

“…Prion diseases are a heterogeneous group of neurodegenerative disorders affecting various mammals including humans. Prion diseases are characterized by a…”
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Preparation and characterization of UV-cured epoxy nanocomposites based on o-montmorillonite modified with maleinized liquid polybutadienes by Malucelli, G., Bongiovanni, R., Sangermano, M., Ronchetti, S., Priola, A.

“…Polymeric nanocomposites based on an epoxy cycloaliphatic resin and o-montmorillonite (Cloisite 30B®) modified by reaction with maleinized liquid…”
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Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking by Atarashi, Ryuichiro, Wilham, Jason M, Christensen, Leah, Hughson, Andrew G, Moore, Roger A, Johnson, Lisa M, Onwubiko, Henry A, Priola, Suzette A, Caughey, Byron

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