Search Results - "Kong, Qingzhong"

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    Amyloid fibrils from the N-terminal prion protein fragment are infectious by Choi, Jin-Kyu, Cali, Ignazio, Surewicz, Krystyna, Kong, Qingzhong, Gambetti, Pierluigi, Surewicz, Witold K.

    “…Recombinant C-terminally truncated prion protein PrP23-144 (which corresponds to the Y145Stop PrP variant associated with a Gerstmann–Sträussler–Scheinker-like…”
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    Novel Strain of the Chronic Wasting Disease Agent Isolated From Experimentally Inoculated Elk With LL132 Prion Protein by Moore, Jo, Tatum, Trudy, Hwang, Soyoun, Vrentas, Catherine, West Greenlee, M. Heather, Kong, Qingzhong, Nicholson, Eric, Greenlee, Justin

    Published in Scientific reports (21-02-2020)
    “…Chronic wasting disease (CWD) is a fatal, progressive disease that affects cervid species, including Rocky mountain elk ( Cervus elaphus nelsoni ). There are 2…”
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    Mammalian Prions Generated from Bacterially Expressed Prion Protein in the Absence of Any Mammalian Cofactors by Kim, Jae-Il, Cali, Ignazio, Surewicz, Krystyna, Kong, Qingzhong, Raymond, Gregory J., Atarashi, Ryuichiro, Race, Brent, Qing, Liuting, Gambetti, Pierluigi, Caughey, Byron, Surewicz, Witold K.

    Published in The Journal of biological chemistry (07-05-2010)
    “…Transmissible spongiform encephalopathies (TSEs) are a group of neurodegenerative diseases that are associated with the conformational conversion of a normal…”
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    Artificial strain of human prions created in vitro by Kim, Chae, Xiao, Xiangzhu, Chen, Shugui, Haldiman, Tracy, Smirnovas, Vitautas, Kofskey, Diane, Warren, Miriam, Surewicz, Krystyna, Maurer, Nicholas R., Kong, Qingzhong, Surewicz, Witold, Safar, Jiri G.

    Published in Nature communications (04-06-2018)
    “…The molecular mechanism that determines under physiological conditions transmissibility of the most common human prion disease, sporadic Creutzfeldt-Jakob…”
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    Molecular biology and pathology of prion strains in sporadic human prion diseases by Gambetti, Pierluigi, Cali, Ignazio, Notari, Silvio, Kong, Qingzhong, Zou, Wen-Quan, Surewicz, Witold K.

    Published in Acta neuropathologica (01-01-2011)
    “…Prion diseases are believed to propagate by the mechanism involving self-perpetuating conformational conversion of the normal form of the prion protein, PrP C…”
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    Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy by Otero, Alicia, Barrio, Tomás, Eraña, Hasier, Charco, Jorge M, Betancor, Marina, Díaz-Domínguez, Carlos M, Marín, Belén, Andréoletti, Olivier, Torres, Juan M, Kong, Qingzhong, Badiola, Juan J, Bolea, Rosa, Castilla, Joaquín

    Published in PLoS pathogens (07-10-2022)
    “…The role of the glycosylation status of PrP C in the conversion to its pathological counterpart and on cross-species transmission of prion strains has been…”
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    Generation of human chronic wasting disease in transgenic mice by Wang, Zerui, Qin, Kefeng, Camacho, Manuel V, Cali, Ignazio, Yuan, Jue, Shen, Pingping, Greenlee, Justin, Kong, Qingzhong, Mastrianni, James A, Zou, Wen-Quan

    Published in Acta neuropathologica communications (26-09-2021)
    “…Chronic wasting disease (CWD) is a cervid prion disease caused by the accumulation of an infectious misfolded conformer (PrP ) of cellular prion protein (PrP…”
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    Transmission characteristics of variably protease-sensitive prionopathy by Notari, Silvio, Xiao, Xiangzhu, Espinosa, Juan Carlos, Cohen, Yvonne, Qing, Liuting, Aguilar-Calvo, Patricia, Kofskey, Diane, Cali, Ignazio, Cracco, Laura, Kong, Qingzhong, Torres, Juan Maria, Zou, Wenquan, Gambetti, Pierluigi

    Published in Emerging infectious diseases (01-12-2014)
    “…Variably protease-sensitive prionopathy (VPSPr), a recently identified and seemingly sporadic human prion disease, is distinct from Creutzfeldt-Jakob disease…”
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    A minimally invasive biomarker for sensitive and accurate diagnosis of Parkinson's disease by Wang, Zerui, Gilliland, Tricia, Kim, Hyun Jo, Gerasimenko, Maria, Sajewski, Kailey, Camacho, Manuel V, Bebek, Gurkan, Chen, Shu G, Gunzler, Steven A, Kong, Qingzhong

    Published in Acta neuropathologica communications (22-10-2024)
    “…Seeding activities of disease-associated α-synuclein aggregates (αSyn ), a hallmark of Parkinson's disease (PD), are detectable by seed amplification assay…”
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    Prion protein (PrP) knock-out mice show altered iron metabolism: a functional role for PrP in iron uptake and transport by Singh, Ajay, Kong, Qingzhong, Luo, Xiu, Petersen, Robert B, Meyerson, Howard, Singh, Neena

    Published in PloS one (01-07-2009)
    “…Despite overwhelming evidence implicating the prion protein (PrP) in prion disease pathogenesis, the normal function of this cell surface glycoprotein remains…”
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    Change in the characteristics of ferritin induces iron imbalance in prion disease affected brains by Singh, Ajay, Qing, Liuting, Kong, Qingzhong, Singh, Neena

    Published in Neurobiology of disease (01-03-2012)
    “…Abstract Prion disease associated neurotoxicity is mainly attributed to PrP-scrapie (PrPSc ), the disease associated isoform of a normal protein, the prion…”
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    Small Protease Sensitive Oligomers of PrPSc in Distinct Human Prions Determine Conversion Rate of PrPC by Kim, Chae, Haldiman, Tracy, Surewicz, Krystyna, Cohen, Yvonne, Chen, Wei, Blevins, Janis, Sy, Man-Sun, Cohen, Mark, Kong, Qingzhong, Telling, Glenn C., Surewicz, Witold K., Safar, Jiri G.

    Published in PLoS pathogens (02-08-2012)
    “…The mammalian prions replicate by converting cellular prion protein (PrPC) into pathogenic conformational isoform (PrPSc). Variations in prions, which cause…”
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