Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Liuting Qing"'
Autor:
Silvio Notari, Xiangzhu Xiao, Juan Carlos Espinosa, Yvonne Cohen, Liuting Qing, Patricia Aguilar-Calvo, Diane Kofskey, Ignazio Cali, Laura Cracco, Qingzhong Kong, Juan Maria Torres, Pierluigi Gambetti
Publikováno v:
Emerging Infectious Diseases, Vol 20, Iss 12, Pp 2006-2014 (2014)
Variably protease-sensitive prionopathy (VPSPr), a recently identified and seemingly sporadic human prion disease, is distinct from Creutzfeldt-Jakob disease (CJD) but shares features of Gerstmann-Sträussler-Scheinker disease (GSS). However, contrar
Externí odkaz:
https://doaj.org/article/465f8e92c0614bcda5457745a06f4d4f
Autor:
Qingzhong Kong, Jeffrey L. Mills, Bishwajit Kundu, Xinyi Li, Liuting Qing, Krystyna Surewicz, Ignazio Cali, Shenghai Huang, Mengjie Zheng, Wieslaw Swietnicki, Frank D. Sönnichsen, Pierluigi Gambetti, Witold K. Surewicz
Publikováno v:
Cell Reports, Vol 4, Iss 2, Pp 248-254 (2013)
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are associated with the conformational conversion of the cellular prion protein, PrPC, into a protease-resistant form, PrPSc. Here, we show that mutation-induced thermodynamic stabi
Externí odkaz:
https://doaj.org/article/078186e630d74d5c88ea9156e40221ed
Publikováno v:
Neurobiology of Disease, Vol 45, Iss 3, Pp 930-938 (2012)
Prion disease associated neurotoxicity is mainly attributed to PrP-scrapie (PrPSc), the disease associated isoform of a normal protein, the prion protein (PrPC). Participation of other proteins and processes is suspected, but their identity and contr
Externí odkaz:
https://doaj.org/article/3fd0183c27004602bda4a80938108280
Autor:
Silvio Notari, Liuting Qing, Maurizio Pocchiari, Ayuna Dagdanova, Kristin Hatcher, Arend Dogterom, Jose F. Groisman, Ib Bo Lumholtz, Maria Puopolo, Corinne Lasmezas, Shu G. Chen, Qingzhong Kong, Pierluigi Gambetti
Publikováno v:
Emerging Infectious Diseases, Vol 18, Iss 1, Pp 21-28 (2012)
Prion diseases are neurodegenerative conditions associated with a misfolded and infectious protein, scrapie prion protein (PrPSc). PrPSc propagate prion diseases within and between species and thus pose risks to public health. Prion infectivity or Pr
Externí odkaz:
https://doaj.org/article/78c7e218ad8142579bbdf9b6b081a0b3
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26635 (2011)
Prion diseases are a family of unique fatal transmissible neurodegenerative diseases that affect humans and many animals. Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common prion disease in humans, accounting for 85-90% of all human prion c
Externí odkaz:
https://doaj.org/article/f660ba566cfb44209c3b6a3a2ae0c2ba
Autor:
Jose F. Groisman, Ib Bo Lumholtz, Arend Dogterom, Liuting Qing, Ayuna Dagdanova, Corinne Ida Lasmézas, Shu G. Chen, Pierluigi Gambetti, Qingzhong Kong, Maria Puopolo, Maurizio Pocchiari, Silvio Notari, Kristin Hatcher
Publikováno v:
Emerging Infectious Diseases
Emerging Infectious Diseases, Vol 18, Iss 1, Pp 21-28 (2012)
Emerging Infectious Diseases, Vol 18, Iss 1, Pp 21-28 (2012)
Intracerebral inoculation of transgenic mice failed to demonstrate prion disease transmission.
Prion diseases are neurodegenerative conditions associated with a misfolded and infectious protein, scrapie prion protein (PrPSc). PrPSc propagate pri
Prion diseases are neurodegenerative conditions associated with a misfolded and infectious protein, scrapie prion protein (PrPSc). PrPSc propagate pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80b454e794e9daa20241ffb47acba6e2
https://doi.org/10.3201/eid1801.110589
https://doi.org/10.3201/eid1801.110589
Autor:
Liuting Qing, Byron Caughey, Ignazio Cali, Pierluigi Gambetti, Krystyna Surewicz, Ryuichiro Atarashi, Witold K. Surewicz, Brent Race, Jae Il Kim, Qingzhong Kong, Gregory J. Raymond
Publikováno v:
Journal of Biological Chemistry. 285:14083-14087
Transmissible spongiform encephalopathies (TSEs) are a group of neurodegenerative diseases that are associated with the conformational conversion of a normal prion protein, PrP(C), to a misfolded aggregated form, PrP(Sc). The protein-only hypothesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eebaedb6fbc038723176bcbc0f5399e
https://doi.org/10.1074/jbc.c110.113464
https://doi.org/10.1074/jbc.c110.113464
Autor:
Wen-Quan Zou, Cristina Casalone, Lan Wang, Liuting Qing, Qingzhong Kong, Bikram Chakraborty, Barbara Iulini, Jingjing Liang, Shenghai Huang, Fusong Chen, Gianluigi Zanusso, Ping Wang, Meiling Wang, Xinyi Li, Pier Luigi Acutis, Francesca Martucci, Salvatore Monaco, Maria Caramelli, Pierluigi Gambetti, Mengjie Zheng, Ignazio Cali, Cristiano Corona
Publikováno v:
Journal of Virology. 82:3697-3701
Bovine spongiform encephalopathy (BSE), the prion disease in cattle, was widely believed to be caused by only one strain, BSE-C. BSE-C causes the fatal prion disease named new variant Creutzfeldt-Jacob disease in humans. Two atypical BSE strains, bov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39f812f6cf8e08d90f6060c6c523cce3
https://doi.org/10.1128/jvi.02561-07
https://doi.org/10.1128/jvi.02561-07
Autor:
Liuting Qing, Xiao-Ling Qu
Publikováno v:
BMB Reports. 37:445-453
We identified apoptosis as being a significant mechanism of toxicity following the exposure of HeLa cell cultures to abrin holotoxin, which is in addition to its inhibition of protein biosynthesis by N-glycosidase activity. The treatment of HeLa cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d226010be5578010c26c467775b06592
https://doi.org/10.5483/bmbrep.2004.37.4.445
https://doi.org/10.5483/bmbrep.2004.37.4.445
Autor:
Emmanuelle Uro-Coste, Gong-Xian Wang, Wen-Quan Zou, Jue Yuan, Xiangzhu Xiao, Qingzhong Kong, Pierluigi Gambetti, James W. Ironside, Ignazio Cali, Paul Brown, Jacqueline Mikol, Dimitris Gazgalis, Marie-Bernadette Delisle, Mai Abouelsaad, Liang Zeng, Liuting Qing, Manuel Camacho Martinez
Publikováno v:
Journal of clinical & cellular immunology
Differentiating iatrogenic Creutzfeldt-Jakob disease (iCJD) from sporadic CJD (sCJD) would be useful for the identification and prevention of human-to-human prion transmission. Currently, the diagnosis of iCJD depends on identification of a recognize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d05b6d2417c893e86827af444669ed
https://pubmed.ncbi.nlm.nih.gov/25419482
https://pubmed.ncbi.nlm.nih.gov/25419482