Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Diane Kofskey"'
Autor:
Romolo Nonno, Silvio Notari, Michele Angelo Di Bari, Ignazio Cali, Laura Pirisinu, Claudia d’Agostino, Laura Cracco, Diane Kofskey, Ilaria Vanni, Jody Lavrich, Piero Parchi, Umberto Agrimi, Pierluigi Gambetti
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 1, Pp 73-81 (2019)
Variably protease-sensitive prionopathy (VPSPr), a recently described human sporadic prion disease, features a protease-resistant, disease-related prion protein (resPrPD) displaying 5 fragments reminiscent of Gerstmann-Sträussler-Scheinker disease.
Externí odkaz:
https://doaj.org/article/ad97e37aa0e14c208f6fcf1cda0903b4
Autor:
Satish Kumar Nemani, Silvio Notari, Ignazio Cali, Victor E Alvarez, Diane Kofskey, Mark Cohen, Robert A. Stern, Brian Appleby, Joseph Abrams, Lawrence Schonberger, Ann McKee, Pierluigi Gambetti
Publikováno v:
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-14 (2018)
Abstract Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease associated with repetitive traumatic brain injury (TBI). CTE is generally found in athletes participating in contact sports and military personnel exposed to explosive bla
Externí odkaz:
https://doaj.org/article/1fe87befe49f4fa68e43dcf39d4af548
Autor:
Chae Kim, Xiangzhu Xiao, Shugui Chen, Tracy Haldiman, Vitautas Smirnovas, Diane Kofskey, Miriam Warren, Krystyna Surewicz, Nicholas R. Maurer, Qingzhong Kong, Witold Surewicz, Jiri G. Safar
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Synthetic prions have previously been generated from recombinant rodent PrP. Here the authors generate synthetic human prions, by seeding human PrP with CJD prions, and characterize its infectivity in mice.
Externí odkaz:
https://doaj.org/article/bde375ffd18941009f755ddc28b0cf33
Autor:
Ignazio Cali, Mark L. Cohen, Stéphane Haїk, Piero Parchi, Giorgio Giaccone, Steven J. Collins, Diane Kofskey, Han Wang, Catriona A. McLean, Jean-Philippe Brandel, Nicolas Privat, Véronique Sazdovitch, Charles Duyckaerts, Tetsuyuki Kitamoto, Ermias D. Belay, Ryan A. Maddox, Fabrizio Tagliavini, Maurizio Pocchiari, Ellen Leschek, Brian S. Appleby, Jiri G. Safar, Lawrence B. Schonberger, Pierluigi Gambetti
Publikováno v:
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-19 (2018)
Abstract The presence of pathology related to the deposition of amyloid-β (Aβ) has been recently reported in iatrogenic Creutzfeldt-Jakob disease (iCJD) acquired from inoculation of growth hormone (GH) extracted from human cadaveric pituitary gland
Externí odkaz:
https://doaj.org/article/b6455469960749f5bf75b7a7b46651b6
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:
Bo Zhang, Daniel Cowden, Fan Zhang, Jue Yuan, Sandra Siedlak, Mai Abouelsaad, Liang Zeng, Xuefeng Zhou, John O'Toole, Alvin S Das, Diane Kofskey, Miriam Warren, Zehua Bian, Yuqi Cui, Tao Tan, Adam Kresak, Robert E Wyza, Robert B Petersen, Gong-Xian Wang, Qingzhong Kong, Xinglong Wang, John Sedor, Xiongwei Zhu, Hua Zhu, Wen-Quan Zou
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0141025 (2015)
Externí odkaz:
https://doaj.org/article/aa31d17b10964f918f046084a1311799
Autor:
Bo Zhang, Daniel Cowden, Fan Zhang, Jue Yuan, Sandra Siedlak, Mai Abouelsaad, Liang Zeng, Xuefeng Zhou, John O'Toole, Alvin S Das, Diane Kofskey, Miriam Warren, Zehua Bian, Yuqi Cui, Tao Tan, Adam Kresak, Robert E Wyza, Robert B Petersen, Gong-Xian Wang, Qingzhong Kong, Xinglong Wang, John Sedor, Xiongwei Zhu, Hua Zhu, Wen-Quan Zou
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0136923 (2015)
The cellular prion protein (PrPC), a protein most noted for its link to prion diseases, has been found to play a protective role in ischemic brain injury. To investigate the role of PrPC in the kidney, an organ highly prone to ischemia/reperfusion (I
Externí odkaz:
https://doaj.org/article/bcb57bbb317d4e0ba912d71adf48e6b8
Autor:
Fabio Moda, Claudio Soto, Fabrizio Tagliavini, Satish K. Nemani, Jody Lavrich, Diane Kofskey, Pierluigi Gambetti, Silvio Notari, Ignazio Cali, Brian S. Appleby
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Scientific Reports
Scientific Reports
The presence of abnormal, disease-related prion protein (PrPD) has recently been demonstrated by protein misfolding cyclic amplification (PMCA) in urine of patients affected with variant Creutzfeldt-Jakob disease (vCJD), a prion disease typically acq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60650f79f7ba6fefb68460538696a18c
http://link.springer.com/article/10.1038/s41598-019-41694-0
http://link.springer.com/article/10.1038/s41598-019-41694-0
Autor:
Ilaria Vanni, Silvio Notari, Laura Cracco, Pierluigi Gambetti, Piero Parchi, Diane Kofskey, Ignazio Cali, Claudia D'Agostino, Jody Lavrich, Umberto Agrimi, Romolo Nonno, Michele Angelo Di Bari, Laura Pirisinu
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 1, Pp 73-81 (2019)
Emerging Infectious Diseases
Emerging Infectious Diseases
Variably protease-sensitive prionopathy (VPSPr), a recently described human sporadic prion disease, features a protease-resistant, disease-related prion protein (resPrPD) displaying 5 fragments reminiscent of Gerstmann-Sträussler-Scheinker disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d18ddcf6cbf018b51b33ba4b8e6c6d42
https://wwwnc.cdc.gov/eid/article/25/1/18-0807_article
https://wwwnc.cdc.gov/eid/article/25/1/18-0807_article
Autor:
Véronique Sazdovitch, Jean-Philippe Brandel, Piero Parchi, Nicolas Privat, Jiri G. Safar, Mark L. Cohen, Brian S. Appleby, Ryan A. Maddox, Steven J. Collins, Ignazio Cali, Charles Duyckaerts, Catriona McLean, Ellen W. Leschek, Diane Kofskey, Stéphane Haїk, Pierluigi Gambetti, Lawrence B. Schonberger, Han Wang, Fabrizio Tagliavini, Ermias D. Belay, Maurizio Pocchiari, Giorgio Giaccone, Tetsuyuki Kitamoto
Publikováno v:
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-19 (2018)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
The presence of pathology related to the deposition of amyloid-β (Aβ) has been recently reported in iatrogenic Creutzfeldt-Jakob disease (iCJD) acquired from inoculation of growth hormone (GH) extracted from human cadaveric pituitary gland or use o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458b8882e8d64d08f1cf1fe0fe3595c0
http://link.springer.com/article/10.1186/s40478-017-0503-z
http://link.springer.com/article/10.1186/s40478-017-0503-z