Zobrazeno 1 - 10 of 28 pro vyhledávání: '"Jan, Langeveld"'
1
Akademický článek
Characterisation of European Field Goat Prion Isolates in Ovine PrP Overexpressing Transgenic Mice (Tgshp IX) Reveals Distinct Prion Strains
Autor: Sonja Ernst, Romolo Nonno, Jan Langeveld, Olivier Andreoletti, Cristina Acin, Penelope Papasavva-Stylianou, Theodoros Sklaviadis, Pier Luigi Acutis, Lucien van Keulen, John Spiropoulos, Markus Keller, Martin H. Groschup, Christine Fast
Publikováno v: Pathogens, Vol 13, Iss 8, p 629 (2024)
After the detection of bovine spongiform encephalopathy (BSE), and a zoonotic transmissible spongiform encephalopathy (TSE) caused by the pathological prion protein (PrPSc) in two goats, the investigation of goat prions became of greater interest. Th
Externí odkaz: https://doaj.org/article/ee3ed78ada134cf6879310ca97c74974
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2
Akademický článek
Prions in Variably Protease-Sensitive Prionopathy: An Update
Autor: Laura Pirisinu, Jan Langeveld, Jue Yuan, Xiangzhu Xiao, Wen-Quan Zou, Pierluigi Gambetti
Publikováno v: Pathogens, Vol 2, Iss 3, Pp 457-471 (2013)
Human prion diseases, including sporadic, familial, and acquired forms such as Creutzfeldt-Jakob disease (CJD), are caused by prions in which an abnormal prion protein (PrPSc) derived from its normal cellular isoform (PrPC) is the only known componen
Externí odkaz: https://doaj.org/article/c0c99bdb04d54ed197bdb0e937cb99ea
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3
Akademický článek
Chronic wasting disease in bank voles: characterisation of the shortest incubation time model for prion diseases.
Autor: Michele Angelo Di Bari, Romolo Nonno, Joaquín Castilla, Claudia D'Agostino, Laura Pirisinu, Geraldina Riccardi, Michela Conte, Juergen Richt, Robert Kunkle, Jan Langeveld, Gabriele Vaccari, Umberto Agrimi
Publikováno v: PLoS Pathogens, Vol 9, Iss 3, p e1003219 (2013)
In order to assess the susceptibility of bank voles to chronic wasting disease (CWD), we inoculated voles carrying isoleucine or methionine at codon 109 (Bv109I and Bv109M, respectively) with CWD isolates from elk, mule deer and white-tailed deer. Ef
Externí odkaz: https://doaj.org/article/feeb8cc3b1234cd3a9a45c125fc23f16
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4
Akademický článek
Glycoform-selective prion formation in sporadic and familial forms of prion disease.
Autor: Xiangzhu Xiao, Jue Yuan, Stéphane Haïk, Ignazio Cali, Yian Zhan, Mohammed Moudjou, Baiya Li, Jean-Louis Laplanche, Hubert Laude, Jan Langeveld, Pierluigi Gambetti, Tetsuyuki Kitamoto, Qingzhong Kong, Jean-Philippe Brandel, Brian A Cobb, Robert B Petersen, Wen-Quan Zou
Publikováno v: PLoS ONE, Vol 8, Iss 3, p e58786 (2013)
The four glycoforms of the cellular prion protein (PrP(C)) variably glycosylated at the two N-linked glycosylation sites are converted into their pathological forms (PrP(Sc)) in most cases of sporadic prion diseases. However, a prominent molecular ch
Externí odkaz: https://doaj.org/article/52b7d62c2bc9412d93e1ea7587a84212
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7
Akademický článek
A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.
Autor: Laura Pirisinu, Michele Di Bari, Stefano Marcon, Gabriele Vaccari, Claudia D'Agostino, Paola Fazzi, Elena Esposito, Roberta Galeno, Jan Langeveld, Umberto Agrimi, Romolo Nonno
Publikováno v: PLoS ONE, Vol 5, Iss 9, p e12723 (2010)
Although proteinacious in nature, prions exist as strains with specific self-perpetuating biological properties. Prion strains are thought to be associated with different conformers of PrP(Sc), a disease-associated isoform of the host-encoded cellula
Externí odkaz: https://doaj.org/article/3c331a062738475e8810756eb013a7d8
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8
Akademický článek
Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease.
Autor: Emmanuelle Uro-Coste, Hervé Cassard, Stéphanie Simon, Séverine Lugan, Jean-Marc Bilheude, Armand Perret-Liaudet, James W Ironside, Stéphane Haik, Christelle Basset-Leobon, Caroline Lacroux, Katell Peoch', Nathalie Streichenberger, Jan Langeveld, Mark W Head, Jacques Grassi, Jean-Jacques Hauw, Francois Schelcher, Marie Bernadette Delisle, Olivier Andréoletti
Publikováno v: PLoS Pathogens, Vol 4, Iss 3, p e1000029 (2008)
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methionine/valine polymorphism at codon 129 of the PRNP gene and the proteinase K (PK) digested abnormal prion protein (PrP(res)) identified on Western blott
Externí odkaz: https://doaj.org/article/b4b622169ff8416bb3e11fae5b8545c4
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