Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Giannantonio Panza"'
Autor:
Giannantonio Panza, Lars Luers, Jan Stöhr, Luitgard Nagel-Steger, Jürgen Weiss, Detlev Riesner, Dieter Willbold, Eva Birkmann
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e14283 (2010)
Prion diseases like Creutzfeldt-Jakob disease in humans, Scrapie in sheep or bovine spongiform encephalopathy are fatal neurodegenerative diseases, which can be of sporadic, genetic, or infectious origin. Prion diseases are transmissible between diff
Externí odkaz:
https://doaj.org/article/b2431ef0d6374eac9693093cffcd8333
Publikováno v:
Rejuvenation Research. 13:220-223
Prion diseases are fatal neurodegenerative diseases that occur either spontaneously or genetically or are caused by infection. Spontaneously occuring prion diseases are age related. The infectious agents, called prions, are proteinaceous infectious p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::982413e140b88b7403b3d72a049632df
https://doi.org/10.1089/rej.2009.0954
https://doi.org/10.1089/rej.2009.0954
Autor:
Lars Luers, Detlev Riesner, Luitgard Nagel-Steger, Jürgen Weiβ, Jan Stöhr, Giannantonio Panza, Dieter Willbold, Eva Birkmann
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e14283 (2010)
PLoS one 5, e14283 (2010). doi:10.1371/journal.pone.0014283
PLoS ONE
PLoS one 5, e14283 (2010). doi:10.1371/journal.pone.0014283
PLoS ONE
Prion diseases like Creutzfeldt-Jakob disease in humans, Scrapie in sheep or bovine spongiform encephalopathy are fatal neurodegenerative diseases, which can be of sporadic, genetic, or infectious origin. Prion diseases are transmissible between diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa5b084d643b58d5951596a465f87d0
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21151607/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21151607/?tool=EBI
Autor:
Lars Luers, Giannantonio Panza, Eva Birkmann, Franziska Henke, J. Weiss, T. Agyenim, Dieter Willbold
Publikováno v:
Rejuvenation research. 13(2-3)
Protein aggregation occurs in many age-related neurodegenerative diseases, where it can lead to deposits of naturally occurring proteins in the brain. In case of Creutzfeldt–Jakob disease (CJD), these deposits consist of prion protein (PrP). CJD ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1511296f03c9da75b6850c86f086072
https://pubmed.ncbi.nlm.nih.gov/20017612
https://pubmed.ncbi.nlm.nih.gov/20017612
Autor:
Dimitrios Papathanassiou, Giannantonio Panza, Christian Dumpitak, Dieter Willbold, Jürgen Weiss, Eva Birkmann, Jan Stöhr, Detlev Riesner
Publikováno v:
Biochemical and biophysical research communications. 373(4)
The conversion of the cellular isoform of the prion protein into the pathogenic isoform PrP(Sc) is the key event in prion diseases. The disease can occur spontaneously genetically or by infection. In earlier studies we presented an in vitro conversio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b12b470a0e6ac487325b3643b0cec74
https://pubmed.ncbi.nlm.nih.gov/18585368
https://pubmed.ncbi.nlm.nih.gov/18585368
Autor:
Tatsuo Terashima, Detlev Riesner, Eva Birkmann, Giannantonio Panza, Otto Baba, Dieter Willbold, Christian Dumpitak, Jan Stöhr
Publikováno v:
Rejuvenation research. 11(2)
Prion diseases like Creutzfeldt-Jakob disease in humans or scrapie in sheep and goats are infectious neurodegenerative diseases. Their infectious agent, called prion, is composed mainly of aggregated and misfolded prion protein and non-proteinaceous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8095ba66853b5c9aaafadac4866aa52
https://pubmed.ncbi.nlm.nih.gov/18341429
https://pubmed.ncbi.nlm.nih.gov/18341429
Autor:
Giannantonio Panza, Luitgard Nagel-Steger, Nicole Weinmann, Tina Kaimann, Eva Birkmann, Holger Wille, Stanley B. Prusiner, Detlev Riesner, Jan Stöhr, Manfred Eigen
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
The conversion of the α-helical, cellular isoform of the prion protein (PrP C ) to the insoluble, β-sheet-rich, infectious, disease-causing isoform (PrP Sc ) is the key event in prion diseases. In an earlier study, several forms of PrP were convert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17eebb49b657dc59839105c4cf3fc6cc
https://europepmc.org/articles/PMC2268150/
https://europepmc.org/articles/PMC2268150/
Publikováno v:
Rejuvenation Research; Apr2010, Vol. 13 Issue 2/3, p220-223, 4p
Autor:
Giannantonio Panza, Jan Stöhr, Eva Birkmann, Detlev Riesner, Dieter Willbold, Otto Baba, Tatsuo Terashima, Christian Dumpitak
Publikováno v:
Rejuvenation Research; Apr2008, Vol. 11 Issue 2, p365-369, 5p