Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Karsten M. Strauss"'
Autor:
Carola Schiesling, Frank P. Marx, Olaf Riess, Christian Melle, Sabine Kautzmann, Simone Engelender, Anne S. Soehn, Thomas Franck, Daniela Berg, Jörg B. Schulz, Jens Pahnke, Karsten M. Strauss, Rejko Krüger, Simon Dawson, Ferdinand von Eggeling, Mira Lang
Publikováno v:
The FASEB Journal. 21:1759-1767
Synphilin-1 is linked to Parkinson's disease (PD), based on its role as an alpha-synuclein (PARK1)-interacting protein and substrate of the ubiquitin E3 ligase Parkin (PARK2) and because of its presence in Lewy bodies (LB) in brains of PD patients. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b97cdbdab119d7b4a509bfda9d1874f
https://doi.org/10.1096/fj.06-6734com
https://doi.org/10.1096/fj.06-6734com
Autor:
Liang Tong, Ludger Schöls, Robert Hering, Christine Klein, Daniela Berg, Bernd Wollnik, Dirk Woitalla, Eva-Maria Mietz, Jörg B. Schulz, Rejko Krüger, Wilhelm Schaible, Xiao Tao, Karsten M. Strauss, Olaf Riess, Peter Bauer, Thomas Müller, Andreas Bauer, Slobodanka Petrovic, Philipp T. Meyer
Publikováno v:
Human Mutation. 24:321-329
Mutations in the parkin gene have been identified as a common cause of autosomal recessive inherited Parkinson disease (PD) associated with early disease manifestation. However, based on linkage data, mutations in other genes contribute to the geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1114f8fc0dcce1e2c45e0a770e29e8a9
https://doi.org/10.1002/humu.20089
https://doi.org/10.1002/humu.20089
Autor:
Matthew J. Farrer, Ludger Schöls, Lei Li, Ellen Gerhardt, Frank P. Marx, Klaus Berger, Olaf Eberhardt, Jennifer M. Kachergus, Mark R. Cookson, Olaf Riess, Carsten Holzmann, Rejko Krüger, Karsten M. Strauss, Jörg B. Schulz, Simone Engelender, Dena G. Hernandez, Christopher A. Ross
Publikováno v:
Human Molecular Genetics. 12:1223-1231
Synphilin-1 is linked to the pathogenesis of Parkinson's disease (PD) based on its identification as an alpha-synuclein (PARK1) and parkin (PARK2) interacting protein. Moreover, synphilin-1 is a component of Lewy bodies (LB) in brains of sporadic PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9324d04cb1f90d5ae33d8f64fbb24b8
https://doi.org/10.1093/hmg/ddg134
https://doi.org/10.1093/hmg/ddg134
Autor:
Sabine Kautzmann, Olaf Riess, Peter Bauer, Guido Krebiehl, Claudia Wahl, Dirk Woitalla, Karsten M. Strauss, Rejko Krüger, Thomas Müller
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 115(8)
Dysfunction of proteasomal protein degradation is involved in neurodegeneration in Parkinson's disease (PD). Recently we identified the regulatory proteasomal subunit S6 ATPase as a novel interactor of synphilin-1, which is a substrate of the ubiquit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e41f9d29e2a082207619d31709a2e99d
https://pubmed.ncbi.nlm.nih.gov/18446261
https://pubmed.ncbi.nlm.nih.gov/18446261
Autor:
Robert, Hering, Karsten M, Strauss, Xiao, Tao, Andreas, Bauer, Dirk, Woitalla, Eva-Maria, Mietz, Slobodanka, Petrovic, Peter, Bauer, Wilhelm, Schaible, Thomas, Müller, Ludger, Schöls, Christine, Klein, Daniela, Berg, Philipp T, Meyer, Jörg B, Schulz, Bernd, Wollnik, Liang, Tong, Rejko, Krüger, Olaf, Riess
Publikováno v:
Human mutation. 24(4)
Mutations in the parkin gene have been identified as a common cause of autosomal recessive inherited Parkinson disease (PD) associated with early disease manifestation. However, based on linkage data, mutations in other genes contribute to the geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d2efbaa38f10d934c5a214db2b21dd4
https://pubmed.ncbi.nlm.nih.gov/15365989
https://pubmed.ncbi.nlm.nih.gov/15365989
Autor:
Jörg T. Epplen, Dirk Woitalla, Olaf Riess, Rejko Krüger, Marcel Hungs, René Gobbelé, Ludger Schöls, Christian Fischer, Thomas Müller, Thorsten Schulte, Karsten M. Strauss, Daniela Berg, Klaus Berger
Publikováno v:
Neuroscience letters. 351(2)
Neurofilament M, a major component of Lewy bodies, represents an interesting candidate in the pathogenesis of Parkinson's disease (PD). We performed detailed mutation analyses of the NF-M gene in 322 familial and sporadic PD patients. Two polymorphis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd7f7eb904ae3e0db8764dd6dd5eda0
https://pubmed.ncbi.nlm.nih.gov/14583397
https://pubmed.ncbi.nlm.nih.gov/14583397