Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Matthias Golla"'
Autor:
Martin Thunemann, Barbara F. Schörg, Susanne Feil, Yun Lin, Jakob Voelkl, Matthias Golla, Angelos Vachaviolos, Ursula Kohlhofer, Leticia Quintanilla-Martinez, Marcus Olbrich, Walter Ehrlichmann, Gerald Reischl, Christoph M. Griessinger, Harald F. Langer, Meinrad Gawaz, Florian Lang, Michael Schäfers, Manfred Kneilling, Bernd J. Pichler, Robert Feil
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Non-invasive cell tracking is a powerful method to visualize cells in vivo under physiological and pathophysiological conditions. Here Thunemann et al. generate a mouse model for in vivo tracking and quantification of specific cell types by combining
Externí odkaz:
https://doaj.org/article/f6168d6482b4443e8fee432ca8cba8f0
Autor:
Cathrine R. Carlson, Christian Johannes Gloeckner, Eleonora Aronica, Jeannette Hübener-Schmid, Ann-Christin Krahl, Stefan Hauser, Olaf Riess, Ludger Schöls, Maike Nagel, Giambattista Guaitoli, Huu P. Nguyen, Matthias Golla, Stefanie N. Hayer, Jonasz J. Weber, Sebastian Samer, Pimthanya Wanichawan
Publikováno v:
Brain 140(5), 1280-1299 (2017). doi:10.1093/brain/awx039
Brain, 140(5), 1280-1299. Oxford University Press
Brain, 140(5), 1280-1299. Oxford University Press
Ataxin-3, the disease protein in Machado-Joseph disease, is known to be proteolytically modified by various enzymes including two major families of proteases, caspases and calpains. This processing results in the generation of toxic fragments of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::727e9d9e95ffaf4bd1fbe7b35cec73f7
https://doi.org/10.1093/brain/awx039
https://doi.org/10.1093/brain/awx039
Autor:
Walter Ehrlichmann, Gerald Reischl, Yun Lin, Martin Thunemann, Michael Schäfers, Christoph M. Griessinger, Matthias Golla, Manfred Kneilling, Jakob Voelkl, Leticia Quintanilla-Martinez, Marcus Olbrich, Meinrad Gawaz, Angelos Vachaviolos, Florian Lang, Susanne Feil, B.F. Schörg, Ursula Kohlhofer, Harald F. Langer, Robert Feil, Bernd J. Pichler
Publikováno v:
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Many pathophysiological processes are associated with proliferation, migration or death of distinct cell populations. Monitoring specific cell types and their progeny in a non-invasive, longitudinal and quantitative manner is still challenging. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d05feff79c98c66b7316437f1af805
https://pubmed.ncbi.nlm.nih.gov/28874662
https://pubmed.ncbi.nlm.nih.gov/28874662
Autor:
Lisa Lehmann, Thorsten Schmidt, Jonasz J. Weber, Jana Schmidt, Olaf Riess, Jeannette Hübener-Schmid, Matthias Golla
Publikováno v:
Journal of neurochemistry. 138(1)
Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominantly inherited neurodegenerative disorder for which no curative therapy is available. The cause of this disease is the expansion of a CAG repeat in the so-called ATXN3 gene leading to an expa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::194c65ce113519778f6734e807aa4215
https://pubmed.ncbi.nlm.nih.gov/26990650
https://pubmed.ncbi.nlm.nih.gov/26990650