Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Karolina Can"'
Autor:
Karolina Can, Christiane Menzfeld, Lena Rinne, Peter Rehling, Sebastian Kügler, Gocha Golubiani, Jan Dudek, Michael Müller
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Rett syndrome (RTT), an X chromosome-linked neurodevelopmental disorder affecting almost exclusively females, is associated with various mitochondrial alterations. Mitochondria are swollen, show altered respiratory rates, and their inner membrane is
Externí odkaz:
https://doaj.org/article/86be88ca0602402c85d149e340a4a190
Publikováno v:
Cells, Vol 9, Iss 12, p 2539 (2020)
Rett syndrome (RTT) is a neurodevelopmental disorder associated with disturbed neuronal responsiveness and impaired neuronal network function. Furthermore, mitochondrial alterations and a weakened cellular redox-homeostasis are considered part of the
Externí odkaz:
https://doaj.org/article/927a51c41c6f4d20b7f5d82eff0b7fb4
Autor:
Karolina, Can, Christiane, Menzfeld, Lena, Rinne, Peter, Rehling, Sebastian, Kügler, Gocha, Golubiani, Jan, Dudek, Michael, Müller
Publikováno v:
Frontiers in Physiology
Rett syndrome (RTT), an X chromosome-linked neurodevelopmental disorder affecting almost exclusively females, is associated with various mitochondrial alterations. Mitochondria are swollen, show altered respiratory rates, and their inner membrane is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51991ad544a1198c1fe81b115f37ee6e
https://pubmed.ncbi.nlm.nih.gov/31114506
https://pubmed.ncbi.nlm.nih.gov/31114506
Publikováno v:
Neuromethods ISBN: 9781493968886
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::790c5b35247cc4223a9a1a221084d998
https://doi.org/10.1007/978-1-4939-6890-9_9
https://doi.org/10.1007/978-1-4939-6890-9_9
Autor:
Michael Müller, Karolina Can
Publikováno v:
Biochemical Society Transactions. 42:959-964
RTT (Rett syndrome) is a severe progressive neurodevelopmental disorder with a monogenetic cause, but complex and multifaceted clinical appearance. Compelling evidence suggests that mitochondrial alterations and aberrant redox homoeostasis result in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::725b4560b2735f44abc6ef0cbb25000c
https://doi.org/10.1042/bst20140071
https://doi.org/10.1042/bst20140071
Publikováno v:
Free radical biologymedicine. 76
Reactive oxygen species mediate cellular signaling and neuropathologies. Hence, there is tremendous interest in monitoring (sub)cellular redox conditions. We evaluated the genetically engineered redox sensor HyPer in mouse hippocampal cell cultures.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b4a04e4058b6e397e7f56f6198038d
https://pubmed.ncbi.nlm.nih.gov/25179473
https://pubmed.ncbi.nlm.nih.gov/25179473
Autor:
Rustam Mollajew, Karolina Can, Jayamuruga P. Arunachalam, S. L. Mironov, Ashraf U. Mannan, Albert Rosenberger, Chiranjeevi Bodda, Hannelore Ehrenreich, Martesa Tantra, Franco Laccone
An intriguing finding about the gene encoding methyl-CpG binding protein 2 (MeCP2) is that the loss-of-function mutations cause Rett syndrome and duplication (gain-of-function) of MECP2 leads to another neurological disorder termed MECP2 duplication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c68d124df37f1fbdeee2ead4a05fd627
https://doi.org/10.1016/j.ajpath.2013.03.019
https://doi.org/10.1016/j.ajpath.2013.03.019