Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Christiane Menzfeld"'
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
Autor:
Oliwa Alicja Janc, Marc Albert Hüser, Katharina Dietrich, Belinda Kempkes, Christiane Menzfeld, Swen Hülsmann, Michael Müller
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 10 (2016)
Rett syndrome (RTT) is a severe neurodevelopmental disorder typically arising from spontaneous mutations in the X-chromosomal methyl-CpG binding protein 2 (MECP2) gene. The almost exclusively female Rett patients show an apparently normal development
Externí odkaz:
https://doaj.org/article/864b8dc6efe64d7bbd07e9e538510f8e
Autor:
Emanuel Großer, Ursula Hirt, Oliwia A. Janc, Christiane Menzfeld, Marc Fischer, Belinda Kempkes, Steffen Vogelgesang, Till U. Manzke, Lennart Opitz, Gabriela Salinas-Riester, Michael Müller
Publikováno v:
Neurobiology of Disease, Vol 48, Iss 1, Pp 102-114 (2012)
Rett syndrome is an X chromosome-linked neurodevelopmental disorder associated with cognitive impairment, motor dysfunction and breathing irregularities causing intermittent hypoxia. Evidence for impaired mitochondrial function is also accumulating.
Externí odkaz:
https://doaj.org/article/d137c3ca17f84a62976a35d9d989855c
Autor:
Simone Wüst, Denise Tischner, Michael John, Jan P Tuckermann, Christiane Menzfeld, Uwe-Karsten Hanisch, Jens van den Brandt, Fred Lühder, Holger M Reichardt
Publikováno v:
PLoS ONE, Vol 4, Iss 12, p e8202 (2009)
BACKGROUND: Dissociating glucocorticoid receptor (GR) ligands hold great promise for treating inflammatory disorders since it is assumed that they exert beneficial activities mediated by transrepression but avoid adverse effects of GR action requirin
Externí odkaz:
https://doaj.org/article/9131bf4fc0fc475bbecdc5ffc8b0ca31
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
Autor:
Christiane Menzfeld, Alexander Götz, Peter Teismann, Denise Tischner, Tommy Regen, Wolfgang Brück, Thomas Herdegen, Martin S. Weber, Philippe Boutin, Sandra Ribes, Shlomo Rotshenker, Michael John, Vanessa Bremes, Angela Borisch, Tobias Pukrop, Jürgen Wienands, Konstantin Neumann, Roland Nau, Helmut Kettenmann, Vicky Waetzig, Fred Lühder, Uwe-Karsten Hanisch, Hana Janova, Iain R. Greig, Alexander Mildner, Denise van Rossum, Holger M. Reichardt, Jörg Scheffel, Michael Müller, Marco Prinz
Publikováno v:
Glia. 63:1083-1099
The putative protein tyrosine kinase (PTK) inhibitor tyrphostin AG126 has proven beneficial in various models of inflammatory disease. Yet molecular targets and cellular mechanisms remained enigmatic. We demonstrate here that AG126 treatment has bene
Autor:
Lennart Opitz, Belinda Kempkes, Ursula Hirt, Steffen Vogelgesang, Gabriela Salinas-Riester, Christiane Menzfeld, Emanuel Großer, Oliwia A. Janc, Marc Fischer, Michael Müller, Till U. Manzke
Publikováno v:
Neurobiology of Disease, Vol 48, Iss 1, Pp 102-114 (2012)
Rett syndrome is an X chromosome-linked neurodevelopmental disorder associated with cognitive impairment, motor dysfunction and breathing irregularities causing intermittent hypoxia. Evidence for impaired mitochondrial function is also accumulating.
Autor:
Oliwia A, Janc, Marc A, Hüser, Katharina, Dietrich, Belinda, Kempkes, Christiane, Menzfeld, Swen, Hülsmann, Michael, Müller
Publikováno v:
Frontiers in Cellular Neuroscience
Rett syndrome (RTT) is a severe neurodevelopmental disorder typically arising from spontaneous mutations in the X-chromosomal methyl-CpG binding protein 2 (MECP2) gene. The almost exclusively female Rett patients show an apparently normal development
Autor:
Christiane, Menzfeld, Michael, John, Denise, van Rossum, Tommy, Regen, Jörg, Scheffel, Hana, Janova, Alexander, Götz, Sandra, Ribes, Roland, Nau, Angela, Borisch, Philippe, Boutin, Konstantin, Neumann, Vanessa, Bremes, Jürgen, Wienands, Holger M, Reichardt, Fred, Lühder, Denise, Tischner, Vicky, Waetzig, Thomas, Herdegen, Peter, Teismann, Iain, Greig, Michael, Müller, Tobias, Pukrop, Alexander, Mildner, Helmut, Kettenmann, Wolfgang, Brück, Marco, Prinz, Shlomo, Rotshenker, Martin S, Weber, Uwe-Karsten, Hanisch
Publikováno v:
Glia. 63(6)
The putative protein tyrosine kinase (PTK) inhibitor tyrphostin AG126 has proven beneficial in various models of inflammatory disease. Yet molecular targets and cellular mechanisms remained enigmatic. We demonstrate here that AG126 treatment has bene
Autor:
Fred Lühder, Uwe-Karsten Hanisch, Denise Tischner, Michael John, Christiane Menzfeld, Holger M. Reichardt, Jan Tuckermann, Jens van den Brandt, Simone Wüst
Publikováno v:
PLoS ONE
PLoS ONE, Vol 4, Iss 12, p e8202 (2009)
PLoS ONE, Vol 4, Iss 12, p e8202 (2009)
Background Dissociating glucocorticoid receptor (GR) ligands hold great promise for treating inflammatory disorders since it is assumed that they exert beneficial activities mediated by transrepression but avoid adverse effects of GR action requiring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1b45d49872e7e73d32e313fbd7c74a
http://resolver.sub.uni-goettingen.de/purl?gs-1/5820
http://resolver.sub.uni-goettingen.de/purl?gs-1/5820