Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Belinda, Kempkes"'
Autor:
Laura Baroncelli, Stefanie Auel, Lena Rinne, Ann-Kathrin Schuster, Victoria Brand, Belinda Kempkes, Katharina Dietrich, Michael Müller
Publikováno v:
Antioxidants, Vol 11, Iss 7, p 1406 (2022)
Rett syndrome (RTT) is a severe neurodevelopmental disorder that typically arises from spontaneous germline mutations in the X-chromosomal methyl-CpG binding protein 2 (MECP2) gene. For the first 6–18 months of life, the development of the mostly f
Externí odkaz:
https://doaj.org/article/da944ab4d6a742a484339464473b084c
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3035718fe2e2100a0778ca31133b9de1
https://pubmed.ncbi.nlm.nih.gov/27895554
https://pubmed.ncbi.nlm.nih.gov/27895554
Autor:
Belinda Kempkes, Kathrin M. Kizina, Benedikt Kolbrink, Lukas S. Terwitte, Katharina Dietrich, Guobin Bao, Michael Müller, Kerstin C. Wagener
Publikováno v:
Antioxidantsredox signaling. 25(1)
Aims: Reactive oxygen species (ROS) and downstream redox alterations not only mediate physiological signaling but also neuropathology. For long, ROS/redox imaging was hampered by a lack of reliable probes. Genetically encoded redox sensors overcame t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3ad6fc7e81dd51864247c9846fa577a
https://pubmed.ncbi.nlm.nih.gov/27059697
https://pubmed.ncbi.nlm.nih.gov/27059697
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff68a6aa50c1dadc5e61ad9aa798bbcb
http://www.sciencedirect.com/science/article/pii/S0969996112002227
http://www.sciencedirect.com/science/article/pii/S0969996112002227
Autor:
Christian, Schnell, Oliwia A, Janc, Belinda, Kempkes, Carolina Araya, Callis, Gabriele, Flügge, Swen, Hülsmann, Michael, Müller
Publikováno v:
Frontiers in Pharmacology, Vol 3 (2012)
Frontiers in Pharmacology
Frontiers in Pharmacology
Chronic stress affects neuronal networks by inducing dendritic retraction, modifying neuronal excitability and plasticity, and modulating glial cells. To elucidate the functional consequences of chronic stress for the hippocampal network, we submitte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::bfa16b9a703a63b4ef5f9c938ac24dde
https://orca.cardiff.ac.uk/id/eprint/67824/1/fphar-03-00053.pdf
https://orca.cardiff.ac.uk/id/eprint/67824/1/fphar-03-00053.pdf
