Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lena Rinne"'
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:
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:
Olusegun L, Adebayo, Ina, Dewenter, Lena, Rinne, Gocha, Golubiani, Revaz, Solomonia, Michael, Müller
Publikováno v:
Archives of Biochemistry and Biophysics. 732:109467
This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/our-business/policies/article-withdrawal). This article has been retracted at the request of the Editor-in-Chief and Authors. Professor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81618659e15f81e05d38c70c418a4647
https://doi.org/10.1016/j.abb.2022.109467
https://doi.org/10.1016/j.abb.2022.109467
Autor:
Gocha Golubiani, Ina Dewenter, Lena Rinne, Michael Müller, Olusegun L. Adebayo, Revaz Solomonia
Publikováno v:
Archives of biochemistry and biophysics. 696
The neurodevelopmental disorder Rett syndrome (RTT) affects mostly females. Upon an apparently normal initial development, cognitive impairment, irregular breathing, motor dysfunction, and epilepsy occur. The complex pathogenesis includes, among othe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54494d9a956c15c345927560cb97b9d8
https://pubmed.ncbi.nlm.nih.gov/36435647
https://pubmed.ncbi.nlm.nih.gov/36435647
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