Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gocha Golubiani"'
Publikováno v:
Biology, Vol 12, Iss 7, p 956 (2023)
Rett syndrome (RTT) is a genetic neurodevelopmental disorder with mutations in the X-chromosomal MECP2 (methyl-CpG-binding protein 2) gene. Most patients are young girls. For 7–18 months after birth, they hardly present any symptoms; later they dev
Externí odkaz:
https://doaj.org/article/a51227f06c75433da5b605d5480ec8ed
Publikováno v:
Cells, Vol 10, Iss 9, p 2494 (2021)
Using unsupervised metabolomics, we defined the complex metabolic conditions in the cortex of a mouse model of Rett syndrome (RTT). RTT, which represents a cause of mental and cognitive disabilities in females, results in profound cognitive impairmen
Externí odkaz:
https://doaj.org/article/506ef2aae3a144dc8e04688e06d2790d
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This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/our-business/policies/article-withdrawal). This article has been retracted at the request of the Editor-in-Chief and Authors.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