Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Liza, Douiev"'
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Omaveloxolone (RTA408) is a second-generation oleanane triterpenoid Nrf2 inducer with antioxidant and anti-inflammatory properties and was reported to improve mitochondrial bioenergetics. It is currently being tested in medical trials for Friedrich a
Externí odkaz:
https://doaj.org/article/f4b131623cb34f1b90ea1ed7bc4925cb
Publikováno v:
Cells, Vol 10, Iss 2, p 452 (2021)
Cytochrome-c-oxidase (COX) subunit 4 (COX4) plays important roles in the function, assembly and regulation of COX (mitochondrial respiratory complex 4), the terminal electron acceptor of the oxidative phosphorylation (OXPHOS) system. The principal CO
Externí odkaz:
https://doaj.org/article/241985c434a546a295baaf9d6479675c
Publikováno v:
Cells, Vol 9, Iss 2, p 301 (2020)
Mitochondria are involved in many cellular processes and their main role is cellular energy production. They constantly undergo fission and fusion, and these counteracting processes are under strict balance. The cytosolic dynamin-related protein 1, D
Externí odkaz:
https://doaj.org/article/7263b2613849447b83de0ca2eb9a4ee7
Autor:
Yun Li, Ruth Sheffer, Peter Nürnberg, Muhannad Daana, Silke Kaulfuss, Hagar Mor-Shakad, Bernd Wollnik, Janine Altmüller, Knut Brockmann, Peter Burfeind, Emrah Kaygusuz, Liza Douiev, Gökhan Yigit
Publikováno v:
Journal of Medical Genetics. 59:549-553
BackgroundDevelopmental and epileptic encephalopathies (DEEs) represent a group of severe neurological disorders characterised by an onset of refractory seizures during infancy or early childhood accompanied by psychomotor developmental delay or regr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::071e868fe3d7984d7b7e5275445c4f05
https://doi.org/10.1136/jmedgenet-2021-107769
https://doi.org/10.1136/jmedgenet-2021-107769
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 8; Pages: 4149
Cytochrome c oxidase (COX), a multimeric protein complex, is the final electron acceptor in the mitochondrial electron transfer chain. Primary COX deficiency, caused by mutations in either mitochondrial DNA or nuclear-encoded genes, is a heterogenous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8ebaf8e119a2591160e9763c2069c51
https://pubmed.ncbi.nlm.nih.gov/35456968
https://pubmed.ncbi.nlm.nih.gov/35456968
Autor:
Aviram Kogot-Levin, Ann Saada, Gil Leibowitz, Devorah Soiferman, Liza Douiev, Itamar Raz, Sarah Weksler-Zangen
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0165417 (2016)
Cytochrome-c-oxidase (COX) deficiency is a frequent cause of mitochondrial disease and is associated with a wide spectrum of clinical phenotypes. We studied mitochondrial function and biogenesis in fibroblasts derived from the Cohen (CDs) rat, an ani
Externí odkaz:
https://doaj.org/article/fcf45543cd3348888841ac549b7b66d6
Cytochrome- c- oxidase (COX), a multimeric protein complex, is the final electron acceptor in the mitochondrial electron transfer chain. Primary COX deficiency, caused by mutations in either mitochondrial DNA or nuclear-encoded genes, is a heterogeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::121a4415ed4c0bb20e05f0f7dd4847ea
https://doi.org/10.21203/rs.3.rs-1026650/v1
https://doi.org/10.21203/rs.3.rs-1026650/v1
Publikováno v:
Cells
Volume 10
Issue 2
Cells, Vol 10, Iss 452, p 452 (2021)
Volume 10
Issue 2
Cells, Vol 10, Iss 452, p 452 (2021)
Cytochrome-c-oxidase (COX) subunit 4 (COX4) plays important roles in the function, assembly and regulation of COX (mitochondrial respiratory complex 4), the terminal electron acceptor of the oxidative phosphorylation (OXPHOS) system. The principal CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc76bf0c1ea2b41bec19cdda2580d28
Autor:
Gökhan, Yigit, Ruth, Sheffer, Muhannad, Daana, Yun, Li, Emrah, Kaygusuz, Hagar, Mor-Shakad, Janine, Altmüller, Peter, Nürnberg, Liza, Douiev, Silke, Kaulfuss, Peter, Burfeind, Bernd, Wollnik, Knut, Brockmann
Publikováno v:
Journal of medical genetics. 59(6)
Developmental and epileptic encephalopathies (DEEs) represent a group of severe neurological disorders characterised by an onset of refractory seizures during infancy or early childhood accompanied by psychomotor developmental delay or regression. DE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3918ff5808c80e6d9b2771fd06a1205b
https://pubmed.ncbi.nlm.nih.gov/34172529
https://pubmed.ncbi.nlm.nih.gov/34172529
Publikováno v:
Prenatal diagnosisREFERENCES. 41(3)
Background Chromosomal-microarray-analysis (CMA) can identify variants of uncertain clinical significance, susceptibility-loci for neurodevelopmental conditions, and risk for adult-onset conditions. We explored choices made by couples undergoing pren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a368aeba8c1d380904c835d8ab1859a
https://pubmed.ncbi.nlm.nih.gov/33128404
https://pubmed.ncbi.nlm.nih.gov/33128404