Zobrazeno 1 - 10
of 186
pro vyhledávání: '"mt-atp6"'
Publikováno v:
Indonesian Journal of Biotechnology, Vol 29, Iss 3, Pp 169-176 (2024)
In addition to the issue of pork contamination, processed meats frequently contain traces of rat meat. Therefore, detection and quantification of the pork and rat DNA in cases of meat and processed meat adulteration are necessary. In the current stud
Externí odkaz:
https://doaj.org/article/f41ac2735f3c4189a410ed789b982bff
Autor:
Daniele Sala, Silvia Marchet, Lorenzo Nanetti, Andrea Legati, Caterina Mariotti, Eleonora Lamantea, Daniele Ghezzi, Alessia Catania, Costanza Lamperti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background MT-ATP6 is a mitochondrial gene which encodes for the intramembrane subunit 6 (or A) of the mitochondrial ATP synthase, also known asl complex V, which is involved in the last step of oxidative phosphorylation to produce cellular
Externí odkaz:
https://doaj.org/article/482c0fe92b70470496f07304e8f01d82
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 14 (2024)
BackgroundSepsis represents a severe manifestation of infection often accompanied by metabolic disorders and mitochondrial dysfunction. Notably, mitochondrial DNA copy number (mtDNA-CN) and the expression of specific mitochondrial genes have emerged
Externí odkaz:
https://doaj.org/article/b06b570070854709b2591b9b7f9cc667
Autor:
Nejira Handžić, Dino Pećar, Selma Durgut, Naida Mulahuseinović, Ivana Čeko, Mirza Izmirlija, Adna Ašić, Lana Salihefendić, Rijad Konjhodžić
Publikováno v:
Genetics & Applications, Vol 8, Iss 1 (2024)
Human mitochondrial genes MT-ATP6 and MT-ATP8 encode the subunits 6 and 8, respectively, of ATP synthase, a vital protein Complex V intricately involved in oxidative phosphorylation and ATP metabolism. This enzyme produces ATP from ADP in the mitocho
Externí odkaz:
https://doaj.org/article/52e25724034845d08d26b1a04104775a
Autor:
Cansu de Muijnck, Mary J. van Schooneveld, Astrid S. Plomp, Richard J. Rodenburg, Maria M. van Genderen, Camiel J.F. Boon
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 34, Iss , Pp 102070- (2024)
Purpose: To describe a case with Leber's hereditary optic neuropathy (LHON) like optic atrophy in the presence of MT-ATP6 gene variant m.8969G > A. Observations: A 20-year-old patient with a history of mild developmental delay, mild cognitive impairm
Externí odkaz:
https://doaj.org/article/4d4355855735408fb4dd3f53ccb8e417
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 11, Pp 2345-2350 (2022)
Episodic weakness is typically associated with a group of disorders so called periodic paralyses. Their major causes are mutation of ion channels, and have rarely been linked to mitochondrial disorders. We report a 20-year-old man with episodic weakn
Externí odkaz:
https://doaj.org/article/0591f6e481814ef6a172aa277306b63a
Akademický článek
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Akademický článek
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Autor:
Emilia Baranowska, Katarzyna Niedzwiecka, Chiranjit Panja, Camille Charles, Alain Dautant, Jarosław Poznanski, Jean-Paul di Rago, Déborah Tribouillard-Tanvier, Roza Kucharczyk
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 4 (2023)
Externí odkaz:
https://doaj.org/article/67af0f6874f24f29be4f95b9a79d1e6c
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundLeigh syndrome (LS; OMIM: 256000) is a progressive neurodegenerative disease caused by genetic mutations resulting in mitochondrial oxidative phosphorylation defects. The prognosis is poor, with most children dying before the age of 2 years
Externí odkaz:
https://doaj.org/article/6106a8409b02407c93205449c4bb61c7