Zobrazeno 1 - 10
of 257
pro vyhledávání: '"mtDNA deletion"'
Akademický článek
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Publikováno v:
Toxicology Reports, Vol 8, Iss , Pp 30-37 (2021)
Millions of people around the world are chronically exposed to Arsenic (As) through food and drinking water. Studies revealed that Arsenic is genotoxic and causes damage to DNA. In this study, we evaluated Corchorus olitorius and Butea monosperma for
Externí odkaz:
https://doaj.org/article/17e8ecbcadcf4c809d2ab259ae6e1226
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract Objectives This study aimed to investigate the clinical and genetic spectrum in Chinese patients with multiple mtDNA deletions presenting with autosomal‐inherited mitochondrial progressive external ophthalmoplegia (PEO). Methods Long‐ran
Externí odkaz:
https://doaj.org/article/2e7d8a23f04d4e82b9161c3002b653ff
Autor:
Carmen Hernández-Ainsa, Ester López-Gallardo, María Concepción García-Jiménez, Francisco José Climent-Alcalá, Carmen Rodríguez-Vigil, Marta García Fernández de Villalta, Rafael Artuch, Julio Montoya, Eduardo Ruiz-Pesini, Sonia Emperador
Publikováno v:
Disease Models & Mechanisms, Vol 15, Iss 3 (2022)
Pearson syndrome is a rare multisystem disease caused by single large-scale mitochondrial DNA deletions (SLSMDs). The syndrome presents early in infancy and is mainly characterised by refractory sideroblastic anaemia. Prognosis is poor and treatment
Externí odkaz:
https://doaj.org/article/36040d500962458b9c10107b2ea0ff9e
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
It is generally accepted that patients with chronic progressive ophthalmoplegia caused by single large-scale deletion (SLD) of mitochondrial DNA (mtDNA) only harbor mutation in skeletal and eye muscles. The aim of this study was to investigate the pr
Externí odkaz:
https://doaj.org/article/06437713c23d4db4b84b982468ffb1a1
Autor:
Mouna Tabebi, Wajdi Safi, Rahma Felhi, Olfa Alila Fersi, Leila Keskes, Mohamed Abid, Mouna Mnif, Faiza Fakhfakh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Mitochondrial diabetes (MD) is a rare monogenic form of diabetes and divided into type l and type 2. It is characterized by a strong familial clustering of diabetes with the presence of maternal transmission in conjunction with bi
Externí odkaz:
https://doaj.org/article/8c8a1057c14b4cd1bd474c4e605bf461
Autor:
Noémi Ágnes Varga, Klára Pentelényi, Péter Balicza, András Gézsi, Viktória Reményi, Vivien Hársfalvi, Renáta Bencsik, Anett Illés, Csilla Prekop, Mária Judit Molnár
Publikováno v:
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-14 (2018)
Abstract Background The etiology of autism spectrum disorders (ASD) is very heterogeneous. Mitochondrial dysfunction has been described in ASD; however, primary mitochondrial disease has been genetically proven in a small subset of patients. The main
Externí odkaz:
https://doaj.org/article/652b60e4f28447cc84307c54a3ca3ccb
Publikováno v:
Neurobiology of Disease, Vol 100, Iss , Pp 30-38 (2017)
Parkinson's disease (PD) is a neurodegenerative condition caused by age-related death of dopaminergic (DA) neurons in the substantia nigra (SN). Mitochondrial DNA (mtDNA) deletions rise exponentially with age in humans and reach their highest levels
Externí odkaz:
https://doaj.org/article/7a50ee06cc174e9eb5f755908c39ec43
Autor:
Abdul Aziz Mohamed Yusoff, Wan Salihah Wan Abdullah, Siti Zulaikha Nashwa Mohd Khair, Siti Muslihah Abd Radzak
Publikováno v:
Oncology Reviews, Vol 13, Iss 1 (2019)
Mitochondria are cellular machines essential for energy production. The biogenesis of mitochondria is a highly complex and it depends on the coordination of the nuclear and mitochondrial genome. Mitochondrial DNA (mtDNA) mutations and deletions are s
Externí odkaz:
https://doaj.org/article/19b9195e74aa44d19183903c944d2ac5
Akademický článek
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