Peroxisomal abnormalities and catalase deficiency in Hutchinson-Gilford Progeria Syndrome

Peroxisomes are small, membrane-enclosed eukaryotic organelles that house various enzymes with metabolic functions. One important feature in both Hutchinson-Gilford Progeria Syndrome (HGPS) and normal aging is the elevated levels of Reactive Oxygen Species (ROS), which are generated from metabolic p...

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Detalles Bibliográficos
Autores principales: Mao, Xiaojing, Bharti, Pratima, Thaivalappil, Abhirami, Cao, Kan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138560/
https://www.ncbi.nlm.nih.gov/pubmed/32186522
http://dx.doi.org/10.18632/aging.102941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138560/
https://www.ncbi.nlm.nih.gov/pubmed/32186522
http://dx.doi.org/10.18632/aging.102941

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