Literature DB >> 11735379

Reactive oxygen species and mitochondrial diseases.

I G Kirkinezos1, C T Moraes.   

Abstract

A variety of diseases have been associated with excessive reactive oxygen species (ROS), which are produced mostly in the mitochondria as byproducts of normal cell respiration. The interrelationship between ROS and mitochondria suggests shared pathogenic mechanisms in mitochondrial and ROS-related diseases. Defects in oxidative phosphorylation can increase ROS production, whereas ROS-mediated damage to biomolecules can have direct effects on the components of the electron transport system. Here, we review the molecular mechanisms of ROS production and damage, as well as the existing evidence of mitochondrial ROS involvement in human diseases. Copyright 2001 Academic Press.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11735379     DOI: 10.1006/scdb.2001.0282

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  99 in total

Review 1.  DNA damage by reactive species: Mechanisms, mutation and repair.

Authors:  N R Jena
Journal:  J Biosci       Date:  2012-07       Impact factor: 1.826

2.  Production of reactive oxygen species by flight muscle mitochondria of the bumblebee (Bombus terrestris L.).

Authors:  M Yu Syromyatnikov; M Yu Chugreev; A V Lopatin; A A Starkov; V N Popov
Journal:  Dokl Biochem Biophys       Date:  2015-09-03       Impact factor: 0.788

Review 3.  Regulation of mitophagy by the ubiquitin pathway in neurodegenerative diseases.

Authors:  Shyamal Desai; Meredith Juncker; Catherine Kim
Journal:  Exp Biol Med (Maywood)       Date:  2018-01-09

4.  Effects of nitric oxide donors on cybrids harbouring the mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) A3243G mitochondrial DNA mutation.

Authors:  Jagdeep K Sandhu; Caroline Sodja; Kevan McRae; Yan Li; Peter Rippstein; Yau-Huei Wei; Boleslaw Lach; Fay Lee; Septimiu Bucurescu; Mary-Ellen Harper; Marianna Sikorska
Journal:  Biochem J       Date:  2005-10-15       Impact factor: 3.857

Review 5.  Exploiting oxidative microenvironments in the body as triggers for drug delivery systems.

Authors:  Shivanjali Joshi-Barr; Caroline de Gracia Lux; Enas Mahmoud; Adah Almutairi
Journal:  Antioxid Redox Signal       Date:  2014-04-15       Impact factor: 8.401

6.  Tissue specificity of a human mitochondrial disease: differentiation-enhanced mis-splicing of the Fe-S scaffold gene ISCU renders patient cells more sensitive to oxidative stress in ISCU myopathy.

Authors:  Daniel R Crooks; Suh Young Jeong; Wing-Hang Tong; Manik C Ghosh; Hayden Olivierre; Ronald G Haller; Tracey A Rouault
Journal:  J Biol Chem       Date:  2012-10-03       Impact factor: 5.157

7.  Quantitative Middle-Down MS Analysis of Parkin-Mediated Ubiquitin Chain Assembly.

Authors:  Kirandeep K Deol; Stephen J Eyles; Eric R Strieter
Journal:  J Am Soc Mass Spectrom       Date:  2020-04-28       Impact factor: 3.109

Review 8.  Links between mitochondrial retrograde response and mitophagy in pathogenic cell signalling.

Authors:  Daniela Strobbe; Soumya Sharma; Michelangelo Campanella
Journal:  Cell Mol Life Sci       Date:  2021-02-23       Impact factor: 9.261

9.  Mitochondrial dysfunctions in myalgic encephalomyelitis/chronic fatigue syndrome explained by activated immuno-inflammatory, oxidative and nitrosative stress pathways.

Authors:  Gerwyn Morris; Michael Maes
Journal:  Metab Brain Dis       Date:  2013-09-10       Impact factor: 3.584

10.  Pitx2 maintains mitochondrial function during regeneration to prevent myocardial fat deposition.

Authors:  Lele Li; Ge Tao; Matthew C Hill; Min Zhang; Yuka Morikawa; James F Martin
Journal:  Development       Date:  2018-09-26       Impact factor: 6.868

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.