Mitochondrial function and Parkinson's disease: from the perspective of the electron transport chain

JL Li, TY Lin, PL Chen, TN Guo, SY Huang… - Frontiers in molecular …, 2021 - frontiersin.org
Parkinson's disease (PD) is known as a mitochondrial disease. Some even regarded it
specifically as a disorder of the complex I of the electron transport chain (ETC). The ETC is …

Premature physiologic aging as a paradigm for understanding increased risk of adverse health across the lifespan of survivors of childhood cancer

KK Ness, JL Kirkland, MM Gramatges… - Journal of Clinical …, 2018 - ascopubs.org
The improvement in survival of childhood cancer observed across the past 50 years has
resulted in a growing acknowledgment that simply extending the lifespan of survivors is not …

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

S Chakrabarty, P Govindaraj, BP Sankaran… - Journal of …, 2021 - Springer
Background Mitochondrial disorders are clinically complex and have highly variable
phenotypes among all inherited disorders. Mutations in mitochon drial DNA (mtDNA) and …

Regional heterogeneity in mitochondrial function underlies region specific vulnerability in human brain ageing: Implications for neurodegeneration

Y Anusha-Kiran, P Mol, G Dey, FA Bhat… - Free Radical Biology …, 2022 - Elsevier
Selective neuronal vulnerability (SNV) of specific neuroanatomical regions such as frontal
cortex (FC) and hippocampus (HC) is characteristic of age-associated neurodegenerative …

Using multi-omics methods to understand dermatomyositis/polymyositis

S Gao, H Luo, H Zhang, X Zuo, L Wang, H Zhu - Autoimmunity Reviews, 2017 - Elsevier
Idiopathic inflammatory myopathies (IIM) are a group of rare and heterogeneous
autoimmune diseases, and the most common subtypes are dermatomyositis (DM) and …

Mitochondrial DNA disturbances and deregulated expression of oxidative phosphorylation and mitochondrial fusion proteins in sporadic inclusion body myositis

M Catalán-García, G Garrabou, C Morén… - Clinical …, 2016 - portlandpress.com
Sporadic inclusion body myositis (sIBM) is one of the most common myopathies in elderly
people. Mitochondrial abnormalities at the histological level are present in these patients …

Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events

N Gowthami, N Pursotham, G Dey… - Journal of …, 2023 - Wiley Online Library
Traumatic brain injury (TBI) causes significant neurological deficits and long‐term
degenerative changes. Primary injury in TBI entails distinct neuroanatomical zones, ie …

Mitochondrial complex I inhibition in dopaminergic neurons causes altered protein profile and protein oxidation: implications for Parkinson's disease

Y Chithra, G Dey, V Ghose, V Chandramohan… - Neurochemical …, 2023 - Springer
Mitochondrial dysfunction and oxidative stress are critical to neurodegeneration in
Parkinson's disease (PD). Mitochondrial dysfunction in PD entails inhibition of the …

An overview of mitochondrial protein defects in neuromuscular diseases

F Marra, P Lunetti, R Curcio, FM Lasorsa… - Biomolecules, 2021 - mdpi.com
Neuromuscular diseases (NMDs) are dysfunctions that involve skeletal muscle and cause
incorrect communication between the nerves and muscles. The specific causes of NMDs are …

Mapping the human skeletal muscle proteome: progress and potential

D Capitanio, M Moriggi, C Gelfi - Expert review of proteomics, 2017 - Taylor & Francis
Introduction: Human skeletal muscle represents 40% of our body mass and deciphering its
proteome composition to further understand mechanisms regulating muscle function under …