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 …
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
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 …
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
Background Mitochondrial disorders are clinically complex and have highly variable
phenotypes among all inherited disorders. Mutations in mitochon drial DNA (mtDNA) and …
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
Selective neuronal vulnerability (SNV) of specific neuroanatomical regions such as frontal
cortex (FC) and hippocampus (HC) is characteristic of age-associated neurodegenerative …
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 …
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 …
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 …
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 …
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 …
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 …
proteome composition to further understand mechanisms regulating muscle function under …