Cargando…

Mitochondrial biology and dysfunction in secondary mitochondrial disease

Mitochondrial diseases are a broad, genetically heterogeneous class of metabolic disorders characterized by deficits in oxidative phosphorylation (OXPHOS). Primary mitochondrial disease (PMD) defines pathologies resulting from mutation of mitochondrial DNA (mtDNA) or nuclear genes affecting either m...

Descripción completa

Detalles Bibliográficos
Autores principales:	Baker, Megan J., Crameri, Jordan J., Thorburn, David R., Frazier, Ann E., Stojanovski, Diana
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Royal Society 2022
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727669/ https://www.ncbi.nlm.nih.gov/pubmed/36475414 http://dx.doi.org/10.1098/rsob.220274

Ejemplares similares

Modelling Mitochondrial Disease in Human Pluripotent Stem Cells: What Have We Learned?
por: McKnight, Cameron L., et al.
Publicado: (2021)

Stimulating Mitochondrial Biogenesis with Deoxyribonucleosides Increases Functional Capacity in ECHS1-Deficient Cells
por: Burgin, Harrison James, et al.
Publicado: (2022)

The TIM22 complex mediates the import of sideroflexins and is required for efficient mitochondrial one-carbon metabolism
por: Jackson, Thomas D., et al.
Publicado: (2021)

Loss of mitochondrial fatty acid β‐oxidation protein short‐chain Enoyl‐CoA hydratase disrupts oxidative phosphorylation protein complex stability and function
por: Burgin, Harrison, et al.
Publicado: (2022)

Mitochondrial Dysfunction in Parkinson’s Disease: Focus on Mitochondrial DNA
por: Buneeva, Olga, et al.
Publicado: (2020)

Targeting redox biology to reverse mitochondrial dysfunction
por: Marcinek, David J., et al.
Publicado: (2013)

Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module
por: Jackson, Thomas D., et al.
Publicado: (2022)

Uremic Myopathy and Mitochondrial Dysfunction in Kidney Disease
por: Serrano, Eurico, et al.
Publicado: (2022)

Mitochondrial dysfunction in Parkinson’s disease
por: Hu, Qingsong, et al.
Publicado: (2016)

Adrenal Dysfunction in Mitochondrial Diseases
por: Corkery-Hayward, Madeleine, et al.
Publicado: (2023)

Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies
por: Stepien, Karolina M., et al.
Publicado: (2022)

Mitochondrial Dysfunction in Parkinson's Disease
por: Keane, P. C., et al.
Publicado: (2011)

Mitochondrial Dysfunction in Parkinson's Disease
por: Moon, Hyo Eun, et al.
Publicado: (2015)

Mitochondrial dysfunction in fibrotic diseases
por: Li, Xinyu, et al.
Publicado: (2020)

Mitochondrial Dysfunction and Chronic Liver Disease
por: Zhang, Chunyan, et al.
Publicado: (2022)

Mitochondrial Dysfunction in Repeat Expansion Diseases
por: Giménez-Bejarano, Alberto, et al.
Publicado: (2023)

Mitochondrial dysfunction in neurological disorders: Exploring mitochondrial transplantation
por: Norat, Pedro, et al.
Publicado: (2020)

The genetic architecture of mitochondrial dysfunction in Parkinson’s disease
por: Larsen, S. B., et al.
Publicado: (2018)

Modeling mitochondrial dysfunctions in the brain: from mice to men
por: Breuer, Megan E., et al.
Publicado: (2011)

Mitochondrial dysfunction in cancer
por: Księżakowska-Łakoma, Kinga, et al.
Publicado: (2014)

Deconstructing Mitochondrial Dysfunction in Alzheimer Disease
por: García-Escudero, Vega, et al.
Publicado: (2013)

Evidence of Oxidative Stress and Secondary Mitochondrial Dysfunction in Metabolic and Non-Metabolic Disorders
por: Stepien, Karolina M., et al.
Publicado: (2017)

Mitochondrial Dysfunction in Alzheimer’s Disease: A Biomarker of the Future?
por: Bell, Simon M., et al.
Publicado: (2021)

Placental Mitochondrial Function and Dysfunction in Preeclampsia
por: Jahan, Fahmida, et al.
Publicado: (2023)

Mitochondrial dysfunction in neurodegenerative diseases and the potential countermeasure
por: Wang, Yan, et al.
Publicado: (2019)

Application of Genome Sequencing from Blood to Diagnose Mitochondrial Diseases
por: Rius, Rocio, et al.
Publicado: (2021)

Assessing mitochondrial dysfunction in cells
por: Brand, Martin D., et al.
Publicado: (2011)

Iron Dysregulation in Mitochondrial Dysfunction and Alzheimer’s Disease
por: Onukwufor, John O., et al.
Publicado: (2022)

Mitochondrial Dysfunction and Therapeutic Perspectives in Cardiovascular Diseases
por: Liu, Yu, et al.
Publicado: (2022)

Dysfunctional Mitochondrial Dynamics in the Pathophysiology of Neurodegenerative Diseases
por: Haun, Florian, et al.
Publicado: (2013)

Mitochondrial Dysfunction in Parkinson’s Disease—Cause or Consequence?
por: Chen, Chun, et al.
Publicado: (2019)

Mitochondrial Dysfunction and Stress Responses in Alzheimer’s Disease
por: Weidling, Ian, et al.
Publicado: (2019)

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases
por: Udhayabanu, Tamilarasan, et al.
Publicado: (2017)

Mitochondrial Dysfunction in Cardiac Diseases and Therapeutic Strategies
por: Huang, Yafei, et al.
Publicado: (2023)

Mitochondrial dysfunction at the crossroad of cardiovascular diseases and cancer
por: Rocca, Carmine, et al.
Publicado: (2023)

Mitochondrial Dysfunction and the Aging Immune System
por: McGuire, Peter J.
Publicado: (2019)

Mitochondrial Dysfunction and Diabetes: Is Mitochondrial Transfer a Friend or Foe?
por: Montgomery, Magdalene K
Publicado: (2019)

ATP Synthase and Mitochondrial Bioenergetics Dysfunction in Alzheimer’s Disease
por: Patro, Somya, et al.
Publicado: (2021)

Mitochondrial Dysfunction in Rheumatoid Arthritis
por: Ma, Chen, et al.
Publicado: (2022)

Mitochondrial Dysfunction and Multiple Sclerosis
por: de Barcelos, Isabella Peixoto, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_kdu96sb9sak7auncp41uj5ue0i