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Topic Review
Mitochondrial Metabolism and Dynamics in Prostate Cancer
Prostate cancer (PCa) is the second leading cause of cancer deaths among men in Western countries. Mitochondria, the “powerhouse” of cells, undergo distinctive metabolic and structural dynamics in different types of cancer. PCa cells experience peculiar metabolic changes during their progression from normal epithelial cells to early-stage and, progressively, to late-stage cancer cells.
  • 300
  • 08 Mar 2023
Topic Review
Mitochondrial Homeostasis
Mitochondria are essential organelles and crucial for cellular survival. Mitochondrial biogenesis and mitophagy are dynamic features that are essential for both maintaining the health of the mitochondrial network and cellular demands. The accumulation of damaged mitochondria has been shown to be related to a wide range of pathologies ranging from neurological to musculoskeletal.
  • 623
  • 18 Oct 2022
Topic Review
Mitochondrial Dysfunction in Repeat Expansion Diseases
Repeat expansion diseases are a group of neuromuscular and neurodegenerative disorders characterized by expansions of several successive repeated DNA sequences. More than 50 repeat expansion diseases have been described. These disorders involve diverse pathogenic mechanisms, including loss-of-function mechanisms, toxicity associated with repeat RNA, or repeat-associated non-ATG (RAN) products, resulting in impairments of cellular processes and damaged organelles. Mitochondria, double membrane organelles, play a crucial role in cell energy production, metabolic processes, calcium regulation, redox balance, and apoptosis regulation.
  • 246
  • 29 Aug 2023
Topic Review
Mitochondrial Dysfunction in FECD
Fuchs endothelial corneal dystrophy (FECD) is a genetically complex, heterogenous, age-related degenerative disease of corneal endothelial cells (CEnCs), occurring in the fifth decade of life with a higher incidence in females. It is characterized by extracellular matrix (ECM) protein deposition called corneal guttae, causing light glare and visual complaints in patients. In FECD, CEnCs exhibit stress-induced senescence, oxidative stress, DNA damage, heightened reactive oxygen species (ROS) production, mitochondrial damage, and dysfunction as well as sustained endoplasmic reticulum (ER) stress. Among all of these, mitochondrial dysfunction involving altered mitochondrial bioenergetics and dynamics plays a critical role in FECD pathogenesis. 
  • 375
  • 27 Aug 2021
Topic Review
Mitochondrial Dynamics in Pulmonary Hypertension
Mitochondria are essential organelles for energy production, calcium homeostasis, redox signaling, and other cellular responses involved in pulmonary vascular biology and disease processes. Mitochondrial homeostasis depends on a balance in mitochondrial fusion and fission (dynamics). Mitochondrial dynamics are regulated by a viable circadian clock.
  • 265
  • 12 Jan 2024
Topic Review
Mitochondrial Disease
Mitochondrial disease is a group of disorders caused by mitochondrial dysfunction. Mitochondria are the organelles that generate energy for the cell and are found in every cell of the human body except red blood cells. They convert the energy of food molecules into the ATP that powers most cell functions. Mitochondrial diseases take on unique characteristics both because of the way the diseases are often inherited and because mitochondria are so critical to cell function. A subclass of these diseases that have neuromuscular symptoms are known as mitochondrial myopathies.
  • 1.0K
  • 25 Oct 2022
Topic Review
Mitochondrial Ca2+ Signaling and Bioenergetics in Alzheimer’s Disease
Alzheimer’s disease (AD) is a hereditary and sporadic neurodegenerative illness defined by the gradual and cumulative loss of neurons in specific brain areas. The processes that cause AD are still under investigation and there are no available therapies to halt it. Progress puts at the forefront the “calcium (Ca2+) hypothesis” as a key AD pathogenic pathway, impacting neuronal, astrocyte and microglial function. An increasing body of evidence points out the early and crucial role of cellular Ca2+ handling dysregulation in AD pathogenesis. Interestingly, Ca2+ is a key regulator of several mitochondrial functions, such as ATP production, and brain cells rely mostly on OXPHOS to match their energy demands.
  • 655
  • 09 Dec 2022
Topic Review
Mitochondria in Oocyte Maturation
Mitochondria are the only animal cell organelles, except for the nucleus, with their own genetic information, called mitochondrial DNA (mtDNA). The mtDNA is a double-stranded, circular, 16,569 bp DNA molecule in humans, which codes 13 essential subunits of the respiratory chain complexes, 22 tRNAs, and two rRNAs, constituting part of the mitochondrial translation machinery.
  • 643
  • 29 Sep 2021
Topic Review
Mitochondria in Maturation of Cardiomyocytes
Cardiomyocytes obtained from pluripotent stem cells (PSCs)differentiation culture are regarded as immature structurally, electrophysiologically, metabolically, and functionally. Mitochondria are organelles responsible for various cellular functions such as energy metabolism, different catabolic and anabolic processes, calcium fluxes, and various signaling pathways. Cells can respond to cellular needs to increase the mitochondrial mass by mitochondrial biogenesis. On the other hand, cells can also degrade mitochondria through mitophagy. Mitochondria are also dynamic organelles that undergo continuous fusion and fission events. 
  • 400
  • 26 Oct 2021
Topic Review
Mitochondria in Health and Disease
Mitochondrial alterations have been implicated in a wide range of diseases, such as neurodegenerative disorders, metabolic disorders, and cancer. 
  • 429
  • 29 May 2023
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