نتایج جستجو برای: mitochondrial damage

تعداد نتایج: 349971  

Journal: :genetics in the 3rd millennium 0
مسعود هوشمند massoud houshmand national institute for genetic engineering and biotechnology / special medical center, tehran, iran حسین صنعتی mohammad hossein sanati بهارک هوشیار کاشانی baharak hooshiar kashani مهدی شفا شریعت پناهی mehdi shafa shariat panahi محمد مهدی بانویی mohammad mehdi banoei آنا عیسائیان anna isaian مصطفی معین

ataxia-telangiectasia (at) is a rare human neurodegenerative autosomal recessive multisystem disease characterized by a wide range of features including progressive cerebellar ataxia during infancy, occulocutaneous telangiectasia, susceptibility to neoplasia, occulomotor disturbances, chromosomal instability and growth and developmental abnormalities. mitochondrial dna (mtdna) has the only non-...

Journal: :the iranian journal of pharmaceutical research 0
jalal pourahmad - farzad kahrizi department of toxicology and pharmacology, faculty of pharmacy, shahid beheshti university of medical sciences nima naderi department of toxicology and pharmacology, faculty of pharmacy, shahid beheshti university of medical sciences ahmad salimi department of toxicology and pharmacology, faculty of pharmacy, shahid beheshti university of medical sciences farshid noorbakhsh department of toxicology and pharmacology, faculty of pharmacy, shahid beheshti university of medical sciences mehrdad faizi department of toxicology and pharmacology, faculty of pharmacy, shahid beheshti university of medical sciences

multiple sclerosis (ms) is a neurodegenerative and autoimmune disease that it’s molecular etiology and factors involving in its progression remains unknown. in this study for evaluation effect of mercuric on progression of ms we investigated the additive effect of mercuric sulfide on the brain mitochondrial dysfunction in experimental autoimmune encephalomyelitis (eae) model of ms in c57bl/6 mi...

Multiple Sclerosis (MS) is a neurodegenerative and autoimmune disease that it’s molecular etiology and factors involving in its progression remains unknown. In this study for evaluation effect of mercuric on progression of MS we investigated the additive effect of mercuric sulfide on the brain mitochondrial dysfunction in experimental autoimmune encephalomyelitis (EAE) model of MS in C57BL/6 mi...

Journal: :Circulation 2002
Cynthia A Knight-Lozano Christal G Young David L Burow Zhao Yong Hu Dale Uyeminami Kent E Pinkerton Harry Ischiropoulos Scott W Ballinger

BACKGROUND A shared feature among cardiovascular disease risk factors is increased oxidative stress. Because mitochondria are susceptible to damage mediated by oxidative stress, we hypothesized that risk factors (secondhand smoke and hypercholesterolemia) are associated with increased mitochondrial damage in cardiovascular tissues. METHODS AND RESULTS Atherosclerotic lesion formation, mitocho...

Journal: :basic and clinical neuroscience 0
shahrzad eftekhar-vaghefi shahid bahonar university of kerman. kerman, iran saeed esmaeili mahani department of biology, faculty of sciences, shahid bahonar university of kerman, kerman, iran leila elyasi neuroscience research center, institute of neuropharmacology, kerman university of medical sciences. kerman, iran mehdi abbasnejad shahid bahonar university of kerman. kerman, iran

introduction: the neuroprotective role of opioid morphine against 6-hydroxydopamineinduced cell death has been demonstrated. however, the exact mechanism(s) underlying such neuroprotection, especially the role of subtype receptors, has not yet been fully clarified. methods: here, we investigated the effects of different opioid agonists on 6-ohda-induced neurotoxicity in human neuroblastoma sh-s...

Multiple Sclerosis (MS) is a neurodegenerative and autoimmune disease that it’s molecular etiology and factors involving in its progression remains unknown. In this study for evaluation effect of mercuric on progression of MS we investigated the additive effect of mercuric sulfide on the brain mitochondrial dysfunction in experimental autoimmune encephalomyelitis (EAE) model of MS in C57BL/6 mi...

Arshi, A., Dehghani-Samani, M., Fadaei, M., Hashemzehi, R., Jamshidian, H., Mahmoudi, E., Noshadi, E.,

Abstract Background and Objectives Mitochondrial biogenesis is a complex process involving the coordinated expression of mitochondrial and nuclear genes, the import of the products of the latter into the organelle and turnover of this process. Mitochondrial malfunction or defects in any of the many pathways involved in mitochondrial biogenesis can lead to degenerative diseases and possibly pla...

Journal: :journal of research in medical sciences 0
reza sharafati?chaleshtori hedayatollah shirzad mahmoud rafieian kopaei amin soltani

mitochondrial dysfunction is one of the main causative factors in a wide variety of complications such as neurodegenerative disorders, ischemia/reperfusion, aging process, and septic shock. decrease in respiratory complex activity, increase in free radical production, increase in mitochondrial synthase activity, increase in nitric oxide production, and impair in electron transport system and/or...

Journal: :the iranian journal of pharmaceutical research 0
jalal pourahmad department of pharmacology and toxicology, school of pharmacy, shahid beheshti university of medical sciences tehran, iran. mir jamal hosseini department of pharmacology and toxicology, school of pharmacy zanjan university of medical sciences zanjan, iran.

mitochondria are unique organelles with major role in cellular function, not only as a major site of atp production, but also by regulating energy expenditure, apoptosis signaling, and production of reactive oxygen species. they play a central role in determining the point-of-no-return for the apoptotic process. there is accumulating evidence supporting a direct link between mitochondria, oxida...

Journal: :genetics in the 3rd millennium 0
صدف کسرایی sadaf kasraie national institute of genetic engineering and biotechnology (nigeb), tehran, iran مسعود هوشمند masoud houshmand محمد مهدی بانویی mommad mehdi banoei سولماز اعتماد اهری soolmaz etemad ahari مهدی شفا شریعت پناهی mehdi shafa shariat panahi پوران شریعتی pouran shariati محمد علی بهار

huntington disease (hd) is a genetically dominant condition caused by expanded cag repeats which code for glutamine in the hd gene product, huntingtin. huntingtin is expressed in almost all tissues, so abnormalities outside the brain can also be expected. involvement of nuclei and mitochondria in hd pathophysiology has been suggested. in fact, mitochondrial dysfunction is reported in brains of ...

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