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Mitochondrial pathways of copper neurotoxicity: focus on mitochondrial dynamics and mitophagy
Aschner M., Skalny A.V., Lu R., Martins A.C., Tizabi Y., Nekhoroshev S.V., Santamaria A., Sinitskiy A.I., Tinkov A.A.
Copper (Cu) is essential for brain development and function, yet its overload induces neuronal
Reciprocal interactions of mitochondria and the neuroimmunoendocrine system in neurodegenerative disorders: An important role for melatonin regulation
Polyakova Victoria O.
of medical conditions. Many factors are involved in the regulation of mitochondrial function, including
Mitochondrial diseases caused by mtDNA mutations: A mini-review
Ryzhkova Anastasia I.
There are several types of mitochondrial cytopathies, which cause a set of disorders, arise as a
Monoacylglycerol Lipase Inhibition Prevents Short-Term Mitochondrial Dysfunction and Oxidative Damage in Rat Brain Synaptosomal/Mitochondrial Fractions and Cortical Slices: Role of Cannabinoid Receptors
Paredes-Ruiz K.J., Chavira-Ramos K., Galvan-Arzate S., Rangel-López E., Karasu Ç., Túnez I., Skalny A.V., Ke T., Aschner M., Orozco-Morales M., Colín-González A.L., Santamaría A.
decreased mitochondrial function and increased lipid peroxidation, JZL184 attenuated both markers
Mitochondrial fusion and fission proteins as novel therapeutic targets for treating cardiovascular disease
Ong S., Kalkhoran S., Cabrera-Fuentes H., Hausenloy D.
BY license. The past decade has witnessed a number of exciting developments in the field of mitochondrial
Diabetes mellitus, mitochondrial dysfunction and ca2+-dependent permeability transition pore
Belosludtsev K.N.
. This review is dedicated to the analysis of recent data regarding the role of mitochondrial dysfunction
The melatonergic pathway and its interactions in modulating respiratory system disorders
Mazzoccoli G.
molecules, oxidant status, lipid raft function, optimized mitochondrial function and reseting of the immune
Hypertrophic Cardiomyopathy Through the Lens of Mitochondria
Kirichenko Tatiana V., Zhivodernikov Ivan V., Kozlova Maria A., Markin Alexander M., Sinyov Vasily V., Markina Yuliya V.
in the sarcomere genes of cardiomyocytes and metabolic disorders of the cell, including mitochondrial dysfunction
ATpase-deficient mitochondrial inner membrane protein ATAD3a disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia
Cooper H., Yang Y., Ylikallio E., Khairullin R., Woldegebriel R., Lin K., Euro L., Palin E., Wolf A., Trokovic R., Isohanni P., Kaakkola S., Auranen M., Lonqvist T., Wanrooij S., Tyynismaa H.
in early childhood may resemble spastic cerebral palsy. The function of ATAD3A, a mitochondrial inner
Mitochondria Donation by Mesenchymal Stem Cells: Current Understanding and Mitochondria Transplantation Strategies
Gomzikova M.O., James V., Rizvanov A.A.
therapeutic approach for the treatment of mitochondrial diseases and mitochondrial function deficiency

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