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Artykuły w czasopismach na temat "NADH-dehydrogenase activity"
Murray, G. I., M. D. Burke i S. W. Ewen. "Enzyme histochemical demonstration of NADH dehydrogenase on resin-embedded tissue." Journal of Histochemistry & Cytochemistry 36, nr 7 (lipiec 1988): 815–19. http://dx.doi.org/10.1177/36.7.3385192.
Pełny tekst źródłaSmall, W. Curtis, i Lee McAlister-Henn. "Identification of a Cytosolically Directed NADH Dehydrogenase in Mitochondria of Saccharomyces cerevisiae". Journal of Bacteriology 180, nr 16 (15.08.1998): 4051–55. http://dx.doi.org/10.1128/jb.180.16.4051-4055.1998.
Pełny tekst źródłaHayashi, Takeshi, Tsuyoshi Kato i Kensuke Furukawa. "Respiratory Chain Analysis of Zymomonas mobilis Mutants Producing High Levels of Ethanol". Applied and Environmental Microbiology 78, nr 16 (1.06.2012): 5622–29. http://dx.doi.org/10.1128/aem.00733-12.
Pełny tekst źródłaThiagalingam, Sam, i Tsanyen Yang. "Purification and characterization of NADH dehydrogenase from Bacillus megaterium". Canadian Journal of Microbiology 39, nr 9 (1.09.1993): 826–33. http://dx.doi.org/10.1139/m93-123.
Pełny tekst źródłaMarchenko, M. M., i O. N. Voloshchuk. "The state of the mitochondrial energy-supplying system of blood leukocytes in the dynamics of guerin's carcinoma growth under the low-level irradiation conditions". Biomeditsinskaya Khimiya 60, nr 6 (2014): 631–35. http://dx.doi.org/10.18097/pbmc20146006631.
Pełny tekst źródłaHuston, Scott, John Collins, Fangfang Sun, Ting Zhang, Timothy D. Vaden, Y. ‐H Percival Zhang i Jinglin Fu. "An activity transition from NADH dehydrogenase to NADH oxidase during protein denaturation". Biotechnology and Applied Biochemistry 65, nr 3 (2.10.2017): 286–93. http://dx.doi.org/10.1002/bab.1607.
Pełny tekst źródłaMiesel, Lynn, Torin R. Weisbrod, Jovita A. Marcinkeviciene, Robert Bittman i William R. Jacobs. "NADH Dehydrogenase Defects Confer Isoniazid Resistance and Conditional Lethality in Mycobacterium smegmatis". Journal of Bacteriology 180, nr 9 (1.05.1998): 2459–67. http://dx.doi.org/10.1128/jb.180.9.2459-2467.1998.
Pełny tekst źródłaChapuy-Regaud, Sabine, Frédérique Duthoit, Laurence Malfroy-Mastrorillo, Pierre Gourdon, Nic D. Lindley i Marie-Claude Trombe. "Competence Regulation by Oxygen Availability and by Nox Is Not Related to Specific Adjustment of Central Metabolism inStreptococcus pneumoniae". Journal of Bacteriology 183, nr 9 (1.05.2001): 2957–62. http://dx.doi.org/10.1128/jb.183.9.2957-2962.2001.
Pełny tekst źródłaPowell, Charles S., i Robert M. Jackson. "Mitochondrial complex I, aconitase, and succinate dehydrogenase during hypoxia-reoxygenation: modulation of enzyme activities by MnSOD". American Journal of Physiology-Lung Cellular and Molecular Physiology 285, nr 1 (lipiec 2003): L189—L198. http://dx.doi.org/10.1152/ajplung.00253.2002.
Pełny tekst źródłaSmyth, G. E., i B. A. Orsi. "Nitroreductase activity of NADH dehydrogenase of the respiratory redox chain". Biochemical Journal 257, nr 3 (1.02.1989): 859–63. http://dx.doi.org/10.1042/bj2570859.
Pełny tekst źródłaRozprawy doktorskie na temat "NADH-dehydrogenase activity"
Boyer, Christian. "Identification et caractérisation de composés circulants d’intérêt dans le sérum d’ours brun hibernant – Étude des effets biologiques du sérum d’ours hibernant sur cellules humaines". Electronic Thesis or Diss., Université Clermont Auvergne (2021-...), 2023. http://www.theses.fr/2023UCFA0012.
Pełny tekst źródłaMuscle atrophy, which is a major public health issue, is a condition that affects the elderly, but also people who are sedentary, immobilized or suffering from chronic inflammation. The use of animal models, in particular laboratory rodents, has made it possible to elucidate the molecular and physiopathological mechanisms at the origin of muscle atrophy. In the search for therapeutic solutions, the exploration of a model of natural resistance to muscle atrophy should open up new and innovative avenues of research. The laboratory is exploring how the hibernating brown bear is able to preserve its muscle tissue during several months of immobility, and how its serum is able to induce changes in the protein balance of human muscle cells. The main objective of my thesis work was to identify compounds or families of compounds circulating in the hibernating bear and responsible for biological effects on human cells. First, I looked for a biological activity that could be easily measured and that could be used to screen the circulating compounds. The measurement of NADH dehydrogenase activity by a colorimetric assay, allows to follow the inhibitory effects of serum and its fractions on human cells in culture, in a robust and reproducible way. Thanks to this tool, we were able to initiate the screening of several fractions from hibernating bear serum, thus starting an unbiased approach in the search for active compounds in hibernating bear serum. This work opens the way to the testing of new fractions, allowing to advance towards the identification of new molecules having a positive effect on the cellular energy balance. According to the same approach, the development of several measurement tools covering other domains of cellular metabolism should allow to complete this approach in the future. In parallel, in the search for active circulating compounds present in the serum of hibernating bears, I focused my research on compounds related to the endocannabinoid system. I was thus able to highlight a global decrease of the endocannabinoid tone, with a decrease of the ligands of the canonical pathway. Surprisingly, the concentration of circulating oleoylethanolamide (OEA) is multiplied by three in winter, suggesting an important role of this compound in the physiology of hibernation in brown bears. The continuation of this work should allow to better identify circulating compounds of interest for human medicine, and to advance towards innovative therapeutic solutions in the fight against certain pathologies, such as muscle atrophy
Peinnequin, André. "La nadh : ubiquinone oxydoréductase de la bactérie photosynthétique Rhodobacter capsulatus : étude et caractérisation de 5 gènes (nuo8, nuo10, nuo11, nuo12 et nuo13) homologues aux gènes mitochondriaux nd1, nd6, nd4L, nd5 et nd4". Université Joseph Fourier (Grenoble ; 1971-2015), 1994. http://www.theses.fr/1994GRE10177.
Pełny tekst źródłaCzęści książek na temat "NADH-dehydrogenase activity"
Sazanov, L. A., P. Burrows i P. J. Nixon. "Presence of a large protein complex containing the ndhK gene product and possessing NADH-specific dehydrogenase activity in thylakoid membranes of higher plant chloroplasts". W Photosynthesis: from Light to Biosphere, 1683–86. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_395.
Pełny tekst źródłaRandall, D. D., J. A. Miernyk, N. R. David, J. Gemel i M. H. Luethy. "Regulation of leaf mitochondrial pyruvate dehydrogenase complex activity by reversible phosphorylation". W Protein Phosphorylation in Plants, 87–104. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780198577775.003.0007.
Pełny tekst źródłaZanella, Alberto, i Paola Bianchi. "Erythrocyte enzymopathies". W Oxford Textbook of Medicine, redaktorzy Chris Hatton i Deborah Hay, 5463–72. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198746690.003.0540.
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