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From Bioblast
- |title=Mahalingam S, Cheviron ZA, Storz JF, McClelland GB, Scott GR (2020) Chronic cold exposur ...bre density and capillarity in the gastrocnemius, and used a comprehensive substrate titration protocol to examine the function of muscle mitochondria by high-r3 KB (376 words) - 06:50, 28 July 2023
- ...rates: 1. Electron transfer pathways and respiratory control. 2. Coupling control. ...Strategically designed SUIT protocols reveal a diversity of mt-respiratory control patterns and pathway additivity depending on species, organs, cell types, a10 KB (1,441 words) - 23:46, 25 January 2021
- ...e absence of cytochrome c. After prolonged ischemia, the adenylate control ratio was significantly reduced, and cytochrome c depletion was detected by the s |pathways=N, S, CIV, ROX2 KB (327 words) - 14:05, 27 December 2021
- ...ficiency were not affected by SuHx or genotype. A higher substrate control ratio for succinate was observed in SuHx fibers and attenuated in ST2<sup>-/-</su |pathways=N, S, NS, ROX3 KB (386 words) - 16:09, 6 December 2021
- ...design of the electron transfer system (ETS) and mitochondrial respiratory control. ...pathway (ET) capacity of mt-preparations depends on (i) substrate type and substrate transport across mt-membranes, (ii) TCA cycle and other mt-matrix dehydroge7 KB (953 words) - 18:33, 10 January 2022
- |title=JΓΈrgensen W, Jelnes P, Rud KA, Hansen LL, Grunnet N, Quistorff B (2012) Progression of type 2 diabetes in GK rats affects muscl |authors=Joergensen W, Jelnes P, Rud KA, Hansen LL, Grunnet N, Quistorff B2 KB (363 words) - 13:00, 9 February 2018
- ...join as coauthors, to provide a balanced view on mitochondrial respiratory control, a fundamental introductory presentation of the concept of the protonmotive ...print website. If you prefer to submit comments in the format of a referee's evaluation rather than a contribution as a coauthor, I will be glad to dist12 KB (1,564 words) - 23:40, 25 January 2021
- |title=NAMPT remodels substrate metabolism in skeletal muscle. ...NAMPT in mice (''Nampt''Tg) would improve muscle respiratory capacity and control and would be additive with endurance exercise training in these mice.5 KB (725 words) - 10:18, 8 November 2016
- ...of ''P''/''E'' by oleoyl-CoA is fully reversed by addition of L-carnitine (control versus recovery with L-carnitine, ''p''=0.338), which facilitates oleoyl-Co |pathways=F, N, S, NS3 KB (354 words) - 23:46, 17 April 2024
- ...de Barros JP, Chevalier S, Dumas JF, Maillot F, Hatch GM, Loyer P, Servais S (2016) Reduced cardiolipin content decreases respiratory chain capacities a ...de Barros JP, Chevalier S, Dumas JF, Maillot F, Hatch GM, Loyer P, Servais S3 KB (392 words) - 23:54, 18 March 2018
- ...on in OXPHOS efficiency. However, with anoxic transition, STZ-diabetic and control heart tissues showed similar ATP hydrolysis capacities through reversal of |pathways=N, S4 KB (547 words) - 17:26, 7 November 2016
- ...g heart may be the result of dysregulation of metabolic pathways, impaired substrate supply or reduced mitochondrial number but not the result of reduced mitoch ...4, pyruvate dehydrogenase subunit B, pyruvateβmalate, respiratory control ratio, reverse transcriptase-polymerized chain reaction, state 3 respiration to t4 KB (532 words) - 17:25, 9 November 2017
- |authors=Bhattacharjee S, Das N, Mandala A, Mukhopadhyay S, Roy SS ...ich is a known factor for insulin resistance. PPARa agonist reinstated the ratio of carnitine palmitoyltransferase (CPT) isoforms in PA-treated muscle cells5 KB (753 words) - 10:40, 20 February 2015
- ...hway (S). Superimposed oxygraph traces (mass-specific oxygen flux [pmol O2βs<sup>-1</sup>βmg<sup>-1</sup> ''m''<sub>w</sub>]) from parallel measuremen ...(succinate&rotenone) restricts ET-capacity and artificially enhances flux control upstream of the Q-cycle, providing diagnostic information on specific branc8 KB (1,056 words) - 10:11, 23 May 2022
- ...rformance (2) provide essential reference points for analysis of metabolic control mechanisms and diagnosis of mitochondrial function in health and disease. ...rformance (2) provide essential reference points for analysis of metabolic control mechanisms and diagnosis of mitochondrial function in health and disease.8 KB (1,121 words) - 19:16, 10 January 2022
- |title=Gnaiger E, SΓΈndergaard H, Munch-Andersen T, Damsgaard R, Hagen C, DΓez-SΓ‘nchez C, Ara I, Wright-Paradis C, Schrauwen P, Hesselink M, Calbet J, Chri ...e in fatty acid oxidation approaching the level of the Inuit, yet coupling control of oxidative phosphorylation was conserved. Our findings reveal that couple10 KB (1,454 words) - 18:29, 10 January 2022
- |title=Menze MA, Marunde MA, Samarajeewa DA, Anderson J, Li S, Hand SC (2013) Group1 LEA protein ameliorates inhibition of mitochondrial |authors=Menze MA, Marunde MA, Samarajeewa DA, Anderson J, Li S, Hand SC5 KB (640 words) - 14:28, 28 March 2018
- |title=Lemieux H, Semsroth S, Antretter H, Hoefer D, Gnaiger E (2011) Increased OXPHOS capacity after co |authors=Lemieux H, Semsroth S, Antretter H, Hoefer D, Gnaiger E6 KB (874 words) - 18:21, 10 January 2022
- |title=[[File:Juhasz L.jpg|left|90px]] Blockade of N-methyl-D-aspartate receptors improves polymicrobial sepsis-evoked mitochond ...with mitochondrial dysfunction and depleted energy supplies [1]. Recently, N-methyl-D-aspartate receptor (NMDA-R)-mediated increase in intracellular cal4 KB (555 words) - 13:33, 28 March 2018
- ...We found a significant (''p''<0,05) relationship between BMI and CI/CI&II ratio, whereas age and training time per week were without significant effects on ...ough these respiratory complexes. However, a significant change of the R/E ratio indicates changes in platelet metabolism. Blood cells emerge as indicators5 KB (755 words) - 15:50, 7 June 2022