[1] Citrate synthase

Tissue sulfhydryl groups

Ellman, G. L. (1959) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(59)90090-6 · Cited by 26,824 · see citing works

A SPECIFIC MICROMETHOD FOR THE DETERMINATION OF ACYL PHOSPHATES

Lipmann, F. A., & Lc, T. (1945) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)51298-4 · Cited by 1,422 · see citing works

The Citrate Condensing Enzyme of Pigeon Breast Muscle and Moth Flight Muscle.

Srere, P. A., Brazil, H., Gonen, L., & Takahashi, M. T. (1963) · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · doi:10.3891/acta.chem.scand.17s-0129 · Cited by 536 · see citing works

MICROESTIMATION OF CITRIC ACID; A NEW COLORIMETRIC REACTION FOR PENTABROMOACETONE

Natelson, S., Pincus, J. B., & Lugovoy, J. K. (1948) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)57193-3 · Cited by 259 · see citing works

Inhibition of citrate-synthase by palmityl-coenzyme A

WIELAND, O. H., & Weiß, L. (1963) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(63)90156-6 · Cited by 222 · see citing works

The membrane systems of the mitochondrion

Bachmann, E., Allmann, D. W., & Green, D. E. (1966) · Archives of Biochemistry and Biophysics · doi:10.1016/s0003-9861(66)81051-2 · Cited by 184 · see citing works

The Purification of Citrate-condensing Enzyme

Srere, P. A., & Kosicki, G. W. (1961) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)61697-2 · Cited by 155 · see citing works

Palmityl-coenzyme a inhibition of the citrate-condensing enzyme

Srere, P. A. (1965) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(65)90061-5 · Cited by 137 · see citing works

Kinetics of regulatory enzymes: Effect of adenosine triphosphate on yeast citrate synthase

Hathaway, J. A., & Atkinson, D. (1965) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(65)90452-3 · Cited by 124 · see citing works

Citrate-condensing Enzyme-Oxalacetate Binary Complex

Srere, P. A. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96679-2 · Cited by 121 · see citing works

Regulation of citrate synthase activity in Escherichia coli

Weitzman, P. D. J. (1966) · Biochimica et Biophysica Acta (BBA) - Enzymology and Biological Oxidation · doi:10.1016/0926-6593(66)90166-4 · Cited by 92 · see citing works

FLUOROACETYL COENZYME A

Brady, R. O. (1955) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)57172-1 · Cited by 86 · see citing works

ATP controlled acetoacetate and citrate synthesis by rat liver mitochondria oxidising palmitoyl-carnitine, and the inhibition of citrate synthase by ATP

Shepherd, D., & Garland, P. B. (1966) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(66)90607-3 · Cited by 81 · see citing works

Effect of Divalent Metal Ions on Nucleotide Inhibition of Pig Heart Citrate Synthase

Kosicki, G. W., & Lee, L. P. K. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99868-6 · Cited by 75 · see citing works

Synthesis of Glutamate and Citrate by Clostridium kluyveri. A New Type of Citrate Synthase*

Gottschalk, G., & Barker, H. A. (1966) · Biochemistry · doi:10.1021/bi00868a003 · Cited by 74 · see citing works

A Source of Error in the Assay of Acetyl-Coenzyme A

PEARSON, D. J. (1965) · Biochemical Journal · doi:10.1042/bj0950023c · Cited by 74 · see citing works

Inhibition of citrate formation by long-chain acyl thioesters of coenzyme A as a possible control mechanism in fatty acid bioxynthesis

Tubbs, P. K. (1963) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(63)90804-7 · Cited by 73 · see citing works

A Coenzyme A analogue, Desulpho-CoA; Preparation and effects on various enzymes

Chase, J. F. A., Middleton, B. S., & Tubbs, P. K. (1966) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(66)90529-8 · Cited by 53 · see citing works

Citryl-CoA and the citrate condensing enzyme

Srere, P. A. (1963) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(63)90565-1 · Cited by 35 · see citing works

A magnetic resonance study of the citrate synthase reaction

Srere, P. A. (1967) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(67)90109-x · Cited by 32 · see citing works

Enzymatic Synthesis of Monofluorocitrate from β-Fluoro-oxaloacetate

Fanshier, D. W., Gottwald, L. K., & Kun, É. (1962) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)84493-9 · Cited by 30 · see citing works

The sulfhydryl groups of citrate-condensing enzyme

Srere, P. A. (1965) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(65)90887-9 · Cited by 22 · see citing works

Glutamate Biosynthesis in Anaerobic Bacteria. II. Stereospecificity of Aconitase and Citrate Synthetase of Clostridium kluyveri*

Stern, J. R., Hegre, C. S., & Bambers, G. (1966) · Biochemistry · doi:10.1021/bi00868a002 · Cited by 20 · see citing works

Relief of palmityl CoA inhibition of citrate synthase by long-chain acylcarnitine derivatives

Fritz, I. B. (1966) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(66)90211-7 · Cited by 19 · see citing works

Ischaemic accumulation of succinate controls reperfusion injury through mitochondrial ROS

Chouchani, E. T., Pell, V. R., Gaude, E., Aksentijević, D., Sundier, S. Y., Robb, E. L., Logan, A., Nadtochiy, S. M., Ord, E. N. J., Smith, A. C., et al. (2014) · Nature · doi:10.1038/nature13909 · Cited by 2,907 · see citing works

SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation

Hirschey, M. D., Shimazu, T., Goetzman, E., Jing, E., Schwer, B., Lombard, D. B., Grueter, C. A., Harris, C., Biddinger, S., Ilkayeva, O. R., et al. (2010) · Nature · doi:10.1038/nature08778 · Cited by 1,687 · see citing works

Brown adipose tissue regulates glucose homeostasis and insulin sensitivity

Stanford, K. I., Middelbeek, R. J. W., Townsend, K. L., An, D., Nygaard, E. B., Hitchcox, K. M., Markan, K. R., Nakano, K., Hirshman, M. F., Tseng, Y.-H., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci62308 · Cited by 1,180 · see citing works

Activation of AMP-activated protein kinase increases mitochondrial enzymes in skeletal muscle

Winder, W. W., Holmes, B. F., Rubink, D. S., Jensen, E. B., Chen, M., & Holloszy, J. O. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.6.2219 · Cited by 709 · see citing works

Lipid oxidation is reduced in obese human skeletal muscle

Kim, J.-Y., Hickner, R. C., Cortright, R. L., Dohm, G. L., & Houmard, J. A. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.279.5.e1039 · Cited by 634 · see citing works

Cardioprotection by S-nitrosation of a cysteine switch on mitochondrial complex I

Chouchani, E. T., Methner, C., Nadtochiy, S. M., Logan, A., Pell, V. R., Ding, S., James, A. M., Cochemé, H. M., Reinhold, J., Lilley, K. S., et al. (2013) · Nature Medicine · doi:10.1038/nm.3212 · Cited by 619 · see citing works

The Charcot-Marie-Tooth type 2A gene product, Mfn2, up-regulates fuel oxidation through expression of OXPHOS system

Pich, S., Bach, D., Briones, P., Liesa, M., Camps, M., Testar, X., Palacín, M., & Zorzano, A. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi149 · Cited by 455 · see citing works

Apoptosis in skeletal muscle with aging

Dirks, A., & Leeuwenburgh, C. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00458.2001 · Cited by 377 · see citing works

Muscle-specific deletion of carnitine acetyltransferase compromises glucose tolerance and metabolic flexibility

Muoio, D. M., Noland, R. C., Kovalik, J.-P., Seiler, S. E., Davies, M. N., DeBalsi, K. L., Ilkayeva, O. R., Stevens, R. D., Kheterpal, I., Zhang, J., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.005 · Cited by 372 · see citing works

Endurance training in obese humans improves glucose tolerance and mitochondrial fatty acid oxidation and alters muscle lipid content

Bruce, C. R., Thrush, A. B., Mertz, V. A., Bezaire, V., Chabowski, A., Heigenhauser, G. J. F., & Dyck, D. J. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00587.2005 · Cited by 328 · see citing works

Daily exercise increases hepatic fatty acid oxidation and prevents steatosis in Otsuka Long-Evans Tokushima Fatty rats

Rector, R. S., Thyfault, J. P., Morris, R. T., Laye, M. J., Borengasser, S. J., Booth, F. W., & Ibdah, J. A. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00428.2007 · Cited by 321 · see citing works

Iron-dependent changes in cellular energy metabolism: influence on citric acid cycle and oxidative phosphorylation

Oexle, H., Gnaiger, E., & Weiss, G. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00088-2 · Cited by 307 · see citing works

Metformin reduces liver glucose production by inhibition of fructose-1-6-bisphosphatase

Hunter, R. W., Hughey, C. C., Lantier, L., Sundelin, E. I., Peggie, M., Zeqiraj, E., Sicheri, F., Jessen, N., Wasserman, D. H., & Sakamoto, K. (2018) · Nature Medicine · doi:10.1038/s41591-018-0159-7 · Cited by 313 · see citing works

High-intensity aerobic interval training increases fat and carbohydrate metabolic capacities in human skeletal muscle

Perry, C. G. R., Heigenhauser, G. J. F., Bonen, A., & Spriet, L. L. (2008) · Applied Physiology Nutrition and Metabolism · doi:10.1139/h08-097 · Cited by 309 · see citing works

Resistance exercise training alters mitochondrial function in human skeletal muscle

PORTER, C., REIDY, P. T., BHATTARAI, N., SIDOSSIS, L. S., & RASMUSSEN, B. B. (2015) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000605 · Cited by 288 · see citing works

Increased Malonyl-CoA Levels in Muscle From Obese and Type 2 Diabetic Subjects Lead to Decreased Fatty Acid Oxidation and Increased Lipogenesis; Thiazolidinedione Treatment Reverses These Defects

Bandyopadhyay, G. K., Yu, J. G., Ofrecio, J., & Olefsky, J. M. (2006) · Diabetes · doi:10.2337/db06-0062 · Cited by 291 · see citing works

Clinical and molecular findings in children with complex I deficiency

Bugiani, M., Invernizzi, F., Alberio, S., Briem, E., Lamantea, E., Carrara, F., Moroni, I., Farina, L., Spada, M., Donati, M. A., et al. (2004) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2004.09.006 · Cited by 264 · see citing works

Nuclear factor erythroid‐derived 2‐like 2 (NFE2L2, Nrf2) mediates exercise‐induced mitochondrial biogenesis and the anti‐oxidant response in mice

Merry, T. L., & Ristow, M. (2016) · The Journal of Physiology · doi:10.1113/jp271957 · Cited by 246 · see citing works

Mitochondria express enhanced quality as well as quantity in association with aerobic fitness across recreationally active individuals up to elite athletes

Jacobs, R. A., & Lundby, C. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01081.2012 · Cited by 222 · see citing works

Peroxisome Proliferator-activated Receptor γ Coactivator 1α or 1β Overexpression Inhibits Muscle Protein Degradation, Induction of Ubiquitin Ligases, and Disuse Atrophy

Brault, J. J., Jespersen, J. G., & Goldberg, A. L. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.113092 · Cited by 217 · see citing works

Cardiomyocyte-Specific BMAL1 Plays Critical Roles in Metabolism, Signaling, and Maintenance of Contractile Function of the Heart

Young, M. E., Brewer, R. A., Peliciari-Garcia, R. A., Collins, H. E., He, L., Birky, T. L., Peden, B. W., Thompson, E. G., Ammons, B.-J., Bray, M. S., et al. (2014) · Journal of Biological Rhythms · doi:10.1177/0748730414543141 · Cited by 220 · see citing works

(–)-Epicatechin enhances fatigue resistance and oxidative capacity in mouse muscle

Nogueira, L., Ramirez‐Sanchez, I., Perkins, G. A., Murphy, A., Taub, P. R., Ceballos, G., Villarreal, F. J., Hogan, M. C., & Malek, M. H. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.209924 · Cited by 205 · see citing works

Increased Reactive Oxygen Species Production and Lower Abundance of Complex I Subunits and Carnitine Palmitoyltransferase 1B Protein Despite Normal Mitochondrial Respiration in Insulin-Resistant Human Skeletal Muscle

Lefort, N., Glancy, B., Bowen, B., Willis, W. T., Bailowitz, Z., De Filippis, E. A., Brophy, C., Meyer, C., Højlund, K., Yi, Z., et al. (2010) · Diabetes · doi:10.2337/db10-0174 · Cited by 174 · see citing works

Vitamin C and E supplementation prevents some of the cellular adaptations to endurance-training in humans

Morrison, D., Hughes, J., Della Gatta, P. A., Mason, S., Lamon, S., Russell, A. P., & Wadley, G. D. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.10.412 · Cited by 171 · see citing works

Exercise training increases sarcolemmal and mitochondrial fatty acid transport proteins in human skeletal muscle

Talanian, J. L., Holloway, G. P., Snook, L. A., Heigenhauser, G. J. F., Bonen, A., & Spriet, L. L. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00073.2010 · Cited by 167 · see citing works

Mitochondrial ATP-synthase in the entorhinal cortex is a target of oxidative stress at stages I/II of Alzheimer’s disease pathology

Terni, B., Boada, J., Portero‐Otin, M., Pamplona, R., & Ferrer, I. (2010) · Brain Pathology · doi:10.1111/j.1750-3639.2009.00266.x · Cited by 159 · see citing works

Metabolic adaptations to a high-fat diet in endurance cyclists

Goedecke, J. H., Christie, C., Wilson, G., Dennis, S. C., Noakes, T. D., Hopkins, W. G., & Lambert, E. V. (1999) · Metabolism · doi:10.1016/s0026-0495(99)90238-x · Cited by 153 · see citing works

Skeletal muscle and heart LKB1 deficiency causes decreased voluntary running and reduced muscle mitochondrial marker enzyme expression in mice.

Thomson, D. M., Porter, B. B., Tall, J. H., Kim, H.-J., Barrow, J. R., & Winder, W. W. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00366.2006 · Cited by 146 · see citing works

Upregulation of Cystathionine-β-Synthase in Colonic Epithelia Reprograms Metabolism and Promotes Carcinogenesis

Phillips, C. M., Zatarain, J. R., Nicholls, M. E., Porter, C., Widen, S. G., Thanki, K., Johnson, P., Jawad, M. U., Moyer, M. P., Randall, J. W., et al. (2017) · Cancer Research · doi:10.1158/0008-5472.can-16-3480 · Cited by 139 · see citing works

Mitochondrial respiratory capacity and coupling control decline with age in human skeletal muscle

Porter, C., Hurren, N. M., Cotter, M. V., Bhattarai, N., Reidy, P. T., Dillon, E. L., Durham, W. J., Tuvdendorj, D., Sheffield-Moore, M., Volpi, E., et al. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00125.2015 · Cited by 134 · see citing works

Effects of aerobic and resistive exercise training on glucose disposal and skeletal muscle metabolism in older men

Ferrara, C. M., Goldberg, A. P., Ortmeyer, H. K., & Ryan, A. S. (2006) · The Journals of Gerontology: Series A · doi:10.1093/gerona/61.5.480 · Cited by 136 · see citing works

Does calorie restriction induce mitochondrial biogenesis? A reevaluation

Hancock, C. R., Han, D., Higashida, K., Kim, S. H., & Holloszy, J. O. (2011) · The FASEB Journal · doi:10.1096/fj.10-170415 · Cited by 131 · see citing works

TNF‐α‐mediated reduction in PGC‐1α may impair skeletal muscle function after cigarette smoke exposure

Tang, K., Wagner, P. D., & Breen, E. C. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.21955 · Cited by 125 · see citing works

Cytochrome c turnover in rat skeletal muscles.

Booth, F. W., & Holloszy, J. O. (1977) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)32731-x · Cited by 116 · see citing works

Nebivolol Improves Diastolic Dysfunction and Myocardial Remodeling Through Reductions in Oxidative Stress in the Zucker Obese Rat

Zhou, X., Ma, L., Habibi, J., Whaley-Connell, A., Hayden, M. R., Tilmon, R. D., Brown, A. N., Kim, J.-A., DeMarco, V. G., & Sowers, J. R. (2010) · Hypertension · doi:10.1161/hypertensionaha.109.145136 · Cited by 116 · see citing works

Cessation of daily exercise dramatically alters precursors of hepatic steatosis in Otsuka Long‐Evans Tokushima Fatty (OLETF) rats

Rector, R. S., Thyfault, J. P., Laye, M. J., Morris, R. T., Borengasser, S. J., Uptergrove, G. M., Chakravarthy, M. V., Booth, F. W., & Ibdah, J. A. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.156745 · Cited by 110 · see citing works

Overexpression of peroxisome proliferator-activated receptor γ co-activator-1α leads to muscle atrophy with depletion of ATP.

Miura, S., Tomitsuka, E., Kamei, Y., Yamazaki, T., Kai, Y., Tamura, M., Kita, K., Nishino, I., & Ezaki, O. (2006) · The American Journal of Pathology · doi:10.2353/ajpath.2006.060034 · Cited by 107 · see citing works

Essential Role for Uncoupling Protein-3 in Mitochondrial Adaptation to Fasting but Not in Fatty Acid Oxidation or Fatty Acid Anion Export

Seifert, E. L., Bézaire, V., Estey, C., & Harper, M.-E. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m803871200 · Cited by 104 · see citing works

Decreased intestinal polyp multiplicity is related to exercise mode and gender in <i>Apc</i>^<i>Min/+</i> mice

Mehl, K. A., Davis, J. M., Clements, J. M., Berger, F. G., Pena, M. M., & Carson, J. A. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00975.2004 · Cited by 99 · see citing works

Chronic psychosocial stress induces reversible mitochondrial damage and corticotropin-releasing factor receptor type-1 upregulation in the rat intestine and IBS-like gut dysfunction

Vicario, M., Alonso, C., Guilarte, M., Serra, J., Martínez, C., González-Castro, A. M., Lobo, B., Antolín, M., Andreu, A. L., García-Arumí, E., et al. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.05.005 · Cited by 92 · see citing works

No decline in skeletal muscle oxidative capacity with aging in long-term calorically restricted rats: Effects are independent of mitochondrial DNA integrity

Baker, D. J., Betik, A. C., Krause, D. J., & Hepple, R. T. (2006) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/61.7.675 · Cited by 89 · see citing works

Regional differences in oxidative capacity of rat white adipose tissue are linked to the mitochondrial content of mature adipocytes.

Deveaud, C., Beauvoit, B., Salin, B., Schaeffer, J., & Rigoulet, M. (2004) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000049374.52989.9b · Cited by 88 · see citing works

Succinate in dystrophic white matter: a proton magnetic resonance spectroscopy finding characteristic for complex II deficiency

Brockmann, K., Bjornstad, A., Dechent, P., Korenke, C. G., Smeitink, J., Trijbels, J. M. F., Athanassopoulos, S., Villagran, R., Skjeldal, O. H., Wilichowski, E., et al. (2002) · Annals of Neurology · doi:10.1002/ana.10232 · Cited by 81 · see citing works

Long-term caloric restriction abrogates the age-related decline in skeletal muscle aerobic function

Hepple, R. T., Baker, D. J., Kaczor, J. J., & Krause, D. J. (2005) · The FASEB Journal · doi:10.1096/fj.04-3535fje · Cited by 80 · see citing works

AMPK activation increases uncoupling protein-3 expression and mitochondrial enzyme activities in rat muscle without fibre type transitions

Putman, C. T., Kiricsi, M., Pearcey, J., MacLean, I. M., Bamford, J. A., Murdoch, G. K., Dixon, W. T., & Pette, D. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.040691 · Cited by 110 · see citing works

Cessation of daily wheel running differentially alters fat oxidation capacity in liver, muscle, and adipose tissue

Laye, M. J., Rector, R. S., Borengasser, S. J., Naples, S. P., Uptergrove, G. M., Ibdah, J. A., Booth, F. W., & Thyfault, J. P. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.91186.2008 · Cited by 77 · see citing works

Long-term administration of L-carnitine to humans: effect on skeletal muscle carnitine content and physical performance

Wächter, S., Vogt, M., Kreis, R., Boesch, C., Bigler, P., Hoppeler, H., & Krähenbühl, S. (2002) · Clinica Chimica Acta · doi:10.1016/s0009-8981(01)00804-x · Cited by 77 · see citing works

Estrogen‐related receptor‐α (ERRα) deficiency in skeletal muscle impairs regeneration in response to injury

LaBarge, S., McDonald, M., Smith‐Powell, L., Auwerx, J., & Huss, J. M. (2014) · The FASEB Journal · doi:10.1096/fj.13-229211 · Cited by 74 · see citing works

Overexpression of carnitine palmitoyltransferase I in skeletal muscle in vivo increases fatty acid oxidation and reduces triacylglycerol esterification

Bruce, C. R., Brolin, C., Turner, N., Cleasby, M. E., van der Leij, F. R., Cooney, G. J., & Kraegen, E. W. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00561.2006 · Cited by 72 · see citing works

Mitochondrial adaptations in skeletal muscle to hindlimb unloading

Wagatsuma, A., Kotake, N., Kawachi, T., Shiozuka, M., Yamada, S., & Matsuda, R. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0677-1 · Cited by 70 · see citing works

Regulation of skeletal muscle oxidative capacity and muscle mass by SIRT3

Lin, L., Chen, K., Khalek, W. A., Ward, J. L., Yang, H., Chabi, B., Wrutniak-Cabello, C., & Tong, Q. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085636 · Cited by 67 · see citing works

Amino acid starvation has opposite effects on mitochondrial and cytosolic protein synthesis

Johnson, M. A., Vidoni, S., Durigon, R., Pearce, S. F., Rorbach, J., He, J., Brea-Calvo, G., Minczuk, M., Reyes, A., Holt, I. J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093597 · Cited by 63 · see citing works

Exercise training and calorie restriction increase SREBP-1 expression and intramuscular triglyceride in skeletal muscle

Nadeau, K. J., Ehlers, L. B., Aguirre, L. E., Moore, R. L., Jew, K. N., Ortmeyer, H. K., Hansen, B. C., Reusch, J. E. B., & Draznin, B. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00543.2005 · Cited by 57 · see citing works

Adenine nucleotide synthesis in exercising and endurance-trained skeletal muscle

Tullson, P. C., & Terjung, R. L. (1991) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1991.261.2.c342 · Cited by 55 · see citing works

Equilibrium constants of the reactions of choline acetyltransferase, carnitine acetyltransferase, and acetylcholinesterase under physiological conditions.

Pieklik, J. R., & Guynn, R. W. (1975) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)41323-9 · Cited by 49 · see citing works

Changes in skeletal muscle mitochondria in response to the development of type 2 diabetes or prevention by daily wheel running in hyperphagic OLETF rats

Rector, R. S., Uptergrove, G. M., Borengasser, S. J., Mikus, C. R., Morris, E. M., Naples, S. P., Laye, M. J., Laughlin, M. H., Booth, F. W., Ibdah, J. A., et al. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00703.2009 · Cited by 48 · see citing works

Mitochondrial and performance adaptations to exercise training in mice lacking skeletal muscle LKB1

Tanner, C. B., Madsen, S. R., Hallowell, D. M., Goring, D. M. J., Moore, T. M., Hardman, S. E., Heninger, M. R., Atwood, D. R., & Thomson, D. M. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00227.2013 · Cited by 47 · see citing works

Dietary restriction increases skeletal muscle mitochondrial respiration but not mitochondrial content in C57BL/6 mice

Hempenstall, S., Page, M. M., Wallen, K. R., & Selman, C. (2012) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.12.002 · Cited by 47 · see citing works

Tissue Oxidative Capacity, Fuel Stores and Skeletal Muscle Fatty Acid Composition In Obesity‐Prone and Obesity‐Resistant Rats

Pagliassotti, M. J., Pan, D. A., Prach, P. A., Koppenhafer, T. A., Storlien, L., & Hill, J. O. (1995) · Obesity Research · doi:10.1002/j.1550-8528.1995.tb00175.x · Cited by 47 · see citing works

Skeletal muscle dysfunction in muscle-specific LKB1 knockout mice.

Thomson, D. M., Hancock, C. R., Evanson, B. G., Kenney, S. G., Malan, B. B., Mongillo, A. D., Brown, J. D., Hepworth, S., Fillmore, N., Parcell, A. C., et al. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01293.2009 · Cited by 45 · see citing works

A chronic increase in physical activity inhibits fed-state mTOR/S6K1 signaling and reduces IRS-1 serine phosphorylation in rat skeletal muscle

Glynn, E. L., Lujan, H. L., Kramer, V. J., Drummond, M. J., DiCarlo, S. E., & Rasmussen, B. B. (2008) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h07-149 · Cited by 45 · see citing works

Dysregulated FXR-FGF19 signaling and choline metabolism are associated with gut dysbiosis and hyperplasia in a novel pig model of pediatric NASH

Hernandez, G. V., Smith, V. A., Melnyk, M., Burd, M. A., Sprayberry, K. A., Edwards, M. S., Peterson, D. G., Bennet, D. C., Fanter, R. K., Columbus, D. A., et al. (2020) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00344.2019 · Cited by 44 · see citing works

In vitro effects of antipsychotics on mitochondrial respiration

Cikánková, T., Fišar, Z., Bakhouche, Y., Ľupták, M., & Hroudová, J. (2019) · Naunyn-Schmiedeberg's Archives of Pharmacology · doi:10.1007/s00210-019-01665-8 · Cited by 44 · see citing works

Dietary Regulation of Fat Oxidative Gene Expression in Different Skeletal Muscle Fiber Types

McAinch, A. J., Lee, J., Bruce, C. R., Tunstall, R. J., Hawley, J. A., & Cameron‐Smith, D. (2003) · Obesity Research · doi:10.1038/oby.2003.197 · Cited by 42 · see citing works

Discovery of an iron-regulated citrate synthase in Staphylococcus aureus

Cheung, J., Murphy, M. E. P., & Heinrichs, D. E. (2012) · Chemistry &amp; Biology · doi:10.1016/j.chembiol.2012.10.003 · Cited by 39 · see citing works

RTG1- and RTG2-dependent retrograde signaling controls mitochondrial activity and stress resistance in Saccharomyces cerevisiae

Torelli, N. Q., Ferreira-Júnior, J. R., Kowaltowski, A. J., & da Cunha, F. M. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.12.025 · Cited by 37 · see citing works

Methylphenidate Decreases ATP Levels and Impairs Glutamate Uptake and Na+,K+-ATPase Activity in Juvenile Rat Hippocampus

Schmitz, F., Pierozan, P., Rodrigues, A. F., Biasibetti, H., Grings, M., Zanotto, B., Coelho, D. M., Vargas, C. R., Leipnitz, G., & Wyse, A. T. S. (2017) · Molecular Neurobiology · doi:10.1007/s12035-016-0289-1 · Cited by 35 · see citing works

The Single Nucleotide Polymorphism Gly482Ser in the PGC-1α Gene Impairs Exercise-Induced Slow-Twitch Muscle Fibre Transformation in Humans

Steinbacher, P., Feichtinger, R. G., Kedenko, L., Kedenko, I., Reinhardt, S., Schönauer, A.-L., Leitner, I., Sänger, A. M., Stoiber, W., Kofler, B., et al. (2015) · PLOS ONE · doi:10.1371/journal.pone.0123881 · Cited by 33 · see citing works

Functional adaptations in the skeletal muscle microvasculature to endurance and interval sprint training in the type 2 diabetic OLETF rat

Martin, J. S., Padilla, J., Jenkins, N. T., Crissey, J. M., Bender, S. B., Rector, R. S., Thyfault, J. P., & Laughlin, M. H. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00823.2012 · Cited by 30 · see citing works

Impairment of insulin signalling in peripheral tissue fails to extend murine lifespan

Merry, T. L., Kuhlow, D., Laube, B., Pöhlmann, D., Pfeiffer, A. F. H., Kahn, C. R., Ristow, M., & Zarse, K. (2017) · Aging Cell · doi:10.1111/acel.12610 · Cited by 30 · see citing works

Aldosterone deficiency in mice burdens respiration and accentuates diet-induced hyperinsulinemia and obesity

Liao, W.-H., Suendermann, C., Steuer, A. E., Pacheco Lopez, G., Odermatt, A., Faresse, N., Henneberg, M., & Langhans, W. (2018) · JCI Insight · doi:10.1172/jci.insight.99015 · Cited by 16 · see citing works

Whole-body and muscle responses to aerobic exercise training and withdrawal in ageing and COPD

Latimer, L. E., Constantin-Teodosiu, D., Popat, B., Constantin, D., Houchen-Wolloff, L., Bolton, C. E., Steiner, M. C., & Greenhaff, P. L. (2022) · European Respiratory Journal · doi:10.1183/13993003.01507-2021 · Cited by 14 · see citing works

Effect of Treadmill Training on Muscle Oxidative Capacity and Accretion in Young Male Obese and Nonobese Zucker Rats

Wardlaw, G. M., Kaplan, M. L., & Lanza-Jacoby, S. (1986) · The Journal of Nutrition · doi:10.1093/jn/116.9.1841 · Cited by 14 · see citing works

Effects of immobilization and aerobic training on proteins related to intramuscular substrate storage and metabolism in young and older men

Vigelsø, A., Gram, M., Wiuff, C., Hansen, C. N., Prats, C., Dela, F., & Helge, J. W. (2016) · European Journal of Applied Physiology · doi:10.1007/s00421-015-3302-x · Cited by 13 · see citing works

Acetyl‐CoA‐Dependent Cleavage of Citrate on Inactivated Citrate Lyase

Buckel, W., Ziegert, K., & Eggerer, H. (1973) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1973.tb02988.x · Cited by 60 · see citing works

The role of citrate in lipid synthesis in developing soybean cotyledons 1

Nelson, D. R., & Rinne, R. W. (1977) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a075512 · Cited by 14 · see citing works

Contributions of Cytosolic and Mitochondrial Acetyl-CoA Syntheses to the Activation of Lipogenic Acetate in Rat Liver

Goldberg, R. P., & Brunengraber, H. (1980) · Springer eBooks · doi:10.1007/978-1-4757-1419-7_41 · Cited by 30 · see citing works

Identification of Catalytic Residues in ATP-Citrate Lyase

Singh, N., Holoweckyj, K., & Fraser, M. E. (2014) · Acta Crystallographica Section A Foundations and Advances · doi:10.1107/s2053273314083260

Molecular basis for acetyl-CoA production by ATP-citrate lyase

Wei, X., Schultz, K. C., Bazilevsky, G. A., Vogt, A. D., & Marmorstein, R. (2019) · Nature Structural & Molecular Biology · doi:10.1038/s41594-019-0351-6 · Cited by 58 · see citing works