Lipid homeostasis in exercise

A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis

Boström, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., Rasbach, K. A., Boström, E. A., Choi, J. H., Long, J. Z., et al. (2012) · Nature · doi:10.1038/nature10777 · Cited by 4,810 · see citing works

Lipid Droplets and Cellular Lipid Metabolism

Walther, T. C., & Farese, R. V. (2012) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-061009-102430 · Cited by 1,668 · see citing works

Skeletal muscle lipid content and insulin resistance: evidence for a paradox in endurance-trained athletes

Goodpaster, B. H. (2001) · Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.86.12.5755 · Cited by 1,194 · see citing works

The effects of increasing exercise intensity on muscle fuel utilisation in humans

van Loon, L. J. C., Greenhaff, P. L., Constantin‐Teodosiu, D., Saris, W. H. M., & Wagenmakers, A. J. M. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00295.x · Cited by 897 · see citing works

Molecular mechanisms of insulin resistance in humans and their potential links with mitochondrial dysfunction

Morino, K., Petersen, K. F., & Shulman, G. I. (2006) · Diabetes · doi:10.2337/db06-s002 · Cited by 853 · see citing works

Perilipin, a major hormonally regulated adipocyte-specific phosphoprotein associated with the periphery of lipid storage droplets

Greenberg, A. S., Egan, J. J., Wek, S. A., Garty, N. B., Blanchette‐Mackie, E. J., & Londos, C. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99168-4 · Cited by 831 · see citing works

ATGL-mediated fat catabolism regulates cardiac mitochondrial function via PPAR-α and PGC-1

Haemmerle, G., Moustafa, T., Wölkart, G., Büttner, S., Schmidt, A. G., van de Weijer, T., Hesselink, M. K. C., Jaeger, D., Kienesberger, P. C., Zierler, K. A., et al. (2011) · Nature Medicine · doi:10.1038/nm.2439 · Cited by 767 · see citing works

Membrane Fatty Acid Transporters as Regulators of Lipid Metabolism: Implications for Metabolic Disease

Glatz, J. F. C., Luiken, J. J. F. P., & Bonen, A. (2010) · Physiological Reviews · doi:10.1152/physrev.00003.2009 · Cited by 757 · see citing works

Exercise and non-alcoholic fatty liver disease: A systematic review and meta-analysis

Keating, S. E., Hackett, D. A., George, J., & Johnson, N. A. (2012) · Journal of Hepatology · doi:10.1016/j.jhep.2012.02.023 · Cited by 536 · see citing works

Resistance exercise reduces liver fat and its mediators in non-alcoholic fatty liver disease independent of weight loss

Hallsworth, K., Fattakhova, G., Hollingsworth, K. G., Thoma, C., Moore, S., Taylor, R., Day, C. P., & Trenell, M. I. (2011) · Gut · doi:10.1136/gut.2011.242073 · Cited by 529 · see citing works

Altered myocardial fatty acid and glucose metabolism in idiopathic dilated cardiomyopathy

Dávila‐Román, V. G., Vedala, G., Herrero, P., Fuentes, L. D. L., Rogers, J. G., Kelly, D. P., & Gropler, R. J. (2002) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(02)01967-8 · Cited by 513 · see citing works

Perilipin 5, a lipid droplet-associated protein, provides physical and metabolic linkage to mitochondria

Wang, H., Sreenivasan, U., Hu, H., Saladino, A. J., Polster, B. M., Lund, L. M., Gong, D., Stanley, W. C., & Sztalryd, C. (2011) · Journal of Lipid Research · doi:10.1194/jlr.m017939 · Cited by 486 · see citing works

Influence of endurance exercise training and sex on intramyocellular lipid and mitochondrial ultrastructure, substrate use, and mitochondrial enzyme activity

Tarnopolsky, M. A., Rennie, C. D., Robertshaw, H. A., Fedak-Tarnopolsky, S. N., Devries, M. C., & Hamadeh, M. J. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00472.2006 · Cited by 457 · see citing works

Adipophilin is a specific marker of lipid accumulation in diverse cell types and diseases

Heid, H., Moll, R., Schwetlick, I., Rackwitz, H., & Keenan, T. W. (1998) · Cell and Tissue Research · doi:10.1007/s004410051181 · Cited by 446 · see citing works

Acute exercise increases triglyceride synthesis in skeletal muscle and prevents fatty acid–induced insulin resistance

Schenk, S., & Horowitz, J. F. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30566 · Cited by 407 · see citing works

Effects of Aerobic Versus Resistance Exercise Without Caloric Restriction on Abdominal Fat, Intrahepatic Lipid, and Insulin Sensitivity in Obese Adolescent Boys

Lee, S., Bacha, F., Hannon, T., Kuk, J. L., Boesch, C., & Arslanian, S. (2012) · Diabetes · doi:10.2337/db12-0214 · Cited by 398 · see citing works

Skeletal Muscle Triglycerides, Diacylglycerols, and Ceramides in Insulin Resistance

Amati, F., Dubé, J. J., Alvarez-Carnero, E., Edreira, M. M., Chomentowski, P., Coen, P. M., Switzer, G. E., Bickel, P. E., Stefanovic-Racic, M., Toledo, F. G. S., et al. (2011) · Diabetes · doi:10.2337/db10-1221 · Cited by 395 · see citing works

Restoration of Muscle Mitochondrial Function and Metabolic Flexibility in Type 2 Diabetes by Exercise Training Is Paralleled by Increased Myocellular Fat Storage and Improved Insulin Sensitivity

Meex, R. C. R., Schrauwen-Hinderling, V. B., Moonen-Kornips, E., Schaart, G., Mensink, M., Phielix, E., van de Weijer, T., Sels, J.-P., Schrauwen, P., & Hesselink, M. K. C. (2010) · Diabetes · doi:10.2337/db09-1322 · Cited by 355 · see citing works

Protection against Fatty Liver but Normal Adipogenesis in Mice Lacking Adipose Differentiation-Related Protein

Chang, B. H., Li, L., Paul, A., Taniguchi, S., Nannegari, V., Heird, W. C., & Chan, L. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.3.1063-1076.2006 · Cited by 309 · see citing works

Adipocyte differentiation-related protein reduces the lipid droplet association of adipose triglyceride lipase and slows triacylglycerol turnover

Listenberger, L. L., Ostermeyer‐Fay, A. G., Goldberg, E. B., Brown, W. J., & Brown, D. A. (2007) · Journal of Lipid Research · doi:10.1194/jlr.m700359-jlr200 · Cited by 301 · see citing works

Isolation and characterization of a full-length cDNA coding for an adipose differentiation-related protein.

Jiang, H., & Serrero, G. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.17.7856 · Cited by 274 · see citing works

Effects of weight loss and exercise on insulin resistance, and intramyocellular triacylglycerol, diacylglycerol and ceramide

Dubé, J. J., Amati, F., Toledo, F. G. S., Stefanović-Račić, M., Rossi, A. P., Coen, P. M., & Goodpaster, B. H. (2011) · Diabetologia · doi:10.1007/s00125-011-2065-0 · Cited by 272 · see citing works

DGAT1 Expression Increases Heart Triglyceride Content but Ameliorates Lipotoxicity

Liu, L., Shi, X., Bharadwaj, K. G., Ikeda, S., Yamashita, H., Yagyu, H., Schaffer, J. E., Yu, Y., & Goldberg, I. J. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.049817 · Cited by 240 · see citing works

Increased intramuscular lipid storage in the insulin-resistant and endurance-trained state

van Loon, L. J. C., & Goodpaster, B. H. (2006) · Pflügers Archiv · doi:10.1007/s00424-005-1509-0 · Cited by 232 · see citing works

Intramyocellular lipids form an important substrate source during moderate intensity exercise in endurance‐trained males in a fasted state

van Loon, L. J. C., Koopman, R., Stegen, J. H. C. H., Wagenmakers, A. J. M., KEIZER, H. A., & Saris, W. H. M. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.052431 · Cited by 231 · see citing works

Proteome of Skeletal Muscle Lipid Droplet Reveals Association with Mitochondria and Apolipoprotein A-I

Zhang, H., Wang, Y., Li, J., Yu, J., Pu, J., Li, L., Zhang, H., Zhang, S., Gong, P., Yang, F., et al. (2011) · Journal of Proteome Research · doi:10.1021/pr200553c · Cited by 211 · see citing works

Sprint interval and traditional endurance training increase net intramuscular triglyceride breakdown and expression of perilipin 2 and 5

Shepherd, S. O., Cocks, M., Tipton, K. D., Ranasinghe, A. M., Barker, T. A., Burniston, J. G., Wagenmakers, A. J. M., & Shaw, C. S. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.240952 · Cited by 207 · see citing works

The lipid droplet coat protein perilipin 5 also localizes to muscle mitochondria

Bosma, M., Minnaard, R., Sparks, L. M., Schaart, G., Losen, M. H., Baets, M. H. D., Duimel, H., Kersten, S., Bickel, P. E., Schrauwen, P., et al. (2011) · Histochemistry and Cell Biology · doi:10.1007/s00418-011-0888-x · Cited by 168 · see citing works

Perilipin 2 improves insulin sensitivity in skeletal muscle despite elevated intramuscular lipid levels

Bosma, M., Hesselink, M. K. C., Sparks, L. M., Timmers, S., Ferraz, M. J., Mattijssen, F., van Beurden, D., Schaart, G., de Baets, M. H., Verheyen, F. K., et al. (2012) · Diabetes · doi:10.2337/db11-1402 · Cited by 149 · see citing works

Overexpression of PLIN5 in skeletal muscle promotes oxidative gene expression and intramyocellular lipid content without compromising insulin sensitivity

Bosma, M., Sparks, L. M., Hooiveld, G. J. E. J., Jörgensen, J. A., Houten, S. M., Schrauwen, P., Kersten, S., & Hesselink, M. K. C. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2013.01.007 · Cited by 135 · see citing works

Re-evaluating lipotoxic triggers in skeletal muscle: Relating intramyocellular lipid metabolism to insulin sensitivity

Bosma, M., Kersten, S., Hesselink, M. K. C., & Schrauwen, P. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.11.003 · Cited by 134 · see citing works

Regular exercise is associated with a protective metabolic phenotype in the rat heart

Burelle, Y., Wambolt, R. B., Grist, M., Parsons, H. L., Chow, J. C. F., Antler, C., Bonen, A., Keller, A., Dunaway, G., Popov, K. M., et al. (2004) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00925.2003 · Cited by 129 · see citing works

Nine months of combined training improves ex vivo skeletal muscle metabolism in individuals with type 2 diabetes

Sparks, L. M., Johannsen, N. M., Church, T. S., Earnest, C. P., Moonen-Kornips, E., Moro, C., Hesselink, M. K. C., Smith, S. R., & Schrauwen, P. (2013) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2012-3874 · Cited by 123 · see citing works

Peroxisome Proliferator-activated Receptor γ Coactivator 1α (PGC-1α) Promotes Skeletal Muscle Lipid Refueling in Vivo by Activating de Novo Lipogenesis and the Pentose Phosphate Pathway*

Summermatter, S., Baum, O., Santos, G., Hoppeler, H. H., & Handschin, C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.145995 · Cited by 114 · see citing works

Post‐exercise adipose tissue and skeletal muscle lipid metabolism in humans: the effects of exercise intensity

Mulla, N. A. L., Simonsen, L., & Bülow, J. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00919.x · Cited by 110 · see citing works

Adipocyte Differentiation-Related Protein and OXPAT in Rat and Human Skeletal Muscle: Involvement in Lipid Accumulation and Type 2 Diabetes Mellitus

Minnaard, R., Schrauwen, P., Schaart, G., Jörgensen, J. A., Lenaers, E., Mensink, M., & Hesselink, M. K. C. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-0352 · Cited by 104 · see citing works

Increased intramuscular lipid synthesis and low saturation relate to insulin sensitivity in endurance-trained athletes

Bergman, B. C., Perreault, L., Hunerdosse, D. M., Koehler, M. C., Samek, A. M., & Eckel, R. H. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00684.2009 · Cited by 103 · see citing works

In Vivo, Fatty Acid Translocase (CD36) Critically Regulates Skeletal Muscle Fuel Selection, Exercise Performance, and Training-induced Adaptation of Fatty Acid Oxidation

McFarlan, J. T., Yoshida, Y., Jain, S. S., Han, X.-X., Snook, L. A., Lally, J., Smith, B. K., Glatz, J. F. C., Luiken, J. J. F. P., Sayer, R. A., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.315358 · Cited by 98 · see citing works

PPARγ coactivator-1α contributes to exercise-induced regulation of intramuscular lipid droplet programming in mice and humans

Koves, T. R., Sparks, L. M., Kovalik, J., Mosedale, M., Arumugam, R., DeBalsi, K. L., Everingham, K., Thorne, L. B., Esther Phielix, E., Meex, R. C. R., et al. (2012) · Journal of Lipid Research · doi:10.1194/jlr.p028910 · Cited by 95 · see citing works

Up-regulation of SREBP-1c and lipogenic genes in skeletal muscles after exercise training

Ikeda, S., Miyazaki, H., Nakatani, T., Kai, Y., Kamei, Y., Miura, S., Tsuboyama-Kasaoka, N., & Ezaki, O. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00883-5 · Cited by 92 · see citing works

Skeletal muscle PLIN proteins, ATGL and CGI-58, interactions at rest and following stimulated contraction

MacPherson, R. E. K., Ramos, S. V., Vandenboom, R., Roy, B. D., & Peters, S. J. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00418.2012 · Cited by 91 · see citing works

Endurance Training Modulates Intramyocellular Lipid Compartmentalization and Morphology in Skeletal Muscle of Lean and Obese Women

Devries, M. C., Samjoo, I. A., Hamadeh, M. J., McCready, C., Raha, S., Watt, M. J., Steinberg, G. R., & Tarnopolsky, M. A. (2013) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-2044 · Cited by 82 · see citing works

Perilipin family (PLIN) proteins in human skeletal muscle: the effect of sex, obesity, and endurance training

Peters, S. J., Samjoo, I. A., Devries, M. C., Stevic, I., Robertshaw, H. A., & Tarnopolsky, M. A. (2012) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h2012-059 · Cited by 81 · see citing works

Improved Ejection Fraction after Exercise Training in Obesity Is Accompanied by Reduced Cardiac Lipid Content

Schrauwen‐Hinderling, V. B., Hesselink, M. K. C., Meex, R. C. R., van der Made, S. M., Schär, M., Lamb, H. J., Wildberger, J. E., Glatz, J. F. C., Snoep, G., Kooi, M. E., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-2076 · Cited by 80 · see citing works

Prolonged exercise training increases intramuscular lipid content and perilipin 2 expression in type I muscle fibers of patients with type 2 diabetes

Shaw, C. S., Shepherd, S. O., Wagenmakers, A. J. M., Hansen, D., Dendale, P., & van Loon, L. J. C. (2012) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00272.2012 · Cited by 72 · see citing works

Basal very low-density lipoprotein metabolism in response to exercise: Mechanisms of hypotriacylglycerolemia

Magkos, F. (2009) · Progress in Lipid Research · doi:10.1016/j.plipres.2009.02.003 · Cited by 71 · see citing works

Adrenaline but not noradrenaline is a determinant of exercise‐induced lipid mobilization in human subcutaneous adipose tissue

de Glisezinski, I., Larrouy, D., Bajzová, M., Koppo, K., Polak, J., Berlan, M., Bülow, J., Langin, D., Marques, M., Crampes, F., et al. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.168906 · Cited by 70 · see citing works

Expression of lipogenic genes is upregulated in the heart with exercise training-induced but not pressure overload-induced left ventricular hypertrophy

Dobrzyń, P., Pyrkowska, A., Duda, M. K., Bednarski, T., Ma̧czewski, M., Langfort, J., & Dobrzyń, A. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00603.2012 · Cited by 64 · see citing works

Cardiac Molecular-Acclimation Mechanisms in Response to Swimming-Induced Exercise in Atlantic Salmon

Castro, V., Grisdale‐Helland, B., Helland, S. J., Torgersen, J. S., Kristensen, T., Claireaux, G., Farrell, A. P., & Takle, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055056 · Cited by 62 · see citing works

Preferential utilization of perilipin 2‐associated intramuscular triglycerides during 1 h of moderate‐intensity endurance‐type exercise

Shepherd, S. O., Cocks, M. S., Tipton, K. D., Ranasinghe, A. M., Barker, T. A., Burniston, J. G., Wagenmakers, A. J. M., & Shaw, C. S. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2012.064592 · Cited by 60 · see citing works

Dual modulation of both lipid oxidation and synthesis by peroxisome proliferator‐activated receptor‐γ coactivator‐1α and ‐1β in cultured myotubes

Espinoza, D., Boros, L. G., Crunkhorn, S., Gami, H., & Patti, M. (2009) · The FASEB Journal · doi:10.1096/fj.09-133728 · Cited by 60 · see citing works

Adipophilin distribution and colocalisation with lipid droplets in skeletal muscle

Shaw, C. S., Sherlock, M., Stewart, P. M., & Wagenmakers, A. J. M. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-009-0558-4 · Cited by 59 · see citing works

Acute exercise-induced changes in basal VLDL-triglyceride kinetics leading to hypotriglyceridemia manifest more readily after resistance than endurance exercise

Magkos, F., Tsekouras, Y. E., Prentzas, K. I., Basioukas, K. N., Matsama, S. G., Yanni, A. E., Kavouras, S. A., & Sidossis, L. S. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90761.2008 · Cited by 59 · see citing works

Effects of exercise and lifestyle modification on fitness, insulin resistance, skeletal muscle oxidative phosphorylation and intramyocellular lipid content in obese children and adolescents

McCormack, S. E., McCarthy, M. A., Harrington, S. G., Farilla, L., Hrovat, M. I., Systrom, D. M., Thomas, B. J., Torriani, M., McInnis, K. J., Grinspoon, S. K., et al. (2013) · Pediatric Obesity · doi:10.1111/j.2047-6310.2013.00180.x · Cited by 57 · see citing works

Hepatic lipid droplets. Isolation, morphology and composition

DiAugustine, R. P., Schaefer, J.-M., & Fouts, J. R. (1973) · Biochemical Journal · doi:10.1042/bj1320323 · Cited by 56 · see citing works

SCD1 activity in muscle increases triglyceride PUFA content, exercise capacity, and PPARΔ expression in mice

Rogowski, M. P., Flowers, M. T., Stamatikos, A., Ntambi, J. M., & Paton, C. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m035865 · Cited by 55 · see citing works

PGC-1α Induces Mitochondrial and Myokine Transcriptional Programs and Lipid Droplet and Glycogen Accumulation in Cultured Human Skeletal Muscle Cells

Mormeneo, E., Jimenez-Mallebrera, C., Palomer, X., Nigris, V. D., Vázquez‐Carrera, M., Orozco, A., Nascimento, A., Colomer, J., Lerín, C., & Gómez-Foix, A. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029985 · Cited by 54 · see citing works

Oxygen consumption, substrate oxidation, and blood pressure following sprint interval exercise

Chan, H. H., & Burns, S. F. (2013) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2012-0136 · Cited by 54 · see citing works

Uptake of chylomicron triglycerides by contracting skeletal muscle in rats

Mackie, B. G., Dudley, G. A., Kaciuba-Uściłko, H., & Terjung, R. L. (1980) · Journal of Applied Physiology · doi:10.1152/jappl.1980.49.5.851 · Cited by 54 · see citing works

Acute endurance exercise increases plasma membrane fatty acid transport proteins in rat and human skeletal muscle

Bradley, N. S., Snook, L. A., Jain, S. S., Heigenhauser, G. J. F., Bonen, A., & Spriet, L. L. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00254.2011 · Cited by 51 · see citing works

Exercise and fat accumulation in the human liver

Magkos, F. (2010) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32833ea912 · Cited by 50 · see citing works

IL-6 Indirectly Modulates the Induction of Glyceroneogenic Enzymes in Adipose Tissue during Exercise

Wan, Z., Ritchie, I. R. W., Beaudoin, M., Castellani, L. N., Chan, C. B., & Wright, D. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041719 · Cited by 43 · see citing works

Contraction‐induced lipolysis is not impaired by inhibition of hormone‐sensitive lipase in skeletal muscle

Alsted, T. J., Ploug, T., Prats, C., Serup, A. K., Høeg, L. D., Schjerling, P., Holm, C., Zimmermann, R., Fledelius, C., Galbo, H., et al. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.260794 · Cited by 43 · see citing works

Exercise training enhances white adipose tissue metabolism in rats selectively bred for low- or high-endurance running capacity

Stephenson, E. J., Lessard, S. J., Rivas, D. A., Watt, M. J., Yaspelkis, B. B., Koch, L. G., Britton, S. L., & Hawley, J. A. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00544.2012 · Cited by 41 · see citing works

Factors regulating fat oxidation in human skeletal muscle

Kiens, B., Alsted, T. J., & Jeppesen, J. (2011) · Obesity Reviews · doi:10.1111/j.1467-789x.2011.00898.x · Cited by 40 · see citing works

Exercise-inducible factors to activate lipolysis in adipocytes

Hashimoto, T., Sato, K., & Iemitsu, M. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00427.2013 · Cited by 36 · see citing works

Expression of perilipins in human skeletal musclein vitroandin vivoin relation to diet, exercise and energy balance

Gjelstad, I. M. F., Haugen, F., Gulseth, H. L., Norheim, F., Jans, A., Bakke, S. S., Raastad, T., Tjønna, A. E., Wisløff, U., Blaak, E. E., et al. (2011) · Archives of Physiology and Biochemistry · doi:10.3109/13813455.2011.630009 · Cited by 32 · see citing works

Skeletal muscle 1H MRSI before and after prolonged exercise. I. muscle specific depletion of intramyocellular lipids

Vermathen, P., Saillen, P., Boss, A., Zehnder, M. G., & Boesch, C. (2012) · Magnetic Resonance in Medicine · doi:10.1002/mrm.24168 · Cited by 28 · see citing works

Lipid droplet dynamics in skeletal muscle

Bosma, M. (2016) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.10.023 · Cited by 91 · see citing works

Targeting Intramyocellular Lipids to Improve Aging Muscle Function

Russ, D. W., Manickam, R., & Tipparaju, S. M. (2025) · Lipids in Health and Disease · doi:10.1186/s12944-025-02622-6 · Cited by 15 · see citing works

Dissection and Lipid Droplet Staining of Oenocytes in Drosophila Larvae

Wei, C., Yan, Y., Miao, X., & Jiao, R. (2019) · Journal of Visualized Experiments · doi:10.3791/60606 · Cited by 4 · see citing works

Lipid droplet metabolism

Khor, V. K., Shen, W., & Kraemer, F. B. (2013) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e3283651106 · Cited by 105 · see citing works

Perilipin-related protein regulates lipid metabolism in C. elegans

Chughtai, A. A., Kaššák, F., Kostrouchová, M., et al. (2015) · PeerJ · doi:10.7717/peerj.1213 · Cited by 32 · see citing works

Lipid droplets: platforms with multiple functions in cancer hallmarks

Cruz, A. L. S., Barreto, E. A., Fazolini, N. P. B., Viola, J. P. B., & Bozza, P. T. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2297-3 · Cited by 539 · see citing works

Another way to get rid of fat

Zechner, R., & Madeo, F. (2009) · Nature · doi:10.1038/4581118a · Cited by 51 · see citing works