Lanza, Ian R.

Exerkines in health, resilience and disease

Chow, L. S., Gerszten, R. E., Taylor, J. M., Pedersen, B. K., van Praag, H., Trappe, S., Febbraio, M. A., Galis, Z. S., Gao, Y., Haus, J. M., et al. (2022) · Nature Reviews Endocrinology

Exercise and Physiological ResponsesAdipokines, Inflammation, and Metabolic Diseases

Cited by 927

A PGC-1α isoform induced by resistance training regulates skeletal muscle hypertrophy

Ruas, J. L., White, J. P., Rao, R. R., Kleiner, S., Brannan, K. T., Harrison, B. C., Greene, N. P., Wu, J., Estall, J. L., Irving, B. A., et al. (2012) · Cell

Muscle Physiology and DisordersAdipose Tissue and Metabolism

Cited by 677

Endurance Exercise as a Countermeasure for Aging

Lanza, I. R., Short, D. K., Short, K. R., Raghavakaimal, S., Basu, R., Joyner, M. J., McConnell, J. P., & Nair, K. S. (2008) · Diabetes

Mitochondrial Function and PathologyAdipose Tissue and Metabolism

Cited by 582

Enhanced Protein Translation Underlies Improved Metabolic and Physical Adaptations to Different Exercise Training Modes in Young and Old Humans

Robinson, M. M., Dasari, S., Konopka, A. R., Johnson, M. L., Manjunatha, S., Esponda, R. R., Carter, R. E., Lanza, I. R., & Nair, K. S. (2017) · Cell Metabolism

Muscle metabolism and nutritionCardiovascular and exercise physiology

Cited by 539

Chronic Caloric Restriction Preserves Mitochondrial Function in Senescence without Increasing Mitochondrial Biogenesis

Lanza, I. R., Zabielski, P., Klaus, K. A., Morse, D. M., Heppelmann, C. J., Bergen, H. R., Dasari, S., Walrand, S., Short, K. R., Johnson, M. L., et al. (2012) · Cell Metabolism

Genetics, Aging, and Longevity in Model OrganismsMitochondrial Function and Pathology

Cited by 227

Characterization of cellular senescence in aging skeletal muscle

Zhang, X., Habiballa, L., Aversa, Z., Ng, Y. E., Sakamoto, A. E., Englund, D. A., Pearsall, V. M., White, T. A., Robinson, M. M., Rivas, D. A., et al. (2022) · Nature Aging

Telomeres, Telomerase, and SenescenceMuscle Physiology and Disorders

Cited by 206

Insulin-sensitizing effects of omega-3 fatty acids: lost in translation?

Lalia, A., & Lanza, I. (2016) · Nutrients

Fatty Acid Research and HealthDiet, Metabolism, and Disease

Cited by 141

Combined Training Enhances Skeletal Muscle Mitochondrial Oxidative Capacity Independent of Age

Irving, B. A., Lanza, I. R., Henderson, G. C., Rao, R. R., Spiegelman, B. M., & Nair, K. S. (2015) · The Journal of Clinical Endocrinology & Metabolism

Cardiovascular and exercise physiologyMitochondrial Function and Pathology

Cited by 139

Influence of fish oil on skeletal muscle mitochondrial energetics and lipid metabolites during high-fat diet

Lanza, I. R., Blachnio-Zabielska, A., Johnson, M. L., Schimke, J. M., Jakaitis, D. R., Lebrasseur, N. K., Jensen, M. D., Sreekumaran Nair, K., & Zabielski, P. (2013) · American Journal of Physiology-Endocrinology and Metabolism

Fatty Acid Research and HealthAdipose Tissue and Metabolism

Cited by 135

Mechanism by Which Caloric Restriction Improves Insulin Sensitivity in Sedentary Obese Adults

Johnson, M. L., Distelmaier, K., Lanza, I. R., Irving, B. A., Robinson, M. M., Konopka, A. R., Shulman, G. I., & Nair, K. S. (2016) · Diabetes

Metabolism, Diabetes, and CancerDietary Effects on Health

Cited by 129

Defects in mitochondrial efficiency and H2O2 emissions in obese women are restored to a lean phenotype with aerobic exercise training

Konopka, A. R., Asante, A., Lanza, I. R., Robinson, M. M., Johnson, M. L., Dalla Man, C., Cobelli, C., Amols, M. H., Irving, B. A., & Nair, K. S. (2015) · Diabetes

Mitochondrial Function and PathologyAdipose Tissue and Metabolism

Cited by 112

Measurement of human skeletal muscle oxidative capacity by 31 P‐MR spectroscopy: A cross‐validation with in vitro measurements

Lanza, I. R., Bhagra, S., Nair, K. S., & Port, J. D. (2011) · Journal of Magnetic Resonance Imaging

Advanced MRI Techniques and ApplicationsCardiovascular and exercise physiology

Cited by 103

TFAM Enhances Fat Oxidation and Attenuates High-Fat Diet–Induced Insulin Resistance in Skeletal Muscle

Koh, J.-H., Johnson, M. L., Dasari, S., LeBrasseur, N. K., Vuckovic, I., Henderson, G. C., Cooper, S. A., Manjunatha, S., Ruegsegger, G. N., Shulman, G. I., et al. (2019) · Diabetes

Metabolism, Diabetes, and CancerAdipose Tissue and Metabolism

Cited by 92

Regulation of skeletal muscle mitochondrial function: genes to proteins

Lanza, I. R., & Sreekumaran Nair, K. (2010) · Acta Physiologica

Mitochondrial Function and PathologyAdipose Tissue and Metabolism

Cited by 83

A size-exclusion-based approach for purifying extracellular vesicles from human plasma

Vanderboom, P. M., Dasari, S., Ruegsegger, G. N., Pataky, M. W., Lucien, F., Heppelmann, C. J., Lanza, I. R., & Nair, K. S. (2021) · Cell Reports Methods

Extracellular vesicles in diseaseAdvanced Proteomics Techniques and Applications

Cited by 75

Effects of dietary n-3 fatty acids on hepatic and peripheral insulin sensitivity in insulin resistant humans

Lalia, A. Z., Johnson, M. L., Jensen, M. D., Hames, K. C., Port, J. D., & Lanza, I. R. (2015) · Diabetes Care

Fatty Acid Research and HealthDiet, Metabolism, and Disease

Cited by 73

Eicosapentaenoic acid but not docosahexaenoic acid restores skeletal muscle mitochondrial oxidative capacity in old mice

Johnson, M. L., Lalia, A. Z., Dasari, S., Pallauf, M., Fitch, M., Hellerstein, M. K., & Lanza, I. R. (2015) · Aging Cell

Fatty Acid Research and HealthMitochondrial Function and Pathology

Cited by 66

Age-associated inflammation and implications for skeletal muscle responses to exercise

Kunz, H. E., & Lanza, I. R. (2023) · Experimental Gerontology

Exercise and Physiological ResponsesMuscle Physiology and Disorders

Cited by 56

Altered Skeletal Muscle Mitochondrial Proteome As the Basis of Disruption of Mitochondrial Function in Diabetic Mice

Zabielski, P., Lanza, I. R., Gopala, S., Holtz Heppelmann, C. J., Bergen, H. R., Dasari, S., & Nair, K. S. (2016) · Diabetes

Mitochondrial Function and PathologyMetabolism, Diabetes, and Cancer

Cited by 54

Impact of insulin deprivation and treatment on sphingolipid distribution in different muscle subcellular compartments of streptozotocin-diabetic C57Bl/6 mice

Zabielski, P., Blachnio-Zabielska, A., Lanza, I. R., Gopala, S., Manjunatha, S., Jakaitis, D. R., Persson, X.-M., Gransee, J., Klaus, K. A., Schimke, J. M., et al. (2014) · American Journal of Physiology-Endocrinology and Metabolism

Sphingolipid Metabolism and SignalingLipid metabolism and biosynthesis

Cited by 30

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Kobren, S. N., Baldridge, D., Velinder, M., Krier, J. B., LeBlanc, K., Esteves, C., Pusey, B. N., Züchner, S., Blue, E., Lee, H., et al. (2021) · Genetics in Medicine

Genomics and Rare DiseasesGenomics and Phylogenetic Studies

Cited by 27

Can dietary nitrates enhance the efficiency of mitochondria?

Nair, K. S., Irving, B. A., & Lanza, I. R. (2011) · Cell Metabolism

Mitochondrial Function and PathologyNitric Oxide and Endothelin Effects

Cited by 13