Myokines: metabolic regulation in obesity and type 2 diabetes

Aerobic Exercise Increases Meteorin-Like Protein in Muscle and Adipose Tissue of Chronic High-Fat Diet-Induced Obese Mice

Bae, J. Y. (2018) · BioMed Research International · doi:10.1155/2018/6283932 · Cited by 77

A Piezo1/KLF15/IL-6 axis mediates immobilization- induced muscle atrophy

Hirata, Y., Nomura, K., 野村, 和., ノムラ, カ., Kato, D., Wake, H., 和氣, 弘., ワケ, ヒ., Ogawa, W., Hirata, Y., et al. (2022) · Institutional Repositories DataBase (IRDB) · Cited by 76

Stressed Liver and Muscle Call on Adipocytes with FGF21

Luo, Y., & McKeehan, W. L. (2013) · Frontiers in Endocrinology · doi:10.3389/fendo.2013.00194 · Cited by 75

Muscle mitochondrial stress adaptation operates independently of endogenous FGF21 action

Ost, M., Coleman, V., Voigt, A., van Schothorst, E. M., Keipert, S., van der Stelt, I., Ringel, S., Graja, A., Ambrosi, T., Kipp, A. P., et al. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2015.11.002 · Cited by 75 · cited 1×

Serum Meteorin-like protein levels decreased in patients newly diagnosed with type 2 diabetes

Lee, J. H., Kang, Y. E., Kim, J. M., Choung, S., Joung, K. H., Kim, H. J., & Ku, B. J. (2018) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2017.10.005 · Cited by 75

Omics approaches for the assessment of biological responses to nanoparticles

Abdelkader, Y., Pérez-Dávalos, L. A., LeDuc, R. D., Zahedi, R. P., & Labouta, H. I. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.114992 · Cited by 75

Thiazolidinediones increase the wingless-type MMTV integration site family (WNT) inhibitor Dickkopf-1 in adipocytes: a link with osteogenesis

Gustafson, B., Eliasson, B., & Smith, U. (2009) · Diabetologia · doi:10.1007/s00125-009-1615-1 · Cited by 74

GDF11 Attenuates Development of Type 2 Diabetes via Improvement of Islet β-Cell Function and Survival

Li, H., Li, Y., Xiang, L., Zhang, J., Zhu, B., Xiang, L., Dong, J., Liu, M., & Xiang, G. (2017) · Diabetes · doi:10.2337/db17-0086 · Cited by 74

Transferrin Receptor 1 Regulates Thermogenic Capacity and Cell Fate in Brown/Beige Adipocytes

Li, J., Pan, X., Pan, G., Song, Z., He, Y., Zhang, S., Ye, X., Xiang, Y., Xie, E., Wang, X., et al. (2020) · Advanced Science · doi:10.1002/advs.201903366 · Cited by 74

Irisin reverses insulin resistance in C2C12 cells via the p38-MAPK-PGC-1α pathway

Ye, X., Shen, Y., Ni, C., Ye, J., Xin, Y., Zhang, W., & Ren, Y. (2019) · Peptides · doi:10.1016/j.peptides.2019.170120 · Cited by 73

Hormones of adipose tissue and their biologic role in lung cancer

Ntikoudi, E., Kiagia, M., Boura, P., & Syrigos, K. N. (2013) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2013.06.005 · Cited by 72

Dkk3 dependent transcriptional regulation controls age related skeletal muscle atrophy

Yin, J., Yang, L., Xie, Y., Liu, Y., Li, S., Yang, W., Xu, B., Ji, H., Ding, L., Wang, K., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04038-6 · Cited by 72

DKK3 expression in hepatocytes defines susceptibility to liver steatosis and obesity

Xie, L., Wang, P., Zhang, P., Zhang, X., Zhao, G., Wang, A., Guo, J., Zhu, X., Zhang, Q., & Li, H. (2016) · Journal of Hepatology · doi:10.1016/j.jhep.2016.03.008 · Cited by 71

The regulation of skeletal muscle fatigability and mitochondrial function by chronically elevated interleukin‐6

VanderVeen, B. N., Fix, D. K., Montalvo, R. N., Counts, B. R., Smuder, A. J., Murphy, E. A., Koh, H., & Carson, J. A. (2018) · Experimental Physiology · doi:10.1113/ep087429 · Cited by 71

Glucose Sensing by Skeletal Myocytes Couples Nutrient Signaling to Systemic Homeostasis

Meng, Z., Gong, J., Chen, Z., Sun, J., Xiao, Y., Wang, L., Li, Y., Liu, J., Xu, X., & Lin, J. D. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.04.007 · Cited by 69

FGF-2–dependent signaling activated in aged human skeletal muscle promotes intramuscular adipogenesis

Mathes, S., Fahrner, A., Ghoshdastider, U., Rüdiger, H. A., Leunig, M., Wolfrum, C., & Krützfeldt, J. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2021013118 · Cited by 69

Myostatin signals through miR-34a to regulate Fndc5 expression and browning of white adipocytes

Ge, X., Sathiakumar, D., Lua, B.-N., Kukreti, H., Lee, M., & McFarlane, C. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.110 · Cited by 67

Growth differentiation factor 11 attenuates liver fibrosis via expansion of liver progenitor cells

Dai, Z., Song, G., Balakrishnan, A., Yang, T., Yuan, Q., Möbus, S., Weiss, A., Bentler, M., Zhu, J., Jiang, X., et al. (2019) · Gut · doi:10.1136/gutjnl-2019-318812 · Cited by 67

The muscle-enriched myokine Musclin impairs beige fat thermogenesis and systemic energy homeostasis via Tfr1/PKA signaling in male mice

Lu, J., Han, S., Lv, X., Li, X., Zhang, Z., Kuang, H., Chen, Z., Lv, C.-A., Peng, W., Yang, Z., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39710-z · Cited by 67

Acute aerobic exercise leads to increased plasma levels of R- and S-β-aminoisobutyric acid in humans

Stautemas, J., Van Kuilenburg, A. B. P., Stroomer, L., Vaz, F., Blancquaert, L., Lefevere, F. B. D., Everaert, I., & Derave, W. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01240 · Cited by 66

Musclin, A Myokine Induced by Aerobic Exercise, Retards Muscle Atrophy During Cancer Cachexia in Mice

Re Cecconi, A. D., Forti, M., Chiappa, M., Zhu, Z., Zingman, L. V., Cervo, L., Beltrame, L., Marchini, S., & Piccirillo, R. (2019) · Cancers · doi:10.3390/cancers11101541 · Cited by 66

Inhibition of in vitro and in vivo brown fat differentiation program by myostatin

Braga, M., Pervin, S., Norris, K. C., Bhasin, S., & Singh, R. (2013) · Obesity · doi:10.1002/oby.20117 · Cited by 65

Chemical and genetic evidence for the involvement of Wnt antagonist Dickkopf2 in regulation of glucose metabolism

Li, X., Shan, J., Chang, W., Kim, I., Bao, J., Lee, H., Zhang, X., Samuel, V. T., Shulman, G. I., Liu, D., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1205015109 · Cited by 63

Asprosin, a novel pleiotropic adipokine implicated in fasting and obesity-related cardio-metabolic disease: Comprehensive review of preclinical and clinical evidence

Shabir, K., Brown, J. E. P., Afzal, I., Gharanei, S., Weickert, M. O., Barber, T. M., Kyrou, I., & Randeva, H. S. (2021) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2021.05.002 · Cited by 63

Hepatocyte-specific fibroblast growth factor 21 overexpression ameliorates high-fat diet-induced obesity and liver steatosis in mice

Yano, K., Yamaguchi, K., Seko, Y., Okishio, S., Ishiba, H., Tochiki, N., Takahashi, A., Kataoka, S., Okuda, K., Liu, Y. X., et al. (2021) · Laboratory Investigation · doi:10.1038/s41374-021-00680-9 · Cited by 63

Exercise improved lipid metabolism and insulin sensitivity in rats fed a high-fat diet by regulating glucose transporter 4 (GLUT4) and musclin expression

Yu, J., Zheng, J., Liu, X. F., Feng, Z., Zhang, X. P., Cao, L., & Zhou, Z. (2016) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x20165129 · Cited by 62

The secretome of the working human skeletal muscle—A promising opportunity to combat the metabolic disaster?

Weigert, C., Lehmann, R., Hartwig, S., & Lehr, S. (2013) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201300094 · Cited by 61

METRNL decreases during adipogenesis and inhibits adipocyte differentiation leading to adipocyte hypertrophy in humans

Löffler, D., Landgraf, K., Rockstroh, D., Schwartze, J. T., Dunzendorfer, H., Kiess, W., & Körner, A. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.180 · Cited by 61

The SWI/SNF chromatin-remodeling factors BAF60a, b, and c in nutrient signaling and metabolic control

Wang, R., Pan, R., Zhang, W., Fu, J., Lin, J. D., & Meng, Z. (2017) · Protein & Cell · doi:10.1007/s13238-017-0442-2 · Cited by 61

Irisin counteracts high glucose and fatty acid-induced cytotoxicity by preserving the AMPK-insulin receptor signaling axis in C2C12 myoblasts

Yano, N., Zhang, L., Wei, D., Dubielecka, P. M., Lei, W., Zhuang, S., Zhu, P., Qin, G., Liu, P. Y., Chin, Y. E., et al. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00219.2019 · Cited by 59

Lactate as a major myokine and exerkine

Brooks, G. A., Osmond, A. D., Arevalo, J. A., Curl, C. C., Duong, J. J., Horning, M. A., Moreno-Santillán, D. D., & Leija, R. G. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-022-00724-0 · Cited by 59

The adipocyte supersystem of insulin and cAMP signaling

Guilherme, A., Rowland, L. A., Wang, H., & Czech, M. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.07.009 · Cited by 59

Exercise-induced Musclin determines the fate of fibro-adipogenic progenitors to control muscle homeostasis

Kang, X., Qian, J., Shi, Y.-X., Bian, X., Zhang, L., Li, G., Wang, L., Zhao, J., Dong, Z., Yang, M., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2023.12.011 · Cited by 59

Lower circulating irisin is associated with nonalcoholic fatty liver disease and type 2 diabetes

Shanaki, M., Moradi, N., Emamgholipour, S., Fadaei, R., & Poustchi, H. (2017) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2017.03.037 · Cited by 57

Plasma Myokine Concentrations After Acute Exercise in Non-obese and Obese Sedentary Women

Garneau, L., Parsons, S. A., Smith, S. R., Mulvihill, E. E., Sparks, L. M., & Aguer, C. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00018 · Cited by 57

SPARC triggers a cell-autonomous program of synapse elimination

López-Murcia, F. J., Terni, B., & Llobet, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1512202112 · Cited by 56

A New Secretory Peptide of Natriuretic Peptide Family, Osteocrin, Suppresses the Progression of Congestive Heart Failure After Myocardial Infarction

Miyazaki, T., Otani, K., Chiba, A., Nishimura, H., Tokudome, T., Takano, H., Matsuo, A., Ishikawa, H. T., Shimamoto, K., Fukui, H., et al. (2018) · Circulation Research · doi:10.1161/circresaha.117.312624 · Cited by 56

Irisin: An anti-inflammatory exerkine in aging and redox-mediated comorbidities

Trettel, C. D. S., Pelozin, B. R. D. A., Barros, M. P., Bachi, A. L. L., Braga, P. G. S., Momesso, C. M., Furtado, G. E., Valente, P. A., de Oliveira, E. M., Hogervorst, E., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1106529 · Cited by 56

The Adipokine Metrnl Ameliorates Chronic Colitis in Il-10–/– Mice by Attenuating Mesenteric Adipose Tissue Lesions During Spontaneous Colitis

Zuo, L., Ge, S., Ge, Y., Li, J., Zhu, B., Zhang, Z., Jiang, C., Li, J., Wang, S., Liu, M., et al. (2019) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjz001 · Cited by 54

Myostatin Regulates Fatty Acid Desaturation and Fat Deposition through MEF2C/miR222/SCD5 Cascade in Pigs

Ren, H., Xiao, W., Qin, X., Cai, G., Chen, H., Hua, Z., Cheng, C., Li, X., Hua, W., Xiao, H., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-01348-8 · Cited by 54

Growth differentiation factor 11 inhibits adipogenic differentiation by activating TGF‐beta/Smad signalling pathway

Luo, H., Guo, Y., Liu, Y., Wang, Y., Zheng, R., Ban, Y., Peng, L., Yuan, Q., & Liu, W. (2019) · Cell Proliferation · doi:10.1111/cpr.12631 · Cited by 53

Exercise-mimicking treatment fails to increase Fndc5 mRNA & irisin secretion in primary human myotubes

Kurdiová, T., Baláž, M., Mayer, A. E., Máderová, D., Belan, V., Wolfrum, C., Ukropec, J., & Ukropcová, B. (2014) · Peptides · doi:10.1016/j.peptides.2014.03.003 · Cited by 52

Opposite changes in meteorin-like and oncostatin m levels are associated with metabolic improvements after bariatric surgery

Pellitero, S., Piquer‐Garcia, I., Ferrer‐Curriu, G., Puig, R., Martínez, E., Moreno, P., Tarascó, J., Balibrea, J. M., Lerín, C., Puig‐Domingo, M., et al. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.268 · Cited by 52

The Baf60c/Deptor Pathway Links Skeletal Muscle Inflammation to Glucose Homeostasis in Obesity

Meng, Z., Wang, L., Xiao, Y., & Lin, J. D. (2014) · Diabetes · doi:10.2337/db13-1061 · Cited by 51

Neurotrophin-targeted therapeutics: A gateway to cognition and more?

Nordvall, G., Forsell, P. K. A. L., & Sandin, J. (2022) · Drug Discovery Today · doi:10.1016/j.drudis.2022.07.003 · Cited by 51

SPARC functions as an inhibitor of adipogenesis

Nie, J., & Sage, E. H. (2009) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-009-0064-4 · Cited by 50

Apelin alleviated neuroinflammation and promoted endogenous neural stem cell proliferation and differentiation after spinal cord injury in rats

Liu, Q., Zhou, S., Wang, X. D., Gu, C., Guo, Q., Li, X., Zhang, C., Zhang, N., Zhang, L., & Huang, F. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02518-7 · Cited by 50

Dkk‐3 is elevated in CSF and plasma of Alzheimer’s disease patients

Zenzmaier, C., Marksteiner, J., Kiefer, A., Berger, P., & Humpel, C. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06158.x · Cited by 49

Inverse relationship between serum Metrnl levels and visceral fat obesity (VFO) in patients with type 2 diabetes

Du, Y., Ye, X., Lu, A., Zhao, D., Liu, J., Cheng, J., & Yang, T. (2020) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2020.108068 · Cited by 49

cGMP rescues mitochondrial dysfunction induced by glucose and insulin in myocytes

Mitsuishi, M., Miyashita, K., & Itoh, H. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.01.017 · Cited by 48

The role of brown and beige adipose tissue in glycaemic control

Klepac, K., Georgiadi, A., Tschöp, M. H., & Herzig, S. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.07.001 · Cited by 48

Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice

Katsimpardi, L., Kuperwasser, N., Camus, C., Moigneu, C., Chiche, A., Tolle, V., Li, H., Kokovay, E., & Lledo, P. (2020) · Aging Cell · doi:10.1111/acel.13038 · Cited by 47

Competitive binding of musclin to natriuretic peptide receptor 3 with atrial natriuretic peptide

Kita, S., Nishizawa, H., Okuno, Y., Tanaka, M., Yasui, A., Matsuda, M., Yamada, Y., & Shimomura, I. (2009) · Journal of Endocrinology · doi:10.1677/joe-08-0551 · Cited by 46

hnRNPU/TrkB Defines a Chromatin Accessibility Checkpoint for Liver Injury and Nonalcoholic Steatohepatitis Pathogenesis

Xiong, J., Liu, T., Mi, L., Kuang, H., Xiong, X., Chen, Z., Li, S., & Lin, J. D. (2019) · Hepatology · doi:10.1002/hep.30921 · Cited by 46

Intestinal Metrnl released into the gut lumen acts as a local regulator for gut antimicrobial peptides

Li, Z., Fan, M.-B., Zhang, S.-L., Qu, Y., Zheng, S., Song, J., & Miao, C. (2016) · Acta Pharmacologica Sinica · doi:10.1038/aps.2016.70 · Cited by 44

Gdf11 gene transfer prevents high fat diet-induced obesity and improves metabolic homeostasis in obese and STZ-induced diabetic mice

Lu, B., Zhong, J., Pan, J., Yuan, X., Ren, M., Jiang, L., Yang, Y., Zhang, G., Liu, D., & Zhang, C. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-02166-1 · Cited by 44

Microproteomic sample preparation

Alexovič, M., Sabó, J., & Longuespée, R. (2021) · PROTEOMICS · doi:10.1002/pmic.202000318 · Cited by 44

Enriched Protein Screening of Human Bone Marrow Mesenchymal Stromal Cell Secretions Reveals MFAP5 and PENK as Novel IL-10 Modulators

Milwid, J. M., Elman, J. S., Li, M., et al. (2014) · Molecular Therapy · doi:10.1038/mt.2014.17 · Cited by 43

Secreted protein acidic and rich in cysteine (SPARC) improves glucose tolerance via AMP‐activated protein kinase activation

Aoi, W., Hirano, N., Lassiter, D. G., Björnholm, M., Chibalin, A., Sakuma, K., Tanimura, Y., Mizushima, K., Takagi, T., Naito, Y., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201900453r · Cited by 43

Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile

Ding, X., Chang, X., Wang, J., Bian, N., An, Y., Wang, G., & Liu, J. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.938341 · Cited by 43

The role of exercise in obesity-related cancers: Current evidence and biological mechanisms

Larson, E. A., Dalamaga, Μ., & Magkos, F. (2023) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2023.02.008 · Cited by 43

Blocking the Myostatin Signal With a Dominant Negative Receptor Improves the Success of Human Myoblast Transplantation in Dystrophic Mice

Fakhfakh, R., Michaud, A., & Tremblay, J. P. (2010) · Molecular Therapy · doi:10.1038/mt.2010.171 · Cited by 42

IL-6: A Potential Role in Cardiac Metabolic Homeostasis

Xu, Y., Zhang, Y., & Ye, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19092474 · Cited by 42

SPARC is required for the maintenance of glucose homeostasis and insulin secretion in mice

Atorrasagasti, C., Onorato, A. M., Gimeno, M. L., et al. (2019) · Clinical Science · doi:10.1042/cs20180714 · Cited by 42

Is Brain-Derived Neurotrophic Factor a Metabolic Hormone in Peripheral Tissues?

Iu, E. C. Y., & Chan, C. B. (2022) · Biology · doi:10.3390/biology11071063 · Cited by 41

Protein Structural Analysis via Mass Spectrometry-Based Proteomics

Artigues, A., Nadeau, O. W., Rimmer, M. A., Villar, M. T., Du, X., Fenton, A. W., & Carlson, G. M. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-41448-5_19 · Cited by 40

Sparc, an EPS-induced gene, modulates the extracellular matrix and mitochondrial function via ILK/AMPK pathways in C2C12 cells

Melouane, A., Yoshioka, M., Kanzaki, M., & St‐Amand, J. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.05.070 · Cited by 40

Circulating Levels of Betatrophin and Irisin Are Not Associated with Pancreaticβ-Cell Function in Previously Diagnosed Type 2 Diabetes Mellitus Patients

Wang, L., Song, J., Wang, C., Lin, P., Liang, K., Sun, Y. S., He, T., Li, W., Zhao, R., Qin, J., et al. (2015) · Journal of Diabetes Research · doi:10.1155/2016/2616539 · Cited by 39

Muscle-derived factors influencing bone metabolism

Gries, K. J., Zysik, V. S., Jobe, T. K., Griffin, N., Leeds, B. P., & Lowery, J. W. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.10.009 · Cited by 39

Myostatin induces mitochondrial metabolic alteration and typical apoptosis in cancer cells

Liu, Y., Cheng, H., Zhou, Y., Zhu, Y., Bian, R., Chen, Y., Li, C., Ma, Q., Zheng, Q., Zhang, Y., et al. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.31 · Cited by 38

Myostatin Knockout Affects Mitochondrial Function by Inhibiting the AMPK/SIRT1/PGC1α Pathway in Skeletal Muscle

Gu, M., Wei, Z., Wang, X., Gao, Y., Wang, D., Liu, X., Bai, C., Su, G., Yang, L., & Li, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232213703 · Cited by 38

The effect of myostatin on proliferation and lipid accumulation in 3T3-L1 preadipocytes

Zhu, H. J., Pan, H., Zhang, X. Z., Li, N., Wang, L. J., Yang, H. B., & Gong, F. (2015) · Journal of Molecular Endocrinology · doi:10.1530/jme-15-0038 · Cited by 37

The Effects of PPAR Stimulation on Cardiac Metabolic Pathways in Barth Syndrome Mice

Schafer, C., Moore, V., Dasgupta, N., Javadov, S. A., James, J. F., Glukhov, A. I., Strauss, A. W., & Khuchua, Z. A. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00318 · Cited by 37

Rheumatoid cachexia: the underappreciated role of myoblast, macrophage and fibroblast interplay in the skeletal muscle niche

Ollewagen, T., Myburgh, K. H., van de Vyver, M., & Smith, C. (2021) · Journal of Biomedical Science · doi:10.1186/s12929-021-00714-w · Cited by 37

Meteorin-Like Protein (Metrnl) in Obesity, during Weight Loss and in Adipocyte Differentiation

Schmid, A., Karrasch, T., & Schäffler, A. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10194338 · Cited by 36

Signaling metabolite β-aminoisobutyric acid as a metabolic regulator, biomarker, and potential exercise pill

Yi, X., Yang, Y., Li, T., Li, M., Yao, T., Hu, G., Wan, G., & Chang, B. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1192458 · Cited by 36

Meteorin-Like Ameliorates β Cell Function by Inhibiting β Cell Apoptosis of and Promoting β Cell Proliferation via Activating the WNT/β-Catenin Pathway

Hu, W., Wang, R., & Sun, B. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.627147 · Cited by 35

Who would have thought—Myokines two decades on

Febbraio, M. A., & Pedersen, B. K. (2020) · Nature Reviews Endocrinology · doi:10.1038/s41574-020-00408-7 · Cited by 34 · cited 1×

Contribution of Liver and Pancreatic Islet Crosstalk to β-Cell Function/Dysfunction in the Presence of Fatty Liver

López-Bermudo, L., Luque‐Sierra, A., Maya‐Miles, D., Gallego‐Durán, R., Ampuero, J., Romero‐Gómez, M., Berná, G., & Martı́n, F. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.892672 · Cited by 34

Reduction of SPARC protects mice against NLRP3 inflammasome activation and obesity

Ryu, S., Spadaro, O., Sidorov, S., Lee, A. H., Caprio, S., Morrison, C. D., Smith, S. R., Ravussin, É., Shchukina, I., Artyomov, M. N., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci169173 · Cited by 34

Inhibition of autocrine secretion of myostatin enhances terminal differentiation in human rhabdomyosarcoma cells

Ricaud, S., Vernus, B., Duclos, M. J. M. J., Bernardi, H., Ritvos, O., Carnac, G., & Bonnieu, A. (2003) · Oncogene · doi:10.1038/sj.onc.1207177 · Cited by 33

Suppressing lipolysis increases interleukin-6 at rest and during prolonged moderate-intensity exercise in humans

Holmes, A. G., Watt, M. J., & Febbraio, M. A. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00195.2004 · Cited by 32

Leucine alters hepatic glucose/lipid homeostasis via the myostatin-AMP-activated protein kinase pathway - potential implications for nonalcoholic fatty liver disease

Zarfeshani, A., Ngo, S., & Sheppard, A. M. (2014) · Clinical Epigenetics · doi:10.1186/1868-7083-6-27 · Cited by 32

SPARC inhibition accelerates NAFLD‐associated hepatocellular carcinoma development by dysregulating hepatic lipid metabolism

Onorato, A. M., Fiore, E. J., Bayo, J., Casali, C. I., Fernández-Tome, M., Rodríguez, M. M., Domínguez, L. M., Argemí, J., Hidalgo, F., Favre, C., et al. (2021) · Liver International · doi:10.1111/liv.14857 · Cited by 32

Mss51 deletion enhances muscle metabolism and glucose homeostasis in mice

Gonzalez, Y. I. R., Moyer, A. L., LeTexier, N. J., Bratti, A. D., Feng, S., Sun, C., Liu, T., Mula, J., Jha, P., Iyer, S. R., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.122247 · Cited by 31

Growth hormone replacement therapy regulates microRNA-29a and targets involved in insulin resistance

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The emerging plasma biomarker Dickkopf-3 (DKK3) and its association with renal and cardiovascular disease in the general population

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Susquehanna Chorale Spring Concert "Roots and Wings"

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