Nampt/PBEF/Visfatin Regulates Insulin Secretion in β Cells as a Systemic NAD Biosynthetic Enzyme

Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase

Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510

Cloning and Characterization of the cDNA Encoding a Novel Human pre-B-Cell Colony-enhancing Factor

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The NAD Biosynthesis Pathway Mediated by Nicotinamide Phosphoribosyltransferase Regulates Sir2 Activity in Mammalian Cells

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NAD+ metabolism in health and disease

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Visfatin, an Adipocytokine with Proinflammatory and Immunomodulating Properties

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Plasma Visfatin Concentrations and Fat Depot–Specific mRNA Expression in Humans

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A phylogenetically conserved NAD + -dependent protein deacetylase activity in the Sir2 protein family

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Elevated Plasma Level of Visfatin/Pre-B Cell Colony-Enhancing Factor in Patients with Type 2 Diabetes Mellitus

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Increased dosage of mammalian Sir2 in pancreatic β cells enhances glucose-stimulated insulin secretion in mice

Moynihan, K. A., Grimm, A. A., Plueger, M. M., Bernal‐Mizrachi, E., Ford, E. L., CRAS-MÉNEUR, C. M. H., Permutt, M. A., & Imai, S. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.07.001 · Cited by 638

Mechanisms of the NAD+ salvage pathway in enhancing skeletal muscle function

Su, M., Qiu, F., Li, Y., Che, T., Li, N., & Zhang, S. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1464815 · Cited by 27

Association of circulating levels of nicotinamide phosphoribosyltransferase (NAMPT/Visfatin) and of a frequent polymorphism in the promoter of the NAMPT gene with coronary artery disease in diabetic and non-diabetic subjects

Saddi-Rosa, P., Oliveira, C. S. V., Crispim, F., Giuffrida, F. M. A., de Lima, V. C., Vieira, J. G. H., Doria, A., Velho, G., & Reis, A. F. (2013) · Cardiovascular Diabetology · doi:10.1186/1475-2840-12-119 · Cited by 24

Combined SIRT3 and SIRT5 deletion is associated with inner retinal dysfunction in a mouse model of type 1 diabetes

Lin, J. B., Lin, J. B., Chen, H. C., Chen, T. H.-T., & Apte, R. S. (2019) · Scientific Reports · doi:10.1038/s41598-019-40177-6 · Cited by 24

Nicotinamide mononucleotide restores oxidative stress‐related apoptosis of oocyte exposed to benzyl butyl phthalate in mice

Jiang, Y., Wang, D., Zhang, C., Jiao, Y., Pu, Y., Cheng, R., Li, C., & Chen, Y. (2023) · Cell Proliferation · doi:10.1111/cpr.13419 · Cited by 24

The relationship between visfatin and metabolic syndrome in postmenopausal women

Kim, J., Kim, S.-H., Im, J., & Lee, D. (2010) · Maturitas · doi:10.1016/j.maturitas.2010.05.002 · Cited by 24

Dynamics of Nampt/visfatin and high molecular weight adiponectin in response to oral glucose load in obese and lean women

Ünlütürk, U., Harmancı, A., Yıldız, B. O., & Bayraktar, M. (2009) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2009.03674.x · Cited by 23

Impact of Metabolic Regulators on the Expression of the Obesity Associated Genes FTO and NAMPT in Human Preadipocytes and Adipocytes

Friebe, D., Löffler, D., Schönberg, M., Bernhard, F., Buttner, P. G., Landgraf, K., Kieß, W., & Körner, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019526 · Cited by 24

NAMPT knockdown attenuates atherosclerosis and promotes reverse cholesterol transport in ApoE KO mice with high-fat-induced insulin resistance

Li, S., Wang, C., Li, K., Li, L., Tian, M., Xie, J., Yang, M., Jia, Y., He, J., Gao, L., et al. (2016) · Scientific Reports · doi:10.1038/srep26746 · Cited by 24

NAMPT-Mediated NAD Biosynthesis as the Internal Timing Mechanism: In NAD+ World, Time Is Running in Its Own Way

Poljšak, B. (2017) · Rejuvenation Research · doi:10.1089/rej.2017.1975 · Cited by 24

A Neutrophil Proteomic Signature in Surgical Trauma Wounds

Bekeschus, S., Lackmann, J., Gümbel, D., Napp, M., Schmidt, A., & Wende, K. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19030761 · Cited by 25

Multiple sub-microscopic genomic lesions are a universal feature of chronic myeloid leukaemia at diagnosis

Khorashad, J. S., Melo, V., Fiegler, H., Gerrard, G., Marin, D., Apperley, J. F., Goldman, J. M., Foroni, L., & Reid, A. G. (2008) · Leukemia · doi:10.1038/leu.2008.210 · Cited by 24

Active visfatin is elevated in serum of maintenance haemodialysis patients and correlates inversely with circulating HDL cholesterol

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Nicotinamide Mononucleotide Supplementation: Understanding Metabolic Variability and Clinical Implications

Benjamin, C., & Crews, R. (2024) · Metabolites · doi:10.3390/metabo14060341 · Cited by 25

Age-Dependent Changes of Adipokine and Cytokine Secretion From Rat Adipose Tissue by Endogenous and Exogenous Toll-Like Receptor Agonists

Peek, V., Neumann, E., Inoue, T., Koenig, S., Pflieger, F. J., Gerstberger, R., Roth, J., Matsumura, K., & Rummel, C. D. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01800 · Cited by 22

Nicotinamide Protects Against Diet‐Induced Body Weight Gain, Increases Energy Expenditure, and Induces White Adipose Tissue Beiging

Méndez‐Lara, K. A., Rodríguez‐Millán, E., Sebastián, D., Blanco‐Soto, R., Camacho, M., Nan, M. N., Diarte‐Añazco, E. M. G., Mato, E., Lope‐Piedrafita, S., Roglans, N., et al. (2021) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202100111 · Cited by 26

Safety and efficacy of long-term nicotinamide mononucleotide supplementation on metabolism, sleep, and nicotinamide adenine dinucleotide biosynthesis in healthy, middle-aged Japanese men

Yamaguchi, S., Irie, J., Mitsuishi, M., Uchino, Y., Nakaya, H., Takemura, R., Inagaki, E., Kosugi, S., Okano, H., Yasui, M., et al. (2024) · Endocrine Journal · doi:10.1507/endocrj.ej23-0431 · Cited by 25

Complex role of nicotinamide adenine dinucleotide in the regulation of programmed cell death pathways

Preyat, N., & Léo, O. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.08.110 · Cited by 23

Nampt/visfatin/PBEF affects expression of myogenic regulatory factors and is regulated by interleukin-6 in chicken skeletal muscle cells

Krzysik-Walker, S. M., Hadley, J. A., Pesall, J. E., McFarland, D. C., VASILATOS-YOUNKEN, R., & Ramachandran, R. (2011) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2011.04.007 · Cited by 23

Metabolic Syndrome in Pediatrics

Kursawe, R., & Santoro, N. (2014) · Advances in clinical chemistry · doi:10.1016/b978-0-12-800141-7.00004-8 · Cited by 23

Nicotinamide phosphoribosyltransferase production in human spermatozoa is influenced by maturation stage

Riammer, S., Garten, A., Schaab, M., Grunewald, S., Kiess, W., Kratzsch, J., & Paasch, U. (2016) · Andrology · doi:10.1111/andr.12252 · Cited by 20

The Role of Adipokines between Genders in the Pathogenesis of Osteoarthritis

Economou, A., Mallia, I., Fioravanti, A., Gentileschi, S., Nacci, F., Bellando-Randone, S., Lepri, G., & Guiducci, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910865 · Cited by 26

Deciphering endocrine function of adipose tissue and its significant influences in obesity-related diseases caused by its dysfunction

Duan, F., Wu, J., Chang, J., Peng, H., Liu, Z., Liu, P., Han, X., Sun, T., Shang, D., Yang, Y., et al. (2024) · Differentiation · doi:10.1016/j.diff.2024.100832 · Cited by 27

Extracellular nicotinamide phosphoribosyltransferase (eNAMPT) neutralization counteracts T cell immune evasion in breast cancer

Travelli, C., Colombo, G., Aliotta, M., Fagiani, F., Fava, N., Sanctis, R. D., Grolla, A. A., Garcia, J. G. N., Clemente, N., Portararo, P., et al. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2023-007010 · Cited by 22

Mitochondrial aldehyde dehydrogenase-2 coordinates the hydrogen sulfide - AMPK axis to attenuate high glucose-induced pancreatic β-cell dysfunction by glutathione antioxidant system

Karunakaran, U., Elumalai, S., Chung, S. M., Maedler, K., Won, K. C., & Moon, J. S. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102994 · Cited by 22

Upregulation of thromboxane synthase mediates visfatin-induced interleukin-8 expression and angiogenic activity in endothelial cells

Kim, S.-R., Jung, Y., Park, H.-J., Kim, M.-K., Jeong, J., Jang, H., Yun, I., Bae, S., & Bae, M. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.072 · Cited by 22

The Value of Visfatin in the Prediction of Metabolic Syndrome: A Multi-Factorial Analysis

Esteghamati, A., Morteza, A., Zandieh, A., Jafari, S., Rezaee, M., Nakhjavani, M., Jamali, A., Esteghamati, A.-R., & Khalilzadeh, O. (2012) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-012-9373-8 · Cited by 22

Involvement of visfatin in palmitate-induced upregulation of inflammatory cytokines in hepatocytes

Choi, Y. J., Choi, S., Ha, E. S., KANG, Y. Y., Han, S. J., Kim, D. J., Lee, K. W., & Kim, H. J. (2011) · Metabolism · doi:10.1016/j.metabol.2011.05.003 · Cited by 22

Identification of potent triazolylpyridine nicotinamide phosphoribosyltransferase (NAMPT) inhibitors bearing a 1,2,3-triazole tail group

Travelli, C., Aprile, S., Mattoteia, D., Colombo, G., Clemente, N., Scanziani, E., Terrazzino, S., Alisi, M. A., Polenzani, L., Grosa, G., et al. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.111576 · Cited by 22

Nicotinamide Phosphoribosyltransferase (Nampt)/Nicotinamide Adenine Dinucleotide (NAD) Axis Suppresses Atrial Fibrillation by Modulating the Calcium Handling Pathway

Feng, D., Xu, D., Murakoshi, N., Tajiri, K., Qin, R., Yonebayashi, S., Okabe, Y., Li, S., Yuan, Z., Aonuma, K., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134655 · Cited by 22

Reproductive roles of novel adipokines apelin, visfatin, and irisin in farm animals

Shokrollahi, B., Shang, J., Saadati, N., Ahmad, H. I., & Yang, C. (2021) · Theriogenology · doi:10.1016/j.theriogenology.2021.06.011 · Cited by 22

Dynamic Aging: Channeled Through Microenvironment

Tan, Q., Liang, N., Zhang, X., & Li, J. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.702276 · Cited by 25

Melatonin inhibits visfatin‐induced inducible nitric oxide synthase expression and nitric oxide production in macrophages

Kang, Y., Kang, Y., Park, H., Wee, H., Jang, H., Bae, M., & Bae, S. (2013) · Journal of Pineal Research · doi:10.1111/jpi.12072 · Cited by 21

Circulating and local visfatin/Nampt/PBEF levels in spontaneously hypertensive rats, stroke-prone spontaneously hypertensive rats and Wistar-Kyoto rats

Wang, P., Du, H., Zhang, R.-Y., Guan, Y., Xu, T., Xu, Q., Su, D., & Miao, C. (2010) · The Journal of Physiological Sciences · doi:10.1007/s12576-010-0103-1 · Cited by 21

NAMPT -3186C/T polymorphism affects repaglinide response in Chinese patients with Type 2 diabetes mellitus

Sheng, F., Dai, X., Qu, J., Lei, G., Lu, H.-B., Wu, J., Xu, X., Pei, Q., Dong, M., Liu, Y., et al. (2011) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2011.05548.x · Cited by 21

The adipokine visfatin induces tissue factor expression in human coronary artery endothelial cells

Cirillo, P. L., Palma, V. D., Maresca, F., Pacifico, F., Ziviello, F., Bevilacqua, M., Trimarco, B., Leonardi, A., & Massimo Chiariello, A. (2012) · Thrombosis Research · doi:10.1016/j.thromres.2012.06.007 · Cited by 21

Récentes adipokines : un lien entre l’obésité et l’athérosclérose

Gauvreau, D., Villeneuve, N., Deshaies, Y., & Cianflone, K. (2011) · Annales d Endocrinologie · doi:10.1016/j.ando.2010.02.025 · Cited by 20

Effect of curcumin on visfatin and zinc-α2-glycoprotein in a rat model of non-alcoholic fatty liver disease

Li, C., Li, J., Chen, Y., Zhong, X., & Kang, M. (2016) · Acta Cirúrgica Brasileira · doi:10.1590/s0102-865020160110000001 · Cited by 21

Adipokine update – neue Moleküle, neue Funktionen

Gelsinger, C., Tschoner, A., Kaser, S., & Ebenbichler, C. F. (2010) · Wiener Medizinische Wochenschrift · doi:10.1007/s10354-010-0781-6 · Cited by 21

The NAMPT enzyme employs a switch that directly senses AMP/ATP and regulates cellular responses to energy stress

Zu, Y., Wu, C., Li, F., Yao, H., Xia, Y., Zhang, R., Li, L., Chen, S., Shi, Q., Xi, S., et al. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.05.022 · Cited by 24

The effects of NAMPT haplotypes and metabolic risk factors on circulating visfatin/NAMPT levels in childhood obesity

Belo, V. D. A., Luizon, M. R., Lacchini, R., de Miranda, J. A., Lanna, C. M. M., Souza-Costa, D. C., & Tanus-Santos, J. E. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.173 · Cited by 20

From Rate-Limiting Enzyme to Therapeutic Target: The Promise of NAMPT in Neurodegenerative Diseases

Zhu, Y., Xu, P., Huang, X., Wen, S., Liu, L., Zhang, S., Zhao, R., Hu, X., & Wang, G. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.920113 · Cited by 21

Impact of circadian clock dysfunction on human health

Samanta, S., & Ali, S. A. (2022) · Exploration of neuroscience · doi:10.37349/en.2022.00002 · Cited by 21

Preclinical Characterization of Pharmacologic NAD + Boosting as a Promising Therapeutic Approach in Rheumatoid Arthritis

Pérez‐Sánchez, C., Escudero‐Contreras, A., Cerdó, T., Sánchez‐Mendoza, L. M., Llamas-Urbano, A., de la Rosa, I. A., Pérez-Rodríguez, M., Muñoz-Barrera, L., Ábalos‐Aguilera, M. C., Barbarroja, N., et al. (2023) · Arthritis & Rheumatology · doi:10.1002/art.42528 · Cited by 20

Nicotinamide mononucleotide (NMN) intake increases plasma NMN and insulin levels in healthy subjects

Yamane, T., Imai, M., Bamba, T., & Uchiyama, S. (2023) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2023.04.031 · Cited by 20

Alternative pathway of bile acid biosynthesis contributes to ameliorate NASH after induction of NAMPT/NAD+/SIRT1 axis

Yang, N., Sun, R., Zhang, X., Wang, J., Wang, L., Zhu, H., Yuan, M., Xu, Y., Ge, C., He, J. B., et al. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114987 · Cited by 20

Genetic variant in visfatin gene promoter is associated with decreased risk of coronary artery disease in a Chinese population

Yan, J.-J., Tang, N., Tang, J.-J., Jia, E., Wang, M., Wang, Q., Zhu, J., Yang, Z., Wang, L., & Huang, J. (2009) · Clinica Chimica Acta · doi:10.1016/j.cca.2009.09.033 · Cited by 20

Plasma visfatin/nicotinamide phosphoribosyltransferase levels in hypertensive elderly – results from the PolSenior substudy

Kocełak, P., Olszanecka‐Glinianowicz, M., Owczarek, A. J., Bożentowicz‐Wikarek, M., Brzozowska, A., Mossakowska, M., Zdrojewski, T. R., Grodzicki, T. K., Więcek, A., & Chudek, J. T. (2014) · Journal of the American Society of Hypertension · doi:10.1016/j.jash.2014.11.002 · Cited by 20

Characterization of chicken visfatin gene: cDNA cloning, tissue distribution, and promoter analysis

Li, J., Meng, F., Song, C., Wang, Y., & Leung, F. C.-C. (2012) · Poultry Science · doi:10.3382/ps.2012-02315 · Cited by 20

The Regulation of the Male Hypothalamic-Pituitary-Gonadal Axis and Testosterone Production by Adipokines

Shpakov, A. O., Ryzhov, J. R., Bakhtyukov, A. A., & Derkach, K. V. (2018) · IntechOpen eBooks · doi:10.5772/intechopen.76321 · Cited by 20

Semaphorin 3 C is a Novel Adipokine Representing Exercise-Induced Improvements of Metabolism in Metabolically Healthy Obese Young Males

Nam, J. S., Ahn, C. W., Park, H. J., & Kim, Y. S. (2020) · Scientific Reports · doi:10.1038/s41598-020-67004-7 · Cited by 20

Tripeptide IRW Upregulates NAMPT Protein Levels in Cells and Obese C57BL/6J Mice

Bhullar, K. S., Son, M., Kerek, E. M., Cromwell, C. R., Wingert, B. M., Wu, K., Jovel, J., Camacho, C. J., Hubbard, B. P., & Wu, J. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c07831 · Cited by 18

Nicotinamide mononucleotide improves spermatogenic function in streptozotocin-induced diabetic mice via modulating the glycolysis pathway

Ma, D., Hu, L., Wang, J., Luo, M., Liang, A., Lei, X., Liao, B., Li, M., Ming, X., Li, H., et al. (2022) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2022099 · Cited by 19

Lipid Profiles and Serum Visfatin Concentrations in Patients with Type II Diabetes in Comparison with Healthy Controls.

Hajianfar, H., Bahonar, A., Entezari, M. H., Askari, G., & Yazdani, M. (2012) · Europe PMC (PubMed Central) · Cited by 19

Circulating visfatin levels in healthy preterm infants are independently associated with high-density lipoprotein cholesterol levels and dietary long-chain polyunsaturated fatty acids

Siahanidou, T., Margeli, A., Kappis, A., Papassotiriou, I., & Mandyla, H. (2010) · Metabolism · doi:10.1016/j.metabol.2010.03.002 · Cited by 19

Inhibition of pre-B cell colony-enhancing factor (PBEF/NAMPT/visfatin) decreases the ability of human neutrophils to generate reactive oxidants but does not impair bacterial killing

Roberts, K. J., Cross, A. L., Vasieva, O., Moots, R. J., & Edwards, S. W. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.1012527 · Cited by 19

Quantitation of NAD+: Why do we need to measure it?

Liu, Y., Clement, J., Grant, R., Sachdev, P. S., & Braidy, N. (2018) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2018.07.023 · Cited by 21

Intestinal Epithelial NAD+ Biosynthesis Regulates GLP-1 Production and Postprandial Glucose Metabolism in Mice

Nagahisa, T., Yamaguchi, S., Kosugi, S., Homma, K., Miyashita, K., Irie, J., Yoshino, J., & Itoh, H. (2022) · Endocrinology · doi:10.1210/endocr/bqac023 · Cited by 19

PBEF/NAMPT/Visfatin: A Promising Drug Target For Treating Rheumatoid Arthritis?

Nowell, M. A., Evans, L., & Williams, A. S. (2012) · Future Medicinal Chemistry · doi:10.4155/fmc.12.34 · Cited by 19

Alterations in adipocyte glucose transporter GLUT4 and circulating adiponectin and visfatin in rat adjuvant induced arthritis

Jur̀čovičová, J., Štofková, A., Škurlová, M., Baculíková, M., Zórad, Š., & Stančíková, M. (2010) · General Physiology and Biophysics · doi:10.4149/gpb_2010_01_79 · Cited by 19

Visfatin and ghrelin: can they be forthcoming biomarkers or new drug targets for asthma?

Toru, Ü., Ayada, C., Genç, O., Şahın, S., Arık, Ö., Acat, M., Bulut, İ., & Çetınkaya, E. (2015) · PubMed Central · Cited by 19

Chronic Administration of Visfatin Ameliorated Diabetic Nephropathy in Type 2 Diabetic Mice

Kang, Y. S., Lee, M., Song, H. K., Kim, J. E., Ghee, J. Y., Cha, J. J., Lee, J. E., Kim, H. W., Han, J., & Cha, D. R. (2016) · Kidney & Blood Pressure Research · doi:10.1159/000443433 · Cited by 19

Ketogenesis and SIRT1 as a tool in managing obesity

Abduraman, M. A., Azizan, N. A., Teoh, S. H., & Tan, M. (2020) · Obesity Research & Clinical Practice · doi:10.1016/j.orcp.2020.12.001 · Cited by 19

Safety Evaluation for Restorin® NMN, a NAD+ Precursor

Turner, J. R., Licollari, A., Mihalcea, E., & Tan, A. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.749727 · Cited by 19

Quantification of localized NAD+ changes reveals unique specificity of NAD+ regulation in the hypothalamus

Johnson, S., Yoshioka, K., Brace, C. S., & Imai, S. (2023) · npj Aging · doi:10.1038/s41514-023-00098-1 · Cited by 18

Technology and functional insights into the nicotinamide mononucleotide for human health

Liu, Y., Gong, J., Marshall, G., Su, C., Shi, J., & Xu, Z. (2023) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-023-12612-2 · Cited by 18

The cytokine trio - visfatin, placental growth factor and fractalkine – and their role in myocardial infarction with non-obstructive coronary arteries (MINOCA)

Stangret, A., Dykacz, W., Jabłoński, K., Wesolowska, A. M., Klimczak‐Tomaniak, D., Kochman, J., & Tomaniak, M. (2023) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2023.08.009 · Cited by 18

Secretion of One Adipokine Nampt/Visfatin Suppresses the Inflammatory Stress‐Induced NF‐κB Activity and Affects Nampt‐Dependent Cell Viability in Huh‐7 Cells

Lin, Y.-C., Wu, H.-C., Liao, C.-C., Chou, Y.-C., Pan, S.-F., & Chiu, C.-M. (2015) · Mediators of Inflammation · doi:10.1155/2015/392471 · Cited by 18

Assessment of serum visfatin levels in girls with anorexia nervosa

Ziora, K. T., Oświęcimska, J. M., Świętochowska, E., Ziora, D. I., Stojewska, M., Suwała, A., Ostrowska, Z., Gorczyca, P. W., Klimacka‐Nawrot, E., Lukas, W., et al. (2011) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2011.04181.x · Cited by 18

Omentin-1 and NAMPT serum concentrations are higher and CK-18 levels are lower in children and adolescents with type 1 diabetes when compared to healthy age, sex and BMI matched controls

Nurten, E., Vogel, M., Kapellen, T. M., Richter, S., Garten, A., Penke, M., Schuster, S., Körner, A., Kieß, W., & Kratzsch, J. (2018) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem-2018-0353 · Cited by 18

Obesity and Cardiovascular Risk: Variations in Visfatin Gene Can Modify the Obesity Associated Cardiovascular Risk. Results from the Segovia Population Based-Study. Spain

Larrad, M. T. M., Anchuelo, A. C., Fernández, C., Barba, M. P., Redondo, Y. L., Serrano‐Ríos, M., & Segovia Insulin Resistance Study Group (SIRSG) (2016) · PLoS ONE · doi:10.1371/journal.pone.0153976 · Cited by 18

Nicotinamide mononucleotide ameliorates adriamycin-induced renal damage by epigenetically suppressing the NMN/NAD consumers mediated by Twist2

Hasegawa, K., Sakamaki, Y., Tamaki, M., & Wakino, S. (2022) · Scientific Reports · doi:10.1038/s41598-022-18147-2 · Cited by 17

Endogenous NAMPT dampens chemokine expression and apoptotic responses in stressed tubular cells

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Integrated Analysis of Crucial Genes and miRNAs Associated with Osteoporotic Fracture of Type 2 Diabetes

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Visfatin is associated with lipid metabolic abnormalities in Lyon hypertensive rats

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Expression and Regulation of Nampt in Human Islets

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