Research Resource: Comprehensive Expression Atlas of the Fibroblast Growth Factor System in Adult Mouse

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837

FGF-21 as a novel metabolic regulator

Kharitonenkov, A., Shiyanova, T. L., Koester, A., Ford, A. M., Micanovic, R., Galbreath, E. J., Sandusky, G. E., Hammond, L. J., Moyers, J. S., Owens, R. A., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23606 · Cited by 2,125

Suppression of Aging in Mice by the Hormone Klotho

Kurosu, H., Yamamoto, M., Clark, J. D., Pastor, J. V., Nandi, A., Gurnani, P., McGuinness, O. P., Chikuda, H., Yamaguchi, M., Kawaguchi, H., et al. (2005) · Science · doi:10.1126/science.1112766 · Cited by 1,935

Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis

Inagaki, T., Choi, M., Moschetta, A., Peng, L., Cummins, C. L., McDonald, J. G., Luo, G., Jones, S. A., Goodwin, B., Richardson, J. A., et al. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.09.001 · Cited by 1,865

Klotho converts canonical FGF receptor into a specific receptor for FGF23

Urakawa, I., Yamazaki, Y., Shimada, T., Iijima, K., Hasegawa, H., Okawa, K., Fujita, T., Fukumoto, S., & Yamashita, T. (2006) · Nature · doi:10.1038/nature05315 · Cited by 1,865

Endocrine Regulation of the Fasting Response by PPARα-Mediated Induction of Fibroblast Growth Factor 21

Inagaki, T., Dutchak, P., Zhao, G., Ding, X., Gautron, L., Parameswara, V., Li, Y., Goetz, R., Mohammadi, M., Esser, V., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.05.003 · Cited by 1,504

Targeted ablation of Fgf23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism.

Shimada, T., Kakitani, M., Yamazaki, Y., Hasegawa, H., Takeuchi, Y., Fujita, T., Fukumoto, S., Tomizuka, K., & Yamashita, T. (2004) · Journal of Clinical Investigation · doi:10.1172/jci19081 · Cited by 1,503

Hepatic Fibroblast Growth Factor 21 Is Regulated by PPARα and Is a Key Mediator of Hepatic Lipid Metabolism in Ketotic States

Badman, M. K., Pissios, P., Kennedy, A. R., Koukos, G., Flier, J. S., & Maratos-Flier, E. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.05.002 · Cited by 1,495

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

Shimada, T., Mizutani, S., Muto, T., Yoneya, T., Hino, R., Takeda, S., Takeuchi, Y., Fujita, T., Fukumoto, S., & Yamashita, T. (2001) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.101545198 · Cited by 1,391

Regulation of Fibroblast Growth Factor-23 Signaling by Klotho

Kurosu, H., Ogawa, Y., Miyoshi, M., Yamamoto, M., Nandi, A., Rosenblatt, K. P., Baum, M. G., Schiavi, S. C., Hu, M. C., Moe, O. W., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.c500457200 · Cited by 1,381

Machine Learning-Based Prediction Model for Predicting the Effect of the Serum γKlotho Level on Susceptibility to Coronary Heart Disease

Guo, Z.-T., Yu, X., Cheng, H., & Naman, T. (2025) · Vascular Health and Risk Management · doi:10.2147/vhrm.s508351 · Cited by 1

Transcriptomic profiling and biomarker discovery in pre-eclampsia: An integrated approach leveraging WGCNA and LASSO with ROC validation

Palanisamy, T. B., & Arumugam, M. (2025) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2025.108546 · Cited by 1

Joint Transcriptomic Analysis of the Effect of Iron Concentration on Piglet Liver and Functional Validation of Iron Regulatory Genes

Qian, H., Wang, P., Li, Y., Zhang, C., Li, J., Wang, Q., Ren, H., Jin, F., Huang, J., Yao, J., et al. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47100843 · Cited by 1

GCGR agonism requires GABAergic signaling in the medial basal hypothalamus to promote weight loss in obese mice

Elmendorf, A. J., Furber, E. C., Lorentz, B., Mahler, C. A., Droz, B. A., Cosgrove, R., Poret, J. M., Knerr, P. J., Samms, R. J., & Flak, J. N. (2026) · Molecular Metabolism · doi:10.1016/j.molmet.2026.102328 · Cited by 1

Metformin increases glycolysis and the stress-induced cytokine GDF15 but not FGF21 in humans

Kolnes, K. J., Møller, P. M., Kruse, R., Christensen, M. H., Kjøbsted, R., Hey-Mogensen, M., Andersen, B., Handberg, A., & Højlund, K. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1797525 · Cited by 2

Site-specific bidirectional regulation of Fgf15 transcription in the mouse ileum

Katafuchi, T., Honda, A., & Makishima, M. (2026) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00026.2026 · Cited by 1

AAV-mediated FGF21 gene therapy promotes health span extension by whole-body tissue-specific adaptations

Jiménez, V., Sacristan, V., García, M., Jambrina, C., Casana, E., MUÑOZ, S. A., Vilà, L., Grass, I., Jaén, M. L., Roca, C., et al. (2026) · Molecular Therapy · doi:10.1016/j.ymthe.2026.05.025 · Cited by 2

Circulating fibroblast growth factor-21 in coronary artery disease: a systematic review and meta-analysis

Shawa, F., Izzeddin, F., & Koç, G. (2026) · Irish Journal of Medical Science (1971 -) · doi:10.1007/s11845-026-04472-2 · Cited by 1

Evaluate the Prognostic Value of serumγKlotho on Long‐Term Prognosis of Patients With Multivessel Coronary Artery Disease and Establish a Prognostic Model

Naman, T., Zhang, Y., Maihemuti, A., Cheng, H., Fu, W., Yu, X., Wang, Z., Yang, Y., & Guo, Z. (2026) · Clinical Cardiology · doi:10.1002/clc.70393 · Cited by 1

Comparison of Swarm Optimization and Genetic Algorithm for Mobile Robot Navigation

Ćurković, P., Jerbić, B., & Stipanĉić, T. (2010) · InTech eBooks · doi:10.5772/8601 · Cited by 1

Role of Perivascular and Visceral Adipose Tissues in Murine Models of Obesity and Atherosclerosis: A Dissertation

Fitzgibbons, T. P. (2012) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/jx6z-xx69 · Cited by 2

The KL genetic polymorphisms Associated with type 2 diabetes Mellitus

Jin, H., & Jung, D. (2022) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-022-01057-5 · Cited by 1

[Research Progress of Klotho in Lung Neoplasms].

Wang, J., Zeng, L., Kong, L., Zhang, L., Chen, J., Zhong, D., & Fan, Y. (2023) · PubMed Central · doi:10.3779/j.issn.1009-3419.2023.101.19 · Cited by 1

Growth factors reviews

Li, X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15793-6.00001-9 · Cited by 1

Low Serum Fibroblast Growth Factor 21 Level and Its Altered Regulation by Thyroid Hormones in Patients with Hashimoto’s Thyroiditis on Levothyroxine Substitution

Berta, E., Halmi, S., Molnár, I., Hutkai, D., Csiha, S., Bhattoa, H. P., Lőrincz, H., Somodi, S., Katkó, M., Harangi, M., et al. (2024) · Metabolites · doi:10.3390/metabo14100565 · Cited by 1

Fibroblast growth factor signaling and spermatogonial stem cell self-renewal.

Yang, M., Whelan, E. C., Zeng, Y., Wei, X., Shi, L., & Yang, F. (2025) · Molecular human reproduction · doi:10.1093/molehr/gaaf039 · Cited by 1

FGF21 Conducts a Metabolic Orchestra and Fat Is a Key Player

Whittle, A. J. (2016) · Endocrinology · doi:10.1210/en.2016-1193 · Cited by 1

Investigating Fibroblast Growth Factor 19 expression in primary and secondary bile acid diarrhoea

Nolan, J. (2016) · doi:10.25560/41879 · Cited by 1

Therapeutic Potential of FGF21 in Alzheimer’s Disease

Sun, A., Xu, B., Wang, X., Liu, L., He, Y., Wang, Z., & Chen, Y. (2017) · Yangtze Medicine · doi:10.4236/ym.2018.21001 · Cited by 1

Brain function of the metabolic hormone fibroblast growth factor 21

Badakhshi, Y., & Jin, T. (2019) · Obesity Medicine · doi:10.1016/j.obmed.2019.100155 · Cited by 1

The Metabolic Effects of FGF21: From Physiology to Pharmacology

Song, P. (2020) · JoLS Journal of Life Sciences · doi:10.5352/jls.2020.30.7.640 · Cited by 1

Paracrine Fibroblast Growth Factor-Based Therapy: An Unexpected Panacea for Metabolic-Dysfunction-Associated Fatty Liver Disease (MAFLD)

Pan, T., Li, T., Shi, L., Su, L., & Chen, Y. (2022) · Infectious Microbes & Diseases · doi:10.1097/im9.0000000000000083 · Cited by 1

The Alpha-Klotho Gene as an Anti-ageing Biomarker: Measures and Applications to the Effects of Nutrition

Jurado‐Fasoli, L. (2022) · Biomarkers in disease · doi:10.1007/978-3-031-07389-2_33 · Cited by 1

Resistance to diet induced obesity in the apolipoprotein E deficient mouse is associated with an attenuated transcriptional response in visceral fatPreprint

Fitzgibbons, T. P., Kelly, M., Kim, J. K., & Czech, M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/494195 · Cited by 1

The Effect of Intracerebroventricular Fibroblast Growth Factor 23 on gene expression in the Rats’ HypothalamusPreprint

Ursem, S. R., Diepenbroek, C., Kool, T., Eggels, L., Heijboer, A. C., & la Fleur, S. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.18.516150 · Cited by 1

Impact of Bmal1 rescue and time-restricted feeding on liver and muscle proteomes during the active phase in micePreprint

Smith, J. G., Molendijk, J., Blazev, R., Chen, W. H., Zhang, Q., Litwin, C., Greco, C. M., Sassone‐Corsi, P., Muñoz‐Cánoves, P., Parker, B. L., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.12.544652 · Cited by 1

Fibroblast growth factor-21 induces skeletal muscle atrophy and increases plasma amino acids in female mice: a potential role for glucocorticoidsPreprint

Larson, K. R., Jayakrishnan, D., Sauza, K. A. S., Goodson, M. L., CHAFFIN, A. T. B., Davidyan, A., Pathak, S. J., Fang, Y., Magaña, D. G., Miller, B. F., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.27.546599 · Cited by 1

Mediators and markers of mammalian lifespan extension: Proteomic, proliferative and hormonal adaptations in mouse models of extended lifespan

Thompson, A. C. S. (2014) · ProQuest Demo Repository

Prox1 and fibroblast growth factor receptors form a novel regulatory loop that promotes lens fiber differentiation and regulates global gene expression

Audette, D. S. (2024) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/zr28-qz49

Stéatose et résistance à l’insuline : implication des hépatokines

Bertrand, C., Valet, P., & Castan‐Laurell, I. (2015) · Obésité · doi:10.1007/s11690-015-0492-7

Phosphate Overload Inhibits Female Fertility in Mice

Dickson, A. S. (2012)

Potensi Terapeutik Fibroblast Growth Factor 21 terhadap Resistensi Insulin

Kurniasari, K., & Arozal, W. (2015) · eJournal Kedokteran Indonesia · doi:10.23886/ejki.3.5049

Possible role of fibroblast growth factor 21 on atherosclerosis via amelioration of endoplasmic reticulum stress-mediated

Wu, X.-M., & Feng, Q. (2015)

Harnessing the Action of Fibroblast Growth Factor21 as a Therapeutic Agent

Brunetti, L., & Kagan, L. (2017) · Current Pharmacology Reports · doi:10.1007/s40495-017-0080-7

Potent stimulation of Fibroblast Growth Factor 19 expression in the human

Zhang, J. H., Nolan, J., Kennie, S. L., Johnston, I. M., Dew, T. K., Dixon, P. H., Williamson, C., & Walters, J. R. F. (2013)

Towards Examining FGF21 Secretion from Pancreatic Islets in a Microfluidic Device

Green, B. J. (2012) · TSpace (University of Toronto)

Hormonal Responses that Regulate the Metabolic Benefits of Exercise: The Contribution of the Melanocortin System and the Fibroblast Growth Factor 21 (FGF21) Signaling Pathway

Loyd, C. (2014) · OhioLink ETD Center (Ohio Library and Information Network)

A pharmacology guided approach for setting limits on product-related impurities for bispecific antibody manufacturing

Rajan, S., Sonoda, J., Tully, T., Williams, A. J., Yang, F., Macchi, F. D., Hudson, T., Chen, M. Z., Liu, S., Valle, N., et al. (2018) · Journal of Pharmacological and Toxicological Methods · doi:10.1016/j.vascn.2018.04.002

Fibroblast Growth Factor 21 is a Novel Protein Sensor in Pregnancy

Sutton, E. F. (2017) · doi:10.31390/gradschool_dissertations.4263

Expression of the hormonal FGF co‐receptor Klotho beta in the Xenopus laevis model

Chen, G., & Tao, Q. (2018) · Cell Biology International · doi:10.1002/cbin.11059

Elucidating the functions of fibroblast growth factor 9 in multiple sclerosis

McElroy, D. (2018) · Enlighten: Theses (The University of Glasgow)

Is ursodeoxycholic acid therapy due to pregnant intrahepatic cholestasis change the adiponectin and fibroblast growth factor‐21 levels?—Pilot study

Kierach, R., Dąbrowski, K., Grabarek, B. O., Kojs‐Mrożkiewicz, M., & Boroń, D. (2020) · Dermatologic Therapy · doi:10.1111/dth.13296

Growth Factor Signaling in the Maintenance of Adult Lung Homeostasis

Araújo-Silva, H., Correia‐Pinto, J., & Moura, R. S. (2020) · Springer eBooks · doi:10.1007/978-3-030-44436-5_13

Intestinal-derived FGF15 preserves muscle and bone mass following sleeve gastrectomyPreprint

Bozadjieva-Kramer, N., Shin, J. H., Shao, Y., Gutiérrez‐Aguilar, R., Li, Z., Heppner, K. M., Chiang, S., Vargo, S. G., Granger, K., Sandoval, D. A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.02.130278

Molecular description of fibroblast growth factor and mechanisms by which fibroblast growth factor-21 mediating biological actions and acting as a biologic biomarker of cardiovascular diseases

Melaku, L. S., & Debela, N. (2020) · Indian Journal of Health Sciences and Biomedical Research (KLEU) · doi:10.4103/kleuhsj.kleuhsj_92_20

REGULATION OF LENS PHENOTYPE VIA TRANSLATIONAL REPRESSION OF RETINAL MARKERS BY LACTASE LIKE & AN INVESTIGATION OF POSTERIOR CAPSULAR OPACIFICATION

Rossi, N. M. (2020)

Mistranslation drives alterations in protein levels and the effects of a synonymous variant at the FGF21 locus

Bayoumi, A. (2020) · The Sydney eScholarship Repository (The University of Sydney)

FGF23 and heart and vascular disease

Leifheit‐Nestler, M., Richter, B., & Haffner, D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818036-5.00009-4

Fibroblast growth factor 23 and pulmonary disease

Krick, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818036-5.00014-8

Aberrant FGF15/FGFR4 Signaling Worsens Nonalcoholic Steatohepatitis Severity in FGF21KO MicePreprint

Yu, Y., Shi, X., Zheng, Q., Wang, X., Liu, X., Tan, M., Lv, G., Zhang, P., Martin, R. C. G., & Li, Y. (2021) · Research Square · doi:10.21203/rs.3.rs-146881/v1

FGF21 Response Varies by Sugar Type and is Associated with Body Weight, Dietary Added Sugar, and Neural Signaling in HumansPreprint

Yunker, A. G., Alves, J. M., LUO, S. H., ANGELO, B. C., DEFENDIS, A. W., Pickering, T. A., Jann, K., Monterosso, J. R., & Page, K. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.29.446318

Role of Fibroblast Growth Factor-23 in Coronary Slow Flow Phenomenon Pathogenesis

Oktaviandani, W., Indrajaya, T., Ghanie, A., & Sukandi, E. (2021) · Bioscientia Medicina Journal of Biomedicine and Translational Research · doi:10.32539/bsm.v5i4.379

Developmental signaling pathways in adult energy homeostasis

Antonellis, P. J. (2021) · Figshare · doi:10.25394/pgs.15062292.v1

Downregulation of WNT8A, LRP5, LRP6 and FGF8 in Malay Non-Syndromic Cleft Lip and/or Palate Patients

Shah, N. S. M., Sulaiman, W. A. W., Sulong, S., & Halim, A. S. (2021) · Sains Malaysiana · doi:10.17576/jsm-2021-5011-14

Faculty Opinions recommendation of Fibroblast growth factor-21 regulates PPARγ activity and the antidiabetic actions of thiazolidinediones.

Means, A. R. (2012) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.13865958.15303059

The commonalities of kidney and eye disease

Schultz, C. L. (2020) · Trends in Diabetes and Metabolism · doi:10.15761/tdm.1000119

The Alpha-Klotho Gene as an Anti-ageing Biomarker: Measures and Applications to the Effects of Nutrition

Jurado‐Fasoli, L. (2022) · Biomarkers in disease · doi:10.1007/978-3-030-81304-8_33-1

Peer Review #3 of "High circulating fibroblast growth factor-21 levels as a screening marker in fatty pancreas patients (v0.1)"

(2023) · PeerJ · doi:10.7287/peerj.15176v0.1/reviews/3

Peer Review #1 of "High circulating fibroblast growth factor-21 levels as a screening marker in fatty pancreas patients (v0.1)"

(2023) · PeerJ · doi:10.7287/peerj.15176v0.1/reviews/1

Peer Review #2 of "High circulating fibroblast growth factor-21 levels as a screening marker in fatty pancreas patients (v0.1)"

(2023) · PeerJ · doi:10.7287/peerj.15176v0.1/reviews/2

Association of plasminogen activator inhibitor-1 and fibroblastic growth factor 21 in 3 groups of type 2 diabetes: Without overweight/obesity, free of insulin resistance, and without hepatosteatosis

Takebe, N., Hasegawa, Y., Matsushita, Y., Chiba, H., Onodera, K., Kinno, H., Oda, T., Nagasawa, K., Segawa, T., Takahashi, Y., et al. (2023) · Medicine · doi:10.1097/md.0000000000034797

Signaling pathway and pharmacology

Li, X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15793-6.00005-6

The FGF metabolic axis

Li, X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15793-6.00000-7

Pharmacological Effects of Fibroblast Growth Factor 21 (FGF21) оn Carbohydrate-Lipid Metabolism: Sex Dependence

Бажан, Н. М., & En, M. (2023) · Успехи физиологических наук · doi:10.31857/s0301179823040033

Cardiokines and cardiac remodeling

Duttaroy, A. K., & Mallick, R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99570-2.00014-x

Effect of Estradiol on Carbohydrate-Fat Metabolism and FGF21 System Activity in Female C57BL/6 Mice with Short-Term Consumption of the Cafeteria Diet

Jakovleva, T., Kazantseva, A., Mamontova, K. Y., & Bazhan, N. (2024) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093024020315

Endocrine fibroblast growth factors in domestic animals

Brinker, E. J., Hardcastle, M., Dittmer, K. E., & Graff, E. C. (2024) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2024.106872

Effect of Estradiol on Carbohydrate-Fat Metabolism and FGF21 System Activity in Female C57BL/6 Mice with Short-Term Consumption of the Cafeteria Diet

Jakovleva, T., Kazantseva, A. Y., Mamontova, K. Y., & Бажан, Н. М. (2024) · Российский физиологический журнал им И М Сеченова · doi:10.31857/s0869813924040054

NASH Cirrhosis: A Systematic Review of Phase 2B Trials

Singh, B., Ramanan, S. P., Singh, W., Kaur, G., Grover, P., & Sridhar, N. (2025) · Open Journal of Gastroenterology · doi:10.4236/ojgas.2025.154014

Can we run away from the metabolic side effects of antipsychotics?

Akcan, M., & Wright, D. C. (2025) · Translational Exercise Biomedicine · doi:10.1515/teb-2025-0016

A molecular tango between chromatin and metabolites orchestrates a feedback switch for alcohol consumption

Schmidt, H. M., Tarling, E. J., & Vallim, T. Q. D. A. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2512733122

Insulin-sensitizing effects of fibroblast growth factor-21 in underfed sheep

dos Santos, A. C. R., McGuckin, M. M., Giesy, S. L., & Boisclair, Y. R. (2025) · Journal of Animal Science · doi:10.1093/jas/skaf217

Fibroblast growth factor 16: Molecular mechanisms, signalling crosstalk, and emerging roles in cardiac biology and metabolic regulation

Hui, X.-D., Lin, Q., Liu, K., Gu, C., Abdelbaset-Ismail, A., Wintergerst, K. A., Deng, Z.-B., Cai, L., & Tan, Y. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107858

Association of FGF Receptor-2rs2981578 SNP with breast cancer in women at the University of Gondar Comprehensive Specialized Hospital, Ethiopia

Abera, M. B., Mengstie, T. A., Tadesse, E., Dejenie, T. A., Teferi, B., Siferih, M., Takle, M. N., Asefa, T., Dessie, G., Tesfaye, W., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0327034

Bases moleculares de las alteraciones del tejido adiposo y cambios metabólicos asociados al síndrome lipodistrófico en pacientes infectados por HIV-1

Escuredo, G., & Miguel, J. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Treatment: Bariatric surgery

Neira, G., Rodríguez, A., Gómez‐Ambrosi, J., Frühbeck, G., & Catalán, V. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00347-2

Effects of Perga on FGF21/Leptin/Insulin in Imparied Glucose Regulation

Acun, A. D., Afşar, E., Aslan, E., & Uslu, S. (2025) · Journal of Research in Veterinary Medicine · doi:10.30782/jrvm.1703629

Exploring the mechanism of Jianpi Guchang recipe and its compound: Inhibition liver metastasis in colorectal carcinoma through regulation of the bile acid-FXR-FGF19 axis

Li, C., Wu, P., Wu, Z., Chen, J., Wang, Z., Zhong, Z., Zhong, Y., & Fu, S. (2026) · Advances in Cancer Biology - Metastasis · doi:10.1016/j.adcanc.2026.100180

Endogenous α-Klotho is a common target in atherosclerosis and calcific aortic valve disease

Martín‐Núñez, E., González-Luis, A., Perdomo-Ramírez, A., Tagua, V. G., Ferri, C. M., Rodriguez, S., Cerro-López, P., López-Castillo, Á., Delgado-Molinos, A., Martín-Olivera, A., et al. (2026) · Biochemical Pharmacology · doi:10.1016/j.bcp.2026.117937 · Cited by 1

The fibroblast growth factor-Klotho endocrine system in health and disease

Makoto, K.-O. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-13683-2.00034-7

Rôle des aminoacides ramifiés dans le déterminisme génétique de la résistance à l’insuline

Haydar, S. (2018) · theses.fr (ABES) · doi:10.70675/5c14c2c4z469bz40fazb55cz985ea78d6c2a

Régulation des canaux Nav1.5 cardiaques par la phosphorylation

Lorenzini, M. (2019) · theses.fr (ABES) · doi:10.70675/98865c7cz5033z4459zba85z6f95070762d4

Impact de la mutation G380R du récepteur FGFR3 responsable de l’achondroplasie sur le métabolisme énergétique et évaluation de l’effet d’un traitement par sFGFR3

Saint-Laurent, C. (2018) · theses.fr (ABES) · doi:10.70675/4009375fzcda1z4b66z89d2z53f370c37d8b

Implication de FGF9 et de FGF19 dans la fibrose pulmonaire idiopathique

Justet, A. (2020) · theses.fr (ABES) · doi:10.70675/6e72f095z0cb6z4dd3zb204z88d1b08b9910

Formes monogéniques de lipomatose de Launois-Bensaude : étude clinique et moléculaire, et modélisation cellulaire

Capel, É. (2019) · theses.fr (ABES) · doi:10.70675/6f3a99cczabfbz442dz9fb2zce28bd32a940

Impact de la déficience en acides aminés indispensables sur le métabolisme protéique et énergétique, et identification de signatures métaboliques

Moro, J. (2021) · theses.fr (ABES) · doi:10.70675/dc31a075z5a7fz49fez8007z3921f49d0edd

Rôle des FGFs endocrines et leurs récepteurs au cours de la fibrose pulmonaire idiopathique

Ghanem, M. (2023) · theses.fr (ABES) · doi:10.70675/fd0d64f8zacf4z4856z9b1az66d4df37a332

Metabolic signatures of indispensable amino acids deficiencies : Identification and validation of urinary biomarkers

Roisné-Hamelin, G. (2024) · theses.fr (ABES) · doi:10.70675/006069a1zb2b5z45e8zbe4fz5af5e3b6e229

The contribution of stem cell factor and its receptor c-Kit to cancer-induced bone pain

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