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ANGPTL8 (betatrophin) role in diabetes and metabolic diseases

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1 of the 63 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1016/j.cell.2013.04.008 (notice 2017-01-01).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/oby.21038openalex-snapshot
Serum betatrophin concentrations are significantly increased in overweight but not in obese or type 2 diabetic individuals
inferredcites →https://doi.org/10.1007/978-1-4614-5441-0_22openalex-snapshot
The Pancreatic β Cells in Human Type 2 Diabetes
inferredcites →https://doi.org/10.1007/s00125-013-3071-1openalex-snapshot
Increased circulating levels of betatrophin in individuals with long-standing type 1 diabetes
inferredcites →https://doi.org/10.1007/s00125-014-3208-xopenalex-snapshot
Circulating betatrophin correlates with atherogenic lipid profiles but not with glucose and insulin levels in insulin-resistant individuals
inferredcites →https://doi.org/10.1007/s00125-014-3346-1openalex-snapshot
An explanation for recent discrepancies in levels of human circulating betatrophin
inferredcites →https://doi.org/10.1007/s00125-015-3590-zopenalex-snapshot
Angiopoietin-like protein 8 (ANGPTL8)/betatrophin overexpression does not increase beta cell proliferation in mice
inferredcites →https://doi.org/10.1007/s10875-008-9242-zopenalex-snapshot
T Regulatory Cells in Autoimmune Diabetes: Past Challenges, Future Prospects
inferredcites →https://doi.org/10.1007/s12020-016-0875-zopenalex-snapshot
Elevated circulating levels of betatrophin are associated with polycystic ovary syndrome
inferredcites →https://doi.org/10.1016/j.bbrc.2012.07.038openalex-snapshot
Lipasin, a novel nutritionally-regulated liver-enriched factor that regulates serum triglyceride levels
inferredcites →https://doi.org/10.1016/j.bbrc.2012.12.025openalex-snapshot
Lipasin, thermoregulated in brown fat, is a novel but atypical member of the angiopoietin-like protein family
inferredcites →https://doi.org/10.1016/j.bbrc.2013.01.129openalex-snapshot
Emerging roles of Lipasin as a critical lipid regulator
inferredcites →https://doi.org/10.1016/j.cell.2012.02.010openalex-snapshot
Diabetes Mellitus and the β Cell: The Last Ten Years
inferredcites →https://doi.org/10.1016/j.cell.2013.01.041openalex-snapshot
The Origins and Drivers of Insulin Resistance
inferredcites →https://doi.org/10.1016/j.cell.2013.04.008openalex-snapshot
RETRACTED: Betatrophin: A Hormone that Controls Pancreatic β Cell Proliferation
inferredcites →https://doi.org/10.1016/j.cell.2014.09.027openalex-snapshot
ANGPTL8/Betatrophin Does Not Control Pancreatic Beta Cell Expansion
inferredcites →https://doi.org/10.1016/j.cell.2014.09.028openalex-snapshot
Perspectives on the Activities of ANGPTL8/Betatrophin
inferredcites →https://doi.org/10.1016/j.cmet.2013.06.006openalex-snapshot
Betatrophin Fuels β Cell Proliferation: First Step toward Regenerative Therapy?
inferredcites →https://doi.org/10.1016/j.diabet.2008.09.007openalex-snapshot
Functional pancreatic beta-cell mass: Involvement in type 2 diabetes and therapeutic intervention
inferredcites →https://doi.org/10.1016/s0140-6736(06)69701-8openalex-snapshot
Sustained reduction in the incidence of type 2 diabetes by lifestyle intervention: follow-up of the Finnish Diabetes Prevention Study
inferredcites →https://doi.org/10.1038/ijo.2015.206openalex-snapshot
Interplay of atherogenic factors, protein intake and betatrophin levels in obese–metabolic syndrome patients treated with hypocaloric diets
inferredcites →https://doi.org/10.1038/nbt.1644openalex-snapshot
A mouse knockout library for secreted and transmembrane proteins
inferredcites →https://doi.org/10.1038/nbt1115openalex-snapshot
New sources of pancreatic β-cells
inferredcites →https://doi.org/10.1038/nrd4058openalex-snapshot
Betatrophin boosts β-cells
inferredcites →https://doi.org/10.1038/nrdp.2015.19openalex-snapshot
Type 2 diabetes mellitus
inferredcites →https://doi.org/10.1038/nrdp.2015.39openalex-snapshot
Type 2 diabetes mellitus
inferredcites →https://doi.org/10.1038/nrendo.2013.98openalex-snapshot
Betatrophin—inducing β-cell expansion to treat diabetes mellitus?
inferredcites →https://doi.org/10.1038/srep05013openalex-snapshot
Elevated circulating lipasin/betatrophin in human type 2 diabetes and obesity
inferredcites →https://doi.org/10.1038/srep10949openalex-snapshot
Higher plasma betatrophin/ANGPTL8 level in Type 2 Diabetes subjects does not correlate with blood glucose or insulin resistance
inferredcites →https://doi.org/10.1038/srep18502openalex-snapshot
A lipasin/Angptl8 monoclonal antibody lowers mouse serum triglycerides involving increased postprandial activity of the cardiac lipoprotein lipase
inferredcites →https://doi.org/10.1042/bst0350033openalex-snapshot
Human obesity and insulin resistance: lessons from experiments of Nature
inferredcites →https://doi.org/10.1046/j.1365-2362.32.s3.3.xopenalex-snapshot
Free fatty acids in obesity and type 2 diabetes: defining their role in the development of insulin resistance and β‐cell dysfunction
inferredcites →https://doi.org/10.1056/nejm200105033441801openalex-snapshot
Prevention of Type 2 Diabetes Mellitus by Changes in Lifestyle among Subjects with Impaired Glucose Tolerance
inferredcites →https://doi.org/10.1073/pnas.1217552109openalex-snapshot
Atypical angiopoietin-like protein that regulates ANGPTL3
inferredcites →https://doi.org/10.1073/pnas.1315292110openalex-snapshot
Mice lacking ANGPTL8 (Betatrophin) manifest disrupted triglyceride metabolism without impaired glucose homeostasis
inferredcites →https://doi.org/10.1097/med.0b013e32835edb89openalex-snapshot
Revisiting the notion of type 1 diabetes being a T-cell-mediated autoimmune disease
inferredcites →https://doi.org/10.1111/dme.12731openalex-snapshot
Increased levels of irisin in people with long‐standing Type 1 diabetes
inferredcites →https://doi.org/10.1152/ajpendo.00084.2012openalex-snapshot
Identification of RIFL, a novel adipocyte-enriched insulin target gene with a role in lipid metabolism
inferredcites →https://doi.org/10.1155/2014/323407openalex-snapshot
Increased Circulating Betatrophin Concentrations in Patients with Type 2 Diabetes
inferredcites →https://doi.org/10.1155/2016/2616539openalex-snapshot
Circulating Levels of Betatrophin and Irisin Are Not Associated with Pancreaticβ-Cell Function in Previously Diagnosed Type 2 Diabetes Mellitus Patients
inferredcites →https://doi.org/10.1155/2016/5090852openalex-snapshot
Circulating Betatrophin Is Increased in Patients with Overt and Subclinical Hypothyroidism
inferredcites →https://doi.org/10.1155/2016/6194750openalex-snapshot
Circulating Betatrophin in Patients with Type 2 Diabetes: A Meta-Analysis
inferredcites →https://doi.org/10.1186/s12933-015-0277-1openalex-snapshot
Lack of associations between betatrophin/ANGPTL8 level and C-peptide in type 2 diabetic subjects
inferredcites →https://doi.org/10.1186/s12933-016-0346-0openalex-snapshot
Circulating angiopoietin-like protein 8 (betatrophin) association with HsCRP and metabolic syndrome
inferredcites →https://doi.org/10.1186/s12944-016-0195-6openalex-snapshot
ANGPTL8/Betatrophin R59W variant is associated with higher glucose level in non-diabetic Arabs living in Kuwaits
inferredcites →https://doi.org/10.1210/er.2008-0015openalex-snapshot
Joint Genetic Susceptibility to Type 1 Diabetes and Autoimmune Thyroiditis: from Epidemiology to Mechanisms
inferredcites →https://doi.org/10.1210/jc.2014-1568openalex-snapshot
Circulating Betatrophin Concentrations Are Decreased in Human Obesity and Type 2 Diabetes
inferredcites →https://doi.org/10.1210/jc.2014-2300openalex-snapshot
Circulating Betatrophin Levels Are Increased in Patients With Type 2 Diabetes and Associated With Insulin Resistance
inferredcites →https://doi.org/10.1371/journal.pone.0131171openalex-snapshot
Increased Maternal and Cord Blood Betatrophin in Gestational Diabetes
inferredcites →https://doi.org/10.1371/journal.pone.0136701openalex-snapshot
Circulating Betatrophin Is Strongly Increased in Pregnancy and Gestational Diabetes Mellitus
inferredcites →https://doi.org/10.1371/journal.pone.0147367openalex-snapshot
Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
inferredcites →https://doi.org/10.1371/journal.pone.0155646openalex-snapshot
Increased Cord Blood Betatrophin Levels in the Offspring of Mothers with Gestational Diabetes
inferredcites →https://doi.org/10.1507/endocrj.ej14-0525openalex-snapshot
Circulating betatrophin is elevated in patients with type 1 and type 2 diabetes
inferredcites →https://doi.org/10.1530/eje-14-0815openalex-snapshot
Betatrophin levels are increased in women with gestational diabetes mellitus compared to healthy pregnant controls
inferredcites →https://doi.org/10.2337/db12-0018openalex-snapshot
Human β-Cell Proliferation and Intracellular Signaling
inferredcites →https://doi.org/10.2337/db13-0246openalex-snapshot
Direct Autocrine Action of Insulin on β-Cells: Does It Make Physiological Sense?
inferredcites →https://doi.org/10.2337/db13-0822openalex-snapshot
Incretin Action in the Pancreas: Potential Promise, Possible Perils, and Pathological Pitfalls
inferredcites →https://doi.org/10.2337/db13-1106openalex-snapshot
Irisin Stimulates Browning of White Adipocytes Through Mitogen-Activated Protein Kinase p38 MAP Kinase and ERK MAP Kinase Signaling
inferredcites →https://doi.org/10.2337/db13-1435openalex-snapshot
Elevated Mouse Hepatic Betatrophin Expression Does Not Increase Human β-Cell Replication in the Transplant Setting
inferredcites →https://doi.org/10.2337/db14-0009openalex-snapshot
Betatrophin Versus Bitter-Trophin and the Elephant in the Room: Time for a New Normal in β-Cell Regeneration Research
inferredcites →https://doi.org/10.2337/dc09-9033openalex-snapshot
International Expert Committee Report on the Role of the A1C Assay in the Diagnosis of Diabetes
inferredcites →https://doi.org/10.2337/dc14-0602openalex-snapshot
Increased Circulating Levels of Betatrophin in Newly Diagnosed Type 2 Diabetic Patients
inferredcites →https://doi.org/10.2337/diabetes.49.8.1325openalex-snapshot
Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy.
inferredcites →https://doi.org/10.3109/09513590.2015.1056142openalex-snapshot
Evaluation of circulating betatrophin levels in gestational diabetes mellitus

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4795161openalex-extracted
Adipose Angptl8 Controls Glucose and Energy Metabolism and its Suppression in Mice Improves Diet Induced Obesity and Inflammation
inferred← citeshttps://doi.org/10.1002/dmrr.3612openalex-snapshot
Maternal and cord blood betatrophin (angiopoietin‐like protein 8) in pregnant women with gestational diabetes and normoglycemic controls: A systematic review, meta‐analysis, and meta‐regression
inferred← citeshttps://doi.org/10.1002/dmrr.3643openalex-snapshot
Plasma insulin is required for the increase in plasma angiopoietin‐like protein 8 in response to nutrient ingestion
inferred← citeshttps://doi.org/10.1002/hep.30030openalex-snapshot
Hepatocellular Carcinoma‐Associated Protein TD26 Interacts and Enhances Sterol Regulatory Element‐Binding Protein 1 Activity to Promote Tumor Cell Proliferation and Growth
inferred← citeshttps://doi.org/10.1007/978-3-030-81303-1_19-1openalex-snapshot
Serum Betatrophin: What It Shows and How It Alters in Gestational Diabetes Mellitus
inferred← citeshttps://doi.org/10.1007/978-3-031-08014-2_19openalex-snapshot
Serum Betatrophin: What It Shows and How It Alters in Gestational Diabetes Mellitus
inferred← citeshttps://doi.org/10.1007/s00289-018-2549-xopenalex-snapshot
SEMI-empirical PM6 method applied in the analysis of thermodynamics properties and molecular orbitals at different temperatures of adsorption drugs on chitosan hydrogels for type 2 diabetes
inferred← citeshttps://doi.org/10.1007/s10930-019-09825-8openalex-snapshot
Bacteria-Derived Recombinant Human ANGPTL8/Betatrophin Significantly Increases the Level of Triglyceride
inferred← citeshttps://doi.org/10.1007/s11033-021-06270-8openalex-snapshot
ANGPTL8 roles in proliferation, metabolic diseases, hypothyroidism, polycystic ovary syndrome, and signaling pathways
inferred← citeshttps://doi.org/10.1007/s11325-022-02736-6openalex-snapshot
The association between biomarker angiopoietin-like protein five and obstructive sleep apnea in patients undergoing bariatric surgery
inferred← citeshttps://doi.org/10.1007/s11332-026-01756-zopenalex-snapshot
Probiotics and exercise modulate hepatic asprosin, betatrophin, Leap-2, and ORM2 gene expression in a high fat diet rat model
inferred← citeshttps://doi.org/10.1007/s12020-022-03285-4openalex-snapshot
Association of serum Tsukushi level with metabolic syndrome and its components
inferred← citeshttps://doi.org/10.1007/s40618-018-0831-2openalex-snapshot
Association of serum betatrophin with fibroblast growth factor-21 in women with polycystic ovary syndrome
inferred← citeshttps://doi.org/10.1016/b978-0-12-819603-8.00004-3openalex-snapshot
Insulin resistance and sleep apnea
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116631openalex-snapshot
New insights into the roles of Irisin in diabetic cardiomyopathy and vascular diseases
inferred← citeshttps://doi.org/10.1016/j.cca.2024.117775openalex-snapshot
The association between plasma angiopoietin-like protein 4, glucose and lipid metabolism during pregnancy, placental function, and risk of delivering large-for-gestational-age neonates
inferred← citeshttps://doi.org/10.1016/j.domaniend.2025.106914openalex-snapshot
Alterations in serum concentrations of visfatin and betatrophin in dogs with diabetes mellitus
inferred← citeshttps://doi.org/10.1016/j.gene.2018.09.041openalex-snapshot
Angiopoietin-like 8 (ANGPTL8) expression is regulated by miR-143-3p in human hepatocytes
inferred← citeshttps://doi.org/10.1016/j.gene.2020.144707openalex-snapshot
ANGPTL8 enhances insulin sensitivity by directly activating insulin-mediated AKT phosphorylation
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111292openalex-snapshot
Adipocyte Angptl8 deletion improves glucose and energy metabolism and obesity associated inflammation in mice
inferred← citeshttps://doi.org/10.1016/j.jpag.2026.05.010openalex-snapshot
Evaluation of Serum Betatrophin Levels in Normal-Weight and Overweight Adolescents with Polycystic Ovary Syndrome
inferred← citeshttps://doi.org/10.1016/j.metabol.2021.154921openalex-snapshot
Angiopoietin-like protein 8 (betatrophin) inhibits hepatic gluconeogenesis through PI3K/Akt signaling pathway in diabetic mice
inferred← citeshttps://doi.org/10.1016/j.numecd.2022.04.006openalex-snapshot
Effect of physical activity in a weight loss program on circulating total ANGPTL8 concentrations in northern Americans with obesity: A prospective randomized controlled trial
inferred← citeshttps://doi.org/10.1038/s41419-022-05029-8openalex-snapshot
ANGPTL8 is a negative regulator in pathological cardiac hypertrophy
inferred← citeshttps://doi.org/10.1038/s41467-019-11513-1openalex-snapshot
Angptl8 mediates food-driven resetting of hepatic circadian clock in mice
inferred← citeshttps://doi.org/10.1038/s41598-019-48371-2openalex-snapshot
Reduced miR-181d level in obesity and its role in lipid metabolism via regulation of ANGPTL3
inferred← citeshttps://doi.org/10.1038/s41598-020-63076-7openalex-snapshot
Correlation of circulating ANGPTL5 levels with obesity, high sensitivity C-reactive protein and oxidized low-density lipoprotein in adolescents
inferred← citeshttps://doi.org/10.1038/s41598-020-69091-yopenalex-snapshot
The circulating ANGPTL8 levels show differences among novel subgroups of adult patients with diabetes and are associated with mortality in the subsequent 5 years
inferred← citeshttps://doi.org/10.1080/14767058.2018.1481382openalex-snapshot
Assessment of circulating betatrophin levels in intrahepatic cholestasis of pregnancy
inferred← citeshttps://doi.org/10.1097/md.0000000000025646openalex-snapshot
Association of betatrophin amounts with 25-(OH)D levels in patients with gestational diabetes mellitus
inferred← citeshttps://doi.org/10.1101/2023.07.04.547624openalex-snapshot
ANGPTL8 R59W variant influences inflammation through modulating NF-κB pathway under TNFα stimulation
inferred← citeshttps://doi.org/10.1111/jcmm.14488openalex-snapshot
Angiopoietin‐like protein 8 expression and association with extracellular matrix metabolism and inflammation during intervertebral disc degeneration
inferred← citeshttps://doi.org/10.1111/jvim.16904openalex-snapshot
Alterations in serum concentrations of visfatin and betatrophin in dogs with hypothyroidism
inferred← citeshttps://doi.org/10.1152/ajpendo.00339.2019openalex-snapshot
Regulation of ANGPTL8 in liver and adipose tissue by nutritional and hormonal signals and its effect on glucose homeostasis in mice
inferred← citeshttps://doi.org/10.1155/2019/5096860openalex-snapshot
The Relationship between Circulating ANGPTL8/Betatrophin Concentrations and Adult Obesity: A Meta-Analysis
inferred← citeshttps://doi.org/10.1155/2020/1621239openalex-snapshot
The ANGPTL8 rs2278426 (C/T) Polymorphism Is Associated with Prediabetes and Type 2 Diabetes in a Han Chinese Population in Hebei Province
inferred← citeshttps://doi.org/10.1155/2022/1113811openalex-snapshot
Angiopoietin-Like 8 in Gestational Diabetes Mellitus: Reduced Levels in Third Trimester Maternal Serum and Placenta, Increased Levels in Cord Blood Serum
inferred← citeshttps://doi.org/10.1172/jci.insight.189371openalex-snapshot
Angiopoietin-like 8 governs osteoblast-adipocyte lineage commitment during skeletal aging
inferred← citeshttps://doi.org/10.1177/0300060518808683openalex-snapshot
Betatrophin for diagnosis and prognosis of mothers with gestational diabetes mellitus
inferred← citeshttps://doi.org/10.1177/14791641241259792openalex-snapshot
The correlations between angiopoietin like 8 and cardiometabolic risk factors in Saudi women with type 2 diabetes mellitus: A pilot study
inferred← citeshttps://doi.org/10.1186/s12887-025-05833-zopenalex-snapshot
Circulating fibroblast growth factor-21, Omentin-1, and betatrophin and their association with metabolic parameters in Saudi adolescents post 12-month lifestyle change program
inferred← citeshttps://doi.org/10.1186/s12933-018-0687-yopenalex-snapshot
Triglyceride-mediated influence of serum angiopoietin-like protein 8 on subclinical atherosclerosis in type 2 diabetic patients: results from the GDMD study in China
inferred← citeshttps://doi.org/10.1186/s12944-018-0659-yopenalex-snapshot
New insights into ANGPLT3 in controlling lipoprotein metabolism and risk of cardiovascular diseases
inferred← citeshttps://doi.org/10.1186/s13213-020-01599-0openalex-snapshot
Liver-specific knockdown of ANGPTL8 alters the structure of the gut microbiota in mice
inferred← citeshttps://doi.org/10.13005/bpj/2764openalex-snapshot
Central Obesity Diminishes Circulating Betatrophin Level in Middle-aged Male Subjects
inferred← citeshttps://doi.org/10.1507/endocrj.ej18-0191openalex-snapshot
Effects of a diet with or without physical activity on angiopoietin-like protein 8 concentrations in overweight/obese patients with newly diagnosed type 2 diabetes: a randomized controlled trial
inferred← citeshttps://doi.org/10.1515/jbcpp-2021-0393openalex-snapshot
Moderate-intensity exercise decreases the circulating level of betatrophin and its correlation among markers of obesity in women
inferred← citeshttps://doi.org/10.2147/dmso.s330700openalex-snapshot
ANGPTL8/Betatrophin Improves Glucose Tolerance in Older Mice and Metabolomic Analysis Reveals Its Role in Insulin Resistance in HepG2 Cells
inferred← citeshttps://doi.org/10.2147/dmso.s455274openalex-snapshot
Association Between rs2278426 Polymorphism of the ANGPTL8 Gene and Polycystic Ovary Syndrome
inferred← citeshttps://doi.org/10.2169/internalmedicine.3609-24openalex-snapshot
Circulating Angiopoietin-like Protein 6 Levels and Clinical Features in Patients with Type 2 Diabetes
inferred← citeshttps://doi.org/10.26740/jossae.v9n1.p1-7openalex-snapshot
Changes in Serum Betatrophin Levels in Obese Women after Two-Weeks of Moderate-intensity Aerobic Exercise
inferred← citeshttps://doi.org/10.29333/ejgm/18521openalex-snapshot
Serum betatrophin and irisin levels in patients with polycystic ovary syndrome with and without insulin resistance
inferred← citeshttps://doi.org/10.3389/fendo.2018.00414openalex-snapshot
Association of Serum Angiopoietin-Like Protein 8 With Albuminuria in Type 2 Diabetic Patients: Results From the GDMD Study in China
inferred← citeshttps://doi.org/10.3389/fendo.2018.00651openalex-snapshot
Increased Level of Angiopoietin Like Proteins 4 and 8 in People With Sleep Apnea
inferred← citeshttps://doi.org/10.3389/fendo.2019.00495openalex-snapshot
Higher Levels of ANGPTL5 in the Circulation of Subjects With Obesity and Type 2 Diabetes Are Associated With Insulin Resistance
inferred← citeshttps://doi.org/10.3389/fpubh.2021.710504openalex-snapshot
Association of Circulating ANGPTL8 Levels With Renal Dysfunction: A Case-Control Study
inferred← citeshttps://doi.org/10.3390/biomedicines12050949openalex-snapshot
Angiopoietin-2 and Angiopoietin-like Proteins with a Prospective Role in Predicting Diabetic Nephropathy
inferred← citeshttps://doi.org/10.3390/cells12212563openalex-snapshot
The Proinflammatory Role of ANGPTL8 R59W Variant in Modulating Inflammation through NF-κB Signaling Pathway under TNFα Stimulation
inferred← citeshttps://doi.org/10.3390/genes12050755openalex-snapshot
ANGPTL3 Variants Associate with Lower Levels of Irisin and C-Peptide in a Cohort of Arab Individuals
inferred← citeshttps://doi.org/10.3390/ijms20174223openalex-snapshot
Loss of Glycine N-Methyltransferase Associates with Angiopoietin-Like Protein 8 Expression in High Fat-Diet-Fed Mice
inferred← citeshttps://doi.org/10.3390/ijms241814244openalex-snapshot
Increased Levels of Circulating IGFBP4 and ANGPTL8 with a Prospective Role in Diabetic Nephropathy
inferred← citeshttps://doi.org/10.3390/jcm14145006openalex-snapshot
Impact of Tumor Necrosis Factor Antagonist Therapy on Circulating Angiopoietin-like Protein 8 (ANGPTL8) Levels in Crohn’s Disease—A Prospective Multi-Center Study
inferred← citeshttps://doi.org/10.3390/metabo10090358openalex-snapshot
Targeted Metabolomics Analysis on Obstructive Sleep Apnea Patients after Multilevel Sleep Surgery
inferred← citeshttps://doi.org/10.3390/metabo12100925openalex-snapshot
Betatrophin and Insulin Resistance
inferred← citeshttps://doi.org/10.3390/metabo13090972openalex-snapshot
Targeted Metabolomics Analysis of Individuals Carrying the ANGPTL8 R59W Variant
inferred← citeshttps://doi.org/10.34172/ajmb.2019.11openalex-snapshot
A Short Review on ANGPTL-8 as an Important Regulator in Diabetes
inferred← citeshttps://doi.org/10.35630/2199-885x/2022/12/5.9openalex-snapshot
INSULIN-PRODUCING CELLS IN THE TREATMENT OF TYPE 1 DIABETES: A LITERATURE REVIEW
inferred← citeshttps://doi.org/10.3892/mmr.2019.10719openalex-snapshot
Recombinant betatrophin (Angptl‑8/lipasin) ameliorates streptozotocin‑induced hyperglycemia and β‑cell destruction in neonatal rats
inferred← citeshttps://doi.org/10.3892/mmr.2023.13099openalex-snapshot
The roles of FLOT1 in human diseases (Review)
inferred← citeshttps://doi.org/10.4254/wjh.v13.i11.1611openalex-snapshot
Newly discovered endocrine functions of the liver
inferred← citeshttps://doi.org/10.70675/52bcdc87z9aedz40abz9459z9019f91b56feopenalex-snapshot
Régulation dépendante du contexte de la morphogenèse et de l’intégrité capillaire par angiopoietin-like 4
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