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Higher plasma betatrophin/ANGPTL8 level in Type 2 Diabetes subjects does not correlate with blood glucose or insulin resistance
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1 of the 41 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/10.1007/978-1-4614-5441-0_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/s10875-008-9242-zopenalex-snapshot
T Regulatory Cells in Autoimmune Diabetes: Past Challenges, Future Prospects
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.2013.04.008openalex-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.celrep.2013.01.007openalex-snapshot
Liver-Derived Systemic Factors Drive β Cell Hyperplasia in Insulin-Resistant States
inferredcites →https://doi.org/10.1016/j.diabres.2011.10.029openalex-snapshot
IDF Diabetes Atlas: Global estimates of the prevalence of diabetes for 2011 and 2030
inferredcites →https://doi.org/10.1016/j.diabres.2013.12.036openalex-snapshot
Comparison of type 2 diabetes prevalence estimates in Saudi Arabia from a validated Markov model against the International Diabetes Federation and other modelling studies
inferredcites →https://doi.org/10.1016/j.diabres.2017.03.024openalex-snapshot
IDF Diabetes Atlas: Global estimates for the prevalence of diabetes for 2015 and 2040
inferredcites →https://doi.org/10.1016/j.pcd.2010.08.002openalex-snapshot
Type 2 diabetes and cardiovascular disease in South Asians
inferredcites →https://doi.org/10.1016/s1097-2765(00)00010-1openalex-snapshot
Loss of Insulin Signaling in Hepatocytes Leads to Severe Insulin Resistance and Progressive Hepatic Dysfunction
inferredcites →https://doi.org/10.1038/srep05013openalex-snapshot
Elevated circulating lipasin/betatrophin in human type 2 diabetes and obesity
inferredcites →https://doi.org/10.1073/pnas.1217552109openalex-snapshot
Atypical angiopoietin-like protein that regulates ANGPTL3
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.12386openalex-snapshot
Cardiovascular disease risk factors in the South Asian population living in Kuwait: a cross‐sectional study
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/10.1155/2014/730472openalex-snapshot
Gender Differences in Ghrelin Association with Cardiometabolic Risk Factors in Arab Population
inferredcites →https://doi.org/10.1159/000350827openalex-snapshot
Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy
inferredcites →https://doi.org/10.1186/1475-2840-13-76openalex-snapshot
Comprehensive analysis of circulating adipokines and hsCRP association with cardiovascular disease risk factors and metabolic syndrome in Arabs
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/10.1258/shorts.2011.011019openalex-snapshot
Prevalences of overweight, obesity, hyperglycaemia, hypertension and dyslipidaemia in the Gulf: systematic review
inferredcites →https://doi.org/10.1371/journal.pone.0040948openalex-snapshot
Prevalence of Type 2 Diabetes in the States of The Co-Operation Council for the Arab States of the Gulf: A Systematic Review
inferredcites →https://doi.org/10.2337/db07-1369openalex-snapshot
β-Cell Replication Is the Primary Mechanism Subserving the Postnatal Expansion of β-Cell Mass in Humans
inferredcites →https://doi.org/10.2337/db08-1198openalex-snapshot
Adaptive β-Cell Proliferation Is Severely Restricted With Advanced Age
inferredcites →https://doi.org/10.2337/db12-1814openalex-snapshot
Sugar, Uric Acid, and the Etiology of Diabetes and Obesity
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/db13-1435openalex-snapshot
Elevated Mouse Hepatic Betatrophin Expression Does Not Increase Human β-Cell Replication in the Transplant Setting
inferredcites →https://doi.org/10.2337/dc08-s055openalex-snapshot
Diagnosis and Classification of Diabetes Mellitus
inferredcites →https://doi.org/10.2337/dc11-s062openalex-snapshot
Diagnosis and Classification of Diabetes Mellitus
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.
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.2919openalex-snapshot
ANGPTL8 (betatrophin) role in diabetes and metabolic diseases
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/10.1007/978-3-030-25057-7_11openalex-snapshot
Biomarkers of Insulin Resistance
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/s00125-016-4066-5openalex-snapshot
ANGPTL2 is associated with an increased risk of cardiovascular events and death in diabetic patients
inferred← citeshttps://doi.org/10.1007/s00125-017-4505-yopenalex-snapshot
Angiopoietin-like protein 8 in early pregnancy improves the prediction of gestational diabetes
inferred← citeshttps://doi.org/10.1007/s00417-017-3676-zopenalex-snapshot
Expression of angiopoietin-like protein 8 correlates with VEGF in patients with proliferative diabetic retinopathy
inferred← citeshttps://doi.org/10.1007/s11010-020-03725-7openalex-snapshot
Higher circulating levels of ANGPTL8 are associated with body mass index, triglycerides, and endothelial dysfunction in patients with coronary artery disease
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/s11033-021-06335-8openalex-snapshot
New insights into ANGPTL8 in modulating the development of cardio-metabolic disorder diseases
inferred← citeshttps://doi.org/10.1007/s11892-015-0676-4openalex-snapshot
Betatrophin in Diabetes Mellitus: the Epidemiological Evidence in Humans
inferred← citeshttps://doi.org/10.1007/s12020-016-0875-zopenalex-snapshot
Elevated circulating levels of betatrophin are associated with polycystic ovary syndrome
inferred← citeshttps://doi.org/10.1007/s13167-019-00180-3openalex-snapshot
The potential role of angiopoietin-like protein-8 in type 2 diabetes mellitus: a possibility for predictive diagnosis and targeted preventive measures?
inferred← citeshttps://doi.org/10.1007/s40618-020-01444-wopenalex-snapshot
Angiopoietin-like 8 (ANGPTL8) as a potential predictor of NAFLD in paediatric patients with Prader-Willi Syndrome
inferred← citeshttps://doi.org/10.1007/s40618-020-01493-1openalex-snapshot
Down-regulation of betatrophin enhances insulin sensitivity in type 2 diabetes mellitus through activation of the GSK-3β/PGC-1α signaling pathway
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2019.11.011openalex-snapshot
High betatrophin in coronary patients protects from cardiovascular events
inferred← citeshttps://doi.org/10.1016/j.bbalip.2024.159461openalex-snapshot
Silencing ANGPTL8 reduces mouse preadipocyte differentiation and insulin signaling
inferred← citeshttps://doi.org/10.1016/j.cca.2021.05.017openalex-snapshot
ANGPTL8 in cardio-metabolic diseases
inferred← citeshttps://doi.org/10.1016/j.diabet.2016.07.029openalex-snapshot
Levels of betatrophin decrease during pregnancy despite increased insulin resistance, beta-cell function and triglyceride levels
inferred← citeshttps://doi.org/10.1016/j.diabres.2017.08.025openalex-snapshot
Angiopoietin-like protein 8: An attractive biomarker for the evaluation of subjects with insulin resistance and related disorders
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145594openalex-snapshot
Analysis of ANGPTL8 promoter activity and screening of related transcription factors in bovine
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148418openalex-snapshot
The minor allele of ANGPTL8 rs2278426 has a protective effect against CAD in T2DM patients
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.jacl.2017.12.011openalex-snapshot
High frequency of type 2 diabetes and impaired glucose tolerance in Japanese subjects with the angiopoietin-like protein 8 R59W variant
inferred← citeshttps://doi.org/10.1016/j.jcjd.2021.07.004openalex-snapshot
A New Clinical Utility for Tubular Markers to Identify Kidney Responders to Saxagliptin Treatment in Adults With Diabetic Nephropathy
inferred← citeshttps://doi.org/10.1016/j.jdiacomp.2016.05.023openalex-snapshot
Circulating betatrophin in healthy control and type 2 diabetic subjects and its association with metabolic parameters
inferred← citeshttps://doi.org/10.1016/j.jfma.2023.12.018openalex-snapshot
Positive correlation of ANGPTL8 expression in human visceral adipose tissue with body mass index
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.116558openalex-snapshot
SIRT6 as a potential target for treating insulin resistance
inferred← citeshttps://doi.org/10.1016/j.peptides.2018.07.001openalex-snapshot
GLP-1 receptor agonists stimulate ANGPTL8 production through the PI3K/Akt pathway in a GLP-1 receptor-dependent manner
inferred← citeshttps://doi.org/10.1016/j.plipres.2020.101067openalex-snapshot
The multi-faces of Angptl8 in health and disease: Novel functions beyond lipoprotein lipase modulation
inferred← citeshttps://doi.org/10.1016/j.soard.2016.01.024openalex-snapshot
Decreased serum betatrophin levels correlate with improved fasting plasma glucose and insulin secretion capacity after Roux-en-Y gastric bypass in obese Chinese patients with type 2 diabetes: a 1-year follow-up
inferred← citeshttps://doi.org/10.1016/j.soard.2018.05.026openalex-snapshot
Biphasic changes in angiopoietin-like 8 level after laparoscopic sleeve gastrectomy and type 2 diabetes remission during a 1-year follow-up
inferred← citeshttps://doi.org/10.1016/j.soard.2018.06.013openalex-snapshot
Paired editorial: biphasic changes in angiopoietin-like 8 level after laparoscopic sleeve gastrectomy and type 2 diabetes remission during a 1-year follow-up
inferred← citeshttps://doi.org/10.1016/j.ygeno.2017.06.006openalex-snapshot
Visualizing the regulatory role of Angiopoietin-like protein 8 (ANGPTL8) in glucose and lipid metabolic pathways
inferred← citeshttps://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
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/s41467-017-02355-wopenalex-snapshot
ANGPTL8 negatively regulates NF-κB activation by facilitating selective autophagic degradation of IKKγ
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/s41598-020-63850-7openalex-snapshot
Association of ANGPTL8 (Betatrophin) Gene Variants with Components of Metabolic Syndrome in Arab Adults
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/10.1038/srep28431openalex-snapshot
The Effects of Serum ANGPTL8/betatrophin on the Risk of Developing the Metabolic Syndrome – A Prospective Study
inferred← citeshttps://doi.org/10.1038/srep39899openalex-snapshot
Hepatic MiR-291b-3p Mediated Glucose Metabolism by Directly Targeting p65 to Upregulate PTEN Expression
inferred← citeshttps://doi.org/10.1055/s-0043-102950openalex-snapshot
ANGPTL8 (Betatrophin) is Expressed in Visceral Adipose Tissue and Relates to Human Hepatic Steatosis in Two Independent Clinical Collectives
inferred← citeshttps://doi.org/10.1055/s-0043-104383openalex-snapshot
Plasma Betatrophin Levels of Subjects Classified with Normal, Impaired, and Diabetic Glucose Tolerance, and Subjects with Impaired Fasting Glucose
inferred← citeshttps://doi.org/10.1055/s-0043-108911openalex-snapshot
The Correlation Between Circulating Betatrophin and Insulin Resistance in General Population: A Meta-Analysis
inferred← citeshttps://doi.org/10.1080/09513590.2016.1252743openalex-snapshot
Association of betatrophin with metabolic characteristics in overweight/obese and lean women with PCOS
inferred← citeshttps://doi.org/10.1080/13813455.2020.1849310openalex-snapshot
The effect of 4-week endurance training on serum levels of irisin and betatrophin in streptozotocin- induced diabetic rats
inferred← citeshttps://doi.org/10.1111/ijcp.13769openalex-snapshot
Saxagliptin and vildagliptin lowered albuminuria in patients with diabetes and hypertension independent on glycaemic control
inferred← citeshttps://doi.org/10.1111/liv.13115openalex-snapshot
Diabetes mellitus in patients with cirrhosis: clinical implications and management
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/10.1155/2015/479157openalex-snapshot
Betatrophin Acts as a Diagnostic Biomarker in Type 2 Diabetes Mellitus and Is Negatively Associated with HDL-Cholesterol
inferred← citeshttps://doi.org/10.1155/2016/4860595openalex-snapshot
The Rise and the Fall of Betatrophin/ANGPTL8 as an Inducer ofβ-Cell Proliferation
inferred← citeshttps://doi.org/10.1155/2017/2316986openalex-snapshot
Serum Concentrations of Betatrophin and Its Association with Indirect Indices of Insulin Resistance and Beta Cell Function in Women with Polycystic Ovary Syndrome
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/10.1177/0300060516680441openalex-snapshot
Serum betatrophin levels are increased and associated with insulin resistance in patients with polycystic ovary syndrome
inferred← citeshttps://doi.org/10.1177/0300060518808683openalex-snapshot
Betatrophin for diagnosis and prognosis of mothers with gestational diabetes mellitus
inferred← citeshttps://doi.org/10.1186/s12933-015-0277-1openalex-snapshot
Lack of associations between betatrophin/ANGPTL8 level and C-peptide in type 2 diabetic subjects
inferred← citeshttps://doi.org/10.1186/s12933-015-0326-9openalex-snapshot
Higher serum betatrophin level in type 2 diabetes subjects is associated with urinary albumin excretion and renal function
inferred← citeshttps://doi.org/10.1186/s12933-016-0346-0openalex-snapshot
Circulating angiopoietin-like protein 8 (betatrophin) association with HsCRP and metabolic syndrome
inferred← citeshttps://doi.org/10.1186/s12933-018-0736-6openalex-snapshot
Associations between circulating full-length angiopoietin-like protein 8 levels and severity of coronary artery disease in Chinese non-diabetic patients: a case–control study
inferred← citeshttps://doi.org/10.1186/s12933-018-0742-8openalex-snapshot
Interaction between endothelial nitric oxide synthase rs1799983, cholesteryl ester-transfer protein rs708272 and angiopoietin-like protein 8 rs2278426 gene variants highly elevates the risk of type 2 diabetes mellitus and cardiovascular disease
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1186/s12944-016-0337-xopenalex-snapshot
Increased ANGPTL3, 4 and ANGPTL8/betatrophin expression levels in obesity and T2D
inferred← citeshttps://doi.org/10.1186/s12944-018-0681-0openalex-snapshot
Increased plasma and adipose tissue levels of ANGPTL8/Betatrophin and ANGPTL4 in people with hypertension
inferred← citeshttps://doi.org/10.1186/s13287-017-0743-7openalex-snapshot
Adipose tissue-derived stem cells ameliorate hyperglycemia, insulin resistance and liver fibrosis in the type 2 diabetic rats
inferred← citeshttps://doi.org/10.1210/clinem/dgab120openalex-snapshot
Genetic and Metabolic Determinants of Plasma Levels of ANGPTL8
inferred← citeshttps://doi.org/10.1210/jc.2016-1788openalex-snapshot
Weight Loss Partially Restores Glucose-Driven Betatrophin Response in Humans
inferred← citeshttps://doi.org/10.13005/bpj/2764openalex-snapshot
Central Obesity Diminishes Circulating Betatrophin Level in Middle-aged Male Subjects
inferred← citeshttps://doi.org/10.1371/journal.pone.0147367openalex-snapshot
Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
inferred← citeshttps://doi.org/10.1371/journal.pone.0173024openalex-snapshot
Plasma and adipose tissue level of angiopoietin-like 7 (ANGPTL7) are increased in obesity and reduced after physical exercise
inferred← citeshttps://doi.org/10.1371/journal.pone.0173197openalex-snapshot
Renal function is independently associated with circulating betatrophin
inferred← citeshttps://doi.org/10.1371/journal.pone.0255147openalex-snapshot
Association between ANGPTL3, 4, and 8 and lipid and glucose metabolism markers in patients with diabetes
inferred← citeshttps://doi.org/10.14740/jem405wopenalex-snapshot
Circulating Betatrophin and Hepatocyte Growth Factor in Type 2 Diabetic Patients: Their Relationship With Disease Prognosis
inferred← citeshttps://doi.org/10.14740/jocmr3114wopenalex-snapshot
Serum Betatrophin Levels and Clinical Features in Patients With Poorly Controlled Type 2 Diabetes
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/10.18203/2320-6012.ijrms20163119openalex-snapshot
Betatrophin is correlated with glucagon and insulin release rather than insulin resistance marker in type 2 diabetes mellitus Iraqi women
inferred← citeshttps://doi.org/10.18502/ijrm.v20i1.10406openalex-snapshot
The association of the betatrophin level with metabolic and inflammatory parameters in infertile women with polycystic ovary syndrome: A case-control study
inferred← citeshttps://doi.org/10.18632/aging.102263openalex-snapshot
MiR-27a promotes insulin resistance and mediates glucose metabolism by targeting PPAR-γ-mediated PI3K/AKT signaling
inferred← citeshttps://doi.org/10.18632/oncotarget.15102openalex-snapshot
Increased circulating full-length betatrophin levels in drug-naïve metabolic syndrome
inferred← citeshttps://doi.org/10.21203/rs.3.rs-11258285/v1openalex-snapshot
Elevated Serum Angiopoietin-Like Protein 6 in New-Onset Diabetes After Kidney Transplantation: A Registry-Based Comparative Study
inferred← citeshttps://doi.org/10.2147/dmso.s411483openalex-snapshot
Association Between Plasma Levels of ANGPTL3, 4, 8 and the Most Common Additional Cardiovascular Risk Factors in Patients with Hypertension
inferred← citeshttps://doi.org/10.21608/ijma.2022.99440.1377openalex-snapshot
Study of serum betatrophin level as a biochemical marker in patients with type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.21608/mjmr.2022.221959openalex-snapshot
A Study of Serum Betatrophin levels in Children with Type 1 Diabetes Mellitus
inferred← citeshttps://doi.org/10.23736/s2724-6507.23.04073-3openalex-snapshot
Association between circulating betatrophin levels and T2DM: a meta-analysis
inferred← citeshttps://doi.org/10.23750/abm.v91i4.8944openalex-snapshot
Effects of vitamin D on apoptosis and betatrophin in the kidney tissue of experimental diabetic rats.
inferred← citeshttps://doi.org/10.26650/istanbuljpharm.2021.933139openalex-snapshot
The inverse association between ANGPTL8 and PI3K-mTOR- PPARγ expressions in adipose tissue of high-fructose- fed rats: The modulatory effect of kefir
inferred← citeshttps://doi.org/10.33140/jgds.07.01.04openalex-snapshot
Impact of Liver Cirrhosis on the Occurrence of Diabetes Mellitus and Glucose Intolerance among Liver Cirrhosis Patients in European Gaza Hospital: A Retroactive Study
inferred← citeshttps://doi.org/10.33545/gynae.2021.v5.i4a.959openalex-snapshot
Betatrophin in polycystic ovary disease and its association with insulin resistance
inferred← citeshttps://doi.org/10.3389/fcvm.2026.1762073openalex-snapshot
Association between serum ANGPLT8 levels and atherogenic index of plasma in Chinese patients with type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.3389/fendo.2018.00169openalex-snapshot
ANGPTL8: An Important Regulator in Metabolic Disorders
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.2018.00423openalex-snapshot
Increased Circulation and Adipose Tissue Levels of DNAJC27/RBJ in Obesity and Type 2-Diabetes
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/fendo.2021.695750openalex-snapshot
Association of ANGPTL8 and Resistin With Diabetic Nephropathy in Type 2 Diabetes Mellitus
inferred← citeshttps://doi.org/10.3389/fendo.2024.1392675openalex-snapshot
Evaluating the correlation of sclerostin levels with obesity and type 2 diabetes in a multiethnic population living in Kuwait
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/cells8101283openalex-snapshot
Increased Expression of Meteorin-Like Hormone in Type 2 Diabetes and Obesity and Its Association with Irisin
inferred← citeshttps://doi.org/10.3390/ijms23158564openalex-snapshot
Increased LRG1 Levels in Overweight and Obese Adolescents and Its Association with Obesity Markers, Including Leptin, Chemerin, and High Sensitivity C-Reactive Protein
inferred← citeshttps://doi.org/10.3390/ijms231810630openalex-snapshot
Adiponectin Intervention to Regulate Betatrophin Expression, Attenuate Insulin Resistance and Enhance Glucose Metabolism in Mice and Its Response to Exercise
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/ijms242216504openalex-snapshot
Gender-Dependent Associations between Serum Betatrophin Levels and Lipoprotein Subfractions in Diabetic and Nondiabetic Obese Patients
inferred← citeshttps://doi.org/10.3390/ijms25116264openalex-snapshot
Associations between Serum Kallistatin Levels and Markers of Glucose Homeostasis, Inflammation, and Lipoprotein Metabolism in Patients with Type 2 Diabetes and Nondiabetic Obesity
inferred← citeshttps://doi.org/10.3390/jcm9020512openalex-snapshot
Evidences for Expression and Location of ANGPTL8 in Human Adipose Tissue
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/10.3390/nu14050915openalex-snapshot
Metabolically Healthy and Unhealthy Obese Phenotypes among Arabs and South Asians: Prevalence and Relationship with Cardiometabolic Indicators
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/10.4081/itjm.q.2018.2openalex-snapshot
L’internista ospedaliero nella gestione del paziente diabetico complesso
inferred← citeshttps://doi.org/10.4093/dmj.2018.42.1.53openalex-snapshot
Serum Betatrophin Concentrations and the Risk of Incident Diabetes: A Nested Case-Control Study from Chungju Metabolic Disease Cohort
inferred← citeshttps://doi.org/10.4103/atm.atm_52_18openalex-snapshot
Betatrophin association with serum triglyceride levels in obstructive sleep apnea patients
inferred← citeshttps://doi.org/10.4103/ijem.ijem_79_18openalex-snapshot
Hepatogenous diabetes: An underestimated problem of liver cirrhosis
inferred← citeshttps://doi.org/10.5223/pghn.2018.21.2.111openalex-snapshot
Investigation of Blood Betatrophin Levels in Obese Children with Non-Alcoholic Fatty Liver Disease
inferred← citeshttps://doi.org/10.5603/dk.2018.0022openalex-snapshot
Insulin resistance and adaptation of pancreatic beta cells during pregnancy
inferred← citeshttps://doi.org/10.5603/dk.2019.0002openalex-snapshot
Wyższe stężenie betatrofiny u pacjentów z noworozpoznaną cukrzycą
inferred← citeshttps://doi.org/10.5812/asjsm-120515openalex-snapshot
The Effect of Four Weeks of Long-Term Endurance Training with and Without Propolis Supplementation on Serum Levels of Betatrophin/ANGPTL8 in Male Athletes
inferred← citeshttps://doi.org/10.7759/cureus.44219openalex-snapshot
Evaluation of Adiponectin and ANGPTL8 in Women With Metabolic Syndrome in the Madinah Region of Saudi Arabia
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