• <em>Single-cell transcriptome dataset of human and mouse</em> in vitro <em>adipogenesis models</em>
• 20 Years with SGBS cells - a versatile in vitro model of human adipocyte biology
• A case of pancreatoblastoma in a child with Simpson-Golabi-Behmel syndrome: Highlighting the importance of alpha fetoprotein monitoring
• Anti-Adipogenic Activity of <em>Rhaponticum carthamoides</em> and Its Secondary Metabolites
• Circulating Levels of Cathelicidin Antimicrobial Peptide (CAMP) Are Affected by Oral Lipid Ingestion
• Differential effects of dolutegravir, bictegravir and raltegravir in adipokines and inflammation markers on human adipocytes
• DIS3L2 Gene Mutation Causes the Perlman Syndrome of Overgrowth and Wilms Tumor Susceptibility
• Divergent effects of the antiretroviral drugs, dolutegravir, tenofovir alafenamide, and tenofovir disoproxil fumarate, on human adipocyte function
• Drug-Initiated Activity Metabolomics Identifies Myristoylglycine as a Potent Endogenous Metabolite for Human Brown Fat Differentiation
• Effects of allicin on human Simpson-Golabi-Behmel syndrome cells in mediating browning phenotype
• Endocrine disruption of adipose physiology: Screening in SGBS cells
• Giant prostatic utricle cyst in a newborn with Simpson-Golabi-Behmel syndrome: Voiding cysturethrography essential for the diagnosis
• Human Genetics of Ventricular Septal Defect
• Hypoxia-driven metabolic reprogramming of adipocytes fuels cancer cell proliferation
• Increased secretion of adipocyte-derived extracellular vesicles is associated with adipose tissue inflammation and the mobilization of excess lipid in human obesity
• Insulin-Induced AKR1C3 Induces Fatty Acid Synthase in a Model of Human PCOS Adipocytes
• Meteorin-like levels are associated with active brown adipose tissue in early infancy
• Myricetin attenuates hypoxia-induced inflammation in human adipocytes
• Novel <em>GPC3</em> Gene Mutation in Simpson-Golabi-Behmel Syndrome with Endocrine Anomalies: A Case Report
• Phenotypic spectrum and tumor risk in Simpson-Golabi-Behmel syndrome: Case series and comprehensive literature review
• Prenatal diagnosis of Simpson-Golabi-Behmel syndrome type 1 with an 814 kb Xq26.2 deletion with the initial presentation of a thick nuchal fold
• SARS-CoV-2 Infection Alters the Phenotype and Gene Expression of Adipocytes
• Simpson-Golabi-Behmel syndrome
• Simpson-Golabi-Behmel Syndrome Type 1
• Simpson-Golabi-Behmel syndrome type 1 with normal birth parameters
• SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis
• Single-cell transcriptome dataset of human and mouse in vitro adipogenesis models
• Stages of preadipocyte differentiation: biomarkers and pathways for extracellular structural remodeling
• Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum