Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) comprise a heterogeneous group of clinically diverse tumors; their management is based on clin...

Congenital adrenal hyperplasia (CAH) is an autosomal recessive condition associated with enzymatic deficiencies affecting the adrenal steroid synthesi...

Phosphomannomutase 2-congenital disorder of glycosylation (PMM2-CDG) is a hereditary defect causing hypoglycosylation of N-linked glycoproteins. It wa...

Abstract not available - data parsing issue resolved

Abstract not available - data parsing issue resolved

Clathrin-mediated endocytosis (CME) is a critical pathway for cellular uptake of metabolites, hormones, and pathogens, including viruses. Recent advan...

UV irradiation stimulates the production of pro-opiomelanocortin (POMC) and its derived peptides, for example, α-melanocyte stimulating hormone (α-MSH...

Abstract not available - data parsing issue resolved

Medullary thyroid carcinoma (MTC) is the most common neuroendocrine carcinoma within the thyroid gland, characterized by strong invasiveness, high met...

Abstract not available - data parsing issue resolved

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This study investigated clinical and genetic characteristics of Chinese pediatric patients with single large-scale mitochondrial DNA deletions (SLSMD)...

While many jurisdictions have phased out use of bisphenol A (BPA), there is increasing exposure to mixtures of BPA alternatives. Like BPA, some altern...