One of the most important inherited metabolic disorders is GM1 gangliosidosis, which is a
progressive neurological disorder. The main cause of this disease is a genetic defect in the …

Identification of features with high levels of confidence in liquid chromatography–mass
spectrometry (LC–MS) lipidomics research is an essential part of biomarker discovery, but …

Background Mucopolysaccharidosis (MPS) and glycoproteinosis are 2 groups of
heterogenous lysosomal storage disorders (LSDs) caused by defective degradation of …

This study explored the potential of Andrographis paniculata in regulating redox imbalance
using planaria as a model organism. Decapitated planaria were regenerated in water, A …

GM1-gangliosidosis and/or Morquio B disease, galactosialidosis (GS), and sialidosis are
three distinct lysosomal storage diseases (LSDs) that arise from dysfunction of one or more …