Ganglioside GD1

Ganglioside GD1 is a lipid of Sphingolipids (SP) class. Ganglioside gd1 is associated with abnormalities such as Sensory neuropathy, Neuropathy, Neuritis, Motor, Autoimmune Syndrome Type II, Polyglandular and protrusion. The involved functions are known as Drug Interactions, inhibitors, Signal Transduction, Baresthesia and Biological function, NOS. Ganglioside gd1 often locates in Membrane, nucleocapsid location, Cell membrane, Cell surface and Face. The associated genes with Ganglioside GD1 are Polypeptides, N-dodecyl-L-lysine amide, anti-IgM, VIP gene and Homologous Gene. The related lipids are sialogangliosides, ganglioside, GD1b, GT1b-ganglioside, ganglioside, GD1a and IV(4)-galactosyl-N-acetylganglioside GD1a.

References related to locations published in Biochim. Biophys. Acta


PMIDJournalPublished DateAuthorTitle
26119566Biochim. Biophys. Acta2015Heredia V et al.Interfacial stabilization of the antitumoral drug Paclitaxel in monolayers of GM1 and GD1a gangliosides.
27806911Biochim. Biophys. Acta2017Ruggiero FM et al.Membrane binding, endocytic trafficking and intracellular fate of high-affinity antibodies to gangliosides GD1a and GM1.
22206893Biochim. Biophys. Acta2012Viljetić B et al.Distribution of mono-, di- and trisialo gangliosides in the brain of Actinopterygian fishes.
15629689Biochim. Biophys. Acta2005Heffer-Lauc M et al.Membrane redistribution of gangliosides and glycosylphosphatidylinositol-anchored proteins in brain tissue sections under conditions of lipid raft isolation.
11278168Biochim. Biophys. Acta2001Tatsumi K et al.Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders.