Apr 26, 2023 · GM1 gangliosidosis is an inherited disorder that destroys nerve cells (neurons) in the brain and spinal cord. This condition can be ...
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GM1 (monosialotetrahexosylganglioside) the "prototype" ganglioside, is a member of the ganglio series of gangliosides which contain one sialic acid residue.
GM1
GM1 the "prototype" ganglioside, is a member of the ganglio series of gangliosides which contain one sialic acid residue. GM1 has important physiological properties and impacts neuronal plasticity and repair mechanisms, and the release of... Wikipedia
Molar mass: 1,546.823 g/mol
Formula: C73H131N3O31
3D model (JSmol): Interactive image
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GM1 Gangliosidosis (GM1) is a rare inherited genetic disorder that primarily affects children. It has many debilitating ramifications, some of which are ...
May 31, 2023 · Overall, GM1 is protective for the CNS and promotes functional recovery of the brain from various diseases and pathological damages [125,384].
GM1 is a protein-associated glycolipid in microdomains. Although GM1 and other gangliosides are known to subserve important intracellular functions, they have ...
GM1 gangliosidosis, also called beta-galactosidase-1 deficiency, is a genetic disorder that progressively destroys nerve cells in the brain and spinal cord.
Apr 26, 2024 · GM1 gangliosidosis (GM1) is a rare but fatal neurodegenerative disease caused by dysfunction or lack of production of lysosomal enzyme, ...
Ganglioside GM1 is a component of neuronal membranes that may enhance the effects of brain-derived nerve growth factor and glial-derived neurotrophic factor ...
Jan 7, 2022 · Monosialotetrahexosylganglioside (GM1) gangliosidosis is an autosomal recessive disorder caused by the lack of ß-galactosidase encoded by GLB1.
GM1 gangliosidosis is a rare inherited lysosomal storage disorder. Molecules accumulate on the brain and spinal cord, causing life-threatening problems.