choline has been researched along with Gangliosidoses in 1 studies
Gangliosidoses: A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
Excerpt | Relevance | Reference |
---|---|---|
"Cholinergic processes were measured in motor cortex, hippocampus, and striatum of cats in the terminal stages of GM1 gangliosidosis and compared to those of control cats." | 1.27 | Increased acetylcholine synthesis and release in brains of cats with GM1 gangliosidosis. ( Baker, HJ; Connor, DJ; Jope, RS, 1986) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Jope, RS | 1 |
Baker, HJ | 1 |
Connor, DJ | 1 |
1 other study available for choline and Gangliosidoses
Article | Year |
---|---|
Increased acetylcholine synthesis and release in brains of cats with GM1 gangliosidosis.
Topics: Acetylcholine; Animals; Biological Transport; Brain; Cats; Choline; Choline O-Acetyltransferase; Cor | 1986 |