choline has been researched along with Adult Sandhoff Disease in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"Sandhoff disease is a progressive neurodegenerative disorder caused by mutations in the HEXB gene which encodes for the beta-subunit of beta-hexosaminidase A and B, resulting in ganglioside GM(2) accumulation in the brain." | 1.32 | Phospholipid synthesis is decreased in neuronal tissue in a mouse model of Sandhoff disease. ( Bodennec, J; Buccoliero, R; Futerman, AH; Sandhoff, K; Van Echten-Deckert, G, 2004) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Buccoliero, R | 1 |
Bodennec, J | 1 |
Van Echten-Deckert, G | 1 |
Sandhoff, K | 1 |
Futerman, AH | 1 |
1 other study available for choline and Adult Sandhoff Disease
Article | Year |
---|---|
Phospholipid synthesis is decreased in neuronal tissue in a mouse model of Sandhoff disease.
Topics: Animals; beta-N-Acetylhexosaminidases; Brain; Carbon Radioisotopes; CDPdiacylglycerol-Serine O-Phosp | 2004 |