4-methylumbelliferyl glucuronide has been researched along with Tay-Sachs Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Guiral, M; Mahuran, D; Reid, SP; Tropak, MB; Withers, SG | 1 |
| Oliveira, P; Pinto, R; Ribeiro, MG; Sá Miranda, MC | 1 |
| Goldman, B; Peleg, L; Shihab, S; Shukry, A | 1 |
3 other study(ies) available for 4-methylumbelliferyl glucuronide and Tay-Sachs Disease
| Article | Year |
|---|---|
Pharmacological enhancement of beta-hexosaminidase activity in fibroblasts from adult Tay-Sachs and Sandhoff Patients.
Topics: Adult; beta-N-Acetylhexosaminidases; Cell Line; Enzyme Activation; Enzyme Inhibitors; Female; Fibroblasts; Hexosaminidase A; Hot Temperature; Humans; Hymecromone; In Vitro Techniques; Lysosomes; Molecular Chaperones; Mutation; Protein Folding; Sandhoff Disease; Tay-Sachs Disease | 2004 |
Identification of GM2-gangliosidosis B1 variant carriers.
Topics: Adolescent; Adult; Aged; beta-N-Acetylhexosaminidases; Child; Child, Preschool; Female; Genetic Carrier Screening; Genetic Variation; Hexosaminidase A; Humans; Hymecromone; Male; Middle Aged; Tay-Sachs Disease | 1993 |
Prenatal and postnatal studies of a late infantile GM2 gangliosidosis in a family of Syrian origin: a possible B1 variant.
Topics: beta-N-Acetylhexosaminidases; Female; Genetic Carrier Screening; Hexosaminidase A; Humans; Hymecromone; Infant, Newborn; Male; Syria; Tay-Sachs Disease | 1993 |