glycine has been researched along with Gangliosidoses in 4 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (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 |
|---|---|
| Aicardi, J | 1 |
| Brady, RO | 1 |
| Paw, BH | 1 |
| Kaback, MM | 1 |
| Neufeld, EF | 1 |
| Raghavan, S | 1 |
| Lyerla, TA | 1 |
| Krusell, A | 1 |
| Kolodny, EH | 1 |
1 review available for glycine and Gangliosidoses
| Article | Year |
|---|---|
[Myoclonias as a manifestation of degenerative disorders of the central nervous system in childhood].
Topics: Adolescent; Age Factors; Brain Diseases; Cerebellar Diseases; Ceroid; Child; Child, Preschool; Diagn | 1982 |
3 other studies available for glycine and Gangliosidoses
| Article | Year |
|---|---|
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors | 1976 |
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidase.
Topics: Adult; Base Sequence; beta-N-Acetylhexosaminidases; Cells, Cultured; Europe; Fibroblasts; G(M2) Gang | 1989 |
Metabolic activities in human skin fibroblasts preloaded with labeled GM2-ganglioside.
Topics: Fibroblasts; G(M1) Ganglioside; Gangliosidoses; Glycine; Humans; Kinetics; Protein Biosynthesis; Ref | 1987 |