glycine has been researched along with Sphingolipid Storage Diseases in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Schlotawa, L | 1 |
| Adang, LA | 1 |
| Radhakrishnan, K | 1 |
| Ahrens-Nicklas, RC | 1 |
| Baenziger, JU | 1 |
| Dierks, T | 2 |
| Schmidt, B | 2 |
| Borissenko, LV | 1 |
| Peng, J | 1 |
| Preusser, A | 1 |
| Mariappan, M | 2 |
| von Figura, K | 2 |
| Dickmanns, A | 1 |
| Preusser-Kunze, A | 1 |
| Ficner, R | 1 |
| Rudolph, MG | 1 |
| Omenn, GS | 1 |
3 reviews available for glycine and Sphingolipid Storage Diseases
| Article | Year |
|---|---|
Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
Topics: Glycine; Humans; Mucopolysaccharidoses; Multiple Sulfatase Deficiency Disease; Mutation; Oxidoreduct | 2020 |
A major step on the road to understanding a unique posttranslational modification and its role in a genetic disease.
Topics: Alanine; Animals; Catalytic Domain; Gene Expression Regulation, Enzymologic; Glycine; Humans; Mutati | 2003 |
Inborn errors of metabolism: clues to understanding human behavioral disorders.
Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter | 1976 |
2 other studies available for glycine and Sphingolipid Storage Diseases
| Article | Year |
|---|---|
Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme.
Topics: Alanine; Amino Acid Sequence; Animals; Base Sequence; Biological Assay; Cattle; CHO Cells; Chromosom | 2003 |
Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme.
Topics: Alanine; Amino Acid Sequence; Binding Sites; Calcium; Catalytic Domain; Crystallography, X-Ray; Cyst | 2005 |