serine has been researched along with Mucopolysaccharidosis I in 2 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Mucopolysaccharidosis I: Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (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 |
---|---|
Matalon, R | 1 |
Dorfman, A | 1 |
Onisawa, J | 1 |
Lee, TY | 1 |
2 other studies available for serine and Mucopolysaccharidosis I
Article | Year |
---|---|
Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture.
Topics: Acetates; Culture Techniques; Fibroblasts; Glycosaminoglycans; Humans; Mucopolysaccharidosis I; Puro | 1966 |
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Pr | 1970 |