Page last updated: 2024-11-08

serine and Mucopolysaccharidosis I

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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Matalon, R1
Dorfman, A1
Onisawa, J1
Lee, TY1

Other Studies

2 other studies available for serine and Mucopolysaccharidosis I

ArticleYear
Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture.
    Proceedings of the National Academy of Sciences of the United States of America, 1966, Volume: 56, Issue:4

    Topics: Acetates; Culture Techniques; Fibroblasts; Glycosaminoglycans; Humans; Mucopolysaccharidosis I; Puro

1966
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
    Biochemical medicine, 1970, Volume: 3, Issue:5

    Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Pr

1970