serine has been researched along with Addison Disease and Cerebral Sclerosis in 3 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.
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 |
---|---|
Perusi, C | 1 |
Gomez-Lira, M | 1 |
Mottes, M | 1 |
Pignatti, PF | 1 |
Bertini, E | 1 |
Cappa, M | 1 |
Vigliani, MC | 1 |
Schiffer, D | 1 |
Rizzuto, N | 1 |
Salviati, A | 1 |
Berger, J | 1 |
Korosec, T | 1 |
Unterrainer, G | 1 |
Molzer, B | 1 |
Cook, HW | 1 |
Thomas, SE | 1 |
Xu, Z | 1 |
1 review available for serine and Addison Disease and Cerebral Sclerosis
Article | Year |
---|---|
Essential fatty acids and serine as plasmalogen precursors in relation to competing metabolic pathways.
Topics: Adrenoleukodystrophy; Fatty Acids, Essential; Fatty Acids, Unsaturated; Glioma; Humans; Infant, Newb | 1991 |
2 other studies available for serine and Addison Disease and Cerebral Sclerosis
Article | Year |
---|---|
Two novel missense mutations causing adrenoleukodystrophy in Italian patients.
Topics: Adrenoleukodystrophy; Adult; ATP Binding Cassette Transporter, Subfamily D, Member 1; ATP-Binding Ca | 1999 |
A de novo adrenoleukodystrophy gene (ABCD1) mutation S636I without detectable ABCD1 protein and a R104C mutation with normal amounts of protein from an Austrian patient collective.
Topics: Adrenal Insufficiency; Adrenoleukodystrophy; Adult; Amino Acid Substitution; Arginine; ATP Binding C | 2000 |