Page last updated: 2024-11-08

serine and Addison Disease and Cerebral Sclerosis

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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Perusi, C1
Gomez-Lira, M1
Mottes, M1
Pignatti, PF1
Bertini, E1
Cappa, M1
Vigliani, MC1
Schiffer, D1
Rizzuto, N1
Salviati, A1
Berger, J1
Korosec, T1
Unterrainer, G1
Molzer, B1
Cook, HW1
Thomas, SE1
Xu, Z1

Reviews

1 review available for serine and Addison Disease and Cerebral Sclerosis

ArticleYear
Essential fatty acids and serine as plasmalogen precursors in relation to competing metabolic pathways.
    Biochemistry and cell biology = Biochimie et biologie cellulaire, 1991, Volume: 69, Issue:7

    Topics: Adrenoleukodystrophy; Fatty Acids, Essential; Fatty Acids, Unsaturated; Glioma; Humans; Infant, Newb

1991

Other Studies

2 other studies available for serine and Addison Disease and Cerebral Sclerosis

ArticleYear
Two novel missense mutations causing adrenoleukodystrophy in Italian patients.
    Molecular and cellular probes, 1999, Volume: 13, Issue:3

    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.
    Human mutation, 2000, Volume: 16, Issue:6

    Topics: Adrenal Insufficiency; Adrenoleukodystrophy; Adult; Amino Acid Substitution; Arginine; ATP Binding C

2000