Page last updated: 2024-11-08

alanine and Genetic Diseases

alanine has been researched along with Genetic Diseases in 2 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
D'Ari, R1
Casadesús, J1
Barbetti, F1
Gejman, PV1
Taylor, SI1
Raben, N1
Cama, A1
Bonora, E1
Pizzo, P1
Moghetti, P1
Muggeo, M1
Roth, J1

Other Studies

2 other studies available for alanine and Genetic Diseases

ArticleYear
Underground metabolism.
    BioEssays : news and reviews in molecular, cellular and developmental biology, 1998, Volume: 20, Issue:2

    Topics: Alanine; Biological Evolution; Energy Metabolism; Enzymes; Genetic Diseases, Inborn; Glutamic Acid;

1998
Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresis.
    Diabetes, 1992, Volume: 41, Issue:4

    Topics: Alanine; Alleles; Arginine; Base Sequence; Child; DNA; Electrophoresis, Polyacrylamide Gel; Exons; F

1992