serine has been researched along with Genetic Diseases, Inborn 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.
Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Fleischhauer, R | 1 |
| Mitrovic, N | 1 |
| Deymeer, F | 1 |
| Lehmann-Horn, F | 1 |
| Lerche, H | 1 |
| Fraser, RA | 1 |
| Goetinck, PF | 1 |
2 other studies available for serine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenita.
Topics: Amino Acid Substitution; Biological Transport; Cell Line; Embryo, Mammalian; Genetic Diseases, Inbor | 1998 |
Reduced synthesis of chondroitin sulfate by cartilage from the mutant, nanomelia.
Topics: Animals; Bone Diseases, Developmental; Carbon Isotopes; Cartilage; Chick Embryo; Chondroitin; Chroma | 1971 |