serine has been researched along with Thalassemias in 4 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 | 3 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Giordano, PC | 1 |
| Zweegman, S | 1 |
| Akkermans, N | 1 |
| Arkesteijn, SG | 1 |
| van Delft, P | 1 |
| Versteegh, FG | 1 |
| Wajcman, H | 1 |
| Harteveld, CL | 1 |
| Honig, GR | 1 |
| Shamsuddin, M | 1 |
| Mason, RG | 1 |
| Vida, LN | 1 |
| Tremaine, LM | 1 |
| Tarr, GE | 1 |
| Shahidi, NT | 1 |
| Chang, JC | 1 |
| Temple, GF | 1 |
| Trecartin, RF | 1 |
| Kan, YW | 1 |
| Rahbar, S | 1 |
| Golban-Moghadam, N | 1 |
| Saoodi, H | 1 |
4 other studies available for serine and Thalassemias
| Article | Year |
|---|---|
The first case of Hb Groene Hart [alpha119(H2)Pro-->Ser, CCT-->TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant.
Topics: Amino Acid Substitution; Genetic Variation; Hemoglobins, Abnormal; Homozygote; Humans; Netherlands; | 2007 |
Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia.
Topics: Absorption; Anemia, Sickle Cell; Chromatography, Ion Exchange; Cysteine; Erythrocytes; Female; Genet | 1980 |
Suppression of the nonsense mutation in homozygous beta 0 thalassaemia.
Topics: Codon; Genes; Mutation; RNA, Transfer; Serine; Suppression, Genetic; Thalassemia | 1979 |
Hemoglobin Lepore Boston in two Iranian families.
Topics: Alanine; Amino Acids; Blood Protein Electrophoresis; Boston; Child; Chromatography, DEAE-Cellulose; | 1974 |