serine has been researched along with A-Thalassemia 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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bisconte, MG | 1 |
| Caldora, M | 1 |
| Musollino, G | 2 |
| Cardiero, G | 1 |
| Flagiello, A | 2 |
| La Porta, G | 1 |
| Lagona, L | 1 |
| Prezioso, R | 1 |
| Qualtieri, G | 1 |
| Gaudiano, C | 1 |
| Medulla, E | 1 |
| Merlino, A | 1 |
| Pucci, P | 2 |
| Lacerra, G | 2 |
| Harteveld, CL | 1 |
| Rozendaal, L | 1 |
| Blom, NA | 1 |
| Lo-A-Njoe, S | 1 |
| Akkerman, N | 1 |
| Arkestijn, S | 1 |
| Van Delft, P | 1 |
| Giordano, PC | 1 |
| Waye, JS | 1 |
| Chui, DH | 1 |
| Scarano, C | 1 |
| Carestia, C | 1 |
4 other studies available for serine and A-Thalassemia
| Article | Year |
|---|---|
α-Thalassemia associated with hb instability: a tale of two features. the case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro.
Topics: Adolescent; Adult; Aged; alpha-Thalassemia; Asparagine; Base Sequence; Child; DNA Mutational Analysi | 2015 |
Hb Oegstgeest [alpha104(G11)Cys-->Ser (alpha1)]. A new hemoglobin variant associated with a mild alpha-thalassemia phenotype.
Topics: alpha-Thalassemia; Amino Acid Substitution; Anemia, Hypochromic; Child; Cysteine; Female; Hemoglobin | 2005 |
Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.
Topics: alpha-Thalassemia; Female; Genetic Variation; Hemoglobins, Abnormal; Humans; Infant, Newborn; Male; | 2007 |
Hb Foggia or alpha 117(GH5)Phe -> Ser: a new alpha 2 globin allele affecting the alpha Hb-AHSP interaction.
Topics: Adolescent; Aged; Alleles; alpha-Thalassemia; Blood Proteins; Female; Globins; Hemoglobins, Abnormal | 2008 |