serine has been researched along with alpha-Thalassemia in 4 studies
| 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; Caldora, M; Cardiero, G; Flagiello, A; Gaudiano, C; La Porta, G; Lacerra, G; Lagona, L; Medulla, E; Merlino, A; Musollino, G; Prezioso, R; Pucci, P; Qualtieri, G | 1 |
| Akkerman, N; Arkestijn, S; Blom, NA; Giordano, PC; Harteveld, CL; Lo-A-Njoe, S; Rozendaal, L; Van Delft, P | 1 |
| Chui, DH; Waye, JS | 1 |
| Carestia, C; Flagiello, A; Lacerra, G; Musollino, G; Pucci, P; Scarano, C | 1 |
4 other study(ies) available for serine and alpha-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 Analysis; Exons; Female; Genotype; Hemoglobins, Abnormal; Humans; Male; Middle Aged; Pedigree; Polymorphism, Single Nucleotide; Proline; Protein Stability; Protein Structure, Quaternary; Protein Structure, Tertiary; RNA, Messenger; Serine; Threonine; Young Adult | 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; Hemoglobins, Abnormal; Humans; Phenotype; Point Mutation; Serine | 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; Phenotype; Proline; Serine | 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; Heterozygote; Humans; Male; Middle Aged; Molecular Chaperones; Mutation; Phenylalanine; Serine | 2008 |