aspartic acid has been researched along with alpha-Thalassemia in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Cao, X; Cao, Y; Chen, H; Chen, X; Li, G; Nie, H; Su, J; Wei, F | 1 |
| Ayukarn, K; Changtrakun, Y; Fucharoen, G; Fucharoen, S; Sanchaisuriya, K; Siriratmanawong, N | 1 |
| Fucharoen, S; Ngiwsara, L; Srisomsap, C; Svasti, J; Winichagoon, P | 1 |
| Akramipour, R; Muniz, A; Nagel, RL; Rahimi, Z; Vaisi-Raygani, A | 1 |
| Altay, C; Baysal, E; Cürük, MA; Dimovski, AJ; Gu, LH; Gürgey, A; Huisman, TH; Kutlar, F; Molchanova, TP; Webber, BB | 1 |
| Arruda, VR; Costa, FF; Grignoli, CR; Kimura, EM; Saad, ST; Sonati, MF; Wenning, MR | 1 |
6 other study(ies) available for aspartic acid and alpha-Thalassemia
| Article | Year |
|---|---|
Amniotic fluid metabolomic and lipidomic alterations associated with hemoglobin Bart's diseases.
Topics: alpha-Thalassemia; Amniotic Fluid; Aspartic Acid; Biomarkers; Female; Glutamates; Hemoglobins, Abnormal; Humans; Hydrops Fetalis; Lipidomics; Pregnancy; Triglycerides | 2021 |
Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
Topics: Adolescent; Adult; Aged; alpha-Thalassemia; Asparagine; Aspartic Acid; Base Sequence; Chromosome Segregation; Female; Gene Deletion; Glutamic Acid; Hemoglobin E; Hemoglobins, Abnormal; Heterozygote; Humans; Lysine; Male; Middle Aged; Pregnancy; Thailand | 2002 |
Two cases of compound heterozygosity for Hb Hekinan [alpha27(B8)Glu-->Asp (alpha1)] and alpha-thalassemia in Thailand.
Topics: Adult; alpha-Thalassemia; Amino Acid Substitution; Aspartic Acid; Female; Genotype; Globins; Glutamic Acid; Hemoglobins, Abnormal; Heterozygote; Humans; Thailand | 2004 |
An Iranian child with HbQ-Iran [alpha75 (EF4) Asp-->His]/-alpha3.7 kb/IVSII.1 G-->A: first report.
Topics: alpha-Thalassemia; Amino Acid Substitution; Aspartic Acid; beta-Thalassemia; Child, Preschool; Hemoglobins, Abnormal; Histidine; Humans; Male; Mutation | 2007 |
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
Topics: Adult; alpha-Thalassemia; Amino Acid Sequence; Aspartic Acid; Base Sequence; Child; Child, Preschool; Erythrocytes; Female; Genetic Variation; Globins; Glycine; Hemoglobins, Abnormal; Humans; Male; Middle Aged; Molecular Sequence Data; Oligonucleotide Probes; Point Mutation; Reticulocytes; Sequence Deletion; Turkey | 1993 |
Hb Rio Claro [beta34(B16)Val-->Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha47(CE5)Asp-->His] and alpha-thalassemia-2(-alpha3.7).
Topics: Adult; alpha-Thalassemia; Aspartic Acid; Child, Preschool; Electrophoresis; Hemoglobins, Abnormal; Histidine; Humans; Male; Methionine; Point Mutation; Valine | 1999 |