aspartic acid has been researched along with Thalassemia in 11 studies
Aspartic Acid: One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
aspartic acid : An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
L-aspartic acid : The L-enantiomer of aspartic acid.
Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (81.82) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (9.09) | 29.6817 |
| 2010's | 1 (9.09) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Basak, J | 1 |
| Bhattacharyya, DM | 1 |
| Mukhopadhyay, A | 1 |
| Brennan, SO | 1 |
| Williamson, D | 1 |
| Smith, MB | 1 |
| Cauchi, MN | 1 |
| Macphee, A | 1 |
| Carrell, RW | 1 |
| Yi-Tao, Z | 1 |
| Headlee, ME | 2 |
| Henson, J | 1 |
| Lam, H | 2 |
| Wilson, JB | 2 |
| Huisman, TH | 2 |
| Salkie, ML | 1 |
| Gordon, PA | 1 |
| Rigal, WM | 1 |
| Honig, GR | 1 |
| Shamsuddin, M | 1 |
| Zaizov, R | 1 |
| Steinherz, M | 1 |
| Solar, I | 1 |
| Kirschmann, C | 1 |
| Agarwal, KN | 1 |
| Lie-Injo, LE | 1 |
| Dozy, AM | 1 |
| Kan, YW | 1 |
| Lopes, M | 1 |
| Todd, D | 1 |
| Reed, RE | 1 |
| Winter, WP | 1 |
| Rucknagel, DL | 1 |
| Sukumaran, PK | 1 |
| Merchant, SM | 1 |
| Desai, MP | 1 |
| Wiltshire, BG | 1 |
| Lehmann, H | 2 |
| Idelson, LI | 1 |
| Didkovsky, NA | 1 |
| Lorkin, PA | 1 |
| Charlesworth, D | 1 |
| Rahbar, S | 1 |
| Tuchinda, S | 1 |
| Eng, LI | 1 |
11 other studies available for aspartic acid and Thalassemia
| Article | Year |
|---|---|
Fannin-Lubbock-I [α₂β₂¹¹⁹(GLY>ASP)], a rare mutation in the beta-globin gene, has been detected for the first time in a Hindu Brahmin family in West Bengal, India.
Topics: Adult; Asian People; Aspartic Acid; Base Sequence; Codon; Female; Glycine; Haplotypes; Hemoglobins, | 2014 |
HbA2 Victoria delta 24 (B6) Gly----Asp. A new delta chain variant occurring with beta-thalassemia.
Topics: Amino Acid Sequence; Aspartic Acid; Female; Genes; Genetic Variation; Glycine; Hemoglobins, Abnormal | 1984 |
Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant.
Topics: Adolescent; Adult; Asparagine; Aspartic Acid; Black People; Child; Female; Genetic Carrier Screening | 1982 |
Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia.
Topics: Adolescent; Amino Acid Sequence; Asparaginase; Aspartic Acid; Canada; Child; Female; Glutamine; Hemo | 1982 |
Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression.
Topics: Alanine; Aspartic Acid; Chemical Phenomena; Chemistry; Child, Preschool; Genetic Variation; Genotype | 1981 |
Iron and the brain: neurotransmitter receptors and magnetic resonance spectroscopy.
Topics: Anemia, Iron-Deficiency; Animals; Aspartic Acid; Brain; Choline; Creatinine; Female; Iron; Iron Defi | 2001 |
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
Topics: Aspartic Acid; Chemical Phenomena; Chemistry; Chromosome Deletion; DNA; Genetic Carrier Screening; G | 1979 |
Haemoglobin inkster (alpha2 85aspartic acid leads to valine beta2) coexisting with beta-thalassaemia in a Caucasian family.
Topics: Amino Acid Sequence; Aspartic Acid; Chromatography, Gel; Chromatography, Ion Exchange; Chromatograph | 1974 |
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families.
Topics: Adult; Amino Acid Sequence; Aspartic Acid; Blood Protein Electrophoresis; Child; Child, Preschool; C | 1972 |
Haemoglobin H disease in a Russian family.
Topics: Adult; Anemia, Hemolytic; Aspartic Acid; Blood Protein Electrophoresis; Carbon Isotopes; Chromium Is | 1971 |
Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine.
Topics: Adult; Amino Acid Sequence; Aspartic Acid; Child; Chromatography, Ion Exchange; Chromatography, Pape | 1970 |