aspartic acid has been researched along with Thalassemias in 11 studies
| 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; Bhattacharyya, DM; Mukhopadhyay, A | 1 |
| Brennan, SO; Carrell, RW; Cauchi, MN; Macphee, A; Smith, MB; Williamson, D | 1 |
| Headlee, ME; Henson, J; Huisman, TH; Lam, H; Wilson, JB; Yi-Tao, Z | 1 |
| Gordon, PA; Headlee, ME; Huisman, TH; Lam, H; Rigal, WM; Salkie, ML; Wilson, JB | 1 |
| Honig, GR; Kirschmann, C; Shamsuddin, M; Solar, I; Steinherz, M; Zaizov, R | 1 |
| Agarwal, KN | 1 |
| Dozy, AM; Kan, YW; Lie-Injo, LE; Lopes, M; Todd, D | 1 |
| Reed, RE; Rucknagel, DL; Winter, WP | 1 |
| Desai, MP; Lehmann, H; Merchant, SM; Sukumaran, PK; Wiltshire, BG | 1 |
| Didkovsky, NA; Idelson, LI | 1 |
| Charlesworth, D; Eng, LI; Lehmann, H; Lorkin, PA; Rahbar, S; Tuchinda, S | 1 |
11 other study(ies) available for aspartic acid and Thalassemias
| 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, Abnormal; Heterozygote; Humans; India; Infant; Middle Aged; Pedigree; Polymorphism, Single Nucleotide; Sequence Analysis, DNA; Thalassemia | 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; Humans; Male; Mutation; Thalassemia | 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; Genetic Variation; Hemoglobins, Abnormal; Humans; Infant; Lysine; Male; Mutation; Pedigree; Peptide Fragments; Thalassemia | 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; Hemoglobin A; Hemoglobin A2; Humans; Male; Middle Aged; Oxygen Consumption; Thalassemia | 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; Globins; Hemoglobin H; Hemoglobins, Abnormal; Hemolysis; Humans; Infant; Thalassemia | 1981 |
Iron and the brain: neurotransmitter receptors and magnetic resonance spectroscopy.
Topics: Anemia, Iron-Deficiency; Animals; Aspartic Acid; Brain; Choline; Creatinine; Female; Iron; Iron Deficiencies; Liver; Magnetic Resonance Spectroscopy; Micronutrients; Models, Animal; Rats; Rats, Sprague-Dawley; Receptors, GABA; Receptors, Glutamate; Receptors, Neurotransmitter; Thalassemia | 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; Globins; Glutamates; Glutamine; Hemoglobin H; Hemoglobins, Abnormal; Histidine; Humans; Hybridization, Genetic; Peptides; Thalassemia | 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; Chromatography, Paper; Cyanogen Bromide; Edetic Acid; Electrophoresis, Paper; Electrophoresis, Starch Gel; Genetics, Medical; Globins; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Models, Structural; Mutation; Thalassemia; Trypsin; Valine | 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; Chromatography, DEAE-Cellulose; Electrophoresis, Starch Gel; Female; Hemoglobins, Abnormal; Histidine; Humans; India; Infant; Male; Pedigree; Thalassemia | 1972 |
Haemoglobin H disease in a Russian family.
Topics: Adult; Anemia, Hemolytic; Aspartic Acid; Blood Protein Electrophoresis; Carbon Isotopes; Chromium Isotopes; Cytoplasmic Granules; Erythrocytes; Female; Hemoglobinometry; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Iron; Levulinic Acids; Pedigree; Peptide Biosynthesis; Porphyrins; Reticulocytes; Splenectomy; Thalassemia; USSR | 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, Paper; Chromatography, Thin Layer; Electrophoresis; Female; Genes; Hemoglobins, Abnormal; Histidine; Humans; Mutation; Peptides; Thalassemia | 1970 |