aspartic acid has been researched along with Anemia, Hemolytic, Acquired in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (75.00) | 18.7374 |
| 1990's | 2 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cianetti, L; Giampaolo, A; Marinucci, M; Musumeci, S; Russo, A; Russo, G; Schilirò, G; Tentori, L | 1 |
| Clegg, JB; Green, B; Morris, M; Ohba, Y; Parker, NE; Rees, DC; Rochette, J; Sasaki, H; Schofield, C; Tanaka, A | 1 |
| Bechtel, KC; Johnson, MH; Moo-Penn, WF; Schmidt, RM; Therrell, BL | 1 |
| Hori, K; Mukai, T; Takahashi, I; Takasaki, Y | 1 |
| Fleming, PJ; Gilbert, AT; Holland, RA; Hughes, WG; Sumner, DR; Tibben, EA | 1 |
| Blanke, S; Johnsen, A; Wimberley, PD | 1 |
| Didkovskiĭ, NA; Idel'son, LI; Kaseĭ, R; Lemann, G; Lorkin, P | 1 |
| Didkovsky, NA; Idelson, LI | 1 |
8 other study(ies) available for aspartic acid and Anemia, Hemolytic, Acquired
| Article | Year |
|---|---|
HB Shepherds Bush (alpha 2 beta 2 74 (E18) Gly replaced by Asp) in two Italian carriers.
Topics: Adult; Anemia, Hemolytic; Aspartic Acid; Electrophoresis, Cellulose Acetate; Female; Genetic Variation; Glycine; Hemoglobins, Abnormal; Humans; Italy; Male | 1981 |
A novel silent posttranslational mechanism converts methionine to aspartate in hemoglobin Bristol (beta 67[E11] Val-Met->Asp).
Topics: Adolescent; Amino Acid Sequence; Anemia, Hemolytic; Aspartic Acid; Base Sequence; DNA Mutational Analysis; Globins; Heinz Bodies; Hemoglobins, Abnormal; Humans; Male; Mass Spectrometry; Methionine; Middle Aged; Molecular Sequence Data; Protein Processing, Post-Translational; Valine | 1996 |
Hemoglobin Lufkin: beta 29 (B11) Gly replaced by Asp. An unstable hemoglobin variant involving an internal amino acid residue.
Topics: Amino Acids; Anemia, Hemolytic; Aspartic Acid; Child; Electrophoresis, Cellulose Acetate; Genetic Variation; Globins; Glycine; Hemoglobins, Abnormal; Humans; Hydrogen-Ion Concentration; Male; Oxygen; Peptides; Texas | 1977 |
Human aldolase A of a hemolytic anemia patient with Asp-128----Gly substitution: characteristics of an enzyme generated in E. coli transfected with the expression plasmid pHAAD128G.
Topics: Amino Acid Sequence; Anemia, Hemolytic; Aspartic Acid; Base Sequence; Circular Dichroism; Escherichia coli; Fructose-Bisphosphate Aldolase; Gene Expression Regulation, Enzymologic; Glycine; Humans; Hydrolysis; Isoenzymes; Molecular Sequence Data; Plasmids; Protein Denaturation; Transfection; Trypsin | 1990 |
Hemoglobin Windsor or beta 11 (A8)Val----Asp: a new unstable beta-chain hemoglobin variant producing a hemolytic anemia.
Topics: Amino Acid Sequence; Amino Acids; Anemia, Hemolytic; Aspartic Acid; Chromatography; Female; Genetic Variation; Hemoglobin A; Hemoglobins, Abnormal; Humans; Infant; Molecular Sequence Data; Peptide Fragments; Trypsin; Valine | 1989 |
Hb Volga [B27 (B9) AlA----AsP], a possible de novo mutation in a Danish person.
Topics: Adult; Alanine; Amino Acid Sequence; Amino Acids; Anemia, Hemolytic; Aspartic Acid; Denmark; Hemoglobins, Abnormal; Humans; Male; Molecular Sequence Data; Mutation | 1989 |
[New unstable hemoglobin "Moskva" beta 24 (B6) glycine-aspartic acid].
Topics: Adolescent; Anemia, Hemolytic; Aspartic Acid; Electrophoresis, Polyacrylamide Gel; Female; Glycine; Hemoglobins, Abnormal; Humans; Leukemia, Myeloid; Peptides | 1974 |
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 |