phenylalanine has been researched along with HbS Disease in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 14 (93.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (6.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Knee, KM; Mukerji, I | 1 |
| Bookchin, RM; Chang, H; Ewert, SM; Nagel, RL | 1 |
| Chiu, DT; Düzgünes, N; Lubin, B; Schwartz, RS | 1 |
| Altman, J; Gorecki, M; Rich, A; Votano, JR; Wilchek, M | 1 |
| Ackerman, S; DiMaio, J; Noguchi, CT; Schechter, AN; Schiller, PW | 1 |
| Acquaye, CT; Gorecki, M; Rich, A; Votano, JR; Wilchek, M | 1 |
| Mamunes, P | 1 |
| Kumpati, J | 3 |
| Acquaye, CT; Ellory, JC; Gorecki, M; Wilchek, M; Young, JD | 1 |
| Levy, HL | 1 |
| Balda, BR; Lukacs, I | 1 |
| Bank, A; Braverman, AS; Marks, PA | 1 |
| Bank, A; Marks, PA | 1 |
4 review(s) available for phenylalanine and HbS Disease
| Article | Year |
|---|---|
Comparative evaluation of fifteen anti-sickling agents.
Topics: Anemia, Sickle Cell; Antisickling Agents; Aspirin; Azepines; Carbamyl Phosphate; Cyanates; Cystamine; Dimethyl Adipimidate; Drug Evaluation; Erythrocyte Indices; Glyceraldehyde; Hemoglobins; Humans; Imidoesters; Mechlorethamine; Oxygen Consumption; Phenylalanine; Pyridoxal; Solubility; Urea | 1983 |
Neonatal screening tests.
Topics: Adenosine Deaminase; Anemia, Sickle Cell; Biological Assay; Costs and Cost Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Tyrosine; United States | 1980 |
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine | 1973 |
[Molecular biologic aspects in dermatology demonstrated by some hereditary enzyme defects].
Topics: Albinism; Alkaptonuria; Anemia, Sickle Cell; Chromosomes; Hartnup Disease; Humans; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Models, Chemical; Molecular Biology; Phenylalanine; Phenylketonurias; Porphyrias; Skin Diseases; Tyrosine | 1968 |
11 other study(ies) available for phenylalanine and HbS Disease
| Article | Year |
|---|---|
Real time monitoring of sickle cell hemoglobin fiber formation by UV resonance Raman spectroscopy.
Topics: Amino Acid Substitution; Anemia, Sickle Cell; Crystallography, X-Ray; Hemoglobin, Sickle; Hemolysis; Humans; Kinetics; Models, Molecular; Mutation; Phenylalanine; Protein Conformation; Protein Subunits; Spectrum Analysis, Raman; Tryptophan; Tyrosine | 2009 |
Interaction of phosphatidylserine-phosphatidylcholine liposomes with sickle erythrocytes. Evidence for altered membrane surface properties.
Topics: Anemia, Sickle Cell; Cell Separation; Diamide; Edetic Acid; Erythrocytes; Humans; Liposomes; Oxygen; Phenylalanine; Phosphatidylcholines; Phosphatidylserines; Pulmonary Surfactants; Sickle Cell Trait; Triolein | 1983 |
Potential use of biaromatic L-phenylalanyl derivatives as therapeutic agents in the treatment of sickle cell disease.
Topics: Anemia, Sickle Cell; Carbon Radioisotopes; Erythrocytes; Hemoglobin, Sickle; Homozygote; Humans; Kinetics; Phenylalanine; Tritium | 1984 |
The effect of phenylalanine derivatives on the solubility of deoxyhemoglobin S. A model class of gelation inhibitors.
Topics: Anemia, Sickle Cell; Antisickling Agents; Colloids; Crystallography; Hemoglobin, Sickle; Humans; Models, Chemical; Phenylalanine; Solubility; Structure-Activity Relationship | 1983 |
Antisickling activity of amino acid benzyl esters.
Topics: Amino Acids; Anemia, Sickle Cell; Antisickling Agents; Benzyl Compounds; Erythrocyte Membrane; Humans; In Vitro Techniques; Osmotic Fragility; Oxygen; Phenylalanine | 1980 |
Inhibition of in vitro sickling by liposome-mediated transport of amino acids into intact human red blood cells.
Topics: Amino Acids; Anemia, Sickle Cell; Antisickling Agents; Erythrocytes; Humans; In Vitro Techniques; Liposomes; Pharmaceutical Vehicles; Phenylalanine; Tryptophan | 1982 |
Mode of transport and possible mechanism of action of L-phenylalanine benzyl ester as an anti-sickling agent.
Topics: Anemia, Sickle Cell; Antisickling Agents; Biological Transport; Erythrocytes; Hemolysis; Humans; Kinetics; Phenylalanine; Structure-Activity Relationship | 1982 |
Liposome-loaded phenylalanine or tryptophan as sickling inhibitor: a possible therapy for sickle cell disease.
Topics: Anemia, Sickle Cell; Erythrocytes; Humans; Liposomes; Osmotic Fragility; Phenylalanine; Tryptophan | 1987 |
Effect of phenylalanine- or tryptophan-loaded liposomes on the rheological properties of AA and SS erythrocytes.
Topics: Anemia, Sickle Cell; Blood Viscosity; Erythrocytes; Humans; Liposomes; Phenylalanine; Tryptophan | 1987 |
Globin chain synthesis in thalassemia.
Topics: Anemia, Sickle Cell; Blood Proteins; Carbon Isotopes; Chromatography; Globins; Humans; Molecular Biology; Phenylalanine; Ribosomes; RNA, Messenger; Thalassemia; Uracil Nucleotides | 1969 |
Protein synthesis in a cell free human reticulocyte system: ribosome function in thalassemia.
Topics: Amino Acids; Anemia, Hemolytic; Anemia, Sickle Cell; Humans; In Vitro Techniques; Phenylalanine; Proteins; Reticulocytes; Ribosomes; Thalassemia | 1966 |