cysteine has been researched along with HbS Disease in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (27.78) | 18.7374 |
| 1990's | 1 (5.56) | 18.2507 |
| 2000's | 8 (44.44) | 29.6817 |
| 2010's | 4 (22.22) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alayash, AI; Kassa, T; Nakagawa, A; Strader, MB; Zapol, WM | 1 |
| Cate, SA; Chen, J; Dominguez, M; Fu, X; Konkle, BA; López, JA; Osborn, W; Özpolat, T | 1 |
| Alayash, AI; Jana, S; Jia, Y; Kassa, T; Meng, F; Strader, MB; Wilson, MT | 1 |
| Abish, S; Alawadi, A; Allard-Coutu, A; Bérubé, D; Dauletbaev, N; Jacob, SV; Lands, LC; Pastore, Y; Robitaille, N; Shilo, NR | 1 |
| Iyamu, EW; Perdew, H; Woods, GM | 1 |
| Bonaventura, C; Ferruzzi, G; Godette, G; Henkens, R; Stevens, RD; Tesh, S | 1 |
| Adams, C; Drane, WE; Kedar, A; Nicole, M; Shaeffer, D | 1 |
| Badaloo, A; Forrester, T; Jahoor, F; Reid, M | 1 |
| Flory, MR; Knee, KM; Mukerji, I; Roden, CK | 1 |
| Bookchin, RM; Nagel, RL; Ranney, HM | 1 |
| Honig, GR; Mason, RG; Shahidi, NT; Shamsuddin, M; Tarr, GE; Tremaine, LM; Vida, LN | 1 |
| Alayash, AI; Cashon, RE; Hrinczenko, BW; Pannell, LK; Schechter, AN; Wojtkowski, TL | 1 |
| Ohnishi, ST; Ohnishi, T | 1 |
| Ellory, JC; Gibson, JS; Kiessling, K; Roberts, N | 1 |
| Zeidan, HM | 1 |
| Cottam, GL; Waterman, MR; Yamaoka, K | 1 |
| Gillette, PN; Manning, JM; Nigen, AM; Peterson, CM | 1 |
| Gerhold, WM; Mandel, EE | 1 |
18 other study(ies) available for cysteine and HbS Disease
| Article | Year |
|---|---|
Targeting βCys93 in hemoglobin S with an antisickling agent possessing dual allosteric and antioxidant effects.
Topics: Anemia, Sickle Cell; Antioxidants; Antisickling Agents; Cysteine; Disulfides; Erythrocytes; Hemoglobin, Sickle; Humans; Hydrogen Peroxide; Oxidants; Oxidation-Reduction; Oxygen; Triazoles | 2017 |
Cysteine Disulfides (Cys-ss-X) as Sensitive Plasma Biomarkers of Oxidative Stress.
Topics: Acetylcysteine; Anemia, Sickle Cell; Antioxidants; Biomarkers; Cysteine; Disulfides; Humans; Oxidative Stress; Sepsis | 2019 |
Sickle Cell Hemoglobin in the Ferryl State Promotes βCys-93 Oxidation and Mitochondrial Dysfunction in Epithelial Lung Cells (E10).
Topics: Anemia, Hemolytic; Anemia, Sickle Cell; Catalysis; Cyclic N-Oxides; Cysteine; Energy Metabolism; Heme; Heme Oxygenase (Decyclizing); Hemoglobin, Sickle; Humans; Hydrogen Peroxide; Iron; Lung; Methemoglobin; Mitochondria; Oxidation-Reduction; Oxygen Consumption; Respiratory Mucosa | 2015 |
Airway hyperreactivity is frequent in non-asthmatic children with sickle cell disease.
Topics: Adolescent; Anemia, Sickle Cell; Bronchial Hyperreactivity; Bronchial Provocation Tests; Child; Cysteine; Female; Humans; Leukotrienes; Male; Methacholine Chloride; Prospective Studies | 2016 |
Cysteine-iron promotes arginase activity by driving the Fenton reaction.
Topics: Anemia, Sickle Cell; Arginase; Cysteine; Enzyme Activation; Erythrocytes; Humans; Iron; Salicylic Acid; Superoxide Dismutase; Superoxides | 2008 |
Responses of normal and sickle cell hemoglobin to S-nitroscysteine: implications for therapeutic applications of NO in treatment of sickle cell disease.
Topics: Anemia, Sickle Cell; Animals; Chelating Agents; Cysteine; Dolphins; Heme; Hemoglobin, Sickle; Hemoglobins; Humans; Nitric Oxide; Oxidation-Reduction; Oxygen; Protein Binding; S-Nitrosothiols; Spectrometry, Mass, Electrospray Ionization; Vasodilator Agents | 2002 |
Measurement of cerebrovascular flow reserve in pediatric patients with sickle cell disease.
Topics: Acetazolamide; Adolescent; Adult; Anemia, Sickle Cell; Anticonvulsants; Brain; Cerebrovascular Circulation; Child; Cysteine; Female; Humans; Male; Organotechnetium Compounds; Oximes; Radiography; Radiopharmaceuticals; Risk Factors; Stroke; Tomography, Emission-Computed, Single-Photon | 2006 |
In vivo rates of erythrocyte glutathione synthesis in adults with sickle cell disease.
Topics: Adult; Anemia, Sickle Cell; Creatinine; Cysteine; Eating; Erythrocytes; Female; Glutathione; Glutathione Disulfide; Glycine; Humans; Hydrogen Peroxide; Isoprostanes; Male; Statistics, Nonparametric; Tyrosine | 2006 |
The role of beta93 Cys in the inhibition of Hb S fiber formation.
Topics: Anemia, Sickle Cell; Cysteine; Ethylmaleimide; Hemoglobin, Sickle; Humans; Methemoglobin; Nitric Oxide; S-Nitrosothiols; Spectrometry, Mass, Electrospray Ionization; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared; Spectrum Analysis, Raman | 2007 |
Formation and properties of hemoglobin beta-2-A-beta-2-S.
Topics: Anemia, Sickle Cell; Benzoates; Blood Protein Electrophoresis; Centrifugation, Zonal; Chemical Phenomena; Chemistry, Physical; Cysteine; Haptoglobins; Hemoglobins, Abnormal; Humans; Oxygen; Protein Binding; Solubility; Sulfhydryl Compounds | 1967 |
Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia.
Topics: Absorption; Anemia, Sickle Cell; Chromatography, Ion Exchange; Cysteine; Erythrocytes; Female; Genetic Variation; Hemoglobin A; Hemoglobin, Sickle; Hemoglobins; Hemoglobins, Abnormal; Humans; Nigeria; Oxygen; Pedigree; Serine; Sulfhydryl Reagents; Thalassemia | 1980 |
Nitric oxide-mediated heme oxidation and selective beta-globin nitrosation of hemoglobin from normal and sickle erythrocytes.
Topics: Anemia, Sickle Cell; Cysteine; Diethylamines; Erythrocytes; Globins; Heme; Hemoglobin A; Hemoglobin, Sickle; Humans; Kinetics; Mass Spectrometry; Methemoglobin; Nitric Oxide; Nitrogen Oxides; Nitroso Compounds; Oxidation-Reduction; Oxygen; S-Nitrosothiols; Spectrophotometry; Thermodynamics | 2000 |
In vitro effects of aged garlic extract and other nutritional supplements on sickle erythrocytes.
Topics: Anemia, Sickle Cell; Antioxidants; Cell Count; Cells, Cultured; Cysteine; Dietary Supplements; Erythrocyte Membrane; Garlic; Humans; Phytotherapy; Plant Extracts; Plants, Medicinal; Reactive Oxygen Species | 2001 |
A comparison in normal individuals and sickle cell patients of reduced glutathione precursors and their transport between plasma and red cells.
Topics: Adult; Amino Acid Transport System ASC; Amino Acid Transport System L; Anemia, Sickle Cell; Biological Transport; Carbon Monoxide; Cysteine; Enzyme Inhibitors; Erythrocytes; Female; Glutamic Acid; Glutamine; Glutathione; Glycine; Humans; Male; Middle Aged; Oxygen; Protein Kinase Inhibitors; Protein Kinases; Serine; Staurosporine | 2000 |
The contact sites of sickle hemoglobin as seen by spin probe-spin label techniques.
Topics: Anemia, Sickle Cell; Binding Sites; Cyclic N-Oxides; Cysteine; Electron Spin Resonance Spectroscopy; Hemoglobin, Sickle; Hemoglobins; Humans; Spin Labels; Tryptophan | 1990 |
Spin-label studies at F9(93)beta of deoxyhemoglobin S aggregation.
Topics: Acetamides; Anemia, Sickle Cell; Chromatography, Gel; Cysteine; Electron Spin Resonance Spectroscopy; Electrophoresis, Disc; Hemoglobins; Hemoglobins, Abnormal; Humans; Iodoacetates; Macromolecular Substances; Mercuribenzoates; Oxyhemoglobins; Protein Binding; Protein Conformation; Pyrrolidines; Spin Labels; Temperature; Viscosity | 1974 |
Determination of the blood concentrations of cyanate after intravenous administration to patients with sickle-cell disease.
Topics: Anemia, Sickle Cell; Carbamates; Carbon Radioisotopes; Chemical Phenomena; Chemistry; Chromatography; Cyanates; Cysteine; Half-Life; Humans; Hydrogen-Ion Concentration; Injections, Intravenous; Methods; Sulfites | 1974 |
Plasma fibrin-stabilizing factor: acquired deficiency in various disorders.
Topics: Acute Disease; Adult; Aged; Anemia, Macrocytic; Anemia, Sickle Cell; Blood Coagulation Disorders; Blood Coagulation Tests; Coronary Disease; Cysteine; Factor XIII; Fibrinogen; Hepatitis; Hot Temperature; Humans; Leukemia; Liver Cirrhosis; Liver Neoplasms; Lupus Erythematosus, Systemic; Lymphoma; Methods; Middle Aged; Myeloproliferative Disorders; Neoplasm Metastasis; Prothrombin Time; Uremia | 1969 |