Page last updated: 2024-08-22

dithiothreitol and HbS Disease

dithiothreitol has been researched along with HbS Disease in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19903 (37.50)18.7374
1990's2 (25.00)18.2507
2000's2 (25.00)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Banerjee, R; Kurthen, A; Vitvitsky, V; Yadav, PK1
Franco, RS; Jiang, M; Joiner, CH; Rettig, RK1
Franco, RS; Jiang, M; Joiner, CH; Rettig, RK; Risinger, M1
Campbell, NF; Gibson, XA; Goodman, SR; McIntyre, J; Monteiro, CA; Shah, A; Shartava, A; Zhang, Y1
Gibson, X; Goodman, SR; Monteiro, CA; Shartava, A1
Bookchin, RM; Fischer, S; Nagel, RL; Roth, EF; Tellez-Nagel, I1
Hebbel, RP; Moyer, NL; Rank, BH1
Carlsson, J; Hebbel, RP; Rank, BH1

Other Studies

8 other study(ies) available for dithiothreitol and HbS Disease

ArticleYear
Sulfide oxidation by a noncanonical pathway in red blood cells generates thiosulfate and polysulfides.
    The Journal of biological chemistry, 2015, Mar-27, Volume: 290, Issue:13

    Topics: Anemia, Sickle Cell; Dithiothreitol; Erythrocytes; Hemoglobin, Sickle; Humans; Hydrogen Sulfide; Kinetics; Methemoglobin; Nitrates; Oxidation-Reduction; Reducing Agents; Sulfides; Thiosulfates

2015
KCl cotransport mediates abnormal sulfhydryl-dependent volume regulation in sickle reticulocytes.
    Blood, 2004, Nov-01, Volume: 104, Issue:9

    Topics: Anemia, Sickle Cell; Biological Transport; Cell Size; Cells, Cultured; Dithiothreitol; Humans; Hydrogen-Ion Concentration; Kinetics; Oxidation-Reduction; Potassium Chloride; Reticulocytes; Sulfhydryl Compounds; Symporters

2004
Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes.
    Blood, 2007, Feb-15, Volume: 109, Issue:4

    Topics: Anemia, Sickle Cell; Biological Transport; Cell Size; Disulfides; Dithiothreitol; Hemoglobins; Humans; Oxidation-Reduction; Potassium Chloride; Reticulocytes; Urea

2007
The efficacy of reducing agents or antioxidants in blocking the formation of dense cells and irreversibly sickled cells in vitro.
    Blood, 1998, Jun-01, Volume: 91, Issue:11

    Topics: Acetylcysteine; Actins; Anemia, Sickle Cell; Antioxidants; Centrifugation, Density Gradient; Dithiothreitol; Erythrocyte Aggregation; Erythrocyte Count; Glutathione; Humans; In Vitro Techniques; Reducing Agents

1998
Preliminary characterization of a structural defect in homozygous sickled cell alpha spectrin demonstrated by a rabbit autoantibody.
    American journal of hematology, 1998, Volume: 58, Issue:3

    Topics: Anemia, Sickle Cell; Animals; Autoantibodies; Blotting, Western; Dithiothreitol; Electrophoresis, Polyacrylamide Gel; Erythrocyte Membrane; Erythrocytes, Abnormal; Homozygote; Humans; Membrane Proteins; Rabbits; Sodium Dodecyl Sulfate; Spectrin

1998
The binding of hemoglobin to membranes of normal and sickle erythrocytes.
    Biochimica et biophysica acta, 1975, Feb-14, Volume: 375, Issue:3

    Topics: Anemia, Sickle Cell; Cell Membrane; Dithiothreitol; Erythrocytes; Hemoglobin, Sickle; Hemoglobins; Humans; Hydrogen-Ion Concentration; Mechlorethamine; Osmolar Concentration; Protein Binding; Temperature

1975
Vesiculation of sickle erythrocytes during thermal stress.
    Blood, 1988, Volume: 72, Issue:3

    Topics: Adult; Anemia, Sickle Cell; Cytoskeletal Proteins; Dinitrochlorobenzene; Dithiothreitol; Erythrocyte Membrane; Erythrocytes, Abnormal; Glutathione; Hot Temperature; Humans; Membrane Proteins; Sulfhydryl Compounds

1988
Abnormal redox status of membrane-protein thiols in sickle erythrocytes.
    The Journal of clinical investigation, 1985, Volume: 75, Issue:5

    Topics: 2,2'-Dipyridyl; Adult; Anemia, Sickle Cell; Chemical Fractionation; Disulfides; Dithiothreitol; Erythrocyte Membrane; Erythrocytes, Abnormal; Filtration; Humans; Membrane Proteins; Oxidation-Reduction; Sulfhydryl Compounds

1985