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bw 12c79 and Anemia, Sickle Cell

bw 12c79 has been researched along with Anemia, Sickle Cell in 7 studies

*Anemia, Sickle Cell: A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. [MeSH]

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's4 (57.14)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kenny, MW; Stuart, J1
Culliford, SJ; Ellory, JC; Mojiminiyi, FB; Stone, PC; Stuart, J1
Beuzard, Y; Chrétien, N; De Paepe, ME; Hoang, T; Jacmain, J; Saadane, N; Sorette, M; Trudel, M1
Nash, GB; Stone, PC; Stuart, J1
Littlewood, T; van Rhee, F; Ware, I1
Johnson, CS; Keidan, AJ; Marwah, SS; Sowter, MC; Stuart, J1
Franklin, IM; Huehns, ER; Joy, M; Keidan, AJ; Stuart, J; White, RD1

Trials

1 trial(s) available for bw 12c79 and Anemia, Sickle Cell

ArticleYear
Effect of BW12C on oxygen affinity of haemoglobin in sickle-cell disease.
    Lancet (London, England), 1986, Apr-12, Volume: 1, Issue:8485

    Topics: Adult; Aldehydes; Anemia, Sickle Cell; Aspartate Aminotransferases; Benzaldehydes; Bilirubin; Binding, Competitive; Clinical Trials as Topic; Dose-Response Relationship, Drug; Erythrocyte Count; Erythrocyte Deformability; Hemoglobin, Sickle; Hemolysis; Humans; Infusions, Parenteral; Leukocyte Count; Male; Oxygen; Oxygen Consumption; Oxyhemoglobins; Thalassemia; Time Factors

1986

Other Studies

6 other study(ies) available for bw 12c79 and Anemia, Sickle Cell

ArticleYear
Preservation of deformability (filterability) of sickle cells by BW12C during progressive deoxygenation.
    British journal of haematology, 1983, Volume: 55, Issue:3

    Topics: Aldehydes; Anemia, Sickle Cell; Benzaldehydes; Dose-Response Relationship, Drug; Erythrocytes; Filtration; Hemoglobin SC Disease; Humans; Oxidation-Reduction; Oxygen; Partial Pressure

1983
Additive in vitro effects of anti-sickling drugs.
    British journal of haematology, 1994, Volume: 86, Issue:4

    Topics: Anemia, Sickle Cell; Antisickling Agents; Benzaldehydes; Calcium; Cells, Cultured; Clotrimazole; Drug Synergism; Erythrocyte Deformability; Erythrocyte Indices; Erythrocytes; Hemorheology; Humans; Nitrendipine; Oxidation-Reduction; Potassium; Potassium Channels; Verapamil

1994
Sickle cell disease of transgenic SAD mice.
    Blood, 1994, Nov-01, Volume: 84, Issue:9

    Topics: Anemia, Sickle Cell; Animals; Antisickling Agents; Benzaldehydes; Disease Models, Animal; Erythrocytes, Abnormal; Erythropoiesis; Hypoxia; Longevity; Lung; Mice; Mice, Transgenic; Microcirculation; Spleen

1994
Substituted benzaldehydes (12C79 and 589C80) that stabilize oxyhaemoglobin also protect sickle cells against calcium-mediated dehydration.
    British journal of haematology, 1992, Volume: 81, Issue:3

    Topics: Anemia, Sickle Cell; Antisickling Agents; Benzaldehydes; Benzoates; Calcium; Dehydration; Erythrocytes, Abnormal; Humans; Oxyhemoglobins; Potassium

1992
Abnormal haemoglobin electrophoresis caused by BW 12C.
    Journal of clinical pathology, 1992, Volume: 45, Issue:10

    Topics: Adenocarcinoma; Anemia, Sickle Cell; Antineoplastic Agents; Benzaldehydes; Blood Protein Electrophoresis; False Negative Reactions; Hemoglobins; Humans; Male; Middle Aged

1992
Pharmacological modification of oxygen affinity improves deformability of deoxygenated sickle erythrocytes: a possible therapeutic approach to sickle cell disease.
    Clinical science (London, England : 1979), 1989, Volume: 76, Issue:4

    Topics: Anemia, Sickle Cell; Benzaldehydes; Benzoates; Erythrocyte Deformability; Hemoglobin, Sickle; Humans; Oxygen

1989