Page last updated: 2024-10-31

ethylmaleimide and Anemia, Sickle Cell

ethylmaleimide has been researched along with Anemia, Sickle Cell in 12 studies

Ethylmaleimide: A sulfhydryl reagent that is widely used in experimental biochemical 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.

Research Excerpts

ExcerptRelevanceReference
"In certain pathologic states, such as sickle cell anemia, phospholipid asymmetry is altered."1.29Detection of altered membrane phospholipid asymmetry in subpopulations of human red blood cells using fluorescently labeled annexin V. ( Discher, D; Ernst, JD; Hua, M; Kuypers, FA; Lewis, RA; Lubin, BH; Schott, MA, 1996)

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19905 (41.67)18.7374
1990's5 (41.67)18.2507
2000's2 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Muzyamba, MC1
Campbell, EH1
Gibson, JS1
Knee, KM1
Roden, CK1
Flory, MR1
Mukerji, I1
Sato, T1
Ohnishi, ST1
Buchanan, GR1
Holtkamp, CA1
Kuypers, FA1
Lewis, RA1
Hua, M1
Schott, MA1
Discher, D1
Ernst, JD1
Lubin, BH1
Godart, H1
Dormandy, A1
Ellory, JC1
al-Rohil Gharaibeh, NS1
al-Sheyyab, M1
Vitoux, D2
Beuzard, Y2
Brugnara, C1
Moore, RB1
Hulgan, TM1
Green, JW1
Jenkins, LD1
Olivieri, O1
Garay, RP1
Cragoe, EJ1
Galacteros, F2
al-Rohil, N1
Jennings, ML1
Leclerc, L1
Girard, F1
Poyart, C1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Sickle Cell Disease (SCD) Biochip': Towards a Simple and Reliable Way to Monitor Sickle Cell Disease[NCT02824471]100 participants (Anticipated)Observational2014-10-31Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

12 other studies available for ethylmaleimide and Anemia, Sickle Cell

ArticleYear
Effect of intracellular magnesium and oxygen tension on K+-Cl- cotransport in normal and sickle human red cells.
    Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2006, Volume: 17, Issue:3-4

    Topics: Anemia, Sickle Cell; Antisickling Agents; Dimethyl Adipimidate; Enzyme Inhibitors; Erythrocytes; Ery

2006
The role of beta93 Cys in the inhibition of Hb S fiber formation.
    Biophysical chemistry, 2007, Volume: 127, Issue:3

    Topics: Anemia, Sickle Cell; Cysteine; Ethylmaleimide; Hemoglobin, Sickle; Humans; Methemoglobin; Nitric Oxi

2007
Effects of sulfhydryl reagents on the anti-sickling activity of some membrane-interacting compounds.
    Biochimica et biophysica acta, 1983, Jan-05, Volume: 727, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Antisickling Agents; Chlorpromazine; Erythrocytes; Ethylmaleimide; Human

1983
Platelet aggregation, malondialdehyde generation and production time in children with sickle cell anaemia.
    Thrombosis and haemostasis, 1981, Dec-23, Volume: 46, Issue:4

    Topics: Adenosine Diphosphate; Adolescent; Anemia, Sickle Cell; Blood Platelets; Child; Child, Preschool; Co

1981
Detection of altered membrane phospholipid asymmetry in subpopulations of human red blood cells using fluorescently labeled annexin V.
    Blood, 1996, Feb-01, Volume: 87, Issue:3

    Topics: Anemia, Sickle Cell; Annexin A5; Calcimycin; Calcium; Cell Separation; Erythrocyte Membrane; Erythro

1996
Do HbSS erythrocytes lose KCl in physiological conditions?
    British journal of haematology, 1997, Volume: 98, Issue:1

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Bicarbonates; Erythrocytes; Ethylmaleimide; Female; Humans;

1997
Inhibition of K+ transport in human sickle cell erythrocytes by okadaic acid and sodium fluoride.
    Clinical and experimental pharmacology & physiology, 1997, Volume: 24, Issue:11

    Topics: Anemia, Sickle Cell; Dose-Response Relationship, Drug; Erythrocytes, Abnormal; Ethylmaleimide; Hemog

1997
The effect of hemoglobin A and S on the volume- and pH-dependence of K-Cl cotransport in human erythrocyte ghosts.
    The Journal of membrane biology, 1999, Feb-01, Volume: 167, Issue:3

    Topics: Anemia, Sickle Cell; Carrier Proteins; Cell Size; Centrifugation, Density Gradient; Chlorides; Eryth

1999
Increased susceptibility of the sickle cell membrane Ca2+ + Mg(2+)-ATPase to t-butylhydroperoxide: protective effects of ascorbate and desferal.
    Blood, 1992, Mar-01, Volume: 79, Issue:5

    Topics: Anemia, Sickle Cell; Ascorbic Acid; Ca(2+) Mg(2+)-ATPase; Calcium-Transporting ATPases; Calmodulin;

1992
Inhibition of K+ efflux and dehydration of sickle cells by [(dihydroindenyl)oxy]alkanoic acid: an inhibitor of the K+ Cl- cotransport system.
    Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:11

    Topics: Anemia, Sickle Cell; Carboxylic Acids; Carrier Proteins; Erythrocytes; Ethylmaleimide; Humans; In Vi

1989
Volume-dependent K+ transport in rabbit red blood cells comparison with oxygenated human SS cells.
    The American journal of physiology, 1989, Volume: 257, Issue:1 Pt 1

    Topics: Anemia, Sickle Cell; Animals; Anions; Biological Transport; Chlorides; Disease Models, Animal; Eryth

1989
The calmodulin-stimulated (Ca2+ + Mg2+)-ATPase in hemoglobin S erythrocyte membranes: effects of sickling and oxidative agents.
    Biochimica et biophysica acta, 1987, Feb-12, Volume: 897, Issue:1

    Topics: Anemia, Sickle Cell; Ca(2+) Mg(2+)-ATPase; Calcium-Transporting ATPases; Calmodulin; Diamide; Erythr

1987