Page last updated: 2024-11-08

serine and Anemia, Sickle Cell

serine has been researched along with Anemia, Sickle Cell in 6 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

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

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gauthier, E1
Rahuel, C1
Wautier, MP1
El Nemer, W1
Gane, P1
Wautier, JL1
Cartron, JP1
Colin, Y1
Le Van Kim, C1
Lee-Stroka, H1
Slezak, SL1
Adams, S1
Martin, J1
Robbins, FM1
Caruccio, L1
Byrne, KM1
Stroncek, DF1
Honig, GR1
Shamsuddin, M1
Mason, RG1
Vida, LN1
Tremaine, LM1
Tarr, GE1
Shahidi, NT1
Bize, I1
Güvenç, B1
Robb, A1
Buchbinder, G1
Brugnara, C1
Kiessling, K1
Roberts, N1
Gibson, JS1
Ellory, JC2
Hall, AC1
Ody, SA1
Poli de Figueiredos, CE1
Chalder, S1
Stuart, J1

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

6 other studies available for serine and Anemia, Sickle Cell

ArticleYear
Protein kinase A-dependent phosphorylation of Lutheran/basal cell adhesion molecule glycoprotein regulates cell adhesion to laminin alpha5.
    The Journal of biological chemistry, 2005, Aug-26, Volume: 280, Issue:34

    Topics: Adrenergic beta-Antagonists; Alanine; Amino Acid Sequence; Anemia, Sickle Cell; Animals; Blotting, W

2005
Another example of a KEL1 variant red cell phenotype due to a threonine to serine change at position 193 of Kell glycoprotein.
    Transfusion, 2008, Volume: 48, Issue:5

    Topics: Anemia, Sickle Cell; Antibodies, Monoclonal; Blood Donors; Blood Transfusion; Genotype; Humans; Immu

2008
Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia.
    Blood, 1980, Volume: 55, Issue:1

    Topics: Absorption; Anemia, Sickle Cell; Chromatography, Ion Exchange; Cysteine; Erythrocytes; Female; Genet

1980
Serine/threonine protein phosphatases and regulation of K-Cl cotransport in human erythrocytes.
    The American journal of physiology, 1999, Volume: 277, Issue:5

    Topics: Anemia, Sickle Cell; Biological Transport; Carrier Proteins; Cell Size; Cytosol; Dehydration; Enzyme

1999
A comparison in normal individuals and sickle cell patients of reduced glutathione precursors and their transport between plasma and red cells.
    The hematology journal : the official journal of the European Haematology Association, 2000, Volume: 1, Issue:4

    Topics: Adult; Amino Acid Transport System ASC; Amino Acid Transport System L; Anemia, Sickle Cell; Biologic

2000
KCl cotransport in HbAA and HbSS red cells: activation by intracellular acidity and disappearance during maturation.
    Advances in experimental medicine and biology, 1991, Volume: 307

    Topics: Anemia, Sickle Cell; Biological Transport; Bumetanide; Carrier Proteins; Choline; Dehydration; Eryth

1991