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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 2 (33.33) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Gauthier, E | 1 |
Rahuel, C | 1 |
Wautier, MP | 1 |
El Nemer, W | 1 |
Gane, P | 1 |
Wautier, JL | 1 |
Cartron, JP | 1 |
Colin, Y | 1 |
Le Van Kim, C | 1 |
Lee-Stroka, H | 1 |
Slezak, SL | 1 |
Adams, S | 1 |
Martin, J | 1 |
Robbins, FM | 1 |
Caruccio, L | 1 |
Byrne, KM | 1 |
Stroncek, DF | 1 |
Honig, GR | 1 |
Shamsuddin, M | 1 |
Mason, RG | 1 |
Vida, LN | 1 |
Tremaine, LM | 1 |
Tarr, GE | 1 |
Shahidi, NT | 1 |
Bize, I | 1 |
Güvenç, B | 1 |
Robb, A | 1 |
Buchbinder, G | 1 |
Brugnara, C | 1 |
Kiessling, K | 1 |
Roberts, N | 1 |
Gibson, JS | 1 |
Ellory, JC | 2 |
Hall, AC | 1 |
Ody, SA | 1 |
Poli de Figueiredos, CE | 1 |
Chalder, S | 1 |
Stuart, J | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Sickle Cell Disease (SCD) Biochip': Towards a Simple and Reliable Way to Monitor Sickle Cell Disease[NCT02824471] | 100 participants (Anticipated) | Observational | 2014-10-31 | Recruiting | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
6 other studies available for serine and Anemia, Sickle Cell
Article | Year |
---|---|
Protein kinase A-dependent phosphorylation of Lutheran/basal cell adhesion molecule glycoprotein regulates cell adhesion to laminin alpha5.
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.
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.
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.
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.
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.
Topics: Anemia, Sickle Cell; Biological Transport; Bumetanide; Carrier Proteins; Choline; Dehydration; Eryth | 1991 |