inositol has been researched along with Malaria in 3 studies
Inositol: An isomer of glucose that has traditionally been considered to be a B vitamin although it has an uncertain status as a vitamin and a deficiency syndrome has not been identified in man. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1379) Inositol phospholipids are important in signal transduction.
inositol : Any cyclohexane-1,2,3,4,5,6-hexol.
1D-chiro-inositol : Belonging to the inositol family of compounds, D-chiro-inositol (DCI) is an isomer of glucose. It is an important secondary messenger in insulin signal transduction.
muco-inositol : An inositol that is cyclohexane-1,2,3,4,5,6-hexol having a (1R,2R,3r,4R,5S,6r)-configuration.
Malaria: A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Glycosylphosphatidylinositol (GPI) glycolipids abound on the cell surface at the merozoite stage of Plasmodium falciparum life cycle are a central toxin in malaria." | 7.76 | Synthetic glycosylphosphatidylinositol microarray reveals differential antibody levels and fine specificities in children with mild and severe malaria. ( Kamena, F; Kwon, YU; Liu, X; Mugasa, JP; Pluschke, G; Seeberger, PH; Tamborrini, M, 2010) |
| "Glycosylphosphatidylinositol (GPI) glycolipids abound on the cell surface at the merozoite stage of Plasmodium falciparum life cycle are a central toxin in malaria." | 3.76 | Synthetic glycosylphosphatidylinositol microarray reveals differential antibody levels and fine specificities in children with mild and severe malaria. ( Kamena, F; Kwon, YU; Liu, X; Mugasa, JP; Pluschke, G; Seeberger, PH; Tamborrini, M, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tamborrini, M | 1 |
| Liu, X | 1 |
| Mugasa, JP | 1 |
| Kwon, YU | 1 |
| Kamena, F | 1 |
| Seeberger, PH | 1 |
| Pluschke, G | 1 |
| Ghosh, S | 1 |
| Sengupta, A | 1 |
| Sharma, S | 1 |
| Sonawat, HM | 1 |
| Vial, HJ | 1 |
| Thuet, MJ | 1 |
| Broussal, JL | 1 |
| Philippot, JR | 1 |
3 other studies available for inositol and Malaria
| Article | Year |
|---|---|
Synthetic glycosylphosphatidylinositol microarray reveals differential antibody levels and fine specificities in children with mild and severe malaria.
Topics: Age Factors; Antibodies; Child, Preschool; Epitope Mapping; Epitopes; Glucosamine; Glycosylphosphati | 2010 |
Metabolic fingerprints of serum, brain, and liver are distinct for mice with cerebral and noncerebral malaria: a ¹H NMR spectroscopy-based metabonomic study.
Topics: Ammonia; Animals; Biomarkers; Brain; Female; Glucose; Host-Parasite Interactions; Inositol; Least-Sq | 2012 |
Phospholipid biosynthesis by Plasmodium knowlesi-infected erythrocytes: the incorporation of phospohlipid precursors and the identification of previously undetected metabolic pathways.
Topics: Animals; Erythrocytes; Glycerophosphates; Inositol; Lysophosphatidylcholines; Macaca fascicularis; M | 1982 |