inositol has been researched along with Ciliary Dyskinesia in 2 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Activation of the inositol cycle by a factor capable of by-passing the normal controls on exocrine secretion by an interaction with a coupling protein could produce effects similar to a calcium ionophore or the ciliary dyskinesia factor." | 7.67 | The end organ defect in cystic fibrosis; a hypothesis: disinhibited inositol cycle activation? ( van Woerkom, AE, 1987) |
| "Activation of the inositol cycle by a factor capable of by-passing the normal controls on exocrine secretion by an interaction with a coupling protein could produce effects similar to a calcium ionophore or the ciliary dyskinesia factor." | 3.67 | The end organ defect in cystic fibrosis; a hypothesis: disinhibited inositol cycle activation? ( van Woerkom, AE, 1987) |
| "Mutants that have only exencephaly are fourfold more frequent than those that have spina bifida aperta with or without exencephaly." | 2.46 | An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. ( Harris, MJ; Juriloff, DM, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Harris, MJ | 1 |
| Juriloff, DM | 1 |
| van Woerkom, AE | 1 |
1 review available for inositol and Ciliary Dyskinesia
| Article | Year |
|---|---|
An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure.
Topics: Animals; Ciliary Motility Disorders; Disease Models, Animal; Epigenomics; Female; Folic Acid; Humans | 2010 |
1 other study available for inositol and Ciliary Dyskinesia
| Article | Year |
|---|---|
The end organ defect in cystic fibrosis; a hypothesis: disinhibited inositol cycle activation?
Topics: Blood Proteins; Calcium; Cell Membrane Permeability; Chlorides; Ciliary Motility Disorders; Cystic F | 1987 |