inositol has been researched along with Congenital Micrognathia in 1 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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lines, MA | 1 |
Ito, Y | 1 |
Kernohan, KD | 1 |
Mears, W | 1 |
Hurteau-Miller, J | 1 |
Venkateswaran, S | 1 |
Ward, L | 1 |
Khatchadourian, K | 1 |
McClintock, J | 1 |
Bhola, P | 1 |
Campeau, PM | 1 |
Boycott, KM | 1 |
Michaud, J | 1 |
van Kuilenburg, AB | 1 |
Ferdinandusse, S | 1 |
Dyment, DA | 1 |
1 other study available for inositol and Congenital Micrognathia
Article | Year |
---|---|
Yunis-VarĂ³n syndrome caused by biallelic VAC14 mutations.
Topics: Alleles; Cells, Cultured; Cleidocranial Dysplasia; Ectodermal Dysplasia; Female; Fibroblasts; Humans | 2017 |