inositol has been researched along with Genetic Predisposition in 7 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 |
|---|---|---|
| "The genetic etiology of late-onset Alzheimer's disease (LOAD) has proven complex, involving clinical and genetic heterogeneity and gene-gene interactions." | 1.40 | Genetic interactions within inositol-related pathways are associated with longitudinal changes in ventricle size. ( Hohman, TJ; Koran, ME; Meda, SA; Thornton-Wells, TA, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Koran, ME | 1 |
| Hohman, TJ | 1 |
| Meda, SA | 1 |
| Thornton-Wells, TA | 1 |
| SanGiovanni, JP | 1 |
| Mehta, S | 2 |
| Burren, KA | 1 |
| Scott, JM | 1 |
| Copp, AJ | 1 |
| Greene, ND | 1 |
| Jain, M | 1 |
| Vélez, JI | 1 |
| Acosta, MT | 1 |
| Palacio, LG | 1 |
| Balog, J | 1 |
| Roessler, E | 1 |
| Pineda, D | 1 |
| Londoño, AC | 1 |
| Palacio, JD | 1 |
| Arbelaez, A | 1 |
| Lopera, F | 1 |
| Elia, J | 1 |
| Hakonarson, H | 1 |
| Seitz, C | 1 |
| Freitag, CM | 1 |
| Palmason, H | 1 |
| Meyer, J | 1 |
| Romanos, M | 1 |
| Walitza, S | 1 |
| Hemminger, U | 1 |
| Warnke, A | 1 |
| Romanos, J | 1 |
| Renner, T | 1 |
| Jacob, C | 1 |
| Lesch, KP | 1 |
| Swanson, J | 1 |
| Castellanos, FX | 1 |
| Bailey-Wilson, JE | 1 |
| Arcos-Burgos, M | 1 |
| Muenke, M | 1 |
| Freedman, ML | 1 |
| Monteiro, AN | 1 |
| Gayther, SA | 1 |
| Coetzee, GA | 1 |
| Risch, A | 1 |
| Plass, C | 1 |
| Casey, G | 1 |
| De Biasi, M | 1 |
| Carlson, C | 1 |
| Duggan, D | 1 |
| James, M | 1 |
| Liu, P | 1 |
| Tichelaar, JW | 1 |
| Vikis, HG | 1 |
| You, M | 1 |
| Mills, IG | 1 |
| Eriksson, UJ | 1 |
| Cederberg, J | 1 |
| Wentzel, P | 1 |
| Prestel, J | 1 |
| Gempel, K | 1 |
| Hauser, TK | 1 |
| Schweitzer, K | 1 |
| Prokisch, H | 1 |
| Ahting, U | 1 |
| Freudenstein, D | 1 |
| Bueltmann, E | 1 |
| Naegele, T | 1 |
| Berg, D | 1 |
| Klopstock, T | 1 |
| Gasser, T | 1 |
2 reviews available for inositol and Genetic Predisposition
| Article | Year |
|---|---|
Variation in lipid-associated genes as they relate to risk of advanced age-related macular degeneration.
Topics: Aging; Diet; Docosahexaenoic Acids; Fatty Acids; Fatty Acids, Omega-3; Genetic Predisposition to Dis | 2009 |
Congenital malformations in offspring of diabetic mothers--animal and human studies.
Topics: Animals; Arachidonic Acid; Congenital Abnormalities; Diabetes Complications; Female; Gene Expression | 2003 |
5 other studies available for inositol and Genetic Predisposition
| Article | Year |
|---|---|
Genetic interactions within inositol-related pathways are associated with longitudinal changes in ventricle size.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Cognitive Dysfunction; Down-Regulation; Enzymes; Female; | 2014 |
The genetic background of the curly tail strain confers susceptibility to folate-deficiency-induced exencephaly.
Topics: Animals; Diet; DNA-Binding Proteins; Female; Folic Acid; Folic Acid Deficiency; Genetic Predispositi | 2010 |
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.
Topics: Aspartic Acid; Attention Deficit Disorder with Hyperactivity; Brain; Case-Control Studies; Choline; | 2012 |
Principles for the post-GWAS functional characterization of cancer risk loci.
Topics: Catechols; Gene Expression; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Associ | 2011 |
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation.
Topics: Adult; Aged; Basal Ganglia; Biomarkers; Cell Line; DNA Mutational Analysis; Energy Metabolism; Femal | 2008 |