2-propanol has been researched along with Genetic Predisposition in 14 studies
2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mechanisms behind pigmentary glaucoma, a form of early-onset glaucoma that may potentially lead to severe visual impairment or blindness, are poorly understood." | 1.56 | Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes. ( Hammond, CJ; Hysi, PG; Simcoe, MJ; Weisschuh, N; Wissinger, B, 2020) |
| "Waardenburg syndrome is a rare genetic disorder characterized by varying degree of deafness associated with pigmentary anomaly and defects of neural crest cell derived structures." | 1.39 | Waardenburg syndrome--a case report. ( Bansal, Y; Goyal, G; Jain, P; Mishra, C; Singh, M, 2013) |
| "Glaucoma is a common disease but its molecular etiology is poorly understood." | 1.31 | Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice. ( Anderson, MG; Chang, B; Davisson, M; Hawes, NL; Heckenlively, JR; John, SW; Savinova, OV; Smith, RS; Wilpan, R; Zabaleta, A, 2001) |
| "DBA/2J (D2) mice develop a form of pigmentary glaucoma involving iris pigment dispersion (IPD) and iris stromal atrophy (ISA)." | 1.31 | Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice. ( Anderson, MG; Chang, B; Hawes, NL; John, SW; Smith, RS; Wiggs, JL; Zabaleta, A, 2002) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 8 (57.14) | 29.6817 |
| 2010's | 5 (35.71) | 24.3611 |
| 2020's | 1 (7.14) | 2.80 |
| Authors | Studies |
|---|---|
| Simcoe, MJ | 1 |
| Weisschuh, N | 1 |
| Wissinger, B | 1 |
| Hysi, PG | 1 |
| Hammond, CJ | 1 |
| Lee, MC | 2 |
| Shei, W | 1 |
| Chan, AS | 2 |
| Chua, BT | 1 |
| Goh, SR | 2 |
| Chong, YF | 1 |
| Hilmy, MH | 2 |
| Nongpiur, ME | 2 |
| Baskaran, M | 1 |
| Khor, CC | 1 |
| Aung, T | 2 |
| Hunziker, W | 2 |
| Vithana, EN | 2 |
| Alías, L | 1 |
| Crespi, J | 1 |
| González-Quereda, L | 1 |
| Téllez, J | 1 |
| Martínez, E | 1 |
| Bernal, S | 1 |
| Gallano, MP | 1 |
| Nasser, LS | 1 |
| Paranaíba, LM | 1 |
| Frota, AC | 1 |
| Gomes, A | 1 |
| Versiani, G | 1 |
| Martelli Júnior, H | 1 |
| Hong, W | 1 |
| Wood, A | 1 |
| Guedes, RA | 1 |
| Guedes, VM | 1 |
| Chaoubah, A | 1 |
| Magdesian, KG | 1 |
| Williams, DC | 1 |
| Aleman, M | 1 |
| Lecouteur, RA | 1 |
| Madigan, JE | 1 |
| Bansal, Y | 1 |
| Jain, P | 1 |
| Goyal, G | 1 |
| Singh, M | 1 |
| Mishra, C | 1 |
| Senatorov, V | 1 |
| Malyukova, I | 1 |
| Fariss, R | 1 |
| Wawrousek, EF | 1 |
| Swaminathan, S | 1 |
| Sharan, SK | 1 |
| Tomarev, S | 1 |
| Dorairaj, SK | 1 |
| Robin, A | 1 |
| Shihadeh, W | 1 |
| Greenberg, S | 1 |
| Liebmann, JM | 1 |
| Ritch, R | 1 |
| Cho, JJ | 1 |
| Hwang, WJ | 1 |
| Hong, SH | 1 |
| Jeong, HJ | 1 |
| Lee, HJ | 1 |
| Kim, HM | 1 |
| Um, JY | 1 |
| Anderson, MG | 2 |
| Smith, RS | 2 |
| Savinova, OV | 1 |
| Hawes, NL | 2 |
| Chang, B | 2 |
| Zabaleta, A | 2 |
| Wilpan, R | 1 |
| Heckenlively, JR | 1 |
| Davisson, M | 1 |
| John, SW | 2 |
| Wiggs, JL | 1 |
14 other studies available for 2-propanol and Genetic Predisposition
| Article | Year |
|---|---|
Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes.
Topics: Aged; Aged, 80 and over; Case-Control Studies; Female; Genetic Predisposition to Disease; Genome-Wid | 2020 |
Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function.
Topics: Blood-Aqueous Barrier; Carrier Proteins; cdc42 GTP-Binding Protein; Cell Movement; Epithelial Cells; | 2017 |
Next-generation sequencing reveals a new mutation in the LTBP2 gene associated with microspherophakia in a Spanish family.
Topics: Adult; Consanguinity; Corneal Diseases; Ectopia Lentis; Exons; Female; Genetic Association Studies; | 2018 |
[Waardenburg syndrome--ophthalmic findings and criteria for diagnosis: case reports].
Topics: Adult; Child, Preschool; Eye Diseases, Hereditary; Female; Genetic Predisposition to Disease; Humans | 2012 |
Expression of the primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 in endothelial and epithelial cell junctions in the eye.
Topics: Actins; Biomarkers; Carrier Proteins; Cells, Cultured; Ciliary Body; Endothelial Cells; Epithelial C | 2014 |
Darwinian medicine: are humans evolving peripheral iridotomies?
Topics: Evolution, Molecular; Eye; Genetic Predisposition to Disease; Humans; Intraocular Pressure; Iris; Ir | 2008 |
Focusing on patients at high-risk for glaucoma in Brazil: a pilot study.
Topics: Adrenal Cortex Hormones; Adult; Aged; Aged, 80 and over; Brazil; Cross-Sectional Studies; Diabetes M | 2009 |
Evaluation of deafness in American Paint Horses by phenotype, brainstem auditory-evoked responses, and endothelin receptor B genotype.
Topics: Animals; Behavior, Animal; Deafness; Evoked Potentials, Auditory, Brain Stem; Female; Genetic Predis | 2009 |
Waardenburg syndrome--a case report.
Topics: Child; Cornea; Diagnosis, Differential; Female; Fundus Oculi; Genetic Predisposition to Disease; Hum | 2013 |
Expression of mutated mouse myocilin induces open-angle glaucoma in transgenic mice.
Topics: Adenosine Triphosphatases; Animals; Cornea; Cytoplasm; Cytoskeletal Proteins; Disease Models, Animal | 2006 |
Phenotypic variability of pigment dispersion syndrome in children.
Topics: Anterior Eye Segment; Child; Exfoliation Syndrome; Female; Genetic Predisposition to Disease; Geneti | 2007 |
Angiotensinogen gene polymorphism predicts hypertension, and iridological constitutional classification enhances the risk for hypertension in Koreans.
Topics: Adult; Angiotensinogen; Chi-Square Distribution; Connective Tissue; Female; Gene Frequency; Genetic | 2008 |
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice.
Topics: Animals; Atrophy; Female; Genetic Predisposition to Disease; Glaucoma; Iris; Male; Mice; Mice, Inbre | 2001 |
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.
Topics: Animals; Atrophy; Chromosome Mapping; Chromosomes, Artificial, Bacterial; Codon, Nonsense; Codon, Te | 2002 |