capsaicin has been researched along with Genetic Diseases, X-Chromosome Linked in 2 studies
| 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 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Davidova, A; Fatima, T; Ferland, CE; Mouchbahani-Constance, S; Orlowski, J; Petitjean, H; Sharif-Naeini, R | 1 |
| Bojang, P; Furukawa, T; Goldberg, AF; Gregg, RG; Hirschtritt, ME; Koike, C; McCall, MA; Nawy, S; Nishina, PM; Peachey, NS; Pearring, JN; Ray, TA; Shen, Y; Sturgill-Short, G | 1 |
2 other study(ies) available for capsaicin and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Loss of SLC9A6/NHE6 impairs nociception in a mouse model of Christianson syndrome.
Topics: Animals; Ataxia; Capsaicin; Epilepsy; Genetic Diseases, X-Linked; Humans; Intellectual Disability; Mice; Mice, Inbred C57BL; Microcephaly; Nociception; Nociceptors; Ocular Motility Disorders; Sodium-Hydrogen Exchangers; TRPV Cation Channels | 2020 |
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
Topics: Action Potentials; Amino Acid Sequence; Amino Acids; Animals; Capsaicin; Chromosome Mapping; Chromosomes, Mammalian; Dendrites; Disease Models, Animal; Exons; Eye Diseases, Hereditary; Genetic Diseases, X-Linked; Heterozygote; Mice; Mice, Transgenic; Molecular Sequence Data; Mutation, Missense; Myopia; Night Blindness; Point Mutation; Retina; Retinal Bipolar Cells; Sequence Analysis, DNA; Threonine; TRPM Cation Channels; Xanthenes | 2012 |