adenine has been researched along with Retinal Diseases in 7 studies
Retinal Diseases: Diseases involving the RETINA.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset." | 1.34 | Frequency of CEP290 c.2991_1655A>G mutation in 175 Spanish families affected with Leber congenital amaurosis and early-onset retinitis pigmentosa. ( Aguirre-Lamban, J; Avila-Fernandez, A; Ayuso, C; Cantalapiedra, D; Lopez-Martinez, MA; Riveiro-Alvarez, R; Trujillo-Tiebas, MJ; Vallespin, E; Villaverde, C, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 3 (42.86) | 2.80 |
| Authors | Studies |
|---|---|
| Pesce, NA | 1 |
| Canovai, A | 1 |
| Plastino, F | 1 |
| Lardner, E | 1 |
| Kvanta, A | 1 |
| Cammalleri, M | 1 |
| André, H | 1 |
| Dal Monte, M | 1 |
| Suh, S | 1 |
| Choi, EH | 1 |
| Leinonen, H | 1 |
| Foik, AT | 1 |
| Newby, GA | 1 |
| Yeh, WH | 1 |
| Dong, Z | 1 |
| Kiser, PD | 1 |
| Lyon, DC | 1 |
| Liu, DR | 1 |
| Palczewski, K | 1 |
| Crunkhorn, S | 1 |
| Loos, D | 1 |
| Hadeler, J | 1 |
| Feucht, N | 1 |
| Spinner, CD | 1 |
| Schwerdtfeger, C | 1 |
| Schmid, RM | 1 |
| Lanzl, I | 1 |
| Vallespin, E | 1 |
| Lopez-Martinez, MA | 1 |
| Cantalapiedra, D | 1 |
| Riveiro-Alvarez, R | 1 |
| Aguirre-Lamban, J | 1 |
| Avila-Fernandez, A | 1 |
| Villaverde, C | 1 |
| Trujillo-Tiebas, MJ | 1 |
| Ayuso, C | 1 |
| Latkany, P | 1 |
| Ciulla, TA | 1 |
| Cacchillo, PF | 1 |
| Malkoff, MD | 1 |
| Alfinito, PD | 1 |
| Townes-Anderson, E | 1 |
7 other studies available for adenine and Retinal Diseases
| Article | Year |
|---|---|
An imbalance in autophagy contributes to retinal damage in a rat model of oxygen-induced retinopathy.
Topics: Adenine; Animals; Autophagy; Biomarkers; Disease Susceptibility; Humans; Infant, Newborn; Oxygen; Ra | 2021 |
Restoration of visual function in adult mice with an inherited retinal disease via adenine base editing.
Topics: Adenine; Animals; Codon, Nonsense; CRISPR-Associated Protein 9; Gene Editing; Genetic Vectors; Lenti | 2021 |
Restoring vision loss with base editing.
Topics: Adenine; Animals; CRISPR-Cas Systems; Gene Editing; Mice; Retinal Diseases | 2020 |
[Ophthalmological alterations at the initial diagnosis of HIV infection].
Topics: Adenine; Adult; Antiretroviral Therapy, Highly Active; Cyclohexanes; Deoxycytidine; Drug Therapy, Co | 2014 |
Frequency of CEP290 c.2991_1655A>G mutation in 175 Spanish families affected with Leber congenital amaurosis and early-onset retinitis pigmentosa.
Topics: Adenine; Age of Onset; Antigens, Neoplasm; Blindness; Cell Cycle Proteins; Cohort Studies; Cytoskele | 2007 |
Mitochondrial maculopathy: geographic atrophy of the macula in the MELAS associated A to G 3243 mitochondrial DNA point mutation.
Topics: Adenine; Atrophy; Deafness; DNA, Mitochondrial; Electroretinography; Female; Guanine; Humans; Macula | 1999 |
Activation of mislocalized opsin kills rod cells: a novel mechanism for rod cell death in retinal disease.
Topics: Adenine; Adenylate Cyclase Toxin; Adenylyl Cyclases; Animals; Apoptosis; Caspase 3; Caspases; Cell D | 2002 |