cytosine has been researched along with Stargardt Disease in 1 studies
Stargardt Disease: A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
| 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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhao, T | 1 |
| Li, Q | 1 |
| Zhou, C | 1 |
| Lv, X | 1 |
| Liu, H | 1 |
| Tu, T | 1 |
| Tang, N | 1 |
| Cheng, Y | 1 |
| Liu, X | 1 |
| Liu, C | 1 |
| Zhao, J | 1 |
| Song, Z | 1 |
| Wang, H | 1 |
| Li, J | 1 |
| Gu, F | 1 |
1 other study available for cytosine and Stargardt Disease
| Article | Year |
|---|---|
Small-molecule compounds boost genome-editing efficiency of cytosine base editor.
Topics: Animals; ATP-Binding Cassette Transporters; CRISPR-Cas Systems; Cytosine; Gene Editing; HEK293 Cells | 2021 |