adenine has been researched along with Progeria in 2 studies
Progeria: An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA.
| 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 | 2 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Whisenant, D | 1 |
| Lim, K | 1 |
| Revêchon, G | 1 |
| Yao, H | 1 |
| Bergo, MO | 1 |
| Machtel, P | 1 |
| Kim, JS | 1 |
| Eriksson, M | 1 |
| Koblan, LW | 1 |
| Erdos, MR | 1 |
| Wilson, C | 1 |
| Cabral, WA | 1 |
| Levy, JM | 1 |
| Xiong, ZM | 1 |
| Tavarez, UL | 1 |
| Davison, LM | 1 |
| Gete, YG | 1 |
| Mao, X | 1 |
| Newby, GA | 1 |
| Doherty, SP | 1 |
| Narisu, N | 1 |
| Sheng, Q | 1 |
| Krilow, C | 1 |
| Lin, CY | 1 |
| Gordon, LB | 1 |
| Cao, K | 1 |
| Collins, FS | 1 |
| Brown, JD | 1 |
| Liu, DR | 1 |
2 other studies available for adenine and Progeria
| Article | Year |
|---|---|
Transient expression of an adenine base editor corrects the Hutchinson-Gilford progeria syndrome mutation and improves the skin phenotype in mice.
Topics: Adenine; Animals; Lamin Type A; Mice; Mutation; Phenotype; Progeria | 2022 |
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice.
Topics: Adenine; Alleles; Alternative Splicing; Animals; Aorta; Base Pairing; Child; Disease Models, Animal; | 2021 |