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 |
RevĂȘchon, 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 |