Page last updated: 2024-10-16

adenine and Progeria

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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's2 (100.00)2.80

Authors

AuthorsStudies
Whisenant, D1
Lim, K1
RevĂȘchon, G1
Yao, H1
Bergo, MO1
Machtel, P1
Kim, JS1
Eriksson, M1
Koblan, LW1
Erdos, MR1
Wilson, C1
Cabral, WA1
Levy, JM1
Xiong, ZM1
Tavarez, UL1
Davison, LM1
Gete, YG1
Mao, X1
Newby, GA1
Doherty, SP1
Narisu, N1
Sheng, Q1
Krilow, C1
Lin, CY1
Gordon, LB1
Cao, K1
Collins, FS1
Brown, JD1
Liu, DR1

Other Studies

2 other studies available for adenine and Progeria

ArticleYear
Transient expression of an adenine base editor corrects the Hutchinson-Gilford progeria syndrome mutation and improves the skin phenotype in mice.
    Nature communications, 2022, 06-02, Volume: 13, Issue:1

    Topics: Adenine; Animals; Lamin Type A; Mice; Mutation; Phenotype; Progeria

2022
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice.
    Nature, 2021, Volume: 589, Issue:7843

    Topics: Adenine; Alleles; Alternative Splicing; Animals; Aorta; Base Pairing; Child; Disease Models, Animal;

2021