Page last updated: 2024-10-17

cytosine and Mitochondrial Diseases

cytosine has been researched along with Mitochondrial Diseases in 2 studies

Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.

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
Cho, SI1
Lee, S2
Mok, YG1
Lim, K1
Lee, J1
Lee, JM1
Chung, E1
Kim, JS2
Lee, H1
Baek, G1
Namgung, E1
Park, JM1
Kim, S1
Hong, S1

Other Studies

2 other studies available for cytosine and Mitochondrial Diseases

ArticleYear
Targeted A-to-G base editing in human mitochondrial DNA with programmable deaminases.
    Cell, 2022, 05-12, Volume: 185, Issue:10

    Topics: Animals; CRISPR-Cas Systems; Cytosine; DNA, Mitochondrial; Escherichia coli; Gene Editing; Humans; M

2022
Enhanced mitochondrial DNA editing in mice using nuclear-exported TALE-linked deaminases and nucleases.
    Genome biology, 2022, 10-12, Volume: 23, Issue:1

    Topics: Animals; Cytosine; DNA, Mitochondrial; Endonucleases; Gene Editing; Humans; Mice; Mitochondria; Mito

2022