Pathological Mutations of the Mitochondrial Human Genome: the Instrumental Role of the Yeast S. cerevisiae
Mitochondrial diseases, which altogether represent not so rare diseases, can be due to mutations either in the nuclear or mitochondrial genomes. Several model organisms or cell lines are usually employed to understand the mechanisms underlying diseases, yeast being one of them. However, in the case...
Main Author: | Monique Bolotin-Fukuhara |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2014-01-01
|
Series: | Diseases |
Subjects: | |
Online Access: | http://www.mdpi.com/2079-9721/2/1/24 |
Similar Items
-
Nuclear and mitochondrial tRNA-lookalikes in the human genome
by: Aristeidis G Telonis, et al.
Published: (2014-10-01) -
MicroRNAs and tRNA-Derived Small Fragments: Key Messengers in Nuclear–Mitochondrial Communication
by: Salvador Meseguer
Published: (2021-05-01) -
The phenotypic expression of mitochondrial tRNA-mutations can be modulated by mitochondrial leucyl-tRNA synthetase and the C-terminal domain thereof.
by: Carla eGiordano, et al.
Published: (2015-03-01) -
Mitochondrial tRNA-Derived Fragments and Their Contribution to Gene Expression Regulation
by: Athanasios-Nasir Shaukat, et al.
Published: (2021-09-01) -
Integrated genomic analysis of mitochondrial RNA processing in human cancers
by: Youssef Idaghdour, et al.
Published: (2017-04-01)