Gene expression in a Drosophila model of mitochondrial disease.
<h4>Background</h4>A point mutation in the Drosophila gene technical knockout (tko), encoding mitoribosomal protein S12, was previously shown to cause a phenotype of respiratory chain deficiency, developmental delay, and neurological abnormalities similar to those presented in many human...
Main Authors: | Daniel J M Fernández-Ayala, Shanjun Chen, Esko Kemppainen, Kevin M C O'Dell, Howard T Jacobs |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2010-01-01
|
Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20066047/?tool=EBI |
Similar Items
-
Phenotypic rescue of a Drosophila model of mitochondrial ANT1 disease
by: Suvi Vartiainen, et al.
Published: (2014-06-01) -
Ligand-Bound GeneSwitch Causes Developmental Aberrations in Drosophila that Are Alleviated by the Alternative Oxidase
by: Ana Andjelković, et al.
Published: (2016-09-01) -
Minimal effects of spargel (PGC-1) overexpression in a Drosophila mitochondrial disease model
by: Jack George, et al.
Published: (2019-07-01) -
Behaviour genetics of the inactive and hypoactive mutants of Drosophila melanogaster
by: O'Dell, K. M. C.
Published: (1986) -
Lethal Interaction of Nuclear and Mitochondrial Genotypes in Drosophila melanogaster
by: Tiina S. Salminen, et al.
Published: (2019-07-01)