Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
European Molecular Biology Laboratory, Meyerhofstrasse 1, Heidelberg, Germany.
Systematic screens for human disease genes have emerged in recent years, due to the wealth of information provided by genome sequences and large scale datasets. Here we review how integration of genomic data in yeast and human is helping to elucidate the genetic basis of mitochondrial diseases. The identification of nearly all yeast mitochondrial proteins and many of their functional interactions provides insight into the role of mitochondria in cellular processes. This information enables prioritization of the candidate genes underlying mitochondrial disorders. In an iterative fashion, the link between predicted human candidate genes and their disease phenotypes can be experimentally tested back in yeast.
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on