|
1
|
Whole-exome sequencing identifies a variant of the mitochondrial MT-ND1 gene associated with epileptic encephalopathy: west syndrome evolving to Lennox-Gastaut syndrome.
|
Hum Mutat
|
2013
|
1.00
|
|
2
|
A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome.
|
BMC Nephrol
|
2013
|
0.89
|
|
3
|
The P1/P2 proteins of the human ribosomal stalk are required for ribosome binding and depurination by ricin in human cells.
|
FEBS J
|
2012
|
0.88
|
|
4
|
Phosphorylation of rat mitochondrial transcription termination factor (mTERF) is required for transcription termination but not for binding to DNA.
|
Nucleic Acids Res
|
2004
|
0.82
|
|
5
|
Expression of the Drosophila melanogaster ATP synthase alpha subunit gene is regulated by a transcriptional element containing GAF and Adf-1 binding sites.
|
Eur J Biochem
|
2004
|
0.79
|
|
6
|
New DNA-binding activity of rat mitochondrial transcription termination factor (mTERF).
|
J Biochem
|
2004
|
0.78
|