Detalhe da pesquisa
1.
Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations.
Am J Hum Genet
; 108(11): 2195-2204, 2021 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34715011
2.
Mutation or knock-down of 17ß-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts.
Hum Mol Genet
; 23(13): 3618-28, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24549042
3.
17ß-Hydroxysteroid dehydrogenase type 10 predicts survival of patients with colorectal cancer and affects mitochondrial DNA content.
Cancer Lett
; 374(1): 149-155, 2016 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26884257