Detalhe da pesquisa
1.
Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation.
Nucleic Acids Res
; 51(14): 7480-7495, 2023 08 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37439353
2.
Within-host evolution of a Klebsiella pneumoniae clone: selected mutations associated with the alteration of outer membrane protein expression conferred multidrug resistance.
J Antimicrob Chemother
; 76(2): 362-369, 2021 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33099622
3.
Tor and the Sin3-Rpd3 complex regulate expression of the mitophagy receptor protein Atg32 in yeast.
J Cell Sci
; 127(Pt 14): 3184-96, 2014 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24838945
4.
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
Hum Mutat
; 36(2): 232-9, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25393721
5.
Drosophila nuclear factor DREF regulates the expression of the mitochondrial DNA helicase and mitochondrial transcription factor B2 but not the mitochondrial translation factor B1.
Biochim Biophys Acta
; 1829(10): 1136-46, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23916463
6.
Generation and maintenance of the circularized multimeric IS26-associated translocatable unit encoding multidrug resistance.
Commun Biol
; 7(1): 597, 2024 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38762617
7.
iMPAQT reveals that adequate mitohormesis from TFAM overexpression leads to life extension in mice.
Life Sci Alliance
; 7(7)2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38664021
8.
Mitochondrial complex III deficiency caused by a homozygous UQCRC2 mutation presenting with neonatal-onset recurrent metabolic decompensation.
Hum Mutat
; 34(3): 446-52, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23281071
9.
Coiled coil domain-containing protein 56 (CCDC56) is a novel mitochondrial protein essential for cytochrome c oxidase function.
J Biol Chem
; 287(29): 24174-85, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22610097
10.
Matrix proteases in mitochondrial DNA function.
Biochim Biophys Acta
; 1819(9-10): 1080-7, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22172992
11.
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).
J Med Genet
; 49(12): 777-84, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23188110
12.
Mitochondrial Lon protease regulates mitochondrial DNA copy number and transcription by selective degradation of mitochondrial transcription factor A (TFAM).
Proc Natl Acad Sci U S A
; 107(43): 18410-5, 2010 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-20930118
13.
Mitochondrial AAA+ proteases.
Enzymes
; 54: 205-220, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37945172
14.
Selective Suppression of Endogenous Gene Expression Using RNAi in Drosophila Schneider S2 Cells.
Methods Mol Biol
; 2281: 303-312, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33847967
15.
Stepwise Evolution of a Klebsiella pneumoniae Clone within a Host Leading to Increased Multidrug Resistance.
mSphere
; 6(6): e0073421, 2021 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34817239
16.
Mitochondrial Lon protease is a gatekeeper for proteins newly imported into the matrix.
Commun Biol
; 4(1): 974, 2021 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34400774
17.
Functional importance of the conserved N-terminal domain of the mitochondrial replicative DNA helicase.
Biochim Biophys Acta
; 1787(5): 290-5, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19063859
18.
Functional analysis by inducible RNA interference in Drosophila melanogaster.
Methods Mol Biol
; 372: 207-17, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-18314728
19.
Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation.
Sci Rep
; 7(1): 8315, 2017 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28814717
20.
Neural-specific deletion of mitochondrial p32/C1qbp leads to leukoencephalopathy due to undifferentiated oligodendrocyte and axon degeneration.
Sci Rep
; 7(1): 15131, 2017 11 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29123152