Detalhe da pesquisa
1.
Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness.
Cell
; 148(4): 716-26, 2012 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22341444
2.
Emerging functions of mitochondria-encoded noncoding RNAs.
Trends Genet
; 39(2): 125-139, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36137834
3.
Planet-compatible pathways for transitioning the chemical industry.
Proc Natl Acad Sci U S A
; 120(8): e2218294120, 2023 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36787351
4.
Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity.
J Biol Chem
; 300(5): 107235, 2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38552739
5.
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy.
Hum Mol Genet
; 32(2): 231-243, 2023 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35947995
6.
Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy.
Hum Mol Genet
; 32(9): 1539-1551, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36611011
7.
Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients.
Hum Mol Genet
; 31(18): 3068-3082, 2022 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35467742
8.
Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy.
Hum Mol Genet
; 31(19): 3299-3312, 2022 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35567411
9.
Comparison of outcomes between stent retriever combined with contact aspiration versus contact aspiration alone in patients without hyperdense artery sign/susceptibility vessel sign.
J Vasc Interv Radiol
; 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38723863
10.
A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism.
Nucleic Acids Res
; 50(16): 9453-9469, 2022 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36039763
11.
Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro.
Nucleic Acids Res
; 50(16): 9368-9381, 2022 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36018806
12.
Long-term voice outcomes of medialization thyroplasty with adjustable implant for unilateral vocal fold paralysis.
Eur Arch Otorhinolaryngol
; 281(3): 1371-1378, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38085304
13.
Assessing the causal relationship between immune traits and systemic lupus erythematosus by bi-directional Mendelian randomization analysis.
Mol Genet Genomics
; 298(6): 1493-1503, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37845373
14.
Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations.
J Biomed Sci
; 30(1): 82, 2023 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37737178
15.
Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation.
J Biomed Sci
; 30(1): 63, 2023 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37537557
16.
Bioinspired Under-Liquid Dual Superlyophobic Surface for On-Demand Oil/Water Separation.
Langmuir
; 39(2): 870-877, 2023 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36602256
17.
An old thrombus may potentially identify patients at higher risk of poor outcome in anterior circulation stroke undergoing thrombectomy.
Neuroradiology
; 65(2): 381-390, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36269335
18.
Low Prealbumin Levels Were Associated with Increased Frequency of Hepatic Encephalopathy in Hepatitis B Virus (HBV)-Related Decompensated Cirrhosis.
Med Sci Monit
; 29: e937772, 2023 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37077040
19.
Bacillus litorisediminis sp. nov., a Thermophilic Bacterium Isolated from Mangrove Sediment.
Curr Microbiol
; 80(2): 79, 2023 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36656344
20.
FARS2 deficiency in Drosophila reveals the developmental delay and seizure manifested by aberrant mitochondrial tRNA metabolism.
Nucleic Acids Res
; 49(22): 13108-13121, 2021 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34878141