Detalhe da pesquisa
1.
Deciphering the "m6A Code" via Antibody-Independent Quantitative Profiling.
Cell
; 178(3): 731-747.e16, 2019 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31257032
2.
Exclusion of m6A from splice-site proximal regions by the exon junction complex dictates m6A topologies and mRNA stability.
Mol Cell
; 83(2): 237-251.e7, 2023 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36599352
3.
Discovery, structure, mechanisms, and evolution of protein-only RNase P enzymes.
J Biol Chem
; 300(3): 105731, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38336295
4.
N1-methylation of adenosine (m1A) in ND5 mRNA leads to complex I dysfunction in Alzheimer's disease.
Mol Psychiatry
; 2024 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38287100
5.
Cleavage kinetics of human mitochondrial RNase P and contribution of its non-nuclease subunits.
Nucleic Acids Res
; 51(19): 10536-10550, 2023 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37779095
6.
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
7.
RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme.
Cell
; 135(3): 462-74, 2008 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-18984158
8.
The m1A landscape on cytosolic and mitochondrial mRNA at single-base resolution.
Nature
; 551(7679): 251-255, 2017 11 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29072297
9.
Functional characterization of the human tRNA methyltransferases TRMT10A and TRMT10B.
Nucleic Acids Res
; 48(11): 6157-6169, 2020 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32392304
10.
YBEY is an essential biogenesis factor for mitochondrial ribosomes.
Nucleic Acids Res
; 48(17): 9762-9786, 2020 09 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32182356
11.
Minimal and RNA-free RNase P in Aquifex aeolicus.
Proc Natl Acad Sci U S A
; 114(42): 11121-11126, 2017 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-29073018
12.
Protein-only RNase P function in Escherichia coli: viability, processing defects and differences between PRORP isoenzymes.
Nucleic Acids Res
; 45(12): 7441-7454, 2017 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28499021
13.
Positioning Europe for the EPITRANSCRIPTOMICS challenge.
RNA Biol
; 15(6): 829-831, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29671387
14.
Substrate recognition and cleavage-site selection by a single-subunit protein-only RNase P.
Nucleic Acids Res
; 44(5): 2323-36, 2016 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26896801
15.
Molecular insights into HSD10 disease: impact of SDR5C1 mutations on the human mitochondrial RNase P complex.
Nucleic Acids Res
; 43(10): 5112-9, 2015 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25925575
16.
Mitochondrial poly(A) polymerase is involved in tRNA repair.
Nucleic Acids Res
; 43(20): 9937-49, 2015 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26354863
17.
Playing RNase P evolution: swapping the RNA catalyst for a protein reveals functional uniformity of highly divergent enzyme forms.
PLoS Genet
; 10(8): e1004506, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25101763
18.
Distribution of Ribonucleoprotein and Protein-Only RNase P in Eukarya.
Mol Biol Evol
; 32(12): 3186-93, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26341299
19.
Repairing tRNA termini: News from the 3' end.
RNA Biol
; 13(12): 1182-1188, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27661287
20.
A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression.
RNA Biol
; 13(5): 477-85, 2016 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26950678