Detalhe da pesquisa
1.
Structure of the mature kinetoplastids mitoribosome and insights into its large subunit biogenesis.
Proc Natl Acad Sci U S A
; 117(47): 29851-29861, 2020 11 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33168716
2.
Decoding the impact of disease-causing mutations in an essential aminoacyl-tRNA synthetase.
J Biol Chem
; 297(6): 101386, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34752820
3.
Peculiarities of aminoacyl-tRNA synthetases from trypanosomatids.
J Biol Chem
; 297(2): 100913, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34175310
4.
Phenotypic diversity of brain MRI patterns in mitochondrial aminoacyl-tRNA synthetase mutations.
Mol Genet Metab
; 133(2): 222-229, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33972171
5.
When a common biological role does not imply common disease outcomes: Disparate pathology linked to human mitochondrial aminoacyl-tRNA synthetases.
J Biol Chem
; 294(14): 5309-5320, 2019 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30647134
6.
How to fold and protect mitochondrial ribosomal RNA with fewer guanines.
Nucleic Acids Res
; 46(20): 10946-10968, 2018 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30215760
7.
Three human aminoacyl-tRNA synthetases have distinct sub-mitochondrial localizations that are unaffected by disease-associated mutations.
J Biol Chem
; 293(35): 13604-13615, 2018 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-30006346
8.
Two proteomic methodologies for defining N-termini of mature human mitochondrial aminoacyl-tRNA synthetases.
Methods
; 113: 111-119, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27793688
9.
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
PLoS Genet
; 11(3): e1005097, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25807530
10.
MiSynPat: An integrated knowledge base linking clinical, genetic, and structural data for disease-causing mutations in human mitochondrial aminoacyl-tRNA synthetases.
Hum Mutat
; 38(10): 1316-1324, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28608363
11.
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation.
Nat Genet
; 39(4): 534-9, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17384640
12.
Thermodynamic properties distinguish human mitochondrial aspartyl-tRNA synthetase from bacterial homolog with same 3D architecture.
Nucleic Acids Res
; 41(4): 2698-708, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23275545
13.
Pathogenic implications of human mitochondrial aminoacyl-tRNA synthetases.
Top Curr Chem
; 344: 247-92, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-23824528
14.
Pathogenic mutations causing LBSL affect mitochondrial aspartyl-tRNA synthetase in diverse ways.
Biochem J
; 450(2): 345-50, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23216004
15.
What is so special about neuronal translation? (comment on DOI 10.1002/bies.201600052).
Bioessays
; 38(9): 816, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27427507
16.
A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondria.
Biochem J
; 433(3): 441-6, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21121901
17.
Purification of Mitochondrial Ribosomal Complexes from Trypanosoma cruzi and Leishmania tarentolae for Cryo-EM Analysis.
Bio Protoc
; 12(10): e4425, 2022 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35865117
18.
Pathology-related mutation A7526G (A9G) helps in the understanding of the 3D structural core of human mitochondrial tRNA(Asp).
RNA
; 15(8): 1462-8, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19535463
19.
Tertiary network in mammalian mitochondrial tRNAAsp revealed by solution probing and phylogeny.
Nucleic Acids Res
; 37(20): 6881-95, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19767615
20.
The rise of RNA: From fundamental research to therapeutic applications.
Biochimie
; 217: 1-2, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38272605