Detalhe da pesquisa
1.
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Am J Hum Genet
; 111(1): 200-210, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38118446
2.
Nuclease-mediated depletion biases in ribosome footprint profiling libraries.
RNA
; 26(10): 1481-1488, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32503920
3.
A small molecule that induces translational readthrough of CFTR nonsense mutations by eRF1 depletion.
Nat Commun
; 12(1): 4358, 2021 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34272367
4.
Stop codon context influences genome-wide stimulation of termination codon readthrough by aminoglycosides.
Elife
; 92020 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31971508
5.
Dynamic Regulation of a Ribosome Rescue Pathway in Erythroid Cells and Platelets.
Cell Rep
; 17(1): 1-10, 2016 09 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27681415
6.
Assessment of erythroid dysplasia by "difference from normal" in routine clinical flow cytometry workup.
Cytometry B Clin Cytom
; 88(2): 125-35, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25490867
7.
Assessment of erythroid dysplasia by "difference from normal" in routine clinical flow cytometry work-up.
Cytometry B Clin Cytom
; 2014 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-25336233