Detalhe da pesquisa
1.
High-fidelity SaCas9 identified by directional screening in human cells.
PLoS Biol
; 18(7): e3000747, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32644995
2.
Association of SARS-CoV-2 viral load with abnormal laboratory characteristics and clinical outcomes in hospitalised COVID-19 patients.
Epidemiol Infect
; 151: e173, 2023 10 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37781778
3.
Efficacy and Safety of Repetitive Transcranial Magnetic Stimulation for Poststroke Memory Disorder: A Meta-Analysis and Systematic Review.
J Integr Neurosci
; 22(5): 131, 2023 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37735134
4.
Engineered FnCas12a with enhanced activity through directional evolution in human cells.
J Biol Chem
; 296: 100394, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33567342
5.
Lb2Cas12a and its engineered variants mediate genome editing in human cells.
FASEB J
; 35(4): e21270, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33715215
6.
Boosting activity of high-fidelity CRISPR/Cas9 variants using a tRNAGln-processing system in human cells.
J Biol Chem
; 294(23): 9308-9315, 2019 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31010827
7.
[Serological feature and molecular mechanism for a case with A307 subgroup].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(6): 677-680, 2020 Jun 10.
Artigo
em Zh
| MEDLINE | ID: mdl-32472551
8.
A 'new lease of life': FnCpf1 possesses DNA cleavage activity for genome editing in human cells.
Nucleic Acids Res
; 45(19): 11295-11304, 2017 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28977650
9.
[Identification and pedigree analysis of ABO subgroup B303].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(3): 440-442, 2018 Jun 10.
Artigo
em Zh
| MEDLINE | ID: mdl-29896751
10.
A serologic weakly reactive RhD is caused by a novel RHD (c.722C>A, p.Thr241Asn) allele.
Transfusion
; 61(4): E31-E33, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33720432
11.
c.543G>C mutation in ABO*A.1.02 allele responsible for a weak A phenotype.
Transfusion
; 59(8): 2756-2757, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31260107
12.
Identification of a novel B allele with multiple missense mutations in a Chinese family with a Bw phenotype.
Transfusion
; 58(11): 2741-2742, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30222859
13.
Effectiveness and safety of repetitive transcranial magnetic stimulation on memory disorder in stroke: A protocol for systematic review and meta-analysis.
Medicine (Baltimore)
; 101(40): e30933, 2022 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36221389
14.
[A novel missense mutation resulting in X-linked adrenoleukodystrophy in female heterozygotes of a Chinese family].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 27(2): 144-8, 2010 Apr.
Artigo
em Zh
| MEDLINE | ID: mdl-20376793
15.
Learning a Single Model with a Wide Range of Quality Factors for JPEG Image Artifacts Removal.
IEEE Trans Image Process
; PP2020 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32886610
16.
[Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 26(1): 50-3, 2009 Feb.
Artigo
em Zh
| MEDLINE | ID: mdl-19199251
17.
[Application and optimization of CRISPR/Cas system in bacteria].
Sheng Wu Gong Cheng Xue Bao
; 35(3): 341-350, 2019 Mar 25.
Artigo
em Zh
| MEDLINE | ID: mdl-30912343
18.
Basic and Clinical Application of Adeno-Associated Virus-Mediated Genome Editing.
Hum Gene Ther
; 30(6): 673-681, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30588843
19.
Efficient cleavage resolves PAM preferences of CRISPR-Cas in human cells.
Cell Regen
; 8(2): 44-50, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31709036
20.
Efficient Human Genome Editing Using SaCas9 Ribonucleoprotein Complexes.
Biotechnol J
; 14(7): e1800689, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30927491