Detalhe da pesquisa
1.
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss.
Am J Hum Genet
; 108(10): 2006-2016, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34626583
2.
ENPP2 inhibitor improves proliferation in AOM/DSS-induced colorectal cancer mice via remodeling the gut barrier function and gut microbiota composition.
Pharmacol Res
; 195: 106877, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37524154
3.
Developing Carbon Dots with Room-Temperature Phosphorescence for the Dual-Signal Detection of Metronidazole.
Langmuir
; 38(49): 15442-15450, 2022 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36455258
4.
Environmentally responsive hydrogels for repair of cardiovascular tissue.
Heart Fail Rev
; 26(5): 1273-1285, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32076909
5.
Room-temperature processed high-quality SnO2 films by oxygen plasma activated e-beam evaporation.
Nanotechnology
; 32(2): 025606, 2021 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32998117
6.
Retrospective investigation of hereditary syndromes in patients with medulloblastoma in a single institution.
Childs Nerv Syst
; 37(2): 411-417, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32930885
7.
The Art of Framework Construction: Core-Shell Structured Micro-Energetic Materials.
Molecules
; 26(18)2021 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34577119
8.
Metabolomics Study Revealing the Potential Risk and Predictive Value of Fragmented QRS for Acute Myocardial Infarction.
J Proteome Res
; 19(8): 3386-3395, 2020 08 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32538096
9.
Novel variants of ABCA4 in Han Chinese families with Stargardt disease.
BMC Med Genet
; 21(1): 213, 2020 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33129279
10.
LYW-6, a novel cryptotanshinone derived STAT3 targeting inhibitor, suppresses colorectal cancer growth and metastasis.
Pharmacol Res
; 153: 104661, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31982491
11.
Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses.
BMC Ophthalmol
; 20(1): 212, 2020 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32487042
12.
Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa.
Ophthalmology
; 126(11): 1549-1556, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31054281
13.
Exome sequencing of Saudi Arabian patients with ADPKD.
Ren Fail
; 41(1): 842-849, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31488014
14.
Revealing Alzheimer's disease genes spectrum in the whole-genome by machine learning.
BMC Neurol
; 18(1): 5, 2018 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29320986
15.
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia.
Hum Mol Genet
; 24(8): 2297-307, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25556185
16.
Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing.
BMC Med Genet
; 18(1): 11, 2017 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28196478
17.
Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy.
Mol Vis
; 23: 605-613, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28867931
18.
CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids.
Brain
; 139(Pt 6): 1666-72, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27190017
19.
Comparative studies on the multi-component pharmacokinetics of Aristolochiae Fructus and honey-fried Aristolochiae Fructus extracts after oral administration in rats.
BMC Complement Altern Med
; 17(1): 107, 2017 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28187732
20.
Screening Hepatotoxic Components in Euodia rutaecarpa by UHPLC-QTOF/MS Based on the Spectrum-Toxicity Relationship.
Molecules
; 22(8)2017 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28749432