Detalhe da pesquisa
1.
Death after High-Dose rAAV9 Gene Therapy in a Patient with Duchenne's Muscular Dystrophy.
N Engl J Med
; 389(13): 1203-1210, 2023 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37754285
2.
A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11.
Clin Genet
; 101(4): 448-453, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34988992
3.
Validation of the simplified Chinese version of the quality of life questionnaire of the European foundation for osteoporosis (QUALEFFO-31).
Eur Spine J
; 25(1): 318-324, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26070551
4.
Relationship between sagittal spinal alignment and the incidence of vertebral fracture in menopausal women with osteoporosis: a multicenter longitudinal follow-up study.
Eur Spine J
; 24(4): 737-43, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25374300
5.
Microwave-assisted synthesis and luminescence properties of Cd(1-x)Eu(x)MoO4 red phosphor.
J Nanosci Nanotechnol
; 14(5): 3618-22, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24734600
6.
Degenerative lumbar scoliosis in Chinese Han population: prevalence and relationship to age, gender, bone mineral density, and body mass index.
Eur Spine J
; 22(6): 1326-31, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23361532
7.
Flavones provide resistance to DUX4-induced toxicity via an mTor-independent mechanism.
Res Sq
; 2023 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36778471
8.
Flavones provide resistance to DUX4-induced toxicity via an mTor-independent mechanism.
Cell Death Dis
; 14(11): 749, 2023 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37973788
9.
Functional Characterization of MC4R Variants in Chinese Morbid Obese Patients and Weight Loss after Bariatric Surgery.
Adv Biol (Weinh)
; 7(9): e2300007, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37140139
10.
Deep Mutational Scanning in Disease-related Genes with Saturation Mutagenesis-Reinforced Functional Assays (SMuRF).
bioRxiv
; 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37873263
11.
Phosphorus- and fluorine-co-doped carbon nitride: modulated visible light absorption, charge carrier kinetics and boosted photocatalytic hydrogen evolution.
Dalton Trans
; 50(40): 14110-14114, 2021 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34604888
12.
Effectiveness of companion-intensive multi-aspect weight management in Chinese adults with obesity: a 6-month multicenter randomized clinical trial.
Nutr Metab (Lond)
; 18(1): 17, 2021 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33536048
13.
Exome sequencing in paediatric patients with movement disorders.
Orphanet J Rare Dis
; 16(1): 32, 2021 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33446253
14.
Double defective group modified nitrogen-deficient carbon nitride with bimetallic PtSn as a cocatalyst for efficient photocatalytic hydrogen evolution up to 765 nm.
Chem Commun (Camb)
; 56(45): 6054-6057, 2020 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32347848
15.
A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis.
NPJ Genom Med
; 5(1): 37, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32963807
16.
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy.
Sci Transl Med
; 12(536)2020 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32213627
17.
Steering Charge Kinetics of Tin Niobate Photocatalysts: Key Roles of Phase Structure and Electronic Structure.
Nanoscale Res Lett
; 13(1): 161, 2018 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29796920
18.
Correction to: Effectiveness of companion-intensive multi-aspect weight management in Chinese adults with obesity: a 6-month multicenter randomized clinical trial.
Nutr Metab (Lond)
; 18(1): 35, 2021 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33785030
19.
Defect-meditated efficient catalytic activity toward p-nitrophenol reduction: A case study of nitrogen doped calcium niobate system.
J Hazard Mater
; 295: 119-26, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25897693
20.
Investigation of the 53 Markers in a DNA-Based Prognostic Test Revealing New Predisposition Genes for Adolescent Idiopathic Scoliosis.
Spine (Phila Pa 1976)
; 40(14): 1086-91, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25811265