Detalhe da pesquisa
1.
Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy.
Graefes Arch Clin Exp Ophthalmol
; 262(1): 337-351, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37584790
2.
Influence of Coal-Fired Fly Ash on Measurement Error of NO2 Electrochemical Sensors.
Sensors (Basel)
; 24(3)2024 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38339616
3.
Increased neural activity of right temporo-parietal junction causes different effect on altruism in situations of advantageous and disadvantageous inequity.
Brain Cogn
; 171: 106061, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37451074
4.
Molecular dynamics study on thermal conductance between a nanotip and a substrate under vertical forces and horizontal sliding.
Phys Chem Chem Phys
; 25(7): 5510-5519, 2023 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36723186
5.
Genetic analysis and clinical features of three Chinese patients with Oguchi disease.
Doc Ophthalmol
; 146(1): 17-32, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36417138
6.
Anomaly Detection of Wind Turbine Driveline Based on Sequence Decomposition Interactive Network.
Sensors (Basel)
; 23(21)2023 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37960662
7.
Leber congenital amaurosis as an initial manifestation in a Chinese patient with thiamine-responsive megaloblastic anemia syndrome.
Am J Med Genet A
; 188(3): 948-952, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34821467
8.
Distinct roles of the medial prefrontal cortex in advantageous and disadvantageous inequity aversion.
Brain Cogn
; 164: 105927, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36343582
9.
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy.
Graefes Arch Clin Exp Ophthalmol
; 260(2): 645-653, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34427740
10.
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Genet Med
; 23(6): 1041-1049, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33531668
11.
Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7.
Mol Vis
; 27: 221-232, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34012225
12.
Clinical and genetic analysis of the ABCA4 gene associated retinal dystrophy in a large Chinese cohort.
Exp Eye Res
; 202: 108389, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33301772
13.
Novel variants in PNPLA6 causing syndromic retinal dystrophy.
Exp Eye Res
; 202: 108327, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33141049
14.
The only-child effect in the neural and behavioral signatures of trust revealed by fNIRS hyperscanning.
Brain Cogn
; 149: 105692, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33540359
15.
Treating Bietti crystalline dystrophy in a high-fat diet-exacerbated murine model using gene therapy.
Gene Ther
; 27(7-8): 370-382, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32483213
16.
Detailed comparison of phenotype between male patients carrying variants in exons 1-14 and ORF15 of RPGR.
Exp Eye Res
; 198: 108147, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32702353
17.
TNFRSF21 mutations cause high myopia.
J Med Genet
; 56(10): 671-677, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31189563
18.
CLINICAL CHARACTERISTICS AND MOLECULAR GENETIC ANALYSIS OF A COHORT OF CHINESE PATIENTS WITH CHOROIDEREMIA.
Retina
; 40(11): 2240-2253, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31922496
19.
[Design and Implementation of Infusion Monitor Software Based on C# Language].
Zhongguo Yi Liao Qi Xie Za Zhi
; 43(6): 429-431, 2019 Nov 30.
Artigo
em Chinês
| MEDLINE | ID: mdl-31854529
20.
Simultaneous pyridine biodegradation and nitrogen removal in an aerobic granular system.
J Environ Sci (China)
; 67: 318-329, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29778165