Detalhe da pesquisa
1.
Allelic phenotype prediction of phenylketonuria based on the machine learning method.
Hum Genomics
; 17(1): 34, 2023 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37004080
2.
Inherited disease-linked arginine76/75 mutants in Cx50 and Cx45 showed impaired homotypic and heterotypic gap junction function, but not Cx43.
Biochem J
; 480(14): 1051-1077, 2023 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37395717
3.
Knowledge, attitude, and practice of patients with major depressive disorder on exercise therapy.
BMC Public Health
; 24(1): 323, 2024 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38287298
4.
[Newborn screening, clinical features and genetic analysis for Citrin deficiency in Henan province].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(4): 461-466, 2024 Apr 10.
Artigo
em Zh
| MEDLINE | ID: mdl-38565513
5.
Identification of phenylketonuria patient genotypes using single-gene full-length sequencing.
Hum Genomics
; 16(1): 23, 2022 07 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35869558
6.
Hyperthermia inhibits growth of nasopharyngeal carcinoma through degradation of c-Myc.
Int J Hyperthermia
; 39(1): 358-371, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35184661
7.
Association of fish oil containing lipid emulsions with retinopathy of prematurity: a retrospective observational study.
BMC Pediatr
; 22(1): 113, 2022 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35236316
8.
Time-dependent Effects of Moderate- and High-intensity Exercises on Myocardial Transcriptomics.
Int J Sports Med
; 43(14): 1214-1225, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36063823
9.
The Hydrophobic Residues in Amino Terminal Domains of Cx46 and Cx50 Are Important for Their Gap Junction Channel Ion Permeation and Gating.
Int J Mol Sci
; 23(19)2022 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36232905
10.
[Analysis of GCH1 gene variant in a consanguineous Chinese pedigree affected with tetrahydrobiopterin deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(7): 713-717, 2022 Jul 10.
Artigo
em Zh
| MEDLINE | ID: mdl-35810427
11.
[Clinical and genetic characteristics of primary carnitine deficiency identified by neonatal screening].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(12): 1167-1170, 2019 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-31813139
12.
Correction to: Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China.
BMC Med Genet
; 19(1): 6, 2018 01 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29316886
13.
Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China.
BMC Med Genet
; 18(1): 108, 2017 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28982351
14.
[Genotype and phenotype correlation of phenylalanine hydroxylase deficiency among patients from Henan].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(3): 300-5, 2016 Jun.
Artigo
em Zh
| MEDLINE | ID: mdl-27264808
15.
Cytokine responses and correlations thereof with clinical profiles in children with enterovirus 71 infections.
BMC Infect Dis
; 15: 225, 2015 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26058678
16.
MD-UNet: a medical image segmentation network based on mixed depthwise convolution.
Med Biol Eng Comput
; 62(4): 1201-1212, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38158549
17.
Antiviral and Anti-Inflammatory Therapeutic Interventions for Treating Herpes Stromal Keratitis: A Systematic Review.
Ophthalmic Epidemiol
; : 1-19, 2023 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37184084
18.
Access to Pediatric Eye Care During a Pandemic: Systematic Review and Meta-Analysis.
Pediatr Ann
; 52(2): e68-e75, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36779881
19.
Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism.
Endocrine
; 79(1): 125-134, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36125728
20.
Acute aerobic exercise regulation of myocardial calcium homeostasis involves CASQ1, CASQ2, and TRDN.
J Appl Physiol (1985)
; 135(4): 707-716, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37589058