Detalhe da pesquisa
1.
Clinical Value of Platelets and Coagulation Parameters in Predicting the Severity of Delta Variant SARS-CoV-2.
Pathobiology
; 90(4): 241-250, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36724757
2.
MnFe2O4/polyaniline/diatomite composite with multiple loss mechanisms towards broadband absorption.
J Chem Phys
; 159(21)2023 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38047515
3.
Effect of different application duration of a venous foot pump on prevention of venous thromboembolism after hip and knee arthroplasty: a multicenter prospective clinical trial.
BMC Musculoskelet Disord
; 24(1): 931, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38041039
4.
Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model.
Molecules
; 28(14)2023 Jul 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37513273
5.
Circ-CBFB exacerbates hypoxia/reoxygenation-triggered cardiomyocyte injury via regulating miR-495-3p in a VDAC1-dependent manner.
J Biochem Mol Toxicol
; 36(11): e23189, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35920438
6.
LncRNA UCA1 remits LPS-engendered inflammatory damage through deactivation of miR-499b-5p/TLR4 axis.
IUBMB Life
; 73(2): 463-473, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33368965
7.
Classification of induced malaria case in an elimination setting: investigation of transfusion-transmitted malaria cases.
Malar J
; 19(1): 136, 2020 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32228585
8.
[A Digital Filtering Method for Eliminating DC Offset in Ambulatory ECG Signals].
Zhongguo Yi Liao Qi Xie Za Zhi
; 43(4): 252-254, 2019 Jul 30.
Artigo
em Zh
| MEDLINE | ID: mdl-31460714
9.
Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study.
Sci Rep
; 14(1): 2271, 2024 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38280885
10.
Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing.
Sci Rep
; 14(1): 9966, 2024 04 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38693200
11.
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population.
Mol Genet Genomic Med
; 12(1): e2365, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38284449
12.
A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the ß-globin Gene: A Possibly Benign Variant.
Indian J Hematol Blood Transfus
; 39(1): 102-106, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36699435
13.
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review.
Mol Genet Genomic Med
; 11(3): e2121, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36504312
14.
Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome.
Mol Genet Genomic Med
; 11(10): e2242, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37485807
15.
Etiology analysis and G6PD deficiency for term infants with jaundice in Yangjiang of western Guangdong.
Front Pediatr
; 11: 1201940, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37492600
16.
Covid-19 omicron variant infection in neonates of Guangdong province-a report of 52 cases.
Front Pediatr
; 11: 1191651, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37416819
17.
Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing.
Front Pediatr
; 10: 816090, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35463886
18.
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication.
Front Genet
; 13: 924573, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35865016
19.
Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing.
Front Genet
; 13: 829613, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35401667
20.
Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report.
Front Genet
; 13: 964098, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36092864