Zhang XY - Search Results

1

Collecting duct NCOR1 controls blood pressure by regulating mineralocorticoid receptor.

Sun K, Wang YL, Hou CC, Shang D, Du LJ, Bai L, Zhang XY, Hao CM, Duan SZ. Sun K, et al. Among authors: zhang xy. J Adv Res. 2024 Feb 8:S2090-1232(24)00053-5. doi: 10.1016/j.jare.2024.02.003. Online ahead of print. J Adv Res. 2024. PMID: 38341030 Free article.

2

Assessment of left ventricular activation conduction during left bundle branch area pacing in heart failure patients: A novel criterion to determine left bundle branch capture.

Zhang W, Chen X, Huang J, Zhang X, Qi Y, Wang J, Zhou X, Su Y, Hou X, Li R. Zhang W, et al. Heart Rhythm. 2024 Nov;21(11):2348-2350. doi: 10.1016/j.hrthm.2024.04.087. Epub 2024 Apr 29. Heart Rhythm. 2024. PMID: 38692341 No abstract available.

3

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.

Lu Y, Zhou Y, Guo J, Qi M, Lin Y, Zhang X, Xiang Y, Fu Q, Wang B. Lu Y, et al. Commun Biol. 2023 Jul 17;6(1):735. doi: 10.1038/s42003-023-05101-9. Commun Biol. 2023. PMID: 37460814 Free PMC article.

4

Novel dominant-negative FOXJ1 mutation in a family with heterotaxy plus mouse model.

Li L, Shi G, Zhang X, Wang T, Wang B, Gao Y, You G, Fu Q, Xiang Y, Zhang X. Li L, et al. Transl Pediatr. 2023 Aug 30;12(8):1476-1489. doi: 10.21037/tp-23-27. Epub 2023 Aug 28. Transl Pediatr. 2023. PMID: 37692537 Free PMC article.

5

Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease.

Lu Y, Fang Q, Qi M, Li X, Zhang X, Lin Y, Xiang Y, Fu Q, Wang B. Lu Y, et al. Commun Biol. 2023 Feb 17;6(1):189. doi: 10.1038/s42003-023-04565-z. Commun Biol. 2023. PMID: 36806749 Free PMC article.

6

FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically.

Zhang X, Gao Y, Zhang X, Zhang X, Xiang Y, Fu Q, Wang B, Xu Z. Zhang X, et al. Front Cell Dev Biol. 2021 May 11;9:630634. doi: 10.3389/fcell.2021.630634. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34046402 Free PMC article.

7

Case Report: Prenatal Diagnosis of a Fetus With Harlequin Ichthyosis Identifies Novel Compound Heterozygous Variants: A Case Report.

Liu J, Zhang X, Wang W, Lan X, Dong M, Yan K, Lei Y, Chen P, Yang M, Shan Q, Jin C. Liu J, et al. Front Genet. 2021 Jan 12;11:608196. doi: 10.3389/fgene.2020.608196. eCollection 2020. Front Genet. 2021. PMID: 33510771 Free PMC article.

8

Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB.

Fa J, Zhang X, Zhang X, Qi M, Zhang X, Fu Q, Xu Z, Gao Y, Wang B. Fa J, et al. Front Cell Dev Biol. 2021 May 10;9:660576. doi: 10.3389/fcell.2021.660576. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34041241 Free PMC article.

9

Characterization and Functional Studies of a Novel Depolymerase Against K19-Type Klebsiella pneumoniae.

Hua Y, Wu Y, Guo M, Ma R, Li Q, Hu Z, Chen H, Zhang X, Li H, Li Q, He P. Hua Y, et al. Front Microbiol. 2022 Jun 22;13:878800. doi: 10.3389/fmicb.2022.878800. eCollection 2022. Front Microbiol. 2022. PMID: 35814656 Free PMC article.

10

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.

Zhang X, Wang B, You G, Xiang Y, Fu Q, Yu Y, Zhang X. Zhang X, et al. BMC Med Genomics. 2021 Oct 9;14(1):243. doi: 10.1186/s12920-021-01090-y. BMC Med Genomics. 2021. PMID: 34627233 Free PMC article.

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