Deyong Xiao
Key Laboratory Of Metabolism And Molecular Medicine
Shanghai, China
Shanghai, China
Last Updated: 09/26/2026
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Found 8 publications
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
Journal: Clinical and translational medicine
Published: February 08, 2022
Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
Journal: Journal of cellular and molecular medicine
Published: November 29, 2018
The Novel Pathogenic Mutation c.849dupT in BRCA2 Contributes to the Nonsense-Mediated mRNA Decay of BRCA2 in Familial Breast Cancer.
Journal: Journal of breast cancer
Published: March 18, 2018
The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafish.
Journal: PLoS genetics
Published: February 15, 2018
Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants.
Journal: European journal of medical genetics
Published: December 29, 2017
Hypomethylation and decreased expression of BRG1 in the myocardium of patients with congenital heart disease.
Journal: Birth defects research
Published: December 09, 2016
Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
Journal: Journal of translational medicine
Published: October 13, 2016
A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer.
Journal: Journal of cancer research and clinical oncology
Published: September 28, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026