Rang Q. Xu

1665 Kongjiang Road
Shanghai, 200092, China

Last Updated: 09/26/2026

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Found 40 publications

Exploration of candidate genes associated with rare SNVs in pulmonary stenosis using whole-exome sequencing and machine learning.

Exploration of candidate genes associated with rare SNVs in pulmonary stenosis using whole-exome sequencing and machine learning.

Journal: Frontiers in genetics

Published: December 11, 2025

Ginkgo biloba extract GBE50 alleviates vascular calcification through inhibiting the NF-κB pathway and the NLRP3 inflammasome.

Ginkgo biloba extract GBE50 alleviates vascular calcification through inhibiting the NF-κB pathway and the NLRP3 inflammasome.

Journal: Journal of ethnopharmacology

Published: October 30, 2025

Slo1 Deficient Myoblast Exosomes-Derived miR-222-3p Inhibits Osteogenic Differentiation via Targeting of STAT3.

Slo1 Deficient Myoblast Exosomes-Derived miR-222-3p Inhibits Osteogenic Differentiation via Targeting of STAT3.

Journal: Journal of cachexia, sarcopenia and muscle

Published: October 11, 2024

Dlc1 deletion activates the canonical Wnt pathway at an early stage and affects subsequent cardiac differentiation in mouse embryonic stem cells.

Dlc1 deletion activates the canonical Wnt pathway at an early stage and affects subsequent cardiac differentiation in mouse embryonic stem cells.

Journal: Genes & diseases

Published: July 30, 2024

Improvement in Tol2 transposon for efficient large-cargo capacity transgene applications in cultured cells and zebrafish ( Danio rerio).

Improvement in Tol2 transposon for efficient large-cargo capacity transgene applications in cultured cells and zebrafish ( Danio rerio).

Journal: Zoological research

Published: May 17, 2024

ccdc141 is required for left-right axis development by regulating cilia formation in the Kupffer's vesicle of zebrafish.

ccdc141 is required for left-right axis development by regulating cilia formation in the Kupffer's vesicle of zebrafish.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: March 22, 2024

Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects.

Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects.

Journal: Genomics

Published: October 24, 2023

Research advances in the treatment of keloid with glucocorticoids

Research advances in the treatment of keloid with glucocorticoids

Journal: Zhonghua shao shang yu chuang mian xiu fu za zhi

Published: October 08, 2023

Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing.

Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing.

Journal: Genomics

Published: March 15, 2023

Novel compound heterozygous CCDC40 mutations in a familial case of primary ciliary dyskinesia.

Novel compound heterozygous CCDC40 mutations in a familial case of primary ciliary dyskinesia.

Journal: Frontiers in pediatrics

Published: July 17, 2022

De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children.

De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children.

Journal: Human genomics

Published: May 31, 2022

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease.

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease.

Journal: PLoS genetics

Published: February 25, 2022

Showing 1-12 of 40

Last Updated: 09/26/2026