Huayang Zhang

180 Fenglin Road
Zhongshan, China

Last Updated: 09/26/2026

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Found 8 publications

Distinct pathogenic mechanisms underlying two protein C variants (p.Arg211Gln and p.Val367Met) in a thrombophilic family: integrated functional and structural analyses.

Distinct pathogenic mechanisms underlying two protein C variants (p.Arg211Gln and p.Val367Met) in a thrombophilic family: integrated functional and structural analyses.

Journal: Human genomics

Published: September 10, 2025

Functional impact of PROC variants on splicing and protein C activity: evidence for clinical reclassification and RNA therapeutic approaches.

Functional impact of PROC variants on splicing and protein C activity: evidence for clinical reclassification and RNA therapeutic approaches.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 09, 2025

Molecular mechanisms and therapeutic strategies for the recurrent F9 (c.520 + 13 A > G) variant in hemophilia B.

Molecular mechanisms and therapeutic strategies for the recurrent F9 (c.520 + 13 A > G) variant in hemophilia B.

Journal: Human genomics

Published: April 19, 2025

A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities.

A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities.

Journal: Journal of thrombosis and haemostasis : JTH

Published: November 18, 2024

Pleiotropic effects of different exonic nucleotide changes at the same position contribute to hemophilia B phenotypic variation.

Pleiotropic effects of different exonic nucleotide changes at the same position contribute to hemophilia B phenotypic variation.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 20, 2023

Tandem and inverted duplications in haemophilia A: Breakpoint characterisation provides insight into possible rearrangement mechanisms.

Tandem and inverted duplications in haemophilia A: Breakpoint characterisation provides insight into possible rearrangement mechanisms.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: January 31, 2023

Effects of 14 F9 synonymous codon variants on hemophilia B expression: Alteration of splicing along with protein expression.

Effects of 14 F9 synonymous codon variants on hemophilia B expression: Alteration of splicing along with protein expression.

Journal: Human mutation

Published: November 09, 2021

The novel mutation p.Asp315Tyr causes severe hemophilia B by impairing coagulation factor IX expression.

The novel mutation p.Asp315Tyr causes severe hemophilia B by impairing coagulation factor IX expression.

Journal: Thrombosis research

Published: July 13, 2020

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Last Updated: 09/26/2026