Fengjiao J. Wang

Key Laboratory Of Clinical Laboratory Diagnosis And Translational Research Of Zhejiang Province
Wenzhou, China

Last Updated: 09/26/2026

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Found 8 publications

Compound heterozygous variants in F7 gene causing severe factor VII deficiency without bleeding: A genotypic and laboratory analysis.

Compound heterozygous variants in F7 gene causing severe factor VII deficiency without bleeding: A genotypic and laboratory analysis.

Journal: Blood cells, molecules & diseases

Published: March 31, 2026

Molecular pathogenesis of a novel p.Cys467Tyr missense variant underlying Hereditary factor Ⅻ deficiency

Molecular pathogenesis of a novel p.Cys467Tyr missense variant underlying Hereditary factor Ⅻ deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 11, 2026

Cerebral venous sinus thrombosis in a family with protein S deficiency: genetic analysis and phenotypic characterization.

Cerebral venous sinus thrombosis in a family with protein S deficiency: genetic analysis and phenotypic characterization.

Journal: Thrombosis journal

Published: February 12, 2026

Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis

Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: February 09, 2026

Analysis of a Chinese pedigree affected with hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene

Analysis of a Chinese pedigree affected with hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: December 26, 2025

Novel compound heterozygous mutations in plasminogen (p.Gly568Arg/p.Ala620Thr) impair protein structure and function in type II deficiency: mechanistic insights into a hereditary thrombogenic disorder.

Novel compound heterozygous mutations in plasminogen (p.Gly568Arg/p.Ala620Thr) impair protein structure and function in type II deficiency: mechanistic insights into a hereditary thrombogenic disorder.

Journal: Orphanet journal of rare diseases

Published: June 26, 2025

Protective role of selenium-enriched supplement on spinal cord injury through the up-regulation of CNTF and CNTF-Ralpha.

Protective role of selenium-enriched supplement on spinal cord injury through the up-regulation of CNTF and CNTF-Ralpha.

Journal: European review for medical and pharmacological sciences

Published: December 05, 2015

Gene expression signature analysis and protein-protein interaction network construction of spinal cord injury.

Gene expression signature analysis and protein-protein interaction network construction of spinal cord injury.

Journal: European review for medical and pharmacological sciences

Published: November 21, 2013

Showing 1-8 of 8

Last Updated: 09/26/2026