Qiyu Xu

Key Laboratory Of Clinical Laboratory Diagnosis And Translational Research Of Zhejiang Province, Shangcai Village, Ouhai District
Wenzhou, 325000, China

Last Updated: 09/26/2026

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Found 11 publications

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

Multiomics and experimental validation reveal theophylline's mechanism targeting IL1A/ACTB/TLR4 and identify synergistic drugs in hepatocellular carcinoma.

Multiomics and experimental validation reveal theophylline's mechanism targeting IL1A/ACTB/TLR4 and identify synergistic drugs in hepatocellular carcinoma.

Journal: The Journal of pharmacology and experimental therapeutics

Published: December 05, 2025

SERPINC1 mutations and thrombotic events in inherited antithrombin deficiency: a study on the han population of East China.

SERPINC1 mutations and thrombotic events in inherited antithrombin deficiency: a study on the han population of East China.

Journal: Orphanet journal of rare diseases

Published: March 05, 2025

Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.

Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.

Journal: Annals of hematology

Published: May 22, 2023

Analysis of the molecular pathogenesis of hereditary protein C deficiency due to a p.Gly86Asp variant of the PROC gene

Analysis of the molecular pathogenesis of hereditary protein C deficiency due to a p.Gly86Asp variant of the PROC gene

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

Published: July 10, 2022

Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.

Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: July 15, 2021

Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.

Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.

Journal: Hamostaseologie

Published: December 29, 2020

Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.

Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: November 16, 2020

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: August 25, 2020

Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).

Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).

Journal: Hamostaseologie

Published: May 26, 2020

Association of polymorphism in the promoter region of PCA3 gene with risk of prosate cancer

Association of polymorphism in the promoter region of PCA3 gene with risk of prosate cancer

Journal: Zhonghua zhong liu za zhi [Chinese journal of oncology]

Published: May 16, 2015

Showing 1-11 of 11

Last Updated: 09/26/2026