Xiaolong Li

301 Yan Chang Zhong Road
Shanghai, 200072, China

Last Updated: 09/26/2026

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Found 25 publications

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

Growth of sulfur-doped bismuth oxybromide nanosheets on carbon fiber cloth for photocatalytically purifying antibiotic wastewater.

Growth of sulfur-doped bismuth oxybromide nanosheets on carbon fiber cloth for photocatalytically purifying antibiotic wastewater.

Journal: Journal of colloid and interface science

Published: May 31, 2024

Fabrication of NH2-MIL-125(Ti) nanodots on carbon fiber/MoS2-based weavable photocatalysts for boosting the adsorption and photocatalytic performance.

Fabrication of NH2-MIL-125(Ti) nanodots on carbon fiber/MoS2-based weavable photocatalysts for boosting the adsorption and photocatalytic performance.

Journal: Journal of colloid and interface science

Published: October 15, 2021

Bismuth oxybromide/bismuth oxyiodide nanojunctions decorated on flexible carbon fiber cloth as easily recyclable photocatalyst for removing various pollutants from wastewater.

Bismuth oxybromide/bismuth oxyiodide nanojunctions decorated on flexible carbon fiber cloth as easily recyclable photocatalyst for removing various pollutants from wastewater.

Journal: Journal of colloid and interface science

Published: August 10, 2021

Corrigendum: First Report of Coexistence of bla SFO-1 and bla NDM-1 β-Lactamase Genes as Well as Colistin Resistance Gene mcr-9 in a Transferrable Plasmid of a Clinical Isolate of Enterobacter hormaechei.

Corrigendum: First Report of Coexistence of bla SFO-1 and bla NDM-1 β-Lactamase Genes as Well as Colistin Resistance Gene mcr-9 in a Transferrable Plasmid of a Clinical Isolate of Enterobacter hormaechei.

Journal: Frontiers in microbiology

Published: July 15, 2021

First Report of Coexistence of bla SFO-1 and bla NDM-1 β-Lactamase Genes as Well as Colistin Resistance Gene mcr-9 in a Transferrable Plasmid of a Clinical Isolate of Enterobacter hormaechei.

First Report of Coexistence of bla SFO-1 and bla NDM-1 β-Lactamase Genes as Well as Colistin Resistance Gene mcr-9 in a Transferrable Plasmid of a Clinical Isolate of Enterobacter hormaechei.

Journal: Frontiers in microbiology

Published: March 04, 2021

Profiling of gut microbial dysbiosis in adults with myeloid leukemia.

Profiling of gut microbial dysbiosis in adults with myeloid leukemia.

Journal: FEBS open bio

Published: February 09, 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

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene

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

Published: September 14, 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

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.

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

Published: August 25, 2020

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

Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by 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: May 31, 2020

Showing 1-12 of 25

Last Updated: 09/26/2026