Yeling Lu
No. 197 Ruijin Second Road
Shanghai, 200025, China
Shanghai, 200025, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 31 publications
Thrombomodulin Gly430Ser mutation attenuates the affinity with thrombin and contributes to thrombosis development.
Journal: Journal of thrombosis and thrombolysis
Published: May 02, 2026
Trp83 is vital to the interaction with phospholipids in γ-carboxyglutamic acid domain of protein C.
Journal: Journal of thrombosis and haemostasis : JTH
Published: February 06, 2026
Asn384Ser Mutation in Protein C is Associated with Multiple-Site Thrombosis in a Young Heterozygous Male.
Journal: Thrombosis and haemostasis
Published: April 18, 2025
Thrombomodulin Arg403Lys mutation impairs protein C activation and increases thrombosis risk.
Journal: Thrombosis research
Published: April 18, 2025
Molecular genetic analysis of two novel ABO∗A alleles causing Ax phenotype in Chinese.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: July 06, 2024
Heterozygous Prothrombin Mutation-Associated Thrombophilia.
Journal: Thrombosis and haemostasis
Published: June 24, 2024
Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome.
Journal: Global medical genetics
Published: June 11, 2024
Molecular mechanisms and clinical manifestations of hereditary hemorrhagic telangiectasia.
Journal: Thrombosis research
Published: May 14, 2024
Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosis.
Journal: Thrombosis research
Published: March 28, 2024
Met343Val mutation disrupts the shuttling of Trp380 leading to a low-activity conformer of activated protein C and causes thrombosis.
Journal: Journal of thrombosis and haemostasis : JTH
Published: February 18, 2024
Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C Deficiency.
Journal: Thrombosis and haemostasis
Published: November 27, 2023
Unraveling the molecular basis underlying nine putative splice site variants of von Willebrand factor.
Journal: Human mutation
Published: September 13, 2021
Last Updated: 09/26/2026