Pengyun Wang
Wuhan, China
Last Updated: 09/26/2026
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Found 16 publications
Association Between Thromboelastography and Coagulation for Disease Severity Evaluation in Patients With Lower Extremity Arteriosclerosis Obliterans.
Journal: Journal of clinical laboratory analysis
Published: September 03, 2024
Association of ApoE gene polymorphisms with serum lipid levels and the risk of type 2 diabetes mellitus in the Chinese Han population of central China.
Journal: PeerJ
Published: December 29, 2022
Two Novel Functional Mutations in Promoter Region of SCN3B Gene Associated with Atrial Fibrillation.
Two Novel Functional Mutations in Promoter Region of SCN3B Gene Associated with Atrial Fibrillation.
Journal: Life (Basel, Switzerland)
Published: September 28, 2022
Hepatocyte Ninjurin2 promotes hepatic stellate cell activation and liver fibrosis through the IGF1R/EGR1/PDGF-BB signaling pathway.
Journal: Metabolism: clinical and experimental
Published: August 19, 2022
Global Limb Anatomic Staging System Score correlates with the clinical outcomes in chronic limb threatening ischemia patients.
Journal: International angiology : a journal of the International Union of Angiology
Published: June 16, 2022
NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling.
Journal: Obesity (Silver Spring, Md.)
Published: April 26, 2022
Gene polymorphism in IL17A and gene-gene interaction in the IL23R/IL17A axis are associated with susceptibility to coronary artery disease.
Journal: Cytokine
Published: March 14, 2022
Annotation of susceptibility SNPs associated with atrial fibrillation.
Journal: Aging
Published: December 16, 2019
Major vault protein plays important roles in viral infection.
Journal: IUBMB life
Published: September 03, 2019
SNP rs2243828 in MPO associated with myeloperoxidase level and atrial fibrillation risk in Chinese Han population.
Journal: Journal of cellular and molecular medicine
Published: August 07, 2019
Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia.
Journal: Molecular genetics and genomics : MGG
Published: September 30, 2018
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation.
Journal: Annals of human genetics
Published: August 06, 2018
Last Updated: 09/26/2026