Yan-ping Q. Zhang
Fuzhou, China
Last Updated: 09/26/2026
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Found 14 publications
Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
Journal: Scientific reports
Published: September 10, 2024
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
Journal: Scientific reports
Published: September 06, 2023
Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis.
Journal: Pediatric rheumatology online journal
Published: August 12, 2023
Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis.
Journal: Scientific reports
Published: April 04, 2023
Eighteen cases of renal aneurysms: Clinical retrospective analysis and experience of endovascular interventional treatment.
Journal: Frontiers in surgery
Published: November 24, 2022
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency.
Journal: Thrombosis journal
Published: August 23, 2022
A clinical analysis of intestinal mucosal necrosis and exfoliation induced by superior mesenteric vein thrombosis: A case report.
Journal: Frontiers in surgery
Published: July 07, 2022
Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation.
Journal: Frontiers in cardiovascular medicine
Published: March 01, 2022
Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization.
Journal: Frontiers in surgery
Published: February 15, 2022
Prevalence of sharp instrument injuries among medical staff in a tertiary general hospital
Journal: Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases
Published: December 10, 2021
Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.
Journal: Cell death & disease
Published: November 30, 2021
A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1.
Journal: Thrombosis journal
Published: July 01, 2021
Last Updated: 09/26/2026