Yao-bin Zhu
Fuzhou, China
Last Updated: 09/26/2026
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Found 17 publications
Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigree.
Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
Published: November 24, 2025
Eleutherococcus senticosus Alleviates Aristolochic-Acid-Induced Acute Kidney Damage by Inhibiting the NLRP3/IL-1β Signaling Pathway in Mice.
Journal: Planta medica
Published: January 24, 2025
The value of computed tomography angiography for evaluation of left atrial enlargement in patients with persistent atrial fibrillation.
Journal: BMC cardiovascular disorders
Published: June 18, 2024
Case Report: Imaging features of a new type double inferior vena cava malformation and review.
Journal: Frontiers in cardiovascular medicine
Published: September 21, 2023
Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome.
Journal: Journal of medical genetics
Published: April 12, 2023
Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: September 09, 2022
Comprehensive analysis of immune ferroptosis gene in renal clear cell carcinoma: prognosis and influence of tumor microenvironment.
Journal: American journal of translational research
Published: May 08, 2022
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
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
Journal: Cardiology research and practice
Published: November 16, 2021
A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
Journal: The journal of gene medicine
Published: May 06, 2021
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.
Journal: BioMed research international
Published: March 18, 2021
Effect of superselective prostatic artery embolization on benign prostatic hyperplasia.
Journal: Abdominal radiology (New York)
Published: May 02, 2020
Last Updated: 09/26/2026