Shan C. Duan
Shenzhen, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 41 publications
Familial Turner Syndrome With Distinct Karyotypes in Two Cousins: Phenotypic Convergence and Genotypic Heterogeneity.
Journal: The American journal of case reports
Published: May 11, 2026
A novel HBD gene mutation associated with normal-range hb A2 in β-thalassemia carriers.
Journal: Annals of hematology
Published: November 07, 2025
Establishment of a Rat Model for Intrauterine Adhesions via Dual Injury: Curettage and Infection.
Journal: Journal of visualized experiments : JoVE
Published: October 20, 2025
Inhibition of ascorbic acid on Pseudomonas bubulae under super-chilled storage.
Journal: World journal of microbiology & biotechnology
Published: October 07, 2025
Enrichment of Zinc-Chelating Peptides from Casein Using IMAC and Their Zinc Binding Modes and Promoting Intestinal Zinc Absorption Activity.
Journal: Journal of agricultural and food chemistry
Published: June 09, 2025
Exploring the causal association between body composition and primary ovarian insufficiency: A retrospective cohort study and Mendelian randomization analyses.
Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics
Published: June 05, 2025
NAALAD2 mutations disrupt the fate of photoreceptor cells and retinal pigment epithelial cells during early retinal development.
Journal: Pharmacological research
Published: December 14, 2024
Protein Kinase C Epsilon Overexpression Protects the Heart Against Doxorubicin-Induced Cardiotoxicity Via Activating SIRT1.
Journal: Cardiovascular toxicology
Published: October 06, 2024
Screening study of hydroxytyrosol metabolites from in vitro fecal fermentation and their interaction with intestinal barrier repair receptor AhR.
Journal: Journal of food science
Published: September 20, 2024
RMRP variants inhibit the cell cycle checkpoints pathway in cartilage‑hair hypoplasia.
Journal: Molecular medicine reports
Published: September 12, 2024
Deficiency in the conserved ECHS1 gene causes Leigh syndrome by impairing mitochondrial respiration efficiency and suppressing ADRB2-PKA signaling.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: September 10, 2024
Adipose tissue may not be a major player in the inflammatory pathogenesis of Autism Spectrum Disorder.
Journal: Brain, behavior, & immunity - health
Published: September 05, 2024
Last Updated: 09/26/2026