Shan Duan

Laboratory of Molecular Medicine, Southern Medical University

Affiliated withSouthern Medical University

Research Area

Biography

Shan Duan has not added Biography.
If you are Shan Duan and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2025

Other Publications

Article	Year
The association between the rs4987105 of 5-lipoxygenase (ALOX5) gene and gestational glucose metabolism in Chinese population. BMC research notes\| PubMed ID: 32093765	2020
mTOR Signaling Pathway Regulates the Release of Proinflammatory Molecule CCL5 Implicated in the Pathogenesis of Autism Spectrum Disorder. Frontiers in immunology\| PubMed ID: 35422816	2022
Corneal histomorphology and electron microscopic observation of R124L mutated corneal dystrophy in a relapsed pedigree. International journal of ophthalmology\| PubMed ID: 36124191	2022
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR. Human heredity\| PubMed ID: 36315991	2023
Lovastatin inhibits the proliferation of human cervical cancer hela cells through the regulation of tp53 pathway by mir-92a-1-5p. Pakistan journal of pharmaceutical sciences\| PubMed ID: 36789815	2022
A mouse model for X-linked Alport syndrome induced by Del-ATGG in the gene. Frontiers in medicine\| PubMed ID: 36968823	2023
A Novel Heterozygous TGFBI c.1613C>A Pathogenic Variant is Associated With Lattice Corneal Dystrophy in a Chinese Family. American journal of ophthalmology\| PubMed ID: 37567434	2023
Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss. BMC medical genomics\| PubMed ID: 38167320	2024
Genetic epidemiology of thalassemia in couples of childbearing age: over 6 years of a thalassemia intervention project. Molecular biology reports\| PubMed ID: 38236368	2024
Adipose tissue may not be a major player in the inflammatory pathogenesis of Autism Spectrum Disorder. Brain, behavior, & immunity - health\| PubMed ID: 39810796	2025
Increased HA/CD44/TGFβ signaling implicates in renal fibrosis of a Col4a5 mutant Alport mice. Molecular medicine (Cambridge, Mass.)\| PubMed ID: 40075271	2025
NAALAD2 mutations disrupt the fate of photoreceptor cells and retinal pigment epithelial cells during early retinal development. Pharmacological research\| PubMed ID: 40185296	2025
Deficiency in the conserved ECHS1 gene causes Leigh syndrome by impairing mitochondrial respiration efficiency and suppressing ADRB2-PKA signaling. Biochimica et biophysica acta. Molecular basis of disease\| PubMed ID: 40446940	2025
Exploring the causal association between body composition and primary ovarian insufficiency: A retrospective cohort study and Mendelian randomization analyses. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics\| PubMed ID: 40734494	2025