Limeng Dai
Chongqing, China
Last Updated: 09/26/2026
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Found 44 publications
A multistage cost-effective strategy for the molecular diagnosis of unexplained vision loss patients: practice in inherited ocular fundus disease.
Journal: Molecular genetics and genomics : MGG
Published: May 09, 2025
Clinical and Genetic Profiles of 11 Chinese Patients With Angelman Syndrome.
Journal: Genetics research
Published: November 30, 2024
Effects of trace element dysregulation on brain structure and function in spinocerebellar Ataxia type 3.
Journal: Neurobiology of disease
Published: November 10, 2024
Gray Matter Asymmetry Alterations in Patients With Spinocerebellar Ataxia Type 3: A Voxel-Based Morphometric Comparison Study.
Journal: CNS neuroscience & therapeutics
Published: September 10, 2024
Imbalanced optimal feedback motor control system in spinocerebellar ataxia type 3.
Journal: European journal of neurology
Published: January 10, 2024
LMNA-related muscular dystrophy involving myoblast proliferation and apoptosis through the FOXO1/GADD45A pathway.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: July 27, 2023
microRNA-130b May Induce Cerebral Vasospasm after Subarachnoid Hemorrhage via Modulating Kruppel-like Factor 4.
Journal: Molecular and cellular biology
Published: June 29, 2023
Supt16 Haploinsufficiency Impairs PI3K/AKT/mTOR/Autophagy Pathway in Human Pluripotent Stem Cells Derived Neural Stem Cells.
Journal: International journal of molecular sciences
Published: December 27, 2022
Disruption of Intracellular Calcium Homeostasis Leads to ERLIN2-Linked Hereditary Spastic Paraplegia in Patient-Derived Stem Cell Models.
Journal: Human mutation
Published: December 23, 2022
Supt16 haploinsufficiency causes neurodevelopment disorder by disrupting MAPK pathway in neural stem cells.
Journal: Human molecular genetics
Published: August 07, 2022
Downregulation of miR-26b attenuates early brain injury induced by subarachnoid hemorrhage via mediating the KLF4/STAT3/HMGB1 axis.
Journal: Experimental neurology
Published: August 03, 2022
X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions.
Journal: Frontiers in genetics
Published: September 24, 2021
Last Updated: 09/26/2026