Publications by authors named "Pengxing Lin"

Article Synopsis
  • - Twin and family studies indicate a significant genetic role in idiopathic generalized epilepsy (IGE), but much about its genetic complexities remains unclear, particularly regarding gene-gene interactions.
  • - The study specifically investigates the CNTN2 gene's interaction with other genetic variants in IGE by analyzing whole-exome sequencing from 114 affected individuals and 296 healthy controls.
  • - Results showed notable gene interaction pairs in the IGE group involving CNTN2, suggesting it may be a candidate pathogenic gene for IGE, thereby highlighting the potential of gene interaction analysis for future research on complex genetic disorders.
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Gene sub-region encoded protein domain is the basic unit for protein structure and function. The DMD gene is the largest coding gene in humans, with its phenotype relevant to idiopathic generalized epilepsy. We hypothesized variants clustered in sub-regions of idiopathic generalized epilepsy genes and investigated the relationship between the DMD gene and idiopathic generalized epilepsy.

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Purpose: Idiopathic generalized epilepsies (IGEs) are a common group of genetic generalized epilepsies with high genetic heterogeneity and complex inheritance. However, the genetic basis is still largely unknown. This study aimed to explore the genetic etiologies in IGEs.

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To evaluate the efficacy and safety of sodium oligomannate in the treatment of Alzheimer's disease. Patients with mild-to-moderate AD were randomly divided into three groups, the scores of ADAS-Cog, ADL, CIBIC-plus, NPI and CSDD were evaluated at the 0th, 12th, 24th, 36th and 48th weeks of medication. Comparing the mean scores of each scale in each cycle of each group.

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Background: Trigeminal neuralgia (TN) is a neuropathic pain that occurs in branches of the trigeminal nerve. MicroRNAs (miRNAs) have been considered key mediators of neuropathic pain. This study was aimed to elucidate the pathophysiological function and mechanisms of miR-223-3p in mouse models of TN.

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