Showing 1 - 19 results of 19 for search 'Wei-Jia Kong', query time: 0.16s Refine Results
  1. 1
    The Compound of Mangiferin-Berberine Salt Has Potent Activities in Modulating Lipid and Glucose Metabolisms in HepG2 Cells
    by Can Wang, Jian-Dong Jiang, Wei Wu, Wei-Jia Kong
    Published 2016-01-01
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    Article
  2. 2
    Antioxidant and Anti-Inflammatory Activities of Berberine in the Treatment of Diabetes Mellitus
    by Zheng Li, Ya-Na Geng, Jian-Dong Jiang, Wei-Jia Kong
    Published 2014-01-01
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    Article
  3. 3
    The risk of cognitive impairment associated with hearing function in older adults: a pooled analysis of data from eleven studies
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    Article
  4. 4
    Gentamicin Blocks the ACh-Induced BK Current in Guinea Pig Type II Vestibular Hair Cells by Competing with Ca2+ at the l-Type Calcium Channel
    by Hong Yu, Chang-Kai Guo, Yi Wang, Tao Zhou, Wei-Jia Kong
    Published 2014-04-01
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    Article
  5. 5
    Local Macrophage-Related Immune Response Is Involved in Cochlear Epithelial Damage in Distinct Gjb2-Related Hereditary Deafness Models
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  6. 6
    Two Distinct Channels Mediated by m2mAChR and α9nAChR Co-Exist in Type II Vestibular Hair Cells of Guinea Pig
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    Article
  7. 7
    The dual role of poly(ADP-ribose) polymerase-1 in modulating parthanatos and autophagy under oxidative stress in rat cochlear marginal cells of the stria vascularis
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  8. 8
    Developmental abnormalities in supporting cell phalangeal processes and cytoskeleton in the Gjb2 knockdown mouse model
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  9. 9
    The Changes in mGluR2 and mGluR7 Expression in Rat Medial Vestibular Nucleus and Flocculus Following Unilateral Labyrinthectomy
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  10. 10
    NLRP3 Inflammasome Sequential Changes in Staphylococcus aureus-Induced Mouse Model of Acute Rhinosinusitis
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    Article
  11. 11
    Berberine Improves Glucose and Lipid Metabolism in HepG2 Cells Through AMPKα1 Activation
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    Article
  12. 12
    Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
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  13. 13
    Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family
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  14. 14
    Increased p66Shc in the inner ear of D-galactose-induced aging mice with accumulation of mitochondrial DNA 3873-bp deletion: p66Shc and mtDNA damage in the inner ear during aging.
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  15. 15
    Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous OTOF Mutations in Two Chinese Families
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  16. 16
    Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Loss in Mice
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  17. 17
    A Novel Spontaneous Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type II
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  18. 18
    Jervell and Lange-Nielsen Syndrome due to a Novel Compound Heterozygous KCNQ1 Mutation in a Chinese Family
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    Article
  19. 19
    The nuclear transcription factor FoxG1 affects the sensitivity of mimetic aging hair cells to inflammation by regulating autophagy pathways
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    Article
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