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Xuemin Wang

Biographic Data

ID7295113
NAMEXuemin Wang
GIVEN NAMESXuemin
FAMILY NAMEWang
SIGNATUREWANG X
AFFILIATIONSTongji University
ORCID0000-0003-2652-6206
VERIFIEDYes
TOTAL WORKS4
TOTAL CITATIONS0
AUTHOR COUNT4
EDITOR COUNT0
FIRST PUBLICATION YEAR2018
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Bazi Bushen improves cognitive dysfunction in 5×FAD mice by targeting amyloid pathology, neuroinflammation and cellular senescence

    Open Access•Huixian Huang, Wensi Lu et al.•ARTICLE•Journal of Ethnopharmacology•2026

  • Sheng-ji Hua-yu Formula promotes diabetic ulcer healing via regulating the cAMP/PKA/CREB signaling pathway

    Open Access•Guomi Wang, Sheng Hu et al.•ARTICLE•Journal of Ethnopharmacology•2025

  • Qinzhuliangxue mixture ameliorates psoriasis by restraining apoptosis in psoriasis via downregulating the MDA-5 pathway

    Open Access•Guomi Wang, Tingting Xue et al.•ARTICLE•Journal of Ethnopharmacology•2024

  • Role of Eukaryotic Initiation Factor eIF2B in Vanishing White Matter Disease

    Truus E M Abbink, Lisanne E Wisse et al.•CHAPTER•Oxford Handbook of Neuronal…•2018

    Vanishing white matter (VWM) disease is a recessive disorder characterized by gradual loss of white matter and of myelin. Its clinical severity is high variable. VWM is caused by mutations in any one of the five genes encoding subunits of eukaryotic initiation factor 2B (eIF2B), a ubiquitous, multimeric protein that plays crucial roles in protein synthesis and its control. There are now known to be at least 160 mutations in eIF2B genes that lead …

No prominent works on this page.

  • Role of Eukaryotic Initiation Factor eIF2B in Vanishing White Matter Disease

    Truus E M Abbink, Lisanne E Wisse et al.•CHAPTER•Oxford Handbook of Neuronal…•2018

    Vanishing white matter (VWM) disease is a recessive disorder characterized by gradual loss of white matter and of myelin. Its clinical severity is high variable. VWM is caused by mutations in any one of the five genes encoding subunits of eukaryotic initiation factor 2B (eIF2B), a ubiquitous, multimeric protein that plays crucial roles in protein synthesis and its control. There are now known to be at least 160 mutations in eIF2B genes that lead …

  • Qinzhuliangxue mixture ameliorates psoriasis by restraining apoptosis in psoriasis via downregulating the MDA-5 pathway

    Open Access•Guomi Wang, Tingting Xue et al.•ARTICLE•Journal of Ethnopharmacology•2024

  • Sheng-ji Hua-yu Formula promotes diabetic ulcer healing via regulating the cAMP/PKA/CREB signaling pathway

    Open Access•Guomi Wang, Sheng Hu et al.•ARTICLE•Journal of Ethnopharmacology•2025

  • Bazi Bushen improves cognitive dysfunction in 5×FAD mice by targeting amyloid pathology, neuroinflammation and cellular senescence

    Open Access•Huixian Huang, Wensi Lu et al.•ARTICLE•Journal of Ethnopharmacology•2026

Medicine (3 works) · Biochemistry (2 works) · Biology (2 works) · Gene (2 works) · Pharmacology (2 works) · Alzheimer's disease research and treatments (1 works) · Amyloid (mycology (1 works) · Amyloidosis (1 works) · Apoptosis (1 works) · Cancer Research (1 works)

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