All Stories

  1. Analysis of Potential Genes and Pathways Involved in the Pathogenesis of Acne by Bioinformatics
  2. Down-regulated SHARPIN may accelerate the development of atopic dermatitis through activating interleukin-33/ST2 signalling
  3. Novel D323G mutation ofDSG4gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
  4. A recurrent R936X mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma
  5. Two novel missense mutations ofATP2A2in two Chinese patients with sporadic Darier Disease
  6. Novel Ala94Thr mutation of keratin 14 in epidermolysis bullosa simplex
  7. A recurrent p.M157R mutation of keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma and literature review
  8. Newly identified phenotypes in aFIP1L1/PDGFRA-associated paediatric HES patient: thrombocytosis, mHPA, young stroke and blindness
  9. Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in theU2HRgene and literature review
  10. Multiple familial trichoepithelioma: report of a Chinese family not associated with a mutation in theCYLDgene and CYLD protein expression in the trichoepithelioma tumor tissue