Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes

Samankaltaisia teoksia

• Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients’ skin fibroblasts
  Tekijä: Chiarelli, Nicola, et al.
  Julkaistu: (2019)
• Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome.
  Tekijä: Nicola Chiarelli, et al.
  Julkaistu: (2018-01-01)
• Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome
  Tekijä: Chiarelli, Nicola, et al.
  Julkaistu: (2018)
• Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts
  Tekijä: Zoppi, Nicoletta, et al.
  Julkaistu: (2018)
• Molecular Genetics and Pathogenesis of Ehlers–Danlos Syndrome and Related Connective Tissue Disorders
  Tekijä: Ritelli, Marco, et al.
  Julkaistu: (2020)