Impaired receptor editing and heterozygous RAG2 mutation in a patient with systemic lupus erythematosus and erosive arthritis

Samankaltaisia teoksia

• Adult-onset manifestation of idiopathic T-cell lymphopenia due to a heterozygous RAG1 mutation
  Tekijä: Abraham, Roshini S., et al.
  Julkaistu: (2012)
• Human RAG mutations: biochemistry and clinical implications
  Tekijä: Notarangelo, Luigi D., et al.
  Julkaistu: (2016)
• Recombination activity of human recombination-activating gene 2 (RAG2) mutations and correlation with clinical phenotype
  Tekijä: Tirosh, Irit, et al.
  Julkaistu: (2018)
• RAG1 reversion mosaicism in a patient with Omenn syndrome
  Tekijä: Crestani, Elena, et al.
  Julkaistu: (2014)
• Engagement of SLAMF2/CD48 prolongs the time frame of effective T cell activation by supporting mature dendritic cell survival()
  Tekijä: Kis-Toth, Katalin, et al.
  Julkaistu: (2014)