Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

Ítems similars

• Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling
  per: Goffart, Steffi, et al.
  Publicat: (2009)
• Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA
  per: Wanrooij, Sjoerd, et al.
  Publicat: (2004)
• Expression of catalytic mutants of the mtDNA helicase Twinkle and polymerase POLG causes distinct replication stalling phenotypes
  per: Wanrooij, Sjoerd, et al.
  Publicat: (2007)
• Overexpression of TFAM or Twinkle Increases mtDNA Copy Number and Facilitates Cardioprotection Associated with Limited Mitochondrial Oxidative Stress
  per: Ikeda, Masataka, et al.
  Publicat: (2015)
• A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions
  per: Tyynismaa, Henna, et al.
  Publicat: (2009)