Differential Phenotypes of Active Site and Human Autosomal Dominant Progressive External Ophthalmoplegia Mutations in Drosophila Mitochondrial DNA Helicase Expressed in Schneider Cells()

Παρόμοια τεκμήρια

• Two families with autosomal dominant progressive external ophthalmoplegia
  ανά: Kiechl, S, κ.ά.
  Έκδοση: (2004)
• Functional importance of the conserved N-terminal domain of the mitochondrial replicative DNA helicase
  ανά: Matsushima, Yuichi, κ.ά.
  Έκδοση: (2008)
• Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM).
  ανά: Black, G C, κ.ά.
  Έκδοση: (1998)
• Physiological and Biochemical Defects in Carboxyl-terminal Mutants of Mitochondrial DNA Helicase
  ανά: Matsushima, Yuichi, κ.ά.
  Έκδοση: (2008)
• Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling
  ανά: Goffart, Steffi, κ.ά.
  Έκδοση: (2009)