Unequal synthesis and differential degradation of propionyl CoA carboxylase subunits in cells from normal and propionic acidemia patients.

Benzer Materyaller

• An unusual insertion/deletion in the gene encoding the beta-subunit of propionyl-CoA carboxylase is a frequent mutation in Caucasian propionic acidemia.
  Yazar:: Tahara, T, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Coding sequence of the precursor of the beta subunit of rat propionyl-CoA carboxylase.
  Yazar:: Kraus, J P, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• High Incidence of Propionic Acidemia in Greenland Is Due to a Prevalent Mutation, 1540insCCC, in the Gene for the β-Subunit of Propionyl CoA Carboxylase
  Yazar:: Ravn, Kirstine, ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• Import of TAT-Conjugated Propionyl Coenzyme A Carboxylase Using Models of Propionic Acidemia
  Yazar:: Collard, Renata, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)
• Human propionyl-CoA carboxylase beta subunit gene: exon-intron definition and mutation spectrum in Spanish and Latin American propionic acidemia patients.
  Yazar:: Rodríguez-Pombo, P, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)