Conservation of the sizes of 53 introns and over 100 intronic sequences for the binding of common transcription factors in the human and mouse genes for type II procollagen (COL2A1).

Benzer Materyaller

• Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouse.
  Yazar:: Vikkula, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.
  Yazar:: Ala-Kokko, L, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Structure of cDNA clones coding for the entire prepro alpha 1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferences.
  Yazar:: Ala-Kokko, L, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)
  Yazar:: Körkkö, J, ve diğerleri
  Baskı/Yayın Bilgisi: (1993)
• Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia.
  Yazar:: Vandenberg, P, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)