Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia.

Παρόμοια τεκμήρια

• An inbred line of transgenic mice expressing an internally deleted gene for type II procollagen (COL2A1). Young mice have a variable phenotype of a chondrodysplasia and older mice have osteoarthritic changes in joints.
  ανά: Helminen, H J, κ.ά.
  Έκδοση: (1993)
• Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral.
  ανά: Pereira, R, κ.ά.
  Έκδοση: (1993)
• Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.
  ανά: Ala-Kokko, L, κ.ά.
  Έκδοση: (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.
  ανά: Ala-Kokko, L, κ.ά.
  Έκδοση: (1989)
• Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy).
  ανά: Ahmad, N N, κ.ά.
  Έκδοση: (1991)