Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17

Lignende værker

• Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome
  af: Gistelinck, Charlotte, et al.
  Udgivet: (2016)
• Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen
  af: Schwarze, Ulrike, et al.
  Udgivet: (2013)
• Lysylhydroxylation and non-reducible crosslinking of human supraspinatus tendon collagen: changes with age and in chronic rotator cuff tendinitis
  af: Bank, R., et al.
  Udgivet: (1999)
• Missense Mutations That Cause Bruck Syndrome Affect Enzymatic Activity, Folding, and Oligomerization of Lysyl Hydroxylase 2
  af: Hyry, Marjo, et al.
  Udgivet: (2009)
• Pyridinium crosslinks as markers of bone resorption in patients with breast cancer.
  af: Paterson, C. R., et al.
  Udgivet: (1991)