Heparan sulfate antagonism alters bone morphogenetic protein signaling and receptor dynamics, suggesting a mechanism in hereditary multiple exostoses

Eitemau Tebyg

• The pathogenic roles of heparan sulfate deficiency in Hereditary Multiple Exostoses
  gan: Pacifici, Maurizio
  Cyhoeddwyd: (2017)
• Perichondrium phenotype and border function are regulated by Ext1 and heparan sulfate in developing long bones: A mechanism likely deranged in Hereditary Multiple Exostoses
  gan: Huegel, Julianne, et al.
  Cyhoeddwyd: (2013)
• Heparan Sulfate in Skeletal Development, Growth, and Pathology: The Case of Hereditary Multiple Exostoses
  gan: Huegel, Julianne, et al.
  Cyhoeddwyd: (2013)
• Domains with highest heparan sulfate–binding affinity reside at opposite ends in BMP2/4 versus BMP5/6/7: Implications for function
  gan: Billings, Paul C., et al.
  Cyhoeddwyd: (2018)
• Identification and characterization of a novel heparan sulfate-binding domain in Activin A longest variants and implications for function
  gan: Yang, Evan, et al.
  Cyhoeddwyd: (2019)