RPTPζ/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1

Ítems similars

• Neurons and Glia Modify Receptor Protein-tyrosine Phosphatase ζ (RPTPζ)/Phosphacan with Cell-specific O-Mannosyl Glycans in the Developing Brain
  per: Dwyer, Chrissa A., et al.
  Publicat: (2015)
• The protein tyrosine phosphatase RPTPζ/phosphacan is critical for perineuronal net structure
  per: Eill, Geoffrey J., et al.
  Publicat: (2020)
• POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease
  per: Diesen, C, et al.
  Publicat: (2004)
• Expression pattern in retinal photoreceptors of POMGnT1, a protein involved in muscle-eye-brain disease
  per: Uribe, Mary Luz, et al.
  Publicat: (2016)
• Biochemical correlation of activity of the α-dystroglycan-modifying glycosyltransferase POMGnT1 with mutations in muscle-eye-brain disease
  per: Voglmeir, Josef, et al.
  Publicat: (2011)