Mutations in HspB1 and hereditary neuropathies

Eitemau Tebyg

• Characterization of Mutants of Human Small Heat Shock Protein HspB1 Carrying Replacements in the N-Terminal Domain and Associated with Hereditary Motor Neuron Diseases
  gan: Muranova, Lydia K., et al.
  Cyhoeddwyd: (2015)
• The Role of the Arginine in the Conserved N-Terminal Domain RLFDQxFG Motif of Human Small Heat Shock Proteins HspB1, HspB4, HspB5, HspB6, and HspB8
  gan: Vladislav M. Shatov, et al.
  Cyhoeddwyd: (2018-07-01)
• The Role of the Arginine in the Conserved N-Terminal Domain RLFDQxFG Motif of Human Small Heat Shock Proteins HspB1, HspB4, HspB5, HspB6, and HspB8
  gan: Shatov, Vladislav M., et al.
  Cyhoeddwyd: (2018)
• Is the small heat shock protein HspB1 (Hsp27) a real and predominant target of methylglyoxal modification?
  gan: Sudnitsyna, Maria V., et al.
  Cyhoeddwyd: (2019)
• Effect of methylglyoxal modification on the structure and properties of human small heat shock protein HspB6 (Hsp20)
  gan: Muranova, Lydia K., et al.
  Cyhoeddwyd: (2016)