LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts and adipose stem cells

Lignende værker

• Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)
  af: Magracheva, Eugenia, et al.
  Udgivet: (2009)
• Mutations in LMNA Modulate the Lamin A - Nesprin-2 Interaction and Cause LINC Complex Alterations
  af: Yang, Liu, et al.
  Udgivet: (2013)
• Atypical Progeroid Syndrome and Partial Lipodystrophy Due to LMNA Gene p.R349W Mutation
  af: Magno, Silvia, et al.
  Udgivet: (2020)
• Monoclonal Antibodies Specific for Disease-Associated Point-Mutants: Lamin A/C R453W and R482W
  af: Roblek, Marko, et al.
  Udgivet: (2010)
• Genotype-phenotype analysis of LMNA-related diseases predicts phenotype-selective alterations in lamin phosphorylation
  af: Lin, Eric W, et al.
  Udgivet: (2020)