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

Ítems similars

• Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)
  per: Magracheva, Eugenia, et al.
  Publicat: (2009)
• Mutations in LMNA Modulate the Lamin A - Nesprin-2 Interaction and Cause LINC Complex Alterations
  per: Yang, Liu, et al.
  Publicat: (2013)
• Atypical Progeroid Syndrome and Partial Lipodystrophy Due to LMNA Gene p.R349W Mutation
  per: Magno, Silvia, et al.
  Publicat: (2020)
• Irisin levels in LMNA-mutated lipodystrophic syndromes
  per: Bensmaine, Faiza, et al.
  Publicat: (2015)
• Monoclonal Antibodies Specific for Disease-Associated Point-Mutants: Lamin A/C R453W and R482W
  per: Roblek, Marko, et al.
  Publicat: (2010)