Bscl2 protein, mouse

Known as: Bernardinelli-Seip congenital lipodystrophy 2 homolog (human), mouse, Gng3lg protein, mouse, seipin protein, mouse 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2013-2015
0120132015

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
UNLABELLED A characteristic phenotype of congenital generalized lipodystrophy 2 (CGL2) that is caused by loss-of-function of… (More)
Is this relevant?
2015
2015
The seipin gene (BSCL2) was originally identified in humans as a loss-of-function gene associated with congenital generalized… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2014
2014
The Seipin gene was originally found to be responsible for type 2 congenital lipodystrophy and involved in lipid droplet… (More)
  • figure 2
  • figure 1
  • figure 3
  • figure 4
Is this relevant?
2013
2013
Mutations affecting the N-glycosylation site in Berardinelli-Seip lipodystrophy (BSCL)-associated gene BSCL2/seipin lead to a… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?