Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Bscl2 protein, mouse

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Seipin gene is originally found in type 2 congenital generalized lipodystrophy (CGL2) to involve lipid droplet formation… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2017
2017
Dental hygienists are often faced with patients wearing lingual orthodontic therapy, as ultrasonic instrumentation (UI) is… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
Is this relevant?
2016
2016
UNLABELLED A characteristic phenotype of congenital generalized lipodystrophy 2 (CGL2) that is caused by loss-of-function of… Expand
Is this relevant?
2014
2014
Gain-of-toxic-function mutations in Seipin (Asparagine 88 to Serine (N88S) and Serine 90 to Leucine (S90L) mutations, both of… Expand
Is this relevant?
2013
2013
Mutations affecting the N-glycosylation site in Berardinelli-Seip lipodystrophy (BSCL)-associated gene BSCL2/seipin lead to a… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?