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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

Related topics

Related topics

1 relation

Broader (1)

Heterotrimeric GTP-Binding Proteins

Related mentions per year

Related mentions per year

1987-2017
19801990200020102020
Bscl2 protein, mouse
Heterotrimeric GTP-Binding Proteins

Papers overview

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2016
2016
Activation of PPARγ Ameliorates Spatial Cognitive Deficits through Restoring Expression of AMPA Receptors in Seipin Knock-Out Mice.
UNLABELLED A characteristic phenotype of congenital generalized lipodystrophy 2 (CGL2) that is caused by loss-of-function of… (More)
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2015
2015
Dmm021550 1615..1624
The seipin gene (BSCL2) was originally identified in humans as a loss-of-function gene associated with congenital generalized… (More)
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2014
2014
Lack of seipin in neurons results in anxiety- and depression-like behaviors via down regulation of PPARγ.
The Seipin gene was originally found to be responsible for type 2 congenital lipodystrophy and involved in lipid droplet… (More)
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2013
2013
Alleviation of seipinopathy-related ER stress by triglyceride storage.
Mutations affecting the N-glycosylation site in Berardinelli-Seip lipodystrophy (BSCL)-associated gene BSCL2/seipin lead to a… (More)
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