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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

Related topics

Related topics

1 relation

Broader (1)

Heterotrimeric GTP-Binding Proteins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Seipin deficiency in mice causes loss of dopaminergic neurons via aggregation and phosphorylation of α-synuclein and neuroinflammation
Seipin gene is originally found in type 2 congenital generalized lipodystrophy (CGL2) to involve lipid droplet formation… Expand
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2017
2017
Dental Hygiene and Orthodontics: Effect of Ultrasonic Instrumentation on Bonding Efficacy of Different Lingual Orthodontic Brackets
Dental hygienists are often faced with patients wearing lingual orthodontic therapy, as ultrasonic instrumentation (UI) is… Expand
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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… Expand
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2014
2014
Motor neuropathy-associated mutation impairs Seipin functions in neurotransmission.
Gain-of-toxic-function mutations in Seipin (Asparagine 88 to Serine (N88S) and Serine 90 to Leucine (S90L) mutations, both of… Expand
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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… Expand
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