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TSC1-TSC2 complex location

Known as: Tuberous sclerosis complex, tuberous sclerosis complex location, tuberin-hamartin complex 
A protein complex consisting of at least tumerin and hamartin; its formation may regulate hamartin homomultimer formation. The complex acts as a… 
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Tuberous sclerosis complex is an autosomal dominant inherited disorder characterized by generalized involvement and variable… 
Review
2009
Review
2009
Among other signals, cell growth is particularly controlled by the target of rapamycin (TOR) pathway that includes the tuberous… 
Review
2004
Review
2004
Tuberous sclerosis complex is an autosomal dominant disease of benign tumors occurring in multiple organ systems of the body… 
2004
2004
Tuberous sclerosis (TSC) is an autosomal dominant disorder caused by mutations in either the TSC1 or TSC2 gene. Both genes are… 
Highly Cited
2003
Highly Cited
2003
The tuberous sclerosis complex (TSC) is a genetic disorder that is caused through mutations in either one of the two tumor… 
Review
2003
Review
2003
The molecular interplay between the phosphoinositide 3-kinase (PI3K) pathway and mammalian target of rapamycin (mTOR) signalling… 
Highly Cited
2002
Highly Cited
2002
Tuberous sclerosis is caused by mutations to either the TSC1 or TSC2 tumor suppressor gene. The disease is characterized by a… 
1996
1996
The Apteronotidae, a family of weakly electric fish from South America (Gymnotiformes), possess a structure called the dorsal…