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TSC1-TSC2 complex location
Known as:
Tuberous sclerosis complex
, tuberous sclerosis complex location
, tuberin-hamartin complex
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A protein complex consisting of at least tumerin and hamartin; its formation may regulate hamartin homomultimer formation. The complex acts as a…
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National Institutes of Health
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Related topics
Related topics
2 relations
TUBEROUS SCLEROSIS 1 (disorder)
Tuberous Sclerosis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Tuberous sclerosis complex: Recent advances in manifestations and therapy
M. Wataya-Kaneda
,
M. Uemura
,
+4 authors
N. Nonomura
International journal of urology
2017
Corpus ID: 21027125
Tuberous sclerosis complex is an autosomal dominant inherited disorder characterized by generalized involvement and variable…
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Review
2013
Review
2013
Tuberous sclerosis.
Paolo Curatolo
,
B. Maria
Handbook of Clinical Neurology
2013
Corpus ID: 41506582
Review
2009
Review
2009
Growth controls connect: Interactions between c-myc and the tuberous sclerosis complex-mTOR pathway
E. Schmidt
,
M. J. Ravitz
,
Li Chen
,
M. Lynch
Cell Cycle
2009
Corpus ID: 27794440
Among other signals, cell growth is particularly controlled by the target of rapamycin (TOR) pathway that includes the tuberous…
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Review
2007
Review
2007
The tuberous sclerosis complex proteins--a GRIPP on cognition and neurodevelopment.
P. D. de Vries
,
C. Howe
Trends in Molecular Medicine
2007
Corpus ID: 30295522
Review
2004
Review
2004
Molecular Genetic Basis of Tuberous Sclerosis Complex: From Bench to Bedside
K. Au
,
Aimee T. Williams
,
M. Gambello
,
H. Northrup
Journal of Child Neurology
2004
Corpus ID: 34819133
Tuberous sclerosis complex is an autosomal dominant disease of benign tumors occurring in multiple organ systems of the body…
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2004
2004
Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosis
K. Mayer
,
M. Goedbloed
,
K. van Zijl
,
M. Nellist
,
H. Rott
Journal of Medical Genetics
2004
Corpus ID: 16006650
Tuberous sclerosis (TSC) is an autosomal dominant disorder caused by mutations in either the TSC1 or TSC2 gene. Both genes are…
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Highly Cited
2003
Highly Cited
2003
Inactivation of the Tuberous Sclerosis Complex-1 and -2 Gene Products Occurs by Phosphoinositide 3-Kinase/Akt-dependent and -independent Phosphorylation of Tuberin*
Andrew R. Tee
,
R. Anjum
,
J. Blenis
Journal of Biological Chemistry
2003
Corpus ID: 46475441
The tuberous sclerosis complex (TSC) is a genetic disorder that is caused through mutations in either one of the two tumor…
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Review
2003
Review
2003
United at last: the tuberous sclerosis complex gene products connect the phosphoinositide 3-kinase/Akt pathway to mammalian target of rapamycin (mTOR) signalling.
B. Manning
,
L. Cantley
Biochemical Society Transactions
2003
Corpus ID: 10655005
The molecular interplay between the phosphoinositide 3-kinase (PI3K) pathway and mammalian target of rapamycin (mTOR) signalling…
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Highly Cited
2002
Highly Cited
2002
Identification and Characterization of the Interaction between Tuberin and 14-3-3ζ*
M. Nellist
,
M. Goedbloed
,
+6 authors
D. Halley
Journal of Biological Chemistry
2002
Corpus ID: 34011941
Tuberous sclerosis is caused by mutations to either the TSC1 or TSC2 tumor suppressor gene. The disease is characterized by a…
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1996
1996
The dorsal filament of the weakly electric Apteronotidae (Gymnotiformes; Teleostei) is specialized for electroreception.
C. R. Franchina
,
C. Hopkins
Brain, Behavior and Evolution
1996
Corpus ID: 3320113
The Apteronotidae, a family of weakly electric fish from South America (Gymnotiformes), possess a structure called the dorsal…
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