TUBEROUS SCLEROSIS 2 (disorder)

Known as: TSC2, TUBEROUS SCLEROSIS 2 
Tuberous sclerosis mapped to chromosome 16p13.3 (TSC2 gene).
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
Axon formation is fundamental for brain development and function. TSC1 and TSC2 are two genes, mutations in which cause tuberous… (More)
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Highly Cited
2005
Highly Cited
2005
Tuberous sclerosis (TSC) is a tumor syndrome caused by mutation in TSC1 or TSC2 genes. TSC tumorigenesis is not always… (More)
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Review
2005
Review
2005
The most exciting advances in the tuberous sclerosis complex (TSC) field occurred in 1993 and 1997 with the cloning of the TSC2… (More)
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Highly Cited
2003
Highly Cited
2003
Mutations in the TSC1 or TSC2 genes cause tuberous sclerosis, a benign tumour syndrome in humans. Tsc2 possesses a domain that… (More)
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Highly Cited
2003
Highly Cited
2003
Mutations in either the TSC1 or TSC2 tumor suppressor gene are responsible for Tuberous Sclerosis Complex. The gene products of… (More)
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Highly Cited
2003
Highly Cited
2003
Tuberous sclerosis complex (TSC) is a genetic disease caused by mutation in either TSC1 or TSC2. The TSC1 and TSC2 gene products… (More)
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Highly Cited
2002
Highly Cited
2002
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterized by the formation of hamartomas in a wide range of human… (More)
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Highly Cited
2001
Highly Cited
2001
Tuberous sclerosis (TSC) is a relatively common hamartoma syndrome caused by mutations in either of two genes, TSC1 and TSC2… (More)
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Highly Cited
2000
Highly Cited
2000
Lymphangioleiomyomatosis (LAM) is a progressive and often fatal interstitial lung disease characterized by a diffuse… (More)
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Review
1999
Review
1999
Tuberous sclerosis (TSC [MIM 191090 and MIM 191100]) is an autosomal dominant disorder characterized by hamartomas in many organs… (More)
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