TUBEROUS SCLEROSIS 1 (disorder)

Known as: TSC1, Tuberous Sclerosis 1 
Tuberous sclerosis mapped to chromosome 9q34 (TSC1 gene).
National Institutes of Health

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Highly Cited
2011
Highly Cited
2011
PURPOSE Renal angiomyolipomas are a frequent manifestation of tuberous sclerosis and sporadic lymphangioleiomyomatosis (LAM… (More)
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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
2008
Highly Cited
2008
Tuberous sclerosis (TSC) is a hamartoma syndrome attributable to mutations in either TSC1 or TSC2 in which brain involvement… (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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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
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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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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Highly Cited
1996
Highly Cited
1996
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterized by seizures, mental retardation, and hamartomatous… (More)
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