Skip to search formSkip to main contentSkip to account menu

TUBEROUS SCLEROSIS 1 (disorder)

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Thymic‐derived CD4+CD25+Foxp3+ natural regulatory T (nTreg) cells are essential for the maintenance of peripheral immune… 
2005
2005
Epilepsy-associated malformations of cortical development (MCDs) comprise a variety of dysplastic and neoplastic lesions of yet… 
2005
2005
Tuberous sclerosis complex is a tumor suppressor syndrome caused by mutations in either the TSC1 or the TSC2 gene. Previous… 
2002
2002
Underrepresentation of chromosome 9 is a common finding in bladder cancer. Frequent loss of the whole chromosome suggests the… 
2001
2001
Abstract Tuberous sclerosis complex (TSC) is a multisystemic disorder characterized by systemic hamartomas. Although the disease… 
1998
1998
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterised by tumour-like malformations (hamartomas) of the brain… 
1998
1998
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterised by the development of benign tumors in multiple… 
1997
1997
The disease gene TSC1 has been genetically mapped to human chromosome region 9q34, in a 4-cM interval between the markers D9S149… 
1993
1993
Pulsed-field gel electrophoresis and flow dot-blot analysis have been used to construct a physical map of the q32-q34 region of…