TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
CTD_human |
|
|
|
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
BEFREE |
This could indicate that TSC2 tumors are more likely than TSC1 tumors to require surgical resection or that TSC2 is more common than TSC1 in our patient population.
|
8755927 |
1996 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosis.
|
9328481 |
1997 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
CLINGEN |
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
|
9242607 |
1997 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
|
9242607 |
1997 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
BEFREE |
The observations indicate that TSC1 mutations are all inactivating, suggest that TSC1 disease occurs in only 15-20% of the sporadic TSC population, and demonstrate that presymptomatic TSC does occur.
|
9924605 |
1998 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
CLINGEN |
Mutations in the TSC1 gene account for a minority of patients with tuberous sclerosis.
|
9863590 |
1998 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.
|
10227394 |
1999 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex.
|
10570911 |
1999 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cyst.
|
10069705 |
1999 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
CLINGEN |
The expression of hamartin, the product of the TSC1 gene, in normal human tissues and in TSC1- and TSC2-linked angiomyolipomas.
|
10349994 |
1999 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
Protein truncation test for screening hamartin gene mutations and report of new disease-causing mutations.
|
10533069 |
1999 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.
|
10227394 |
1999 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
Tuberous sclerosis type 1: three novel mutations detected in exon 15 by a combination of HDA and TGGE.
|
10874311 |
2000 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
BEFREE |
A combination of linkage analysis and direct sequencing eliminate several likely candidate genes, including tuberous sclerosis 1 and 2 genes (TSC1 and TSC2) and the tumor suppressor gene TP53.
|
10759551 |
2000 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
CLINGEN |
Hamartin expression and interaction with tuberin in tumor cell lines and primary cultures.
|
11170177 |
2001 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
BEFREE |
We have isolated a mutation in the Drosophila homolog of TSC1 (Tsc1).
|
11348592 |
2001 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
However, our study indicates that a fraction of sporadic LAM can be a TSC1 disease; therefore, both TSC genes should be examined, even for patients with sporadic LAM.
|
11829138 |
2002 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Focal cortical dysplasia of Taylor's balloon cell type: mutational analysis of the TSC1 gene indicates a pathogenic relationship to tuberous sclerosis.
|
12112044 |
2002 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
AlteredExpression
|
disease |
BEFREE |
In an effort to provide support for this hypothesis and to identify specific markers of aberrant neuroglial cell differentiation in TSC, we employed gene expression profiling on Tsc1 conditional knockout (Tsc1(GFAP)CKO) mouse astrocytes.
|
14999811 |
2004 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Inherited interstitial lung disease.
|
15331184 |
2004 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
CLINGEN |
A mouse model of tuberous sclerosis 1 showing background specific early post-natal mortality and metastatic renal cell carcinoma.
|
15888477 |
2005 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States.
|
17304050 |
2007 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
GeneticVariation
|
disease |
UNIPROT |
Missense mutations to the TSC1 gene cause tuberous sclerosis complex.
|
18830229 |
2009 |
TUBEROUS SCLEROSIS 1 (disorder)
|
0.690 |
AlteredExpression
|
disease |
BEFREE |
We show by cDNA array and immunohistochemical analysis that EGF, EGFR, HGF, c-Met, and VEGF, but not Flt-1, mRNA, and protein expression was up-regulated in Tsc1 conditional knockout (Tsc1(GFAP)CKO) mouse cortex.
|
21224066 |
2011 |