|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex.
|
15595939 |
2005 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
Conversely, in patients with known TSC, enlarged and polycystic kidneys should signal the possibility of the TSC2/ADPKD1 contiguous gene syndrome and not simply TSC.
|
25355409 |
2015 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Tuberous sclerosis complex (TSC) is a tumor suppressor gene disorder characterized by mutations in the TSC1 or TSC2 genes.
|
16192644 |
2005 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Intellectual ability in tuberous sclerosis complex correlates with predicted effects of mutations on TSC1 and TSC2 proteins.
|
26408672 |
2015 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
In this study, we analyzed TSC1 and TSC2 in 57 Japanese patients with TSC (8 familial and 49 sporadic; 46 definite and 11 suspect TSC) and identified 31 mutations including 11 TSC1 mutations (two familial and nine sporadic; all definite TSC) and 20 TSC2 mutations (2 familial and 18 sporadic; 19 definite and 1 suspect TSC).
|
23389244 |
2013 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Our findings confirm and supplement existing literature that TSC2 mutation is likely to be associated with a more severe, earlier presenting TSC phenotype, including infantile spasms.
|
24917535 |
2014 |
|
Tuberous Sclerosis
|
1.000 |
AlteredExpression
|
disease |
BEFREE |
Collectively, these data reveal a novel function of TSC2 and Rheb in the regulation of EP3 expression and cell viability.<b>Implications:</b> Therapeutic targeting of an aberrant PGE2-EP3 signaling axis may have therapeutic benefit for TSC patients and for other mTOR-hyperactive neoplasms.<i></i>.
|
28710231 |
2017 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Here we report a new approach for detecting mutations in TSC: a denaturing gradient gel electrophoresis (DGGE) analysis for small TSC2 mutations, a multiplex ligation-dependent probe amplification (MLPA) analysis for large deletions and duplications in TSC1 or TSC2, and a long-range PCR/sequencing-based analysis for small TSC1 mutations.
|
16114042 |
2005 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Blood DNA samples from 61 patients with definite (n = 53) or probable (n = 8) clinical diagnosis of TS were tested for mutations in TSC1 and TSC2 genes using Sanger sequencing and MLPA analysis.
|
29476190 |
2018 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in the TSC1 or TSC2 genes.
|
22161988 |
2012 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
The dependence of Tsc2-deficient cells on exogenous nutrients may provide novel approaches for the treatment of TSC.
|
30242175 |
2018 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
These phenotypes only become apparent when differentiating TSC2+/+ and TSC2-/- cultures in more physiologically relevant conditions of 5 mM glucose suggesting that the careful consideration of culture conditions is vital to ensuring biological relevance and translatability of stem cell models for neurological disorders such as TSC.
|
31761686 |
2019 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Tuberous sclerosis (TSC) is a tumor syndrome caused by TSC1 or TSC2 mutations that lead to aberrant activation of mTOR and tumor formation in multiple organs.
|
28844017 |
2017 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
To investigate whether these lipids are generated in a TSC2-dependent manner, we profiled in vitro preclinical models of TSC/LAM and found significant LPC accumulation in TSC2-deficient cells relative to TSC2-expressing control cells.
|
25780943 |
2015 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
Recent work has indicated that the TSC1-TSC2 complex plays a role in the pathobiology of a number of tumor predisposition syndromes, including tuberous sclerosis (TSC1/2), Peutz-Jeghers syndrome (LKB1), and Cowden's syndrome (PTEN), in which the TSC/Rheb/mTOR axis is inappropriately active secondary to loss of tumor suppressor function.
|
15611656 |
2005 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
We have sequenced 1949 kb from the terminal Giemsa light band of human chromosome 16p, enabling us to fully annotate the region extending from the telomeric repeats to the previously published tuberous sclerosis disease 2 (TSC2) and polycystic kidney disease 1 (PKD1) genes.
|
11157797 |
2001 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Tuberous sclerosis complex (TSC) is an autosomal-dominant or sporadic multisystem disorder that results from mutations in either TSC1 or TSC2.
|
29478616 |
2018 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder that results from mutations in the TSC1 or TSC2 genes and is associated with hamartoma formation in multiple organ systems.
|
20146692 |
2010 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
TSC1/TSC2 variants were found in 60% patients with tuberous sclerosis complex patients.
|
30185235 |
2018 |
|
Tuberous Sclerosis
|
1.000 |
Biomarker
|
disease |
BEFREE |
Analysis of second, somatic events in tumors for which the status of both TSC1 and TSC2 is known is essential for exploration of the pathogenesis of TSC-lesion development.
|
11468687 |
2001 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Tuberous sclerosis complex (TSC) is an inherited disorder resulting from mutations in one of two genes, TSC1 (Hamartin) and TSC2 (Tuberin).
|
18345974 |
2008 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Testing for tuberous sclerosis was negative for deletion or duplications of genes TSC1 and TSC2.
|
29336632 |
2018 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Here, we report a pathogenic TSC2 variant, c.1864C>T, p.(Arg622Trp), associated with a mild phenotype, with most carriers meeting fewer than two major clinical diagnostic criteria for TSC.
|
28211972 |
2017 |
|
Tuberous Sclerosis
|
1.000 |
AlteredExpression
|
disease |
BEFREE |
Kidney angiomyolipoma tissue from TSC patients expresses significant levels of phopho-tuberin and low levels of tuberin compared to control kidney tissue.
|
19265534 |
2009 |
|
Tuberous Sclerosis
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype--phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex.
|
15798777 |
2005 |