Nephronophthisis
|
0.200 |
Biomarker
|
disease |
MGD |
|
|
|
Mammary Neoplasms
|
0.020 |
Biomarker
|
group |
LHGDN |
A role for TAZ in migration, invasion, and tumorigenesis of breast cancer cells.
|
18413727 |
2008 |
Polycystic Kidney Diseases
|
0.010 |
Biomarker
|
group |
BEFREE |
Glis3 is associated with primary cilia and Wwtr1/TAZ and implicated in polycystic kidney disease.
|
19273592 |
2009 |
Thyroid Dysgenesis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis.
|
19542741 |
2009 |
Polycystic Kidney, Autosomal Dominant
|
0.010 |
Biomarker
|
disease |
BEFREE |
These results implicate TAZ and PATJ as novel regulatory elements of the PC2 channel and might thus be involved in ADPKD pathology.
|
20833712 |
2010 |
Multiple Chronic Conditions
|
0.010 |
Biomarker
|
disease |
BEFREE |
Here we describe a novel interaction of TAZ with the multi-PDZ-containing PALS1-associated tight junction protein (PATJ).
|
20833712 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In addition, short-hairpin RNA (shRNA)-mediated knockdown of TAZ expression in NSCLC cells suppresses their proliferation and anchorage-independent growth in vitro, and tumor growth in mice in vivo, which can be reversed by re-introduction of shRNA-resistant TAZ into TAZ-knockdown NSCLC cells.
|
21258416 |
2011 |
Malignant neoplasm of breast
|
0.090 |
Biomarker
|
disease |
BEFREE |
Recently, TAZ has also been identified as a major component of the novel Hippo-LATS tumor suppressor pathway and to function as an oncogene in breast cancer.
|
21258416 |
2011 |
Breast Carcinoma
|
0.090 |
Biomarker
|
disease |
BEFREE |
Recently, TAZ has also been identified as a major component of the novel Hippo-LATS tumor suppressor pathway and to function as an oncogene in breast cancer.
|
21258416 |
2011 |
Malignant neoplasm of lung
|
0.060 |
Biomarker
|
disease |
BEFREE |
Therefore, TAZ may present a novel target for the future diagnosis, prognosis and therapy of lung cancer.
|
21258416 |
2011 |
Carcinoma of lung
|
0.060 |
Biomarker
|
disease |
BEFREE |
Therefore, TAZ may present a novel target for the future diagnosis, prognosis and therapy of lung cancer.
|
21258416 |
2011 |
Primary malignant neoplasm of lung
|
0.060 |
Biomarker
|
disease |
BEFREE |
Therefore, TAZ may present a novel target for the future diagnosis, prognosis and therapy of lung cancer.
|
21258416 |
2011 |
Non-Small Cell Lung Carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
In addition, short-hairpin RNA (shRNA)-mediated knockdown of TAZ expression in NSCLC cells suppresses their proliferation and anchorage-independent growth in vitro, and tumor growth in mice in vivo, which can be reversed by re-introduction of shRNA-resistant TAZ into TAZ-knockdown NSCLC cells.
|
21258416 |
2011 |
Epithelioid hemangioendothelioma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Subsequent reverse transcription-polymerase chain reaction (RT-PCR) confirmed in three EHE the WWTR1-CAMTA1 fusion product.
|
21584898 |
2011 |
Epithelioid hemangioendothelioma, malignant
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Subsequent reverse transcription-polymerase chain reaction (RT-PCR) confirmed in three EHE the WWTR1-CAMTA1 fusion product.
|
21584898 |
2011 |
Carcinogenesis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
CAMTA1 and WWTR1 have been previously shown to play important roles in oncogenesis.
|
21584898 |
2011 |
Childhood Epithelioid Hemangioendothelioma
|
0.090 |
AlteredExpression
|
disease |
BEFREE |
Subsequent reverse transcription-polymerase chain reaction (RT-PCR) confirmed in three EHE the WWTR1-CAMTA1 fusion product.
|
21584898 |
2011 |
Adult Epithelioid Hemangioendothelioma
|
0.090 |
AlteredExpression
|
disease |
BEFREE |
Subsequent reverse transcription-polymerase chain reaction (RT-PCR) confirmed in three EHE the WWTR1-CAMTA1 fusion product.
|
21584898 |
2011 |
Epithelioid hemangioendothelioma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
The chimeric WWTR1/CAMTA1 transcription factor may represent a therapeutic target for EHE and offers the opportunity to shed light on the functions of two poorly characterized proteins.
|
21885404 |
2011 |
Epithelioid hemangioendothelioma, malignant
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
The chimeric WWTR1/CAMTA1 transcription factor may represent a therapeutic target for EHE and offers the opportunity to shed light on the functions of two poorly characterized proteins.
|
21885404 |
2011 |
Childhood Epithelioid Hemangioendothelioma
|
0.090 |
AlteredExpression
|
disease |
BEFREE |
The chimeric WWTR1/CAMTA1 transcription factor may represent a therapeutic target for EHE and offers the opportunity to shed light on the functions of two poorly characterized proteins.
|
21885404 |
2011 |
Adult Epithelioid Hemangioendothelioma
|
0.090 |
AlteredExpression
|
disease |
BEFREE |
The chimeric WWTR1/CAMTA1 transcription factor may represent a therapeutic target for EHE and offers the opportunity to shed light on the functions of two poorly characterized proteins.
|
21885404 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The coexpression of TAZ, but not a mutated form of TAZ that lacks TEAD binding, with platelet-derived growth factor-B (PDGF-B) resulted in high-grade tumors with MES features in a murine model of glioma.
|
22190458 |
2011 |
Glioblastoma
|
0.050 |
PosttranslationalModification
|
disease |
BEFREE |
TAZ expression was lower in proneural (PN) GBMs and lower-grade gliomas, which correlated with CpG island hypermethylation of the TAZ promoter compared with MES GBMs.
|
22190458 |
2011 |
Glioma
|
0.050 |
Biomarker
|
disease |
BEFREE |
The coexpression of TAZ, but not a mutated form of TAZ that lacks TEAD binding, with platelet-derived growth factor-B (PDGF-B) resulted in high-grade tumors with MES features in a murine model of glioma.
|
22190458 |
2011 |