Browse our anti-WWTR1 (WWTR1) Antibodies

Zebrafish WW Domain Containing Transcription Regulator 1 (WWTR1) interaction partners

1. Altogether, the data suggest that Wwtr1 establishes the compact wall architecture necessary for trabeculation, and that Nrg/Erbb2 (show ERBB2 Antibodies) signaling negatively regulates its nuclear localization and therefore its activity.

2. Yap (show YAP1 Antibodies)/Taz (show TAZ Antibodies)-Tead activity is necessary and sufficient for optic vesicle progenitors to adopt retinal pigment epithelium identity in zebrafish.

3. Taz (show TAZ Antibodies) is required in the anteroposterior patterning of the pronephric progenitor domain in the intermediate mesoderm, acting in part by regulating retinoic acid signaling in the pronephric progenitor field in the intermediate mesoderm.

4. Taz (show TAZ Antibodies)-depleted larvae displayed patterning defects in ventral cranial vessels that correlate with lateral displacement of thyroid follicles

5. When transcriptional coactivators Yap (show YAP1 Antibodies) and Taz (show TAZ Antibodies) were restricted from interacting with Tead transcription factors through expression of a dominant negative transgene, cardiac precursors failed to migrate completely to the midline.

6. TAZ (show TAZ Antibodies) has a critical role in osteoblast differentiation in vivo

Human WW Domain Containing Transcription Regulator 1 (WWTR1) interaction partners

1. functional evaluation of a HTM cell monolayer using a permeability assay demonstrated that the inhibition of YAP (show YAP1 Antibodies) and TAZ (show TAZ Antibodies) attenuated the DEX-induced impairment of permeability. These findings suggest that YAP (show YAP1 Antibodies) and TAZ (show TAZ Antibodies) play pivotal roles in the DEX-induced cytoskeletal changes of HTM cells, and reveal novel potential mechanisms for the development and progression of glaucoma

2. WWTR1 promotes cell proliferation and inhibits apoptosis of GC cells by regulating cell cycle/apoptosisassociated factors, and effectors in the TGFbeta (show TGFB1 Antibodies) pathway.

3. EphA2 (show EPHA2 Antibodies)-mediates glutaminolysis through YAP (show YAP1 Antibodies)/TAZ (show TAZ Antibodies) activation in HER2 (show ERBB2 Antibodies)-positive breast cancer and may serve as potential therapeutic targets in patients.

4. Depletion of either YES-associated protein (YAP (show YAP1 Antibodies)) or transcriptional coactivator with PDZ (show INADL Antibodies)-motif (TAZ (show TAZ Antibodies)) sensitised cancer cell lines to MLN8237, resulting in apoptosis and reduction in aurora-A (show AURKA Antibodies).

5. High TAZ (show TAZ Antibodies) expression is associated with breast cancer.

6. Nuclear localization of YAP (show YAP1 Antibodies) and TAZ (show TAZ Antibodies) was reduced in DMOG-treated primary tubular epithelial cells.

7. SnoN (show SKIL Antibodies) interacts with multiple components of the Hippo pathway to inhibit the binding of Lats2 to TAZ (show TAZ Antibodies) and the subsequent phosphorylation of TAZ (show TAZ Antibodies), leading to TAZ (show TAZ Antibodies) stabilization.

8. Results show that YAP (show YAP1 Antibodies) and TAZ (show TAZ Antibodies) transcription are regulated by Cbx7 (show CBX7 Antibodies) inhibiting glioblasoma cell migration.

9. Besides its role in normal tissue development, TAZ (show TAZ Antibodies) plays critical roles in cell proliferation, differentiation, apoptosis, migration, invasion, epithelial-mesenchymal transition (EMT (show ITK Antibodies)), and stemness in multiple human cancers.

10. Together, these data illustrate that YAP (show YAP1 Antibodies)/TAZ (show TAZ Antibodies) signaling is responsive to hydrogel stiffness and degradability, but the outcome is dependent on the dimensionality of cell-biomaterial interactions.

Mouse (Murine) WW Domain Containing Transcription Regulator 1 (WWTR1) interaction partners

1. MOB1 (show HOPX Antibodies)-dependent YAP1 (show YAP1 Antibodies)/TAZ (show TAZ Antibodies)-TEAD complex functions as a transcriptional repressor of SOX9 (show SOX9 Antibodies) and thereby negatively regulates chondrogenesis.

2. TAZ (show TAZ Antibodies) regulates cell fate depends on not only the cell type but also its subcellular localization.

3. The results suggested that TAZ (show TAZ Antibodies) may suppress apoptosis and premature senescence in spermatogenic cells by inhibiting the p53 (show TP53 Antibodies)-p21 (show D4S234E Antibodies) signaling pathway, thus playing important roles in the maintenance and control of reproductive function.

4. The role of Yap (show YAP1 Antibodies) and Wwtr1 in the Hippo signaling pathway and the regulation of spermatogenesis in mice are reported.

5. Taz (show TAZ Antibodies) and Yap (show YAP1 Antibodies) have overlapping functions in promoting myoblast proliferation but Taz (show TAZ Antibodies) then switches to enhance myogenic differentiation.

6. A crucial role for YAP (show YAP1 Antibodies) and TAZ (show TAZ Antibodies) in the maintenance of the postnatal adrenal cortex.

7. TAZ (show TAZ Antibodies) is a critical factor for SRC kinase (show CSK Antibodies)-mediated intestinal tumor formation and regeneration.

8. YAP (show YAP1 Antibodies)/TAZ (show TAZ Antibodies) plays multifaceted roles for endothelial cell behaviors, proliferation, junction assembly, and metabolism in sprouting angiogenesis and barrier formation

9. Yap (show YAP1 Antibodies) and Taz (show TAZ Antibodies) leads to impaired epicardial epithelial-to-mesenchymal transition (EMT (show ITK Antibodies)) and a reduction in epicardial cell proliferation and differentiation into coronary endothelial cells.

10. This study identifies YAP (show YAP1 Antibodies)/TAZ (show TAZ Antibodies) as central mediators of VEGF (show VEGFA Antibodies) signaling