basic FUNCTION
| may be participating to apoptosis |
|
involved in vessel development and/or maturation |
|
involved in modulation of ERK signaling mediated by MST4, and could be a regulatory adaptor necessary for MST4 function |
|
having both necessary and sufficient role to induce apoptosis |
|
identified in the vascular endothelium of placenta, suggesting that they might play roles during angiogenesis and vasculogenesis |
|
novel function for PDCD10/CCM3, acting as a critical regulator of neuronal survival during development |
|
important function of PDCD10/CCM3 in the regulation of apoptosis during vertebrate neural development |
|
key component in PCDH-gamma-mediated regulation of neuronal survival |
|
key regulator of neuronal survival in the PCDH-gamma pathway during development |
|
has both neural cell autonomous and nonautonomous functions |
|
can participate in a protein complex also containing KRIT1 and CCM2 |
|
required for normal physiologic function in nonvascular cells and implicate a cell nonautonomous mechanism in disease pathogenesis |
|
PDCD10 and striatins exhibit opposing functions on the targeting of MST4 to the Golgi and Golgi positioning |
|
able to bridge interactions between the GCKIII protein MST4 and STRN3 |
|
PDCD10 and striatin exhibit opposing roles on the localization of the kinase MST4 to the Golgi, with striatins favoring a Golgi localization and PDCD10 promoting cytosolic location |
|
might be a regulatory adaptor required for STK25 functions, which differ distinctly depending on the redox status of the cells that may be potentially related to tumor progression |
|
crucial role in vascular development and in regulation of angiogenesis and apoptosis |
|
KRIT1, PDCD10, and CCM2 are critical regulators of endothelial cell-cell contact and vascular homeostasis |
|
PDCD10 expression in the absence of CCM2 is sufficient to support normal cell growth, revealing complex-independent roles for PDCD10 |
|
both CCM2 and PDCD10 are required for normal endothelial cell network formation |
|
CCM2 and PDCD10 genes could likely play a role in the regulation of mouse gonadogenesis translational activation upon testicular and ovarian development |
|
|