| basic FUNCTION
| ras-like GTP-binding protein dispensable for survival, but required for anchorage-independent proliferation |
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RALA and RALB are important, functionally distinct targets for geranylgeranyltransferase I inhibitors-mediated tumor apoptosis and growth inhibition  |
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mediate both common and specific transcriptional programs that are associated with human cancer and identify RREB1 as a novel transcriptional effector of RAL (Oxford 2007) |
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required to tether the exocyst to the cytokinetic furrow in early cytokinesis |
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with RALB, make critical non-overlapping contributions to the generation of a tumorigenic regulatory network, supporting bypass of the normal restraints on both cell proliferation and survival  |
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with its activator RALGDS participate in nutrient sensing and are indispensable for activation of mammalian target of rapamycin complex 1 (MTOR) induced by extracellular nutrients  |
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calmodulin (CaM)-binding protein, having a role in the regulation of PLC-delta1 function  |
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control neurite branching, but also regulates neuronal polarity  |
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suppresses early stages of Ras-induced squamous cell carcinoma progression  |
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its activation elicited by the exchange factor RALGDS in response to a rise in intracellular Ca2+ and cAMP controls hormone release from pancreatic beta-cell by coordinating the execution of different events in the secretory pathway  |
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with RALB contribute to KRas-dependent ionizing radiation resistance  |
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its function in dermal fibroblasts is required for tumor progression of neighboring neoplastic keratinocytes  |
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RALA and RALBP1 regulate mitochondrial fission at mitosis  |