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The effect on cell growth was assessed as a percentage of cell viability, with vehicle-treated cells considered 100% viable

they promote the proliferation, migration and survival of endometriotic cells by activating signaling pathways such as Raf/MEK/ERK and mTOR

IP3 triggers intracellular calcium release from the endoplasmic reticulum, which initiates GH exocytosis from secretory granules

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