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Mechanistically, we find ABHD11 removes glutaryl adducts from lipoatean essential fatty acid modification required for the TCA cycle

In addition, second-line treatments such as GnRH agonists effectively reduce pain but are compromised by significant menopausal side effects and challenges with long-term tolerability, which has prompted the development of novel oral GnRH antagonists like elagolix, linzagolix, and relugolix that offer dose-dependent estrogen suppression and rapid reversibility