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Neurologists seeking a way to treat the fatal neurodegenerative disorder amyotrophic lateral sclerosis (ALS) have identified the EPHA4 (ephrin type-A receptor 4) gene as a likely target for drug or
A molecular signaling pathway based on the cytokine interleukin-1 (IL-1) has been found to play a critical regulatory role in the formation and growth of bone mass in the developing individual.
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