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It is well appreciated that certain mutant p53 proteins exhibit stark decreases in the stability of their core DBD domain [5,6,7]

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In individuals with low blood eosinophil levels, this medication, which targets the IL-33 pathway, resulted in a marginally better reduction in exacerbation

The most commonly reported adverse events in the Phase 2 trial were gastrointestinal in nature, including nausea, vomiting, and diarrhoea consistent with the GLP-1 receptor agonist class

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