Associated Papers
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
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Medcomm, 2025
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Supplement: MCO2-6-e70394-s001.xlsx › TableS13
Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry.
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Journal of Molecular Medicine (berlin, Germany), 2025
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Supplement: 109_2024_2510_MOESM2_ESM.xlsx › Sheet1
PRIMA-1MET-induced neuroblastoma cell death is modulated by p53 and mycn through glutathione level.
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Journal of Experimental & Clinical Cancer Research : Cr, 2019
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Supplement: 13046_2019_1066_MOESM1_ESM.xlsx › SK-N-SH
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