Málstofa: Genetcis I

Using genetic information to understand the pathogenesis and improve management of essential tremor

KMT2D-deficiency drives hypoxia responses in normoxia and causes precocious differentiation.

Whole proteome analysis of endothelial cells in response to catecholamine stimulation using an untargeted approach

Characterization of TGFß signaling and mechanotransduction as potential inducers of epithelial-to-mesenchymal transition in placentation

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