Using genetic information to understand the pathogenesis and improve management of essential tremor
- Flytjandi: Astros Thorarensen Skuladottir
- Höfundar - í stafrófsröð: Astros Thorarensen Skuladottir and Kari Stefansson
- Lykilorð: Genetics Molecular Biology Pathology
KMT2D-deficiency drives hypoxia responses in normoxia and causes precocious differentiation.
- Flytjandi: Sara Þöll Halldórsdóttir
- Höfundar - í stafrófsröð: Sara Þöll Halldórsdóttir and Hans Tómas Björnsson
- Lykilorð: Genetics Stem Cells
Characterization of TGFß signaling and mechanotransduction as potential inducers of epithelial-to-mesenchymal transition in placentation
- Flytjandi: Sophia Mähr
- Höfundar - í stafrófsröð: Sophia Mähr and Gudrun Valdimarsdottir
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