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Egln1 protein, mouse

Known as: PHD2 protein, mouse, prolyl hydroxylase domain 2 protein, mouse, EGL nine homolog 1 (C. elegans) protein, mouse 
National Institutes of Health

Papers overview

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2019
2019
Background Loss of function mutations in the EGLN1 gene are a cause of erythrocytosis. EGLN1 encodes for prolyl hydroxylase… 
2019
2019
In diabetes-associated chronic wounds, the normal response to hypoxia is impaired and many cellular processes involved in wound… 
2006
2006
Purpose: Hypoxia in tumors is associated with poor prognosis and resistance to treatment. The outcome of hypoxia is largely…