Matches in Nanopublications for { ?s ?p "[RUNX1 and NF-E2 overexpression was not detected in patients with EPO receptor (EPOR) gain-of-function, suggesting distinct mechanisms by which erythroid progenitors in polycythemias with defects of hypoxia sensing and EPOR mutations exert their EPO hypersensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_assertion description "[RUNX1 and NF-E2 overexpression was not detected in patients with EPO receptor (EPOR) gain-of-function, suggesting distinct mechanisms by which erythroid progenitors in polycythemias with defects of hypoxia sensing and EPOR mutations exert their EPO hypersensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- assertion description "[RUNX1 and NF-E2 overexpression was not detected in patients with EPO receptor (EPOR) gain-of-function, suggesting distinct mechanisms by which erythroid progenitors in polycythemias with defects of hypoxia sensing and EPOR mutations exert their EPO hypersensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1133478.RAFoTEG-Qj24eLC2pQ8qBryQ4TgZyO5dWjJFtooXGlPYM130_assertion description "[RUNX1 and NF-E2 overexpression was not detected in patients with EPO receptor (EPOR) gain-of-function, suggesting distinct mechanisms by which erythroid progenitors in polycythemias with defects of hypoxia sensing and EPOR mutations exert their EPO hypersensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1133478.RAFoTEG-Qj24eLC2pQ8qBryQ4TgZyO5dWjJFtooXGlPYM130_provenance.