Matches in Nanopublications for { ?s ?p "[Other variants, identified in controls, included c.2089G>A (p.Gly697Ser) and c.2097T>C. Our identification of potentially defective NPAS3 variants supports recent studies that implicate perturbations in NPAS3 pathways in impaired neurogenesis and psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_assertion description "[Other variants, identified in controls, included c.2089G>A (p.Gly697Ser) and c.2097T>C. Our identification of potentially defective NPAS3 variants supports recent studies that implicate perturbations in NPAS3 pathways in impaired neurogenesis and psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- NP811931.RA7Dqy9QeCPmEBg7RSb7ePL85i5WjDnBZkah1KoURSiEw130_assertion description "[Other variants, identified in controls, included c.2089G>A (p.Gly697Ser) and c.2097T>C. Our identification of potentially defective NPAS3 variants supports recent studies that implicate perturbations in NPAS3 pathways in impaired neurogenesis and psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811931.RA7Dqy9QeCPmEBg7RSb7ePL85i5WjDnBZkah1KoURSiEw130_provenance.
- NP811930.RANf1cNMrIl2PxSkHmgCMXQwM_C9JXMtclZRErt0fEP84130_assertion description "[Other variants, identified in controls, included c.2089G>A (p.Gly697Ser) and c.2097T>C. Our identification of potentially defective NPAS3 variants supports recent studies that implicate perturbations in NPAS3 pathways in impaired neurogenesis and psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811930.RANf1cNMrIl2PxSkHmgCMXQwM_C9JXMtclZRErt0fEP84130_provenance.
- NP936882.RAuBcM5rKFg4LY-xSmsuXLcWoXOCYZwgz9cy2H6cCX4xU130_assertion description "[Other variants, identified in controls, included c.2089G>A (p.Gly697Ser) and c.2097T>C. Our identification of potentially defective NPAS3 variants supports recent studies that implicate perturbations in NPAS3 pathways in impaired neurogenesis and psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936882.RAuBcM5rKFg4LY-xSmsuXLcWoXOCYZwgz9cy2H6cCX4xU130_provenance.