Matches in Nanopublications for { ?s ?p "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP316289.RAdcYmwvh_GPxYjzzb4srScrLajBdxYsjLuzyp84YUtoI130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316289.RAdcYmwvh_GPxYjzzb4srScrLajBdxYsjLuzyp84YUtoI130_provenance.
- NP327217.RAGBBVX5bdhyIJv5ZQFjA-SIZGUzxyOa8nQkw0dSZ0wTc130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327217.RAGBBVX5bdhyIJv5ZQFjA-SIZGUzxyOa8nQkw0dSZ0wTc130_provenance.
- NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_provenance.
- NP304360.RAAG5MCoSd7PK_Gs2-B3XaPNXHQNT3O23jGvom0ZJxliY130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304360.RAAG5MCoSd7PK_Gs2-B3XaPNXHQNT3O23jGvom0ZJxliY130_provenance.
- NP304364.RAy8ZKIjVVtthNbiB2aP2M5Vt-oVzTgnpNPjjanN58b3E130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304364.RAy8ZKIjVVtthNbiB2aP2M5Vt-oVzTgnpNPjjanN58b3E130_provenance.
- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.