Matches in Nanopublications for { ?s ?p "[These data provide the first evidence that the ER-retention of mutant FKRP may play a role in the pathogenesis of CMD and potentially explain why the allelic disorder LGMD2I is milder, because the mutated protein is able to reach the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_assertion description "[These data provide the first evidence that the ER-retention of mutant FKRP may play a role in the pathogenesis of CMD and potentially explain why the allelic disorder LGMD2I is milder, because the mutated protein is able to reach the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion description "[These data provide the first evidence that the ER-retention of mutant FKRP may play a role in the pathogenesis of CMD and potentially explain why the allelic disorder LGMD2I is milder, because the mutated protein is able to reach the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_provenance.
- NP942766.RAncGgW0_FiPDm5yDT_cFkrVO8D2Kuc7WqAaUaXBdcTfo130_assertion description "[These data provide the first evidence that the ER-retention of mutant FKRP may play a role in the pathogenesis of CMD and potentially explain why the allelic disorder LGMD2I is milder, because the mutated protein is able to reach the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP942766.RAncGgW0_FiPDm5yDT_cFkrVO8D2Kuc7WqAaUaXBdcTfo130_provenance.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion description "[These data provide the first evidence that the ER-retention of mutant FKRP may play a role in the pathogenesis of CMD and potentially explain why the allelic disorder LGMD2I is milder, because the mutated protein is able to reach the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_provenance.