Matches in Nanopublications for { ?s ?p "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP356666.RAXw4odgx2WKrH6CamhlIXsz62jz9VBQXHQESe8D-UwT8130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356666.RAXw4odgx2WKrH6CamhlIXsz62jz9VBQXHQESe8D-UwT8130_provenance.
- NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP507126.RAtiuyHB-kYbYiTCzuPHbIlEgmb4wcyvknnSQXIHuAq9w130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507126.RAtiuyHB-kYbYiTCzuPHbIlEgmb4wcyvknnSQXIHuAq9w130_provenance.
- NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- NP507125.RAyuzdcnZg184_nrtHl_VciN7DG2ABhxNy0q5egA3FiXM130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507125.RAyuzdcnZg184_nrtHl_VciN7DG2ABhxNy0q5egA3FiXM130_provenance.
- NP507127.RAwMZtGWkvEHdu6mzfdsAhJM2Dxlu-n0eixodvqrvsoIs130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507127.RAwMZtGWkvEHdu6mzfdsAhJM2Dxlu-n0eixodvqrvsoIs130_provenance.