Showing 821 - 840 results of 100,108 for search '(( 5 ((ppm decrease) OR (a decrease)) ) OR ( 5 ((point decrease) OR (nn decrease)) ))', query time: 1.28s Refine Results
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    A391V is a potential pathogenic allele. by Wesley R. Lewis (3144372)

    Published 2016
    “…<p>(A) Sanger Sequence confirmation of the 1172 C>T point mutation in Gas8<sup>AV</sup> mice reproducing the A391V missense mutation found in the human patient. …”
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    A tropomyosin point mutant recapitulates the <i>rng8/9</i> deletion phenotype. by Omaya Dudin (3926825)

    Published 2017
    “…(G) Kymographs of Myo52-tdTomato showing multiple stable dots over >60s in <i>cdc8</i><sup><i>E104A</i></sup> mutant. (H) Myo51-3YFP fluorescence at the fusion site is decreased in <i>cdc8</i><sup><i>E104A</i></sup> mutant (N = 15); (***) P < 3 × 10<sup>−5</sup>, t-test. …”
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