Search alternatives:
point decrease » point increase (Expand Search)
ppm decrease » _ decrease (Expand Search), pa decreased (Expand Search), 026 decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
point decrease » point increase (Expand Search)
ppm decrease » _ decrease (Expand Search), pa decreased (Expand Search), 026 decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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A391V is a potential pathogenic allele.
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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823
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824
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HoxA9 represses and C/EBPα activates the <i>Cebpa</i> +8 kb enhancer in immature myeloid cells.
Published 2019Subjects: -
832
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833
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834
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835
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836
A tropomyosin point mutant recapitulates the <i>rng8/9</i> deletion phenotype.
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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