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The mutation also affected seminal and crown root elongation at early growth stage.
We asked if the E457Q mutation also affected phlorizin inhibition of hSGLT3.
Strikingly, the KKGRR/AAGAA mutation also affected the segregation of ClC-6 and ClC-7.
The same tim ΔNLS mutation also affected nuclear accumulation of PER and TIM when expressed in cultured Drosophila cells and caused delays in the onset of PER/TIM nuclear accumulation that are well correlated with the long-period circadian rhythms of tim ΔNLS flies.
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Kinetic and equilibrium unfolding experiments indicate that the VH mutation also affects VL unfolding, possibly by partially destabilizing the interface provided by VH, even though the mutation is distant from the interface.
It could be that the L302P mutation also affects this orientation - the mutation affects both polymerization and GTP hydrolysis activity.
The E1103G mutation also affects the pausing kinetics.
The p. Gly211Val mutation also affects the mobile actuator domain.
We cannot however exclude the possibility that this mutation also affects other yet-unidentified function of the SADH domain.
Additionally, the atrad21.3 mutation also affects the kinetics of DNA dsb damage repair after the induction of DNA dsb.
In addition, the accessibility of a resistance-conferring mutation also affects the kinetics of the evolution of resistance.
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