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Interestingly p160 is also shown to interact with TEAD but this interaction does not appear to involve the LxxLL motif.
These data suggest that analogues 1 and 2 are able to interact with CYP2B6 although this interaction does not result in metabolism of these molecules.
PGRPs also interact directly with Imd, but this interaction does not seem to be required for signaling [14], [15].
Here we show that Zyx102 and Enabled (Ena), the Drosophila member of the Ena/VASP family, can interact specifically in vitro and that this interaction does not occur when a particular mutant form of Ena, encoded by the lethal ena210 allele, is used.
Together it is possible that ARTD10(435–528) interacts with a karyopherin but it would appear that this interaction does not follow any of the known rules.
NIPA1 physically interacts with the type II BMP receptor (BMPRII) and we demonstrate that this interaction does not require the cytoplasmic tail of BMPRII.
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Similarly, the wild type TAK1 (Fig. 7B, upper panel) or MKK7β1 (Fig. 7C, upper panel), were able to stably interact with JIP1, and this interaction did not appear to be affected by any of the VRK2 isoforms.
This interaction did not occur with nonconjugated nanoparticles used as control.
When sucrose 0,2 M was combined with DMSO, similar viable cell number in proliferation to non-cryopreserved conditions were detected (Fig. 3A C), but this interaction did not overtake the effects obtained by only DMSO (Table 2).
This interaction did not occur in earlier years because analytic philosophers, at least until the later Wittgenstein, had almost always considered their study of language to be a priori and thus unconcerned with empirical facts about particular languages.
Normally, the DISC1 protein binds to a specific region of the PDE4B protein, but this interaction did not take place in the schizophrenic subjects.
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