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The scIHF variants described here will help to explore further how flexible these requirements are.
The variants described here are dramatically slowed down in PT efficiency and provide excellent models to resolve the individual steps.
The variants described here are not rare mutations, rather they are polymorphisms that are common in normal populations.
The three variants described here have been submitted to the Clinvar database, http://www.ncbi.nih.gov/clinvar.nih.gov/clinvar
Interestingly, these genetic studies, together with the rare variants described here, are reflected in the phenotype of SYN2 KO mice.
The genetic variants described here will be a useful resource for future studies of genetic variation regulating performance traits and diseases in equids.
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The MRC variant described here then attempts to compensate for this effect by combining weighted estimates of the SOF from each receiver.
The single missense mutation, arginine 225 to glutamine (R225Q) results in a dominant mutation that is homologous to the γ3 R225W variant described here.
Since the translation start in the previously reported IL4I1 transcript differs from that in the variant described here, the two protein products differ at their N termini.
Gastropexy with the technical variant described here is easy to be performed and was feasible and safe in the present study.
It is possible that the lower band is the brain-specific PIPKIγ splice variant (PIPKIγ_i3), identified by Giudici et al. [ 32, 33], which shares partial sequence homology with the human PIPKIγ_i5 variant described here [ 32, 33].
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