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Exact(5)
The indirectly conformational variations of the inhibitors, which caused by the E119G mutation, are responsible for the loss of the binding free energies.
These results indicate that the identified gene deletions (and not an acquired second site mutation) are responsible for the diploid-specific hypersensitivity to DOX.
In a small number of individuals with FXS, mechanisms other than trinucleotide expansion, such as deletion or point mutation, are responsible for the syndrome.
DNMT3b germline mutation are responsible for the immunodeficiency centromeric instability-facial anomalies (ICF) syndrome, the cancer risk of which is not known, while no DNMT1 germline mutation in any genetic syndrome has so far been reported.
Previous studies have confirmed that KIT regulatory mutations including the gene duplication and splice mutation are responsible for the dominant white phenotype in pigs and have pleiotropic effects on peripheral blood cell measures in Western commercial pigs [ 23, 24].
Similar(55)
We hypothesized that the NS mutation is responsible for the differential bm12-cGVHD response between B6 and B6.
To determine whether the G92D mutation is responsible for the loss of AI-2 production, we mutated the Asp-92 back to a glycine by site-directed mutagenesis.
Recently, it has been demonstrated that a single point mutation is responsible for the acquisition of transforming properties by the EJ and T24 human bladder carcinoma gene1 3.
Researchers found that a single genetic mutation is responsible for a relatively large percentage of cases in the two groups under study.
Researchers now say that the same gene mutation is responsible for both the wrinkles and the fever.
Here, we report that incomplete penetrance of the mutation is responsible for partial bulb innervation in a small fraction of Klf7 null mice.
Related(15)
evolution are responsible
mutagenesis are responsible
variation are responsible
deployment are responsible
transformation are responsible
rotation are responsible
mutation are dominant
mutation are heterozygous
mutation are highlighted
mutation are immune
mutation are cross-resistant
mutation are unclear
mutation are low
mutation are tRNALeu UUR
mutation are indispensable
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