Sentence examples for mutation is specific from inspiring English sources

Exact(7)

The effect of Nlgn2 mutation is specific for inhibitory synapses from fast-spiking (parvalbumin-positive) but not from somatostatin-positive interneurons [ 126].

Our finding that the BBS3 A89V missense mutation is specific for vision demonstrates that this region is important for proper function of the protein in the eye.

Dideoxysequencing confirmed that this mutation is specific to AS-30CQ and does not appear in either AS-15MF or AS-ATN.

However, it is not known whether this mutation is specific to the Cana-dian population or is frequent in other Caucasian populations.

The effect of the swd mutation is specific to the exocrine pancreas and skin (hypopigmentation), because the other digestive organs, including intestine and liver, of the swd mutants seem grossly normal on histological sections (Fig. 1N,O).

This mutation is specific to the 129 strain, because two ES cell lines derived from C57BL/6 mice, Bruce4 and JM8.N4, were found to be wild-type for the caspase 11 locus.

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Similar(53)

This mutation was specific to the hydroquinones, as it was not observed with quinones and other components of the redox cycling (semiquinones and reactive oxygen species).

Results showed that in most cases the mutation was specific to all of the different clusters analysed from within the lineage, although several instances of within-lineage and even within-cluster variation was observed.

IDH1 mutations were not associated with NADP+-dependent G6PDH activity (P = 0.60; Fig.  3c) or with NAD+-dependent IDH activity (P = 0.639; Fig.  3d), indicating that the correlation with IDH1 mutations is specific for the NADP+-dependent IDH activity.

At this point it is not clear if the loss of DNA methylation associated with KDM5C mutations is specific to KDM5C loss of function or would also be observed in the context of loss of function of other H3K4 demethylases.

In this study, sequence analysis has revealed that, among a variety of mutations, the HA-S220T and NA-N248D mutations are specific for the dominant variant(s) of the 2009 pdm influenza A(H1N1) viruses.

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