Sentence examples for mutations become available from inspiring English sources

Once hiPSC lines from multiple patients with sarcomeric mutations become available, those could be used for large-scale high-throughput screens for drug discovery.

Until similar comprehensive neuropsychological data on the I810N patients and other AHC patients with identified ATP1A3 mutations become available, it would be unreliable to draw specific parallels with aspects of the Myk/+ cognitive phenotype at this stage.

Should a larger set of β-mannosidosis associated mutations become available in the future, it would be very interesting to apply this structural analysis procedure to authenticate our genotype-phenotype correlation.

This is because incident case numbers are not expected to increase rapidly because of the increasing uptake of prophylactic surgery among unaffected BRCA1/2 mutation carriers and the relatively short follow-up since DNA testing for BRCA mutations became available (1995), together with the fact that many newly identified carriers were tested because they (already) had breast cancer.

As the virus will continue to evolve, new mutations will become available and the best way we have found to allow quick mapping and update of new sequence variation in respect to drug and antibody binding sites is to give full access to users/readers via a 3D structure visualization tool at the supplementary webpage (instructions to map new mutations are given, including an example).

It will be interesting to see whether the conclusions made in mouse hold in general when more invertebrate null mutation phenotypic data become available for such analyses.

As clinical practice is rapidly shifting toward digital breast imaging, this work should set the stage for applying the strategies described herein to newer images from mutation carriers as they become available.

This type of mutation produces new structures that become available for further experimentation and potential new uses.

An additional 15 samples have become available for mutation testing from the original ⩽30 series.

In the past few years several spontaneous or engineered mouse models with mutations in Ca2+ channel genes have become available, providing a powerful approach to defining Ca2+ channel function in vivo.

As the number of MEFV mutations discovered continues to increase, more data will become available revealing further relationships among the many different MEFV missense mutations and their phenotypic expression in various ethnic groups.