Sentence examples for mutations with all from inspiring English sources

All microdissected targets histologically classified as HGD and LGD had mutations with all targets falling into the low ML or high ML levels.

This conclusion follows from three observations: 1) The previously unexamined basal lineages of grasses (represented by Anomochloa, Streptochaeta, and Pharus) contain a pseudogene copy of rps14 in the mitochondrial genome that shares two frameshift mutations with all other grasses.

The impact of RAS mutations in KRAS exon 3 and 4 and NRAS exons 2, 3 and 4 appears to be similar to that of KRAS exon 2 mutations, with all mutations being predictive of a lack of response to panitumumab therapy.

Using this flexible approach, we model the mutations as deriving from an unknown number of subclones, each of which is present at an unknown fraction of tumor cells and contributes an unknown proportion of all somatic mutations, with all the unknown parameters to be jointly estimated in the model (Extended Experimental Procedures).

Modeling Subclonal Structure Using Bayesian Dirichlet Processes We model somatic mutations within the tumor as deriving from an unknown number of subclones, each of which is present at an unknown fraction of tumor cells and contributes an unknown proportion of all somatic mutations, with all the unknown parameters to be jointly estimated.

Chromosome 9 showed linkage with the mutation, with all ten affected mice being homozygous for the B6 allele of D9Mit182 (101.431 Mb), while no unaffected mice were homozygous for B6 at that marker (Chi square test 1.4e−6).

In this study, genetic analysis of 44 patients from different Caucasian ethnic backgrounds confirmed a founder effect for the p.Ala467Thr of this mutation, with all patients having an identical POLG haplotype, including the predicted promoter region polymorphism.

Mutations occur with all three possible outcomes: neutral, deleterious, and beneficial.

This co-transporter may play a major role in determining seizure-susceptibility based on our observations that kcc is a powerful seizure-enhancer mutation, interacting with all other mutants in our collection to exacerbate seizure phenotypes.

Another possible direction is integrating the proposed novel mutation scheme with all compared and other self-adaptive DE variants plus combining the proposed self-adaptive crossover with other DE mutation schemes.

This mutation cosegregated with all affected individuals and was not observed in unaffected family members.