Examples of using Mutation in English and their translations into German
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Political
His mutation.
Evolution of miRNA by duplication and mutation in animals.
Evidence of the mutation f508del and r117h heterozygous!
Don't listen to the mutation, Joey.
With one gene mutation we do sin against the Mother.
People also translate
White canaries in Germanys appeared, got thanks to mutation also.
You will eradicate that mutation and then your weapon's intact.
Mutation, right, took us from single-celled organisms to the dominant form.
Genetics==The origin of the Oregon Rex breed is a result of mutation.
AID HFE Kit enables detection of mutation C282Y and H63D in HFE gene.
Mekinist should only be used to treat melanomas with the BRAF mutation.
In the case of 0-20% mutation we could not detect any problems with fertilization.
No doubt the adaptation to desert soil produces a mutation in colour.
An AR mutation is found in more than 95% of patients with CAIS; 30% are de novo mutations.
IB Biotech offers two levels of study of the BRCA1 and 2 gene mutation.
Another possibility for mutation correction is the use of a suppressor mutation.
The involvement of the lung is however as severe as with the most common mutation F508del.
Site selected mutation by lanthanides was discovered in 1995 and possibly earlier.
One tool for JVM-based programming languages that automates mutation testing is Pitest.
Patients with confirmed mutation have a poor outcome after renal transplantation.
Phenotype variability within members of a family carrying a novel mutation in the CRX gene.
Contrary to what is claimed, this mutation is obviously neither beneficial nor evolution-triggering.
You could view this as the allele frequency of that mutation on the X chromosome.
This lesson presents mutation types, their frequency and underlying causes.
ISBN 3-910074-67-7* Michael Fuchs:"Methoden der Frühdiagnostik des Eintrittszeitpunktes der Mutation bei Knabenstimmen.
People with this mutation were better able to reproduce successfully than those without the mutation.
A mutation in the 3' UTR of the myostatin gene in Texel sheep creates target sites for the microRNAs miR-1 and miR-206.
The group of patients with inactivation of p53 by mutation overlaps largely with the group of patients showing a del17p13, but is not identical.
Mutation in the HFE gene are causing a defective interaction of the HFE protein with transferrin receptor with negative impact on iron absorption.
Overactivation of src, however, such as by mutation, can lead to increased activity of src, which can cause overgrowth and malignancy of cells.