Examples of using Same mutation in English and their translations into Slovak
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Evan Lee suffered the same mutation as those animals.
This creates many new cells that all have that same mutation.
If that poor man has the same mutation as the animals, you have to find out why.
We have seen plenty of animals with the same mutation, right?
If there is even a chance that I have the same mutation, Mitch needs to know that there's another phase two subject.
This creates many new cells, each of which has the same mutation.
This is important information, because the same mutation are hiding in the cells of different parts of the body.
This leads to the creation of numerous new cell with the same mutations.
If all the tumours in a patient with multiple types of cancer have the same mutation pattern, this is a strong indication that there is a genetic cause.
I compared your blood to our one-armed friend, and… you have the same mutation.
If all the tumors in a patient with multiple types of cancer have the same mutation pattern, this is a strong indication that a genetic aspect is involved.
The signs may evendiffer between members of the same family who have the same mutation.
Letters are also used to denote amino acids, so the same mutation might also be written as p. A40V.
Diagnosis for other family members then involves a relatively simple blood test,which looks for the same mutation.
The use of emtricitabine in patient with chronic HBV induces the same mutation pattern in the YMDD motif observed with lamivudine therapy.
The same mutation in different individuals can manifest differently regardless of what level assess its effects: molecular, biochemical or phenotypic.
It is shared among the primates only,in the exact chromosomal location, with the same mutations that render it nonfunctional.
I mean, if they have the same mutation, and they get this genetic test and they understand it, then they can get regular screens and can catch cancer early, and potentially live a significantly longer life.
The team identified DNA mutations, which were present at the time of diagnosis and looked for those same mutations at each sampling point.
At the same time, due to the high number of unique mutations andthe wide variety of clinical features for the same mutation, knowledge of the particular type and position of the mutation in the gene can only predict very little the development and severity of the disease.
Next, the researchers identified mutations in DNA thatwere present at the time of diagnosis, and were looking for the same mutation in each sampling point.
This is because parents who are closely relatedare more likely to be carrying the same mutation, so a child may inherit from both sides, causing the mutation to take effect.
Next, the researchers identified mutations in DNA, which are present at the time of diagnosis,and were looking for the same mutation in each sampling point.