Voorbeelden van het gebruik van These mutations in het Engels en hun vertalingen in het Nederlands
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Some patients do not harbor these mutations.
These mutations were, in most cases, hereditary.
We are born with some of these mutations.
People who have these mutations often have dry skin.
These mutations can be passed on from parent to child.
And we don't know what causes these mutations but.
What are these mutations, and what is their added value?
The Alliance could have thousands of soldiers with these mutations.
Of course, these mutations are not an isolated phenomenon.
And are often triggered by periods of heightened emotional stress. These mutations manifest at puberty.
These mutations can be easily searched,
And… And whatever is causing these mutations is not from outer space.
These mutations are in humans mostly derived from the father.
Isolates containing these mutations remain sensitive to stavudine.
These mutations lead to defective inactivation of the channel.
One example of a method that is used to identify these mutations is whole exome sequencing.
We find these mutations in approximately a quarter of the families.
These mutations most likely are compensatory mutations. .
Most of these mutations are in N-ras,
These mutations are changes in our genome that happen spontaneously.
These mutations are then visible on the Mutation Dashboard.
These mutations lead to abnormal proplatelets and thrombocytopenia.
And these mutations accumulate approximately as a function of time.
These mutations are believed to have a causative role in the NSCLC.
These mutations manifest at puberty,
These mutations were either spontaneous
These mutations manifest at puberty, often triggered by periods of emotional stress.
These mutations featured maximum emission
These mutations inhibit mitotic exit,
Each of these mutations ultimately leads to the formation of amyloid plaques,