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Acquired mutation
Causing genetic mutation
Frame-shift mutation
Frameshift mutation
Frameshift mutations in the genome of the organism
Mutagenic
Mutation
Phase-shift mutation
Point mutation
Reading frameshift
Single site mutation
Somatic cell mutation
Somatic mutation

Traduction de «frameshift mutation » (Anglais → Néerlandais) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
frameshift mutation | frame-shift mutation | phase-shift mutation | reading frameshift

leesraammutatie | leesraamverschuiving


Frameshift mutation | Reading frameshift

Frameshift-mutatie


frameshift mutations in the genome of the organism

frameshift-mutaties in het genetisch materiaal van het organisme


Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

erfelijke plaatsspecifieke eierstokkanker-syndroom


acquired mutation | somatic cell mutation | somatic mutation

somatische celmutatie | somatische mutatie,knopmutatie


A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL

metabole myopathie door lactaattransporterdefect




A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd

Eiken-syndroom




mutagenic | causing genetic mutation

mutageen | wat verandering teweegbrengt
TRADUCTIONS EN CONTEXTE
Frameshift mutation : a genetic mutation caused by insertions or deletions of a number of nucleotides that is not evenly divisible by three within a DNA sequence that codes for a protein/peptide.

Frameshift-mutatie : een genetische mutatie veroorzaakt door insertie of deletie van een aantal nucleotiden dat niet gelijkmatig deelbaar is door drie binnen een DNA-sequentie die voor een eiwit/peptide codeert.


15. The mutations scored in the lacI, lacZ, cII and gpt point mutation assays consist primarily of base pair substitution mutations, frameshift mutations and small insertions/deletions.

15. De mutaties die worden bepaald in de lacI-, lacZ-, cII- en gpt-puntmutatietesten bestaan hoofdzakelijk uit basenpaarsubstitutiemutaties, frameshift-mutaties en kleine inserties/deleties.


4. The weight of evidence suggests that transgenes respond to mutagens in a similar manner to endogenous genes, especially with regard to the detection of base pair substitutions, frameshift mutations, and small deletions and insertions(24).

4. De bewijskracht wijst erop dat transgenen op vergelijkbare wijze reageren op mutagenen als op endogene genen, in het bijzonder met betrekking tot de detectie van basenpaarsubstituties, frameshift-mutaties en kleine deleties en inserties (24).




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Date index: 2024-04-12
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