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KünyeVeri korumaGizlilik ayarları
mlud
Genommutation
ge·nom·ic [ʤi:ˈnɒmɪk, Amerİng -ˈnɑ:mɪk] SıFAT
genomic
genomisch meslek dili
genomic
des Genoms meslek dili nach isim
genomic
Erb-
the genomic information
die Informationen pl des Genoms meslek dili
the genomic information
die Erbinformationen pl
mu·ta·tion [mju:ˈteɪʃən] ISIM
mutation
Veränderung dişil <-, -en>
mutation
Mutation dişil <-, -en> meslek dili
genomic mutation ISIM
genomic mutation
Genommutation
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Tek dilli örnekler (PONS yazı işleri tarafından onaylanmamıştır)
Note also that the form often used instead of after vowels does not cause nasal mutation.
en.wikipedia.org
The gene has been found to have missense mutation in exon 9.
en.wikipedia.org
However, he also describes a self-correcting meme, highly resistant to mutation.
en.wikipedia.org
When combined, these factors will result in a variable phenotype for iminoglycinuria depending on which mutations are present.
en.wikipedia.org
If there is a known mutation in the family, prenatal testing is available.
en.wikipedia.org
İnternetten örnekler (PONS yazı işleri tarafından onaylanmamıştır)
[...]
Prominent amongst the Institute ’ s research topics are the signaling pathways that normally regulate aspects of embryogenesis and organogenesis along with the mechanisms orchestrating cell division and the maintenance of genomic integrity during cell proliferation.
www.isrec.ch
[...]
Die Forschungsprogramme konzentrieren sich auf die Signalwege, die die verschiedenen Aspekte der Embryogenese und der Organogenese regulieren sowie auf die Mechanismen, die den Zellzyklus der Zellteilung sowie die Integrität des Genoms während der Zellproliferation kontrollieren.
www.isrec.ch
[...]
Because miRNAs are frequently located at sites of genomic aberrations, we plan to identify small regions of genomic imbalances using array-CGH on DNA-microarrays and to correlate this information with clinically relevant prognostic markers and differentially expressed miRNAs.
[...]
www.ngfn.de
[...]
Da miRNAs häufig an Stellen des Genoms lokalisiert sind, die sich auch durch chromosomale Veränderungen auszeichnen hat unser Forschungsvorhaben weiterhin zum Ziel genomische Veränderungen mit Hilfe der Mikroarray-basierten CGH Methode zu untersuchen um dann wiederum diese Information mit den miRNA Expressionsprofilen sowie dem klinisch relevantem Therapieansprechen und dem Langzeitüberleben zu korrelieren.
[...]
www.ngfn.de

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