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of hereditary BC cases. This study aimed to identify missing genetic determinants of BC. Methods: Whole exome

(BC). In this study, we performed Targeted Next-Generation Sequencing of MMR pathway genes MLH1, MSH2

to establish the viability of microorganisms by amplification of specific sequences of nucleic acids, both

and their binding sites, noncoding RNAs and their targets in protein-coding gene sequences evolutionarily originated

the influence of current and past trends in stochastic sequences on future trends. We find that the discussed

Роль генетических мутаций в профилактике злокачественных новообразований у здорового населения (обзор литературы)
О. Н. Липатов, O. N. Lipatov, К. Т. Ахметгареева, K. T. Akhmetgareeva (Креативная хирургия и онкология, №4, 2020)

СОВРЕМЕННЫЕ ПОДХОДЫ К ДИФФЕРЕНЦИАЦИИ ЖИВЫХ И МЕРТВЫХ БАКТЕРИЙ С ПОМОЩЬЮ ИЗБИРАТЕЛЬНОЙ АМПЛИФИКАЦИИ НУКЛЕИНОВЫХ КИСЛОТNASBA (NUCLEIC ACID SEQUENCE BASED AMPLIFICATION)

. The results of international sequencing of the human genome were analyzed in 2004. These data revealed about

) tripeptide sequence anchored to the surface with a bisphosphonate linker. In terms of wear resistance

) tripeptide sequence anchored to the surface with a bisphosphonate linker. In terms of wear resistance

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