Human-genome single nucleotide polymorphisms affecting transcription factor binding and their role in pathogenesis

Human-genome single nucleotide polymorphisms affecting transcription factor binding and their role in pathogenesis

Single nucleotide polymorphisms (SNPs) are the most common type of variation in the human genome. The vast majority of SNPs identified in the human genome do not have any effect on the phenotype; however, some can lead to changes in the function of a gene or the level of its expression. Most SNPs as...

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Bibliographic Details
Main Authors: E. V. Antontseva, A. O. Degtyareva, E. E. Korbolina, I. S. Damarov, T. I. Merkulova
Format: Article
Language:English
Published: Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders 2023-11-01
Series:Вавиловский журнал генетики и селекции
Subjects:
regulatory single-nucleotide polymorphism
transcription factor-binding sites
gene expression
genome-wide studies
Online Access:https://vavilov.elpub.ru/jour/article/view/3938

Internet

https://vavilov.elpub.ru/jour/article/view/3938

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