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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Detalles Bibliográficos
Autores principales: Antontseva, E.V., Degtyareva, A.O., . Korbolina, E.E, Damarov, I.S., Merkulova, T.I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641029/
https://www.ncbi.nlm.nih.gov/pubmed/37965371
http://dx.doi.org/10.18699/VJGB-23-77

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641029/
https://www.ncbi.nlm.nih.gov/pubmed/37965371
http://dx.doi.org/10.18699/VJGB-23-77

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