An exome-wide association study of nearly 38,000 smokers from the Mexico City Prospective Study identified rare coding ...
Variants in a nicotine receptor gene are associated with a lower likelihood of heavy smoking, according to a study published ...
EL MUNDO on MSN
Discovery: People with certain genetic variants are less likely to get hooked on tobacco
The variant of the CHRNB3 gene, involved in the regulation of the substance, is starting to be considered as a possible ...
A massive genomics effort has identified thousands of single nucleotide non-coding variants, which alter gene activity, that link to disease and health.
In recent years, the development of large-scale sequencing projects has identified numerous genomic variants in the human genome. For instance, the NyuWa genome resource (Cell Reports, 2021), led by ...
Genetic studies now identify millions of variants across human populations, yet most disease-associated signals fall outside protein-coding regions. This ...
EMBL scientists created SDR-seq, a tool for single-cell DNA-RNA-sequencing that studies both DNA and RNA simultaneously, linking coding and non-coding genetic variants to gene expression in the same ...
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