Previous genetic studies have examined the association of aspirin, NSAIDs, or both with colorectal cancer according to a limited
number of candidate genes or pathways.6 - 10 Thus, to comprehensively identify common genetic markers that characterize individuals who may obtain differential benefit from aspirin and NSAIDs, we conducted a discovery - based, genome - wide analysis of gene × environment interactions between regular use of aspirin, NSAIDs, or both and single - nucleotide polymorphisms (SNPs) in relation to risk of colorectal cancer.
Not exact matches
The system can yield dose - response curves for
candidate drugs, screen the phenotypes
of large
numbers of gene mutations, or execute complex custom protocols for completely new experiments.
VAAST, also developed in Yandell's laboratory, identified a
number of mutations that might have caused the syndrome, but couldn't identify an individual
candidate as the causative
gene.
As mRNA isolation is simple and since DNA microarrays are a proven genomics reagent for monitoring differential
gene expression, a genome - wide expression analysis may be the fastest and most efficient method for identifying additional
candidate effectors
of colony queen
number.
Vaccine
candidates for preventing SARS have been developed by various groups and include inactivated whole virus, spike (S) protein preparations, virus - like particles (VLPs), plasmid DNA and a
number of vectors containing
genes for SARS - CoV proteins [13]--[28].
Linkage and
candidate gene studies have been highly successful in the identification
of genes that cause the monogenic variants
of diabetes and, although progress in the more common forms
of T2D has been slow, a
number of genes have now been reproducibly associated with T2D risk in multiple studies.
This section invites manuscripts describing (a) Linkage, association, substitution or positional mapping and epigenetic studies in any species; (b) Validation studies
of candidate genes using genetically - engineered mutant model organisms; (c) Studies focused on epistatis and
gene - environment interactions; (d) Analysis
of the functional implications
of genomic sequence variation and aim to attach physiological or pharmacogenomic relevance to alterations in
genes or proteins; (e) Studies
of DNA copy
number variants, non-coding RNA, genome deletions, insertions, duplications and other single nucleotide polymorphisms and their relevance to physiology or pharmacology in humans or model organisms, in vitro or in vivo; and (f) Theoretical approaches to analysis
of sequence variation.
The Human Genome Scrubber maps ASD
candidate genes by their location along the human genome and provides users with information including the assigned
gene score and the
number of reports associated with the
gene.