Results 251 to 260 of about 5,755,630 (299)
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Single Nucleotide Polymorphisms
2006The identification of DNA variation or gene mutations, which contributes to or determines a disease, has been a major research focus, as it describes the underlying inherited disease components. With the human genome being sequenced, the reference sequence is now at hand, facilitating the systematic identification of DNA variation and its subsequent ...
Ulrich Broeckel, Martin J. Hessner
+7 more sources
Hypertension and single nucleotide polymorphisms
Current Hypertension Reports, 2000Hypertension is a common, complex disease phenotype that has been intensively studied to identify susceptibility loci in humans. Candidate genes continue to be uncovered via genetic analysis in model organisms through linkage analysis with families and/or sib-pairs and through association studies using sequence variants in genes that play a role in key
M J, Rieder, D A, Nickerson
openaire +2 more sources
Single-Nucleotide Polymorphism Mapping
2006Single-nucleotide polymorphism (SNP) mapping is the easiest and most reliable way to map genes in Caenorhabditis elegans. SNPs are extremely dense and usually have no associated phenotype, making them ideal markers for mapping. SNP mapping has three steps.
M Wayne, Davis, Marc, Hammarlund
openaire +2 more sources
single nucleotide polymorphism
2009(SNP, pronounced “snips”) variation at just a single base of a four-bases (syn. nucleotides) long codon; it is assumed that SNPs predispose individuals to develop certain diseases but also to respond or not to certain drugs; → see also genom, pharmacogenetics.
openaire +1 more source
The single nucleotide polymorphism story
Pharmacogenetics, 2003Sandrine, Barbaux, François, Cambien
openaire +2 more sources

