Results 271 to 280 of about 441,146 (309)
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Single nucleotide polymorphisms: aging and diseases

Biogerontology, 2004
Differences of more than 3 million nucleotides can bee seen comparing the genomes of two individuals as a result of single nucleotide polymorphism (SNP). More and more SNPs can be identified and it seems that these alterations are behind of several biological phenomena.
Margit Zeher   +4 more
openaire   +3 more sources

Shares in single nucleotide polymorphisms

Expert Opinion on Therapeutic Patents, 1999
The announcement of a consortium between the public and private sectors to produce a public single nucleotide polymorphism (SNP) map of the human genome is a unique development which acknowledges the need for research tools to be widely available. The human genome project has been characterised by public-private tensions over information access and ...
openaire   +2 more sources

Single Nucleotide Polymorphism Typing

2019
Single nucleotide polymorphism (SNP) typing process utilizes biochemical techniques to determine the sequential order of nucleotide bases in a DNA strand using sequencing machines. Last decade has witnessed a tremendous expansion since the invention of the Sanger sequencing.
Srinivasan, Srilakshmi, Batra, Jyotsna
openaire   +2 more sources

Methods for Genotyping Single Nucleotide Polymorphisms

Annual Review of Genomics and Human Genetics, 2001
One of the fruits of the Human Genome Project is the discovery of millions of DNA sequence variants in the human genome. The majority of these variants are single nucleotide polymorphisms (SNPs). A dense set of SNP markers opens up the possibility of studying the genetic basis of complex diseases by population approaches.
openaire   +2 more sources

‘Other’ applications of single nucleotide polymorphisms

Trends in Biotechnology, 2007
Single nucleotide polymorphisms (SNPs) are the most frequent form of sequence variation in the human genome, occurring on average every 300 base pairs. Owing to their high density, SNPs are considered useful for identifying the genes associated with complex diseases. The focus of this Opinion article is the recent applications of SNPs that fall outside
openaire   +3 more sources

Genetic susceptibility and single-nucleotide polymorphisms

Seminars in Fetal and Neonatal Medicine, 2005
The completion of the Human Genome Project has provided insight into human genetic variation, most commonly represented by single-nucleotide polymorphisms. There is presently a great deal of interest in linking genetic and phenotypic variation in the form of severity of, and susceptibility to, common multifactorial diseases.
openaire   +3 more sources

Molecular imaging in oncology: Current impact and future directions

Ca-A Cancer Journal for Clinicians, 2022
Martin G Pomper, Steven P Rowe
exaly  

The single nucleotide polymorphism story

Pharmacogenetics, 2003
Sandrine Barbaux, Fran ois Cambien
openaire   +3 more sources

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