Evaluation of Candidate Reference Genes for Gene Expression NormalizationStudy performed in Brassica juncea using real time quantitative RT-PCR.
Reliable and Rapid Characterization of Functional FCN2 Gene Variants Reveals Diverse Geographical PatternsIn this study, scientists genotyped and characterized four FCN2 functional SNP variants in West Africans, South Americans, South East Asians from Vietnam and Caucasians from Germany using an available rapid, reliable and cost effective FRET-RTPCR methodology.
Good News for NanomedicineQuantum dots appear safe in pioneering study on primates.
Research on Butterflies Reveals Genetic SharingLandmark effort to sequence the genome of a South American butterfly has revealed the key behind its ability to mimic other butterflies.
Zooming in on Early Embryonic DevelopmentBroad Institute researchers show a high-resolution view of mouse embryogenesis, down to individual bases, showing genetic changes.
New Technique Reveals Unseen Information in DNA CodeScientists have developed and tested a technique to distinguish between two modified forms of cytosine.
NIH Study Finds that Coffee Drinkers have Lower Risk of DeathOlder adults who drank coffee — caffeinated or decaffeinated — had a lower risk of death overall than others who did not drink coffee.
Finnish Researchers Discover Genes Inhibiting the Spread of Prostate CancerResearchers utilize the cell spot micro array technology to study the impacts of all genes in an entire genome in a single experiment.
Stabilizing Fanconi Anemia with AntioxidantsFanconi anemia (FA) is a rare genetic disorder which affects one person in 350,000.
Scientists Make Groundbreaking Discovery Of Mutation Causing Genetic Disorder In HumansScientists at A*STAR's Institute of Medical Biology (IMB), in collaboration with doctors and scientists in Jordan, Turkey, Switzerland and USA, have identified the genetic cause of a birth defect known as Hamamy syndrome.
