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Genomics is the branch of molecular biology concerned with the structure, function, evolution, and mapping of genomes.
In this application note, BMG Labtech discuss how the Bioluminescence resonance energy transfer (BRET) is a versatile tool to study interactions and trafficking in proteins.
Scientists have identified a gene that in women is linked to the creation and location of new fat cells and therefore is thought to contribute to the risk of type 2 diabetes...
Researchers have found that a gene that makes humans eat more sugar can also lower body fat...
Broad data analysis points to genetic similarities between Lou Gehrig's Disease and a form of dementia...
There are no short-cuts in the complex field of lipidomics, explains Cristina Legido-Quigley, a Principal Investigator in Systems Medicine at Steno Diabetes Center Copenhagen in Denmark and at King’s College London.
Discovery allows scientists to index thousands of cells simultaneously, a 40-fold increase from the current method...
A type 1 diabetes genetic score can identify infants at risk for pre-symptomatic type 1 diabetes...
Scientists have found a genetic trigger that may improve the brain's ability to heal from a range of debilitating conditions...
A new computational method allows scientists to identify rare gene mutations in cancer cells with greater accuracy and sensitivity...
An international team of researchers has identified a new gene associated with the development of amyotrophic lateral sclerosis...
Researchers have identified two genes that are responsible for governing the replication of the Epstein-Barr virus, an infection that drives the growth of several types of cancer...
Neuroscientists have identified a specific molecular mechanism that appears to undermine the ability of neurons to properly incorporate changes driven by experience...
Next generation sequencing (NGS) has transformed biological research, invigorating the field of genomics, and has increased understanding of our genetic basis.
Researchers have uncovered new answers about why cells rapidly age in children with the rare and fatal disease, Hutchinson-Gilford Progeria Syndrome (HGPS).
A team of scientists in the UK and Italy has discovered a switch that instructs blood vessel cells to become blood stem cells during embryonic development in mice. These findings could aid research into new blood cell creation for transplants.
