Genomics

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A genetic variation makes sugar healthy for some Greenlanders

A genetic variation among some Greenlanders makes sugar healthy – significantly more than for most people.

23 Dec 2021

Researchers identify genes responsible for “spinach teeth”

People are generally familiar with “spinach teeth,” the harmless but gritty-chalky mouthfeel triggered because of a vegetable.

23 Dec 2021

Experts carry out the first major genetic study into cortical folding patterns

The brain’s surface, the cortex, is folded into an intricate pattern of grooves (sulci) and bumps (gyri). Individual differences in this pattern are associated with cognitive performance and brain disorders, however very little is known on how the “bumpiness and grooviness” of the cortex is determined.

23 Dec 2021

Revealing a Cell's Components through Artificial Intelligence

We speak to Professor Trey Ideker and Yue Qin about their latest in cell biology and how artificial intelligence could be used to discover new components within cells.

From UC San Diego 23 Dec 2021

Experts identify proteins that regulate dual processes

According to recent research, the protein UBR7 acts as a histone chaperone and controls histone re-deposition at certain sites at the time of DNA replication.

22 Dec 2021

Study provides evidence of human to animal transmission of SARS-CoV-2

A geographic and genetic analysis of variants of SARS-CoV-2 and related viruses in animals and humans might offer proof of interspecies transmission globally.

21 Dec 2021

DNA analyses reveals insights into ancestry, social organization of ancient people in the Nile Valley

The first genome-wide ancient human DNA data from Sudan reveals new insights into the ancestry and social organization of people who lived more than 1,000 years ago in the Nile Valley, an important genetic and cultural crossroads.

20 Dec 2021

Gene mutation for Parkinson's disease drives mislocalization of iron in activated microglia

A common gene mutation for Parkinson's disease drives mislocalization of iron in activated microglia, according to a new study publishing December 16th in the open-access journal PLOS Biology, by Mark Cookson of the National Institute on Aging and colleagues.

17 Dec 2021

Novel tool can efficiently map new genome sequences to a "pangenome"

Since the first sequencing of the human genome more than 20 years ago, the study of human genomes has relied almost exclusively on a single reference genome to which others are compared to identify genetic variations.

From University of California Santa Cruz 17 Dec 2021

Services to accelerate genome editing research

AMSBIO has expanded its range of custom gene editing services to complement its extensive portfolio of off-the-shelf CRISPR/Cas9 products.

From AMS Biotechnology 17 Dec 2021

Researchers develop novel technique to monitor remote immune mechanisms

The human immune system works hard to maintain an individual’s health and protect against viruses, bacteria, parasites, fungi, and cancerous cells.

17 Dec 2021

Study employs gene reactivation to treat Fragile X syndrome

Fragile X syndrome, or FXS—a principal genetic cause of autism—impacts around one in 6,000 females and one in 4,000 males.

17 Dec 2021

Adults with rare genetic changes have poorer health, says study

According to a study, grown-ups with certain genetic causes of mental health and other brain disorders had substantially increased rates of chronic disease.

17 Dec 2021

Lack of genetic switch results in malformations during embryonic development

A group of researchers identified how a minor disturbance in the activation mechanism of this gene triggers the origin of clubfoot, a common foot malformation.

17 Dec 2021

What Role do Genes Play in the Development of Antibodies?

In this interview, we speak to researchers from the University of Toronto about their latest research that investigated the role genes play in the development of antibodies.

From University of Toronto 16 Dec 2021

Study paves the way for more accurate prenatal genetic testing for congenital heart disease

One in every 100 babies is born with a congenital heart disease (CHD), and CHD is the major cause of death in newborns – however the genetic cause of these developmental disorders is not fully understood, hindering the development of accurate pre-natal genetic testing.

15 Dec 2021

Clemson-led research on unlocking the cotton genome bound for International Space Station

Clemson researcher Chris Saski admits sending the University's iconic Tiger Paw to space aboard a SpaceX Dragon spacecraft is, quite literally, "an out-of-this-world experience."

15 Dec 2021

Genetic mutation appears to be a predisposing factor for COPD independent of smoking

In 2019, the WHO positioned chronic obstructive pulmonary disease (COPD) third in the global ranking of causes of death.

From Institut Pasteur 15 Dec 2021

Detecting high-impact rare genetic variants in individuals with severe schizophrenia

New research published in the Proceedings of the National Academy of Sciences shows that examining genetic mutations in individuals with severe schizophrenia can improve the ability to detect disease-associated rare genetic variants.

15 Dec 2021

Gene writing helps develop advanced therapies safely and effectively

An international, multidisciplinary team of researchers from the Translational Synthetic Biology Laboratory at Pompeu Fabra University (Barcelona, Spain), led by Dr. Marc Güell, has published an article in the scientific journal Nature Communications.

14 Dec 2021

Genomics

A genetic variation makes sugar healthy for some Greenlanders

Researchers identify genes responsible for “spinach teeth”

Experts carry out the first major genetic study into cortical folding patterns

Revealing a Cell's Components through Artificial Intelligence

Experts identify proteins that regulate dual processes

Study provides evidence of human to animal transmission of SARS-CoV-2

DNA analyses reveals insights into ancestry, social organization of ancient people in the Nile Valley

Gene mutation for Parkinson's disease drives mislocalization of iron in activated microglia

Novel tool can efficiently map new genome sequences to a "pangenome"

Services to accelerate genome editing research

Researchers develop novel technique to monitor remote immune mechanisms

Study employs gene reactivation to treat Fragile X syndrome

Adults with rare genetic changes have poorer health, says study

Lack of genetic switch results in malformations during embryonic development

What Role do Genes Play in the Development of Antibodies?

Study paves the way for more accurate prenatal genetic testing for congenital heart disease

Clemson-led research on unlocking the cotton genome bound for International Space Station

Genetic mutation appears to be a predisposing factor for COPD independent of smoking

Detecting high-impact rare genetic variants in individuals with severe schizophrenia

Gene writing helps develop advanced therapies safely and effectively

Driving Support for Pharmaceutical Testing Through Continuous Innovation

From Memory to Metaplasticity: Unraveling the Brain's Secrets

Revolutionizing Mass Spectrometry: A Deep Dive into Plasmion’s SICRIT® Technology

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