Genome News and Research

RSS

Study shows an unusual mechanism could have thwart the invasion of human genome by junk DNA

In the January 7th edition of Communications Biology, researchers at InsideOutBio argue that an unusual form of DNA with a reverse twist may have helped thwart the invasion of the human genome by junk DNA.

11 Jan 2019

Staphylococcus aureus: Study describes development of resistance to antibiotic for the first time

The Staphylococcus aureus bacterium is one of the commonest pathogens and can even cause sepsis. The new antibiotic dalbavancin is very effective against many bacterial pathogens.

10 Jan 2019

New biomarker may help better predict outcomes in patients with HPV-related head and neck cancers

By analyzing variations in the level of human papillomavirus (HPV) in head and neck cancers, researchers at The University of Texas MD Anderson Cancer Center have discovered a gene signature associated with treatment response and survival in patients.

10 Jan 2019

Novel biomarker links tumor progression to genome instability

Our DNA is under constant attack. The delicate molecule that contains our genetic information is extremely vulnerable to everything from environmental agents, such as radiation, to the chemicals in the air we breathe and the food we eat.

10 Jan 2019

Viral replication not necessary to cause lethal disease by food-borne pathogen

The replication of a bacterial virus is not necessary to cause lethal disease in a mouse model of a food-borne pathogen called Enterohemorrhagic Escherichia coli, according to a study published January 10 in the open-access journal PLOS Pathogens by Sowmya Balasubramanian, John Leong and Marcia Osburne of Tufts University School of Medicine, and colleagues.

10 Jan 2019

NYSCF announce partnership with Ngene to develop new disease treatments

The New York Stem Cell Foundation Research Institute today announced a partnership with Ngene Therapeutics Inc. to develop new disease treatments that leverage human stem cell research and novel gene editing techniques.

10 Jan 2019

NorthShore and Color partner to deliver the power of genomics in routine primary care

NorthShore University HealthSystem and Color today announced a groundbreaking partnership to deliver the power of genomics to routine primary care at population scale.

9 Jan 2019

Researchers identify and overcome barrier in CRISPR gene editing to treat muscular dystrophy

The gene editing technique known as CRISPR is a revolutionary approach to treating inherited diseases. However, the tool has yet to be used to effectively treat long-term, chronic conditions.

9 Jan 2019

Genetic variations may influence whether vitamin E decreases or increases cancer risk

Almost half of all Americans take a vitamin supplement, and yet many large-scale, placebo-controlled clinical trials of various supplements have found little or no benefit.

8 Jan 2019

Scientists identify evolutionary formula for monogamy

U.S. biologists have conducted a study showing that the evolution of a universal transcriptomic code underlies monogamous behavior in various species of vertebrates.

8 Jan 2019

PAC1R mutation in children with autism may be linked to severity of social problems

A mutation of the gene PAC1R may be linked to the severity of social deficits experienced by kids with autism spectrum disorder, finds a study from a multi-institutional research team led by Children's faculty.

8 Jan 2019

Scientists identify new bat-borne virus related to Ebola

Researchers from Singapore's Duke-NUS Medical School, in collaboration with scientists in China, have identified and characterized a new genus of filovirus from a Rousettus bat in China. Their findings were published in the journal Nature Microbiology.

7 Jan 2019

Scientists highlight lack of diversity in genomic studies

A growing number of genomic studies have generated important discoveries regarding human health and behavior, but new research from the University of Oxford suggests that scientific advancement is limited by a lack of diversity.

7 Jan 2019

Research reveals factors at play in genetic incompatibility of different species

Most evolutionary biologists distinguish one species from another based on reproductivity: members of different species either won't or can't mate with one another, or, if they do, the resulting offspring are often sterile, unviable, or suffer some other sort of reduced fitness.

4 Jan 2019

Bulldogs' screw tails linked to rare inherited syndrome in humans

With their small size, stubby faces and wide-set eyes, bulldogs, French bulldogs and Boston terriers are among the most popular of domestic dog breeds. Now researchers at the University of California, Davis, School of Veterinary Medicine have found the genetic basis for these dogs' appearance, and linked it to a rare inherited syndrome in humans.

3 Jan 2019

Researchers reveal cause of possible genetic problems in mitochondria

A group of researchers from the Andalusian Centre for Molecular Biology and Regenerative Medicine has revealed the importance of eliminating any excess of defective products that might have accumulated in the mitochondria, as its presence generates mitochondrial instability and information loss on the mitochondrial genome.

3 Jan 2019

Researchers identify genes that drive male-female brain differences, trigger initiation of puberty

Researchers have identified a group of genes that induces differences in the developing brains of male and female roundworms and triggers the initiation of puberty, a genetic pathway that may have the same function in controlling the timing of sual maturation in humans.

3 Jan 2019

Nature-based antibiotic molecules for treatment of infections

New developments in antimicrobial peptides (AMPs) with antibiofilm properties are rapidly materializing.

2 Jan 2019

Study provides new insights into how genes are activated

In a study in Nature, researchers at Karolinska Institutet present a new method for analyzing how instructions in the genome control how our genes are activated in individual cells.

2 Jan 2019

Scientists solve mystery of Yemen cholera epidemic

The most likely source of the cholera epidemic in Yemen has been discovered by scientists. Through the use of genomic sequencing, scientists at the Wellcome Sanger Institute and Institut Pasteur estimate the strain of cholera causing the current outbreak in Yemen - the worst cholera outbreak in recorded history - came from Eastern Africa and entered Yemen with the migration of people in and out of the region.

2 Jan 2019

Genome News and Research

Study shows an unusual mechanism could have thwart the invasion of human genome by junk DNA

Staphylococcus aureus: Study describes development of resistance to antibiotic for the first time

New biomarker may help better predict outcomes in patients with HPV-related head and neck cancers

Novel biomarker links tumor progression to genome instability

Viral replication not necessary to cause lethal disease by food-borne pathogen

NYSCF announce partnership with Ngene to develop new disease treatments

NorthShore and Color partner to deliver the power of genomics in routine primary care

Researchers identify and overcome barrier in CRISPR gene editing to treat muscular dystrophy

Genetic variations may influence whether vitamin E decreases or increases cancer risk

Scientists identify evolutionary formula for monogamy

PAC1R mutation in children with autism may be linked to severity of social problems

Scientists identify new bat-borne virus related to Ebola

Scientists highlight lack of diversity in genomic studies

Research reveals factors at play in genetic incompatibility of different species

Bulldogs' screw tails linked to rare inherited syndrome in humans

Researchers reveal cause of possible genetic problems in mitochondria

Researchers identify genes that drive male-female brain differences, trigger initiation of puberty

Nature-based antibiotic molecules for treatment of infections

Study provides new insights into how genes are activated

Scientists solve mystery of Yemen cholera epidemic

The art of CRISPR: The power and promise of gene editing eBook

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

Latest News