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Current surveillance system does not quickly pick up most listeriosis cases in the EU, study reveals

More than half of the severe listeriosis cases in the European Union belong to clusters, many of which are not being picked up fast enough by the current surveillance system, suggests a new article published in Eurosurveillance.

20 Aug 2018

Study shows that rogue proteins may underlie some ALS and frontotemporal dementia cases

ALS -- amyotrophic lateral sclerosis -- is a neurodegenerative disease that attacks motor neurons in the brain and spinal cord, slowly robbing its victims of their ability to walk, talk, breathe and swallow.

20 Aug 2018

Scientists identify pathways that reveal insights into mechanism of lung cancer etiology

Lung cancer is the leading cause of preventable cancer death. A disease of complex origin, lung cancer is usually considered to result from effects of smoking and from multiple genetic variants.

17 Aug 2018

New CRISPR technology may help eliminate mutated gene sequence

In a new study in cells, University of Illinois researchers have adapted CRISPR gene-editing technology to cause the cell's internal machinery to skip over a small portion of a gene when transcribing it into a template for protein building.

17 Aug 2018

New project to combat DMD-related fibrosis receives major funding boost

Duchenne muscular dystrophy is one of the most common congenital diseases in the world, affecting one in 3,500 Canadian males. DMD is caused by mutations in the dystrophin gene that results in progressive muscle degeneration and there are currently no effective treatments for DMD.

17 Aug 2018

Female mosquitoes quickly evolve selective mating behavior when faced with threats

Certain female mosquitoes quickly evolve more selective mating behavior when faced with existential threats from other invasive mosquito species, with concurrent changes to certain genetic regions, according to new research from North Carolina State University.

17 Aug 2018

Research uncovers miscarriage cause, identifies potential targets for treatment

Tragic miscarriages for a couple have led to a discovery with potentially broad implications for future disease treatments, according to a team of researchers at the University of North Carolina School of Medicine. They identified a previously undiscovered gene mutation underlying hydrops fetalis – a fatal condition to fetuses due to fluid buildup in the space between organs.

16 Aug 2018

Study finds role of autoimmunity in development of COPD

Autoimmunity plays a role in the development of chronic obstructive pulmonary disease (COPD), according to a study led by Georgia State University and Vanderbilt University Medical Center that analyzed human genome information stored in Vanderbilt's DNA biobank.

16 Aug 2018

Experts advise against universal genomic screening of newborns

In a new report, experts at The Hastings Center advise against genomic screening of newborns, despite it's potential for providing life long personalized care.

16 Aug 2018

Report discusses whether all newborns should undergo genetic sequencing

As the cost of genome sequencing decreases, researchers and clinicians are debating whether all newborns should be sequenced at birth, facilitating a lifetime of personalized medical care.

16 Aug 2018

Tufts researchers win grant to study integration of genomic sequencing into neonatal care

Tufts Medical Center researchers have received a five-year grant award for more than $8 million from the National Center For Advancing Translational Sciences of the National Institutes of Health to study the integration of targeted genomic sequencing into neonatal diagnosis and care.

16 Aug 2018

Researchers develop novel statistical method to evaluate gene-to-gene interactions linked with cancer

Research led by Hui-Yi Lin, PhD, Associate Professor of Biostatistics at LSU Health New Orleans School of Public Health, has developed another novel statistical method for evaluating gene-to-gene interactions associated with cancer and other complex diseases.

15 Aug 2018

Study reveals role of RUNX proteins in DNA repair

A study by researchers from the Cancer Science Institute of Singapore at the National University of Singapore has revealed that RUNX proteins are integral to efficient DNA repair via the Fanconi Anemia pathway.

15 Aug 2018

Researchers move closer to finding potential soft spot in drug-resistant tuberculosis

Antibiotic-resistant tuberculosis is a public health threat. TB and other bacteria become resistant to antibiotics by evolving genetic changes over time, which they can do quite quickly because bacterial lifecycles are short.

15 Aug 2018

Scientists reveal role of 'junk DNA' in cancer dissemination

The more scientists explore so-called "junk" DNA, the less the label seems to fit.

14 Aug 2018

Study identifies potential guidance to treat gastric cancer patients

Researchers from Wake Forest Baptist Medical Center and Tianjin Medical University Cancer Institute and Hospital have discovered that gastric cancer tissue samples bearing mutation of a specific gene, MUC16, too are associated with higher tumor mutation loads.

14 Aug 2018

New method provides a 'big picture' of genetic influences on traits and diseases

Scientists at Johns Hopkins Bloomberg School of Public Health have developed a powerful method for characterizing the broad patterns of genetic contributions to traits and diseases. The new method provides a "big picture" of genetic influences that should be particularly helpful in designing future genetic studies and understanding potential for genetic risk prediction.

14 Aug 2018

Neural stem cells are the key to tail regeneration

Cut off a salamander's tail and, in a few weeks, a near-perfect replacement grows. Do the same to a lizard and a new tail will regrow, but it won't be the same as the original. By comparing tail regeneration between the two animals, researchers at the University of Pittsburgh School of Medicine found that stem cells in the spinal cord are the ultimate limiting factor.

14 Aug 2018

New genome analysis could identify people at higher risk of common deadly diseases

A research team at the Broad Institute of MIT and Harvard, Massachusetts General Hospital (MGH), and Harvard Medical School reports a new kind of genome analysis that could identify large fractions of the population who have a much higher risk of developing serious common diseases, including coronary artery disease, breast cancer, or type 2 diabetes.

13 Aug 2018

New test predicts the risk of serious disease months before symptoms appear

Researchers have developed a new genetic test that can identify people who are at an increased risk of serious disease, long before they develop any symptoms.

13 Aug 2018

Genome News and Research

Current surveillance system does not quickly pick up most listeriosis cases in the EU, study reveals

Study shows that rogue proteins may underlie some ALS and frontotemporal dementia cases

Scientists identify pathways that reveal insights into mechanism of lung cancer etiology

New CRISPR technology may help eliminate mutated gene sequence

New project to combat DMD-related fibrosis receives major funding boost

Female mosquitoes quickly evolve selective mating behavior when faced with threats

Research uncovers miscarriage cause, identifies potential targets for treatment

Study finds role of autoimmunity in development of COPD

Experts advise against universal genomic screening of newborns

Report discusses whether all newborns should undergo genetic sequencing

Tufts researchers win grant to study integration of genomic sequencing into neonatal care

Researchers develop novel statistical method to evaluate gene-to-gene interactions linked with cancer

Study reveals role of RUNX proteins in DNA repair

Researchers move closer to finding potential soft spot in drug-resistant tuberculosis

Scientists reveal role of 'junk DNA' in cancer dissemination

Study identifies potential guidance to treat gastric cancer patients

New method provides a 'big picture' of genetic influences on traits and diseases

Neural stem cells are the key to tail regeneration

New genome analysis could identify people at higher risk of common deadly diseases

New test predicts the risk of serious disease months before symptoms appear

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

Lab Matters host Harriet Gould on building a more connected lab community

The Critical Role of Sample Storage in Drug Discovery and Development

Advancing Neuroscience Research Through Collaboration and Patient-Centered Innovation

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