Genetic News and Research

RSS

TGen study identifies potential new drug targets to alleviate pain in pancreatic cancer patients

The Translational Genomics Research Institute has discovered potential drug targets to reduce pain in pancreatic cancer patients.

7 Nov 2016

Scientists identify new way to block action of genetic mutations found in most cancers

Researchers at the University of Illinois at Chicago have identified a new way to block the action of genetic mutations found in nearly 30 percent of all cancers.

7 Nov 2016

Proteins in the blood of children can predict risk for incipient type 1 diabetes

Certain proteins in the blood of children can predict incipient type 1 diabetes, even before the first symptoms appear. A team of scientists at the Helmholtz Zentrum München, partners in the German Center for Diabetes Research, reported these findings in the 'Diabetologia' journal.

7 Nov 2016

New treatment with therapeutic short interfering RNA could help thwart cancer

In the fight against cancer, doctors dish out combination-blows of surgery, chemotherapy and other drugs to beat back a merciless foe. Now, scientists have taken early steps toward adding a stinging punch to clinicians' repertoire.

7 Nov 2016

UNC scientists find clue that may help explain why people differ in ability to survive arterial blockages

Researchers at the University of North Carolina School of Medicine have found a major clue that may explain why some people sustain relatively little damage from strokes or heart attacks despite severe arterial blockages.

7 Nov 2016

Vaccine-related rubella virus causes harm in some patients with primary immunodeficiency disorders

Some patients with rare primary immunodeficiency disorders may be at risk for infection by rubella virus, and possibly serious skin inflammation, after receiving the rubella vaccine, usually administered as part of the measles-mumps-rubella (MMR) vaccine.

7 Nov 2016

Researchers map two gene mutations that trigger retinal disease leading to macular degeneration

Two gene mutations that trigger a retinal disease that causes blindness in one in 5,000 males have been mapped, leading to the potential for new therapeutic treatments.

7 Nov 2016

E-cigarette vapour does not induce DNA mutations linked to tobacco smoke exposures

E-cigarette vapour does not induce DNA mutations commonly observed with tobacco smoke exposures in lab-based tests.

7 Nov 2016

Age, genetic disposition play important role in susceptibility to Lyme disease

People react very differently to an infection with the Borrelia bacterium that causes Lyme disease.

7 Nov 2016

New study examines genetic factors underlying poor tolerance to shift work

Some people adapt easily to shift work, but not everyone can handle constant disruptions to their daily rhythm. Finnish researchers have now found that a melatonin receptor gene influences tolerance to shift work.

5 Nov 2016

WSU researcher finds a way to reduce development of cancer cells

A Washington State University researcher has developed a way to reduce the development of cancer cells that are an infrequent but dangerous byproduct of gene therapy.

5 Nov 2016

Smoking causes added mutations in DNA of lung cells

A paper published today in Science shows that smoking tobacco causes added mutations in the DNA of lung cells and in the DNA of other cells in the body. This is the first study to show the process by which smoking causes these cancers.

4 Nov 2016

Rutgers Cancer Institute researcher receives grant to explore cell pathway in triple-negative breast cancer

Rutgers Cancer Institute of New Jersey researcher Michael L. Gatza, PhD, has received a $200,000 V Scholar Grant from The V Foundation for Cancer Research to explore a cell pathway in triple-negative breast cancer.

4 Nov 2016

Ebola mutation increased infectivity

New research finds a genetic mutation in the Ebola virus that enabled it to target human cells more effectively during the recent Ebola epidemic.

4 Nov 2016

Genetic variation, environmental conditions can have significant impact on human health

Scientists at the Wayne State University School of Medicine's Center for Molecular Medicine and Genetics have shown for the first time the extent by which interactions between environmental exposures and genetic variation across individuals have a significant impact on human traits and diseases like diabetes, heart disease and obesity, strengthening the case for precision medicine initiatives.

4 Nov 2016

TB bacteria can be divided into generalists and specialists, study finds

Tuberculosis (TB) is a major global public health problem. Treatment often takes many months and till this day there is no effective vaccine. Various TB bacterial strains exist globally, with different geographical spread. Only the so-called Lineage 4 occurs on all continents.

4 Nov 2016

Llama antibodies can detect cerebral lesions that characterize Alzheimer's disease

The major challenge facing physicians treating Alzheimer's is the ability to detect markers of the disease as early as possible. These markers, located in the brain, are difficult to access, hampering diagnosis.

4 Nov 2016

Genetic mutation confers risk for development of Parkinson's disease earlier than usual

A collaboration of 32 researchers in seven countries, led by scientists at Mayo Clinic's campus in Florida, has found a genetic mutation they say confers a risk for development of Parkinson's disease earlier than usual.

3 Nov 2016

Researchers identify first two core genes that regulate deep sleep and dreaming

Researchers have identified the first two core genes that regulate the amount of deep sleep and dreaming, a key development they believe will lead to the discovery of a network of related genes controlling sleep.

3 Nov 2016

Researchers identify marker of aggressive disease for papillary thyroid cancer

A new discovery from University of Alberta scientists represents an important milestone in the fight against thyroid cancer. In a study published in EBioMedicine and recently presented at the American Thyroid Association annual meeting, the team has identified a marker of aggressive disease for papillary thyroid cancer, which comprises about 90 per cent of all thyroid cancers.

3 Nov 2016

Genetic News and Research

TGen study identifies potential new drug targets to alleviate pain in pancreatic cancer patients

Scientists identify new way to block action of genetic mutations found in most cancers

Proteins in the blood of children can predict risk for incipient type 1 diabetes

New treatment with therapeutic short interfering RNA could help thwart cancer

UNC scientists find clue that may help explain why people differ in ability to survive arterial blockages

Vaccine-related rubella virus causes harm in some patients with primary immunodeficiency disorders

Researchers map two gene mutations that trigger retinal disease leading to macular degeneration

E-cigarette vapour does not induce DNA mutations linked to tobacco smoke exposures

Age, genetic disposition play important role in susceptibility to Lyme disease

New study examines genetic factors underlying poor tolerance to shift work

WSU researcher finds a way to reduce development of cancer cells

Smoking causes added mutations in DNA of lung cells

Rutgers Cancer Institute researcher receives grant to explore cell pathway in triple-negative breast cancer

Ebola mutation increased infectivity

Genetic variation, environmental conditions can have significant impact on human health

TB bacteria can be divided into generalists and specialists, study finds

Llama antibodies can detect cerebral lesions that characterize Alzheimer's disease

Genetic mutation confers risk for development of Parkinson's disease earlier than usual

Researchers identify first two core genes that regulate deep sleep and dreaming

Researchers identify marker of aggressive disease for papillary thyroid cancer

Sequencing & Genomics: Elevating Science and Healthcare 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