Genetics News and Research

Latest Genetics News and Research

Scientists identify mutational signatures in ovarian cancer

Scientists have identified distinct patterns of genetic mutation among patients with ovarian cancer that could help them personalise treatment in the future.

14 Aug 2018

Researchers transform research tool to study neuronal function

Puzzled by their experimental results, a team of scientists from Baylor College of Medicine and Texas Children's Hospital investigated why a research tool that was expected to suppress neuronal activity actually was stimulating it.

14 Aug 2018

New study focuses on promise of gene therapy for Amish nemaline myopathy

A new comprehensive natural history study about Amish nemaline myopathy in the Old Order Amish population focuses on the promise of gene therapy for this lethal disorder.

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

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

Altered nitrogen metabolism may contribute to emergence of new cancer mutations

Nitrogen is a basic building block of all the body's proteins, RNA and DNA, so cancerous tumors are greedy for this element. Researchers at the Weizmann Institute of Science, in collaboration with colleagues from the National Cancer Institute and elsewhere, have now shown that in many cancers, the patient's nitrogen metabolism is altered, producing detectable changes in the body fluids and contributing to the emergence of new mutations in cancerous tissue.

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

Researchers develop revolutionary zebrafish model to gain more insight into bone diseases

Although much scientific research has been done into the development of the skeleton, the underlying mechanisms that drive the formation and maintenance of our bones are still not very well understood, and research into the development of our bone remains of enormous importance.

13 Aug 2018

Scientists pinpoint the cause of a rare childhood seizure disorder

Scientists have developed a set of computational tools that pinpoint the cause of Early Infantile Epileptic Encephalopathy (EIEE), a rare childhood disorder.

13 Aug 2018

Genetically modified mosquitoes and special bed nets help tackle deadly diseases

Researchers at the Imperial College’s South Kensington campus have successfully created genetically modified mosquitoes that would stop them from multiplying and spreading dreaded diseases such as malaria, Dengue, Chikungunya and Zika that kill millions worldwide annually.

13 Aug 2018

Reduced levels of chaperone protein may have implications for development of Parkinson’s disease

Reduced levels of a chaperone protein might have implications for the development and progression of neurodegenerative diseases such as Parkinson's disease and Lewy body dementia, according to new research from investigators at the University of Alabama at Birmingham.

10 Aug 2018

Scientists uncover mechanisms responsible for development of fibrosis

Idiopathic pulmonary fibrosis is an incurable lung disease of unknown origin with limited treatment options. Research suggests that the signaling molecule WNT5A plays a key role in the pathogenic process.

10 Aug 2018

Study yields new insights into why the system needs sleep

Sleep is essential for brain functionality and overall health but understanding how sleep delivers its beneficial effects remains largely unknown. In an article publishing on August 9 in the open access journal PLOS Biology, Shanaz Diessler and Maxime Jan at the University of Lausanne and the SIB Swiss Institute of Bioinformatics (Switzerland), sleep researchers are exploring new and unbiased approaches that can take sleep to a systems level.

10 Aug 2018

Helmholtz Zentrum München appoints Professor Matthias Tschöp as new CEO

Professor Matthias Tschöp, MD, has been appointed the new CEO of Helmholtz Zentrum München. He took over from Professor Günther Wess, who led the center for the past 13 years.

10 Aug 2018

OGT announces launch of updated SureSeq Interpret NGS analysis software

Oxford Gene Technology, The Molecular Genetics Company, has announced the launch of the eagerly-anticipated update to its SureSeq Interpret software, included with purchases of SureSeq NGS panels.

From Oxford Gene Technology 10 Aug 2018

Researchers describe underlying mechanisms of congestive heart failure

Congestive heart failure is a terminal disease that affects nearly 6 million Americans. Yet its management is limited to symptomatic treatments because the causal mechanisms of congestive heart failure -- including its most common form, ischemic cardiomyopathy -- are not known.

10 Aug 2018

New discovery could pave way for improved leukemia treatment

Previous research has revealed that patients with acute myeloid leukemia who also have a particular mutation in a gene called NPM1 have a higher rate of remission with chemotherapy. About one-third of leukemia patients possess this favorable mutation, but until now, how it helps improve outcomes has remained unknown.

9 Aug 2018

Researchers discover genetic mutation underlying debilitating childhood brain disorder

Ashleigh Schaffer, PhD, assistant professor of genetics at Case Western Reserve University School of Medicine, and a team of global genetics experts have discovered a genetic mutation and the faulty development process it triggers, causing a debilitating brain-based disorder in children.

9 Aug 2018

Dietary carbohydrates linked to increased risk of osteoarthritis

Do your knees ache? According to new findings from the Oklahoma Medical Research Foundation, your diet could be a culprit.

9 Aug 2018

New 3D-printed device could help spinal cord injury patients regain some function

Engineers and medical researchers at the University of Minnesota have teamed up to create a groundbreaking 3D-printed device that could someday help patients with long-term spinal cord injuries regain some function.

9 Aug 2018

Genetics News and Research

Latest Genetics News and Research

Scientists identify mutational signatures in ovarian cancer

Researchers transform research tool to study neuronal function

New study focuses on promise of gene therapy for Amish nemaline myopathy

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

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

Altered nitrogen metabolism may contribute to emergence of new cancer mutations

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

Researchers develop revolutionary zebrafish model to gain more insight into bone diseases

Scientists pinpoint the cause of a rare childhood seizure disorder

Genetically modified mosquitoes and special bed nets help tackle deadly diseases

Reduced levels of chaperone protein may have implications for development of Parkinson’s disease

Scientists uncover mechanisms responsible for development of fibrosis

Study yields new insights into why the system needs sleep

Helmholtz Zentrum München appoints Professor Matthias Tschöp as new CEO

OGT announces launch of updated SureSeq Interpret NGS analysis software

Researchers describe underlying mechanisms of congestive heart failure

New discovery could pave way for improved leukemia treatment

Researchers discover genetic mutation underlying debilitating childhood brain disorder

Dietary carbohydrates linked to increased risk of osteoarthritis

New 3D-printed device could help spinal cord injury patients regain some function

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