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Study shows misfiring brain cells can create swallowing problems in children with neurodevelopmental disorders

According to neuroscientists, misfiring brain cells that regulate vital parts of the tongue and mouth might be creating swallowing problems in kids.

2 Sep 2020

New method accurately detects single gene mutation in a pool of 10,000 cells

Rare genetic mutations occurring in cells cannot be detected by existing sequencing techniques because these methods do not have the required sensitivity.

1 Sep 2020

Researchers explore the structure and dynamics of biological nanomachine

Cells that are infected by a virus or carry a carcinogenic mutation, for example, produce proteins foreign to the body.

31 Aug 2020

Largely ignored 'housekeeping' gene plays unexpected role in neurological diseases

Within cells, molecules known as transfer RNAs, or "tRNAs," play an important but unglamorous workhorse role in keeping the genetic translation process moving along from codes of DNA to functional proteins.

27 Aug 2020

Re-designed natural enzyme shows promise in promoting the regrowth of nerve tissue injury

A team of researchers from University of Toronto Engineering and the University of Michigan has redesigned and enhanced a natural enzyme that shows promise in promoting the regrowth of nerve tissue following injury.

From University of Toronto 25 Aug 2020

Lipid-based nanoparticles can help treat genetic disorders

Introducing genetic material into the body to treat diseases can work, but making sure that those materials are safely sent to the right location is complicated.

24 Aug 2020

Programmable DNA nanoswitches can rapidly detect emerging viruses, including SARS-CoV-2

Programmable DNA nanoswitches that bind to viral RNA in human body fluids may provide an inexpensive platform to rapidly detect a wide variety of emerging viruses, including SARS-CoV-2, according to a new study.

24 Aug 2020

Genetic background influences cancer risk in individuals with single-gene variants

Life can change dramatically when someone learns they are genetically predisposed to a disease, such as a condition called familial hypercholesterolemia, where a mutated gene can lead to elevated cholesterol and increased risk for a premature heart attack.

21 Aug 2020

Study investigates how Ebola virus adapts to bat and human cells

A new study by researchers from The University of Texas Medical Branch at Galveston uncovered new information on why the Ebola virus can live within bats without causing them harm, while the same virus wreaks deadly havoc to people.

19 Aug 2020

RNA-based therapeutic approach could be used to cure hereditary diseases

Short RNA molecules can be used as medication. Their effectiveness is based on the genetic information they carry: therapeutic RNA can bind to the body's own RNA and thus influence how it functions.

19 Aug 2020

'Survival of the fittest': How meiotic drivers shape the evolution of gamete formation

It can be hard to dispute the common adage 'survival of the fittest'. After all, "most of the genes in the genome are there because they're doing something good," says Sarah Zanders, PhD, assistant investigator at the Stowers Institute for Medical Research

18 Aug 2020

Genome analysis helps identify 568 cancer driver genes

Analysis of the genomes of 28,000 tumors from 66 types of cancer has led to the identification of 568 cancer driver gene.

18 Aug 2020

Detection of cancer using different kind of liquid biopsy

Because cancer is easier to successfully treat when it's caught early, a major goal in cancer research is to develop new ways to find tumors at early stages, before they start to spread. One approach that's being studied are liquid biopsies.

14 Aug 2020

Researchers use supercomputer to gain new insights into hepatitis B virus

Researchers at the University of Delaware, using supercomputing resources and collaborating with scientists at Indiana University, have gained new understanding of the virus that causes hepatitis B and the "spiky ball" that encloses the virus's genetic blueprint.

14 Aug 2020

A genetic link discovered to predict treatment response for patients with rare, aggressive cancer

A Singapore team led by clinician-scientists and researchers from the National Cancer Centre Singapore (NCCS) discovered a genetic link to better predict treatment response for relapsed/refractory patients with natural- killer T-cell lymphoma (NKTCL), a highly aggressive form of blood cancer.

13 Aug 2020

Genetic analysis could be used to counsel parents after stillbirth

Columbia researchers have uncovered an array of new genes that cause stillbirth, significantly increasing the understanding of the condition's genetic foundations.

13 Aug 2020

Study reveals key biochemical processes that advance understanding of colorectal cancer

A new insight into cell signals that control cancer growth and migration could help in the search for effective anti-cancer drugs. A McGill-led study reveals key biochemical processes that advance our understanding of colorectal cancer, the third most common cancer among Canadians.

13 Aug 2020

Study may reduce transmissible cancer in Tasmanian devils, offers hope for treating human cancers

A rare, transmissible tumor has brought the iconic Tasmanian devil to the brink of extinction, but new research by scientists at Washington State University and the Fred Hutchinson Cancer Research Center in Seattle indicates hope for the animals' survival and possibly new treatment for human cancers.

10 Aug 2020

Test pinpoints which people with gonorrhea can be treated with ciprofloxacin

A test designed by UCLA researchers can pinpoint which people with gonorrhea will respond successfully to the inexpensive oral antibiotic ciprofloxacin, which had previously been sidelined over concerns the bacterium that causes the infection was becoming resistant to it.

10 Aug 2020

Gut dysbiosis in people with Huntington's disease may offer a potential target for future treatment

A world first clinical study of the gut microbiome in people with Huntington's disease (HD) has found that it is not just a disease of the brain, but also of the body.

7 Aug 2020

Mutation News and Research

Study shows misfiring brain cells can create swallowing problems in children with neurodevelopmental disorders

New method accurately detects single gene mutation in a pool of 10,000 cells

Researchers explore the structure and dynamics of biological nanomachine

Largely ignored 'housekeeping' gene plays unexpected role in neurological diseases

Re-designed natural enzyme shows promise in promoting the regrowth of nerve tissue injury

Lipid-based nanoparticles can help treat genetic disorders

Programmable DNA nanoswitches can rapidly detect emerging viruses, including SARS-CoV-2

Genetic background influences cancer risk in individuals with single-gene variants

Study investigates how Ebola virus adapts to bat and human cells

RNA-based therapeutic approach could be used to cure hereditary diseases

'Survival of the fittest': How meiotic drivers shape the evolution of gamete formation

Genome analysis helps identify 568 cancer driver genes

Detection of cancer using different kind of liquid biopsy

Researchers use supercomputer to gain new insights into hepatitis B virus

A genetic link discovered to predict treatment response for patients with rare, aggressive cancer

Genetic analysis could be used to counsel parents after stillbirth

Study reveals key biochemical processes that advance understanding of colorectal cancer

Study may reduce transmissible cancer in Tasmanian devils, offers hope for treating human cancers

Test pinpoints which people with gonorrhea can be treated with ciprofloxacin

Gut dysbiosis in people with Huntington's disease may offer a potential target for future treatment

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