Genetics News and Research

Latest Genetics News and Research

New technique reveals how the brain responds to light signals received by the retina

In recent decades, scientists have learned a great deal about how different neurons connect and send signals to each other. But it's been difficult to trace the activity of individual nerve fibers known as axons, some of which can extend from the tip of the toe to the head.

15 Oct 2019

New molecular "clock" could help monitor life-altering development disorders in children

Scientists have developed a molecular "clock" that could reshape how pediatricians measure and monitor childhood growth and potentially allow for an earlier diagnosis of life-altering development disorders.

15 Oct 2019

Gene mutations in the ClC-2 chloride channel cause high blood pressure, kidney damage

When the adrenal gland produces too much aldosterone, this often leads to high blood pressure and kidney damage (hyperaldosteronism). It has only recently emerged that several patients harbor a mutation in the gene for the ClC-2 chloride channel.

15 Oct 2019

New UCL-developed mathematical model could help predict next Ebola outbreak

The next Ebola outbreak could be predicted using a new UCL-developed model that tracks how changes to ecosystems and human societies combine to affect the spread of the deadly infectious disease.

15 Oct 2019

Ophthalmologists honored at AAO 2019 for exceptional service in medical and surgical eye care

The American Academy of Ophthalmology is honoring ophthalmologists who have improved eye care for millions worldwide through their commitment to their patients and their profession. The honorees will be recognized during AAO 2019, the 123rd Annual Meeting of the American Academy of Ophthalmology.

15 Oct 2019

Advances in translational genetics unlocked by Bio-Rad technologies to be presented at ASHG 2019

Scientists will present 24 abstracts and three talks, highlighting research driven in part by Bio-Rad Laboratories' Droplet Digital PCR and single-cell ATAC-Seq (scATAC-Seq) technologies, at the 2019 American Society of Human Genetics Annual Meeting in Houston, October 15-19.

15 Oct 2019

Study suggesting that CRISPR babies are likely to die early has been retracted

A research paper that sparked concerns about the lifespan of China's first gene-edited babies has been retracted due to technical errors.

15 Oct 2019

New system can help the immune system spot and eliminate tumors

Cancer cells are masters at avoiding detection, but a new system developed by Yale scientists can make them stand out from the crowd and help the immune system spot and eliminate tumors that other forms of immunotherapies might miss, the researchers report Oct. 14 in the journal Nature Immunology.

14 Oct 2019

Cleveland Clinic-led researchers develop novel genetic-based epilepsy risk scores

An international team of researchers led by Cleveland Clinic has developed new genetic-based epilepsy risk scores which may lay the foundation for a more personalized method of epilepsy diagnosis and treatment.

14 Oct 2019

SOX9 broadly modifies the severity of Alagille syndrome liver disease in mice

Alagille syndrome is a rare pediatric genetic disorder that can affect the liver, heart, kidneys, blood vessels, skeleton and other tissues.

11 Oct 2019

$RESILIENT study tests benefit of ETA guided treatments for patients with advanced refractory cancers$

RESILIENT study tests benefit of ETA guided treatments for patients with advanced refractory cancers

RESILIENT was a single arm, open label, phase II/III study to test if label agnostic therapy regimens guided by Encyclopedic Tumor Analysis can offer meaningful clinical benefit for patients with relapsed refractory metastatic malignancies.

11 Oct 2019

Jumping genes can contribute to rare childhood developmental disorders

The largest study of its kind into childhood developmental disorders has discovered that jumping genes cause genetic changes in some patients with undiagnosed neurodevelopmental diseases.

11 Oct 2019

Researchers develop customized drug treatment to bypass patient’s unique mutation

An unprecedented case at Boston Children's Hospital shows that it's possible to do something that's never been done before: identify a patient's unique mutation, design a customized drug to bypass it, manufacture and test the drug, and obtain permission from the Food and Drug Administration (FDA) to begin treating the patient -- all in less than one year.

11 Oct 2019

Genetic mechanisms could serve as a road map for screening new drugs to prolong healthy lifespan

The discovery in the 1990s that a mutation in a single gene of an experimental worm could double its lifespan set off a stampede of research on the molecular biology of aging and triggered hopes that drug therapies or other interventions could be developed to extend healthy human lifespan. But as is often the case in science, the genetic regulation of aging is more complicated than it first appeared.

10 Oct 2019

Kazan University researchers study the genetics of nephropathia epidemica

This particular inquiry pertains to CCR5 - a gene which has lately been on the focuses of research worldwide. In particular, CCR5 deletion was used in China to perform the first ever genetic editing on human embryos. It's also known that a CCR5-Δ32 mutation can make people immune to HIV.

10 Oct 2019

Osteoarthritis has no cure, but symptoms can be managed

Osteoarthritis can't be ignored. On a grand scale, it is the most common form of arthritis (which actually isn't a specific disease but rather a general term for inflammation in a joint), accounting for more cases than all the other forms combined. It affects an estimated 31 million Americans and is a leading cause of disability among adults.

10 Oct 2019

Scientists identify strong genetic markers for PTSD

Post-traumatic stress disorder (PTSD) is the most commonly occurring and seriously debilitating disorder that happens when a person gets exposed to traumatic events, including sexual assault, combat, and natural disaster.

9 Oct 2019

Siblings of people with gambling disorder display increased impulsivity, risky decision-making

Biological siblings of people with gambling disorder also display markers of increased impulsivity and risk-taking, according to a new UBC psychology study. The findings, published today in Neuropsychopharmacology, suggest people with gambling disorder - a psychiatric term for serious gambling problems - may have pre-existing genetic vulnerabilities to the illness.

9 Oct 2019

New discovery brings scientists closer to developing an RSV vaccine

Scientists have made an important discovery that could lead to a vaccine that will protect against respiratory syncytial virus (RSV).

9 Oct 2019

Vaccine for deadly RSV could be on the way, scientists say

A vaccine for the common and sometimes deadly RSV (respiratory syncytial virus) has been elusive, but scientists say a new discovery puts them much closer to success.

9 Oct 2019

Genetics News and Research

Latest Genetics News and Research

New technique reveals how the brain responds to light signals received by the retina

New molecular "clock" could help monitor life-altering development disorders in children

Gene mutations in the ClC-2 chloride channel cause high blood pressure, kidney damage

New UCL-developed mathematical model could help predict next Ebola outbreak

Ophthalmologists honored at AAO 2019 for exceptional service in medical and surgical eye care

Advances in translational genetics unlocked by Bio-Rad technologies to be presented at ASHG 2019

Study suggesting that CRISPR babies are likely to die early has been retracted

New system can help the immune system spot and eliminate tumors

Cleveland Clinic-led researchers develop novel genetic-based epilepsy risk scores

SOX9 broadly modifies the severity of Alagille syndrome liver disease in mice

RESILIENT study tests benefit of ETA guided treatments for patients with advanced refractory cancers

Jumping genes can contribute to rare childhood developmental disorders

Researchers develop customized drug treatment to bypass patient’s unique mutation

Genetic mechanisms could serve as a road map for screening new drugs to prolong healthy lifespan

Kazan University researchers study the genetics of nephropathia epidemica

Osteoarthritis has no cure, but symptoms can be managed

Scientists identify strong genetic markers for PTSD

Siblings of people with gambling disorder display increased impulsivity, risky decision-making

New discovery brings scientists closer to developing an RSV vaccine

Vaccine for deadly RSV could be on the way, scientists say

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