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Brain protein plays a prominent role in the maintenance of chronic pain

A protein called RGS4 (Regulator of G protein signaling 4) plays a prominent role in the maintenance of long-term pain states and may serve as a promising new target for the treatment of chronic pain conditions, according to research conducted at the Icahn School of Medicine at Mount Sinai and published in print October 16, in The Journal of Neuroscience.

11 Oct 2019

Live-cell, genetically engineered pig skin used for temporary closure of a burn wound

Burn specialists at Massachusetts General Hospital announced today they have successfully used live-cell, genetically engineered pig skin (xenograft) for the temporary closure of a burn wound.

11 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

Simple way to effectively transport medication into the brain identified

For the first time, scientists have identified a simple way that can effectively transport medication into the brain - which could lead to improved treatments for neurological and neurodegenerative diseases.

11 Oct 2019

Blood test can improve diagnosis and monitoring of aortic aneurysms

It is the 'silent killer' that claimed the life of Albert Einstein and affects 1% of men over the age of 65, but researchers at the University of Dundee believe they may be able to reduce the number of fatalities caused by abdominal aortic aneurysms.

11 Oct 2019

Male and female mice show decreased exploratory behavior with age, study finds

Due to strain-specific behavioral idiosyncrasies, inbred mouse strains are suboptimal research models for behavioral aging studies.

11 Oct 2019

New genomics technique can be used to track down the causes of rare genetic diseases

A team led by a scientist at Scripps Research has invented a new genomics technique for tracking down the causes of rare genetic diseases.

11 Oct 2019

Genetic oscillator captures changes in gut microbiome growth patterns

For all the attention the human microbiome has been getting over the last few years, one aspect of such research rarely makes headlines: the difficulty of observing how it changes over time in response to various stimuli.

11 Oct 2019

New gene therapy for wet age-related macular degeneration is on the horizon

Gene therapy is showing promise for one of the most common causes of blindness. Data presented today shows that six patients with wet age-related macular degeneration have, so far, gone at least six months without the need for continued injections to control a disease that typically requires treatment every four to six weeks.

11 Oct 2019

Medical and surgical eye care experts gather in San Francisco for AAO 2019

More than 25,000 are expected to attend the American Academy of Ophthalmology's 123rd annual meeting, AAO 2019, from Oct. 12-15 at the Moscone Center in San Francisco.

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

New study finds genetic link for some forms of SIDS

A genetic link has now been found for some instances of Sudden Infant Death Syndrome, or SIDS. The new UW Medicine research study is the first to make an explainable link tracking the mechanism between a genetic anomaly and some forms of the devastating syndrome, which claims the lives of more than 3,000 infants a year.

11 Oct 2019

New tool records and tracks microbiome growth

Over the past years, the human microbiome has gained immense popularity due to its role in shaping one’s health. It is essential for human development, nutrition, and immunity. That’s why many studies have focused on how to improve one’s health by targeting or enhancing the microbiome.

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

Harvard University receives $20 million gift to establish new center for autism research

Autism and related disorders-a constellation of neurodevelopmental conditions affecting one in 59 children in the United States alone - have become one of modern medicine's most confounding mysteries.

11 Oct 2019

Structural biology reveals 3D structure of asthma-linked receptor

A new study has laid bare the structure of a protein receptor called the CysLT1 receptor that is implicated in a range of allergic and cardiovascular conditions as well as some types of cancer. Published in Science Advances, the paper shows how the researchers used structural biology techniques to accomplish this feat.

10 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

Study pinpoints a gene that allows chlamydia to pick up DNA from host environment

According to the Centers for Disease Control and Prevention, chlamydia trachomatis is the most commonly reported sexually transmitted bacterial disease in the U.S., totaling 1.7 million cases in 2017. Rates are highest among teenagers and young adults. Left untreated, chlamydia can cause blindness and sterility.

10 Oct 2019

Serum neurofilament levels can be used to differentiate between frontotemporal dementia and psychiatric disorders

Early symptoms of frontotemporal dementia are often confused with symptoms occurring in psychiatric disorders.

10 Oct 2019

Imperial scientists aim to re-engineer stump skin for more comfortable prosthetics

People who have had limbs removed often use false arms and legs, known as prosthetics, to improve mobility and independence - but 75 per cent of prosthetic-wearing amputees encounter problems like skin tears, ulceration, and blisters.

10 Oct 2019

Genetic News and Research

Brain protein plays a prominent role in the maintenance of chronic pain

Live-cell, genetically engineered pig skin used for temporary closure of a burn wound

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

Simple way to effectively transport medication into the brain identified

Blood test can improve diagnosis and monitoring of aortic aneurysms

Male and female mice show decreased exploratory behavior with age, study finds

New genomics technique can be used to track down the causes of rare genetic diseases

Genetic oscillator captures changes in gut microbiome growth patterns

New gene therapy for wet age-related macular degeneration is on the horizon

Medical and surgical eye care experts gather in San Francisco for AAO 2019

Jumping genes can contribute to rare childhood developmental disorders

New study finds genetic link for some forms of SIDS

New tool records and tracks microbiome growth

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

Harvard University receives $20 million gift to establish new center for autism research

Structural biology reveals 3D structure of asthma-linked receptor

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

Study pinpoints a gene that allows chlamydia to pick up DNA from host environment

Serum neurofilament levels can be used to differentiate between frontotemporal dementia and psychiatric disorders

Imperial scientists aim to re-engineer stump skin for more comfortable prosthetics

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

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