Gene News and Research

Latest Gene News and Research

Researchers develop new technique to image cell populations and genetic contents

Researchers have come up with a new way to image cell populations and their genetic contents. Their study, appearing June 20 in the journal Cell, describes how a technique called DNA microscopy helps illuminate the spatial organization of genetic material within cells and tissues without specialized, expensive optical equipment.

24 Jun 2019

New study could change our understanding of how stem cells differentiate

A pioneering new study led by Florida State University biologists could fundamentally change our understanding of how embryonic stem cells differentiate into specific cell types.

24 Jun 2019

Study identifies proteins that interact with processes regulating gene p53

Scientists at VCU Massey Cancer Center have discovered that the loss of a protein called DBC1 in breast cancer cells leads to the dysregulation of normal anti-cancer functions, contributing to cancer cell growth and resistance to therapies.

24 Jun 2019

FDA expands approval of cystic fibrosis treatment to include pediatric patients as young as 6 years old

The U.S. Food and Drug Administration today expanded the indication for Symdeko (a combination of tezacaftor/ivacaftor) tablets for treatment of pediatric patients ages 6 years and older with cystic fibrosis who have certain genetic mutations.

22 Jun 2019

New mutation discovered in the leptin gene

The global obesity epidemic is so far-reaching it now has an overarching name: globesity. Texas Biomed Staff Scientist Raul Bastarrachea, M.D., is part of a team that discovered a new mutation in the gene that regulates the key hormone suppressing hunger called leptin.

22 Jun 2019

Study reveals genetic signature of failed immune response to cancer

Our immune system is programmed to destroy cancer cells. Sometimes it has trouble slowing disease progression because it doesn't act quickly or strongly enough.

21 Jun 2019

Study offers new clues to autism's underlying biology

Over the past decade, autism spectrum disorder has been linked to mutations in a variety of genes, explaining up to 30 percent of all cases to date.

21 Jun 2019

Researchers develop model of intestinal infection that could advance vaccine development

The intestinal parasite Cryptosporidium, which causes a diarrheal disease, is very good at infecting humans. It's the leading cause of waterborne disease from recreational waters in the United States.

21 Jun 2019

Bad gene associated with sudden death in epilepsy and breathing problems

In sudden death in epilepsy, people stop breathing for no apparent reason and die. Now, a group of UConn neuroscientists have a lead as to why, they report in the journal eLife.

21 Jun 2019

Scientists develop a stable platform to reprogram scar tissue into healthy heart cells

Every year 790,000 Americans suffer a heart attack, which leaves damaged scar tissue on the heart and limits its ability to beat efficiently.

21 Jun 2019

People with family history of Alzheimer's do not perform as well as their peers

Results from a study of nearly 60,000 individuals suggest those at higher risk of developing Alzheimer's disease due to family history may demonstrate changes in memory performance as early as their 20s.

21 Jun 2019

New genetic marker linked to higher risk of premenopausal breast cancer

University of Alberta researchers have added a new genetic marker to the breast cancer map, helping to expand the list of genetic mutations clinicians can watch for in cancer screenings.

20 Jun 2019

Scientists identify early signs of Parkinson’s disease years before symptoms develop

Scientists have identified the earliest signs of Parkinson’s disease in the brain up to 20 years before patients present with any symptoms.

20 Jun 2019

Dangerous brain parasite invades host cell, maintains steady nutrient supply

A team of researchers has found that a dangerous type of parasite that affects the brain, maintains a stable supply of essential nutrients as it replicates in the host cell. In an unexpected turn of events, the body itself delivers food to the harmful predator.

20 Jun 2019

Researcher employs people who inject drugs to study factors influencing acquisition of HIV

In recent years, the HIV infection rate in Estonia has continued to be around 200 new cases each year, which is still one of the highest incidence rates per 100,000 inhabitants in Europe.

20 Jun 2019

New laser treatment aims to stop the development of age-related vision loss

There are 200 million people in the world living with AMD, and in approximately a fifth of these cases, the disease progresses to an advanced stage, leading to visual impairment.

19 Jun 2019

Dietary supplement improves neuronal function of a patient with atypical Rett syndrome

A multicentric translational research study carried out by groups of the Bellvitge Biomedical Research Institute, Sant Joan de Déu Hospital, the University of Barcelona, Hospital Clínic, the University of Vic, Sant Pau i la Santa Creu Hospital, the Rare Diseases Networking Biomedical Research Centre and the Commissariat à l'Énergie Atomique, has demonstrated the potential of the amino acid L-serine - administered as a dietary supplement - to improve the neuronal function of a patient with a mutation of glutamate receptors associated with atypical Rett syndrome with severe encephalopathy.

19 Jun 2019

Scientists pinpoint cause of fatal respiratory disorder that turns babies' lips and skin blue

Scientists used a gene editing method called CRISPR/Cas9 to generate mice that faithfully mimic a fatal respiratory disorder in newborn infants that turns their lips and skin blue. The new laboratory model allowed researchers to pinpoint the ailment's cause and develop a potential and desperately needed nanoparticle-based treatment.

19 Jun 2019

Three signs of real progress against sickle cell disease

A decade ago, the United Nations declared June 19 to be World Sickle Cell Awareness Day- and for good reason.

19 Jun 2019

Researchers identify genes linked with survival in children with biliary atresia

Scientists at Cincinnati Children's Hospital Medical Center have identified an expression pattern of 14 genes at the time of diagnosis that predicts two year, transplant-free survival in children with biliary atresia – the most common diagnosis leading to liver transplants in children.

19 Jun 2019

Gene News and Research

Latest Gene News and Research

Researchers develop new technique to image cell populations and genetic contents

New study could change our understanding of how stem cells differentiate

Study identifies proteins that interact with processes regulating gene p53

FDA expands approval of cystic fibrosis treatment to include pediatric patients as young as 6 years old

New mutation discovered in the leptin gene

Study reveals genetic signature of failed immune response to cancer

Study offers new clues to autism's underlying biology

Researchers develop model of intestinal infection that could advance vaccine development

Bad gene associated with sudden death in epilepsy and breathing problems

Scientists develop a stable platform to reprogram scar tissue into healthy heart cells

People with family history of Alzheimer's do not perform as well as their peers

New genetic marker linked to higher risk of premenopausal breast cancer

Scientists identify early signs of Parkinson’s disease years before symptoms develop

Dangerous brain parasite invades host cell, maintains steady nutrient supply

Researcher employs people who inject drugs to study factors influencing acquisition of HIV

New laser treatment aims to stop the development of age-related vision loss

Dietary supplement improves neuronal function of a patient with atypical Rett syndrome

Scientists pinpoint cause of fatal respiratory disorder that turns babies' lips and skin blue

Three signs of real progress against sickle cell disease

Researchers identify genes linked with survival in children with biliary atresia

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