Gene News and Research

Latest Gene News and Research

Researchers develop new technology to inhibit the development of Alzheimer's disease

Researchers at the Technion-Israel Institute of Technology and their partners at Bar Ilan University have developed new technology to inhibit the development of Alzheimer's disease.

18 Nov 2019

Potential new therapy for progeria

Aging is a complex and natural process that affects all living organisms. As people age, normal biological processes are affecting, resulting in a decline in various organs and age-related conditions. Though aging is normal, some children affected by a disease called Progeria may age way faster than others.

18 Nov 2019

Tailored T-cells safe, may be effective in preventing and treating multiple viral infections

Tailored T-cells specially designed to combat a half dozen viruses are safe and may be effective in preventing and treating multiple viral infections, according to research led by Children's National Hospital faculty.

18 Nov 2019

Teenage drinking increases risk of anxiety and alcohol problems in adulthood

A recent study suggests that teenage drinking may predispose a person to anxiety and alcohol abuse in later life.

18 Nov 2019

BGU researchers discover gene that causes nighttime atrial fibrillation

Genetic studies spanning three generations of a Persian Jewish family by researchers at Ben-Gurion University of the Negev. have identified a gene that causes nighttime atrial fibrillation (AFib).

18 Nov 2019

High-fat maternal diet can cause life-long changes in the fetal brain

A study team at MedUni Vienna’s Center for Brain Research has found that high-fat maternal diets can cause life-long changes in the brain of the unborn offspring.

18 Nov 2019

Study: Almost 10% of diverse Latino populations meet the criteria for mild cognitive impairment

A study of over 6,300 Latinos of Dominican, Central American, Cuban, Mexican Puerto Rican and South American heritage estimates that nearly 10% of middle-age and older Latinos in the U.S. meet the criteria for mild cognitive impairment.

18 Nov 2019

Sudden death due to heart disease – it could be in the genes

More than 220,000 American adults die suddenly of cardiac causes – a phenomenon called sudden cardiac death. Some sources put it as closer to 400,000. Both inexplicable and distressing, this has been the subject of a new study published in the Journal of the American College of Cardiology and presented at the American Heart Association’s scientific session.

17 Nov 2019

Experimental drug found to be effective at reducing bad cholesterol

Twice-yearly injections of an experimental cholesterol-lowering drug, inclisiran, were effective at reducing low-density lipoprotein (LDL) cholesterol, often called bad cholesterol, in patients already taking the maximum dose of statin drugs, according to data of the ORION-10 trial presented Saturday, Nov. 16, at the American Heart Association's Scientific Sessions 2019.

17 Nov 2019

Rare DNA variants linked to sudden cardiac death

Sudden cardiac death affects 220,000 U.S. adults annually, most of whom have no prior symptoms of a heart issue.

17 Nov 2019

UCLA Health pulmonologist describes the signs and symptoms of lung cancer

Nikki Moreno, a 42-year-old mother of two, was not expecting to hear she had advanced lung cancer when she ended up in the emergency room at the UCLA Medical Center, Santa Monica, last October. She hadn't been feeling well for over a year but didn't think too much of her symptoms.

15 Nov 2019

Yale-led study provides roadmap to discover new treatment for idiopathic pulmonary fibrosis

A Yale-led collaborative study boosts scientific understanding of how the lung disease idiopathic pulmonary fibrosis (IPF) progresses, providing a roadmap for researchers to discover new treatment targets for the disease.

15 Nov 2019

Research breakthrough may lead to new therapeutic targets for cancers

Computational modeling is the use of computers to simulate and study the behavior of complex systems. Computational approaches are widely adopted in the bioimedical sciences and can be used to sift through large volumes of complex data to extract recurrent patterns that may point to a disease's causes and effects.

15 Nov 2019

Study: 15,000 cases of hypophosphatasia potentially undetected in Spanish population

Hypophosphatasia (HPP) is a rare and serious hereditary disease that is potentially life-threatening and is caused by one or more mutations in the gene coding for alkaline phosphatase (ALPL). It is frequently misdiagnosed.

15 Nov 2019

Mining 'darkest' parts of the genome in cancer cells yields gold

Mining the rich uncharted territory of the genome or genetic material of a cancer cell has yielded gold for Princess Margaret scientists: new protein targets for drug development against prostate cancer.

15 Nov 2019

Broccoli's effects on kidney health may depend on individual's genetics

New research indicates that the benefits of a dietary compound on kidney health may depend on an individual's genetics. The findings, which appear in an upcoming issue of JASN, may be helpful for tailoring interventions to prevent or treat kidney disease.

15 Nov 2019

Key Alzheimer's gene variants act differently among Caribbean Hispanics based on ancestry

Researchers looking to uncover the mysteries of Alzheimer's disease have revealed new insights from old variants.

15 Nov 2019

Scientists reverse learning and memory deficits with drugs in animal model of Down syndrome

In a surprising finding using the standard animal model of Down syndrome (DS), scientists were able to correct the learning and memory deficits associated with the condition -- the leading genetic cause of cognitive disability and the most frequently diagnosed chromosomal disorder in the U.S. -- with drugs that target the body's response to cellular stresses.

15 Nov 2019

Non-coding enhancer DNA may be key for identifying genetic risk in neurological conditions

One might think that the primary cause of most genetically linked diseases comes from mutations in coding DNA -- alterations in coding regions of the genome that can lead directly to changes in the expression of particular proteins important for a healthy body.

14 Nov 2019

Altering malarial parasite genes to prevent malaria

Malaria is a mosquito-borne disease caused by the parasitic organism called Plasmodium, of which there are several types that cause the different kinds of malarial fever. This age-old infection still kills over 400,000 people every year, all over the world. A new study published in the journal Cell on November 14, 2019, shows how a simple tweaking of the genes of this organism could quite conceivably lead to the elimination of this disease altogether.

14 Nov 2019

Gene News and Research

Latest Gene News and Research

Researchers develop new technology to inhibit the development of Alzheimer's disease

Potential new therapy for progeria

Tailored T-cells safe, may be effective in preventing and treating multiple viral infections

Teenage drinking increases risk of anxiety and alcohol problems in adulthood

BGU researchers discover gene that causes nighttime atrial fibrillation

High-fat maternal diet can cause life-long changes in the fetal brain

Study: Almost 10% of diverse Latino populations meet the criteria for mild cognitive impairment

Sudden death due to heart disease – it could be in the genes

Experimental drug found to be effective at reducing bad cholesterol

Rare DNA variants linked to sudden cardiac death

UCLA Health pulmonologist describes the signs and symptoms of lung cancer

Yale-led study provides roadmap to discover new treatment for idiopathic pulmonary fibrosis

Research breakthrough may lead to new therapeutic targets for cancers

Study: 15,000 cases of hypophosphatasia potentially undetected in Spanish population

Mining 'darkest' parts of the genome in cancer cells yields gold

Broccoli's effects on kidney health may depend on individual's genetics

Key Alzheimer's gene variants act differently among Caribbean Hispanics based on ancestry

Scientists reverse learning and memory deficits with drugs in animal model of Down syndrome

Non-coding enhancer DNA may be key for identifying genetic risk in neurological conditions

Altering malarial parasite genes to prevent malaria

eBook: Using iPSCs models for human disease research and drug discovery eBook

Real-time Raman monitoring for pharmaceutical hot melt extrusion

Synthetic Psychedelics: A Growing Public Health Concern

How the Vutara VXL simplifies single-molecule imaging