Genetic News and Research

RSS

Coimbra Pediatric Hospital selects Congenica's Sapientia software platform for In2Genome project

Congenica, a global provider of clinical genomics interpretation software, today announced a new customer partnership with the Coimbra Paediatric Hospital, a leading paediatric hospital in Portugal and part of the Coimbra Hospital and University Centre.

7 Sep 2017

New microfluidic device offers insights on cancer metastasis

As cancer grows, it evolves. Individual cells become more aggressive and break away to flow through the body and spread to distant areas.

7 Sep 2017

Myriad Genetics introduces new precision medicine tool to enhance myRisk Hereditary Cancer test

Myriad Genetics, Inc., a leader in molecular diagnostics and personalized medicine, announced today that it has launched riskScore, a new clinically validated precision medicine tool to enhance its myRisk Hereditary Cancer test. riskScore quantifies a woman's risk of developing breast cancer by combining genetic markers throughout the genome with her family and clinical history.

7 Sep 2017

Study identifies genes that regulate gestational length and likelihood of preterm delivery

The genes that regulate gestational length and the likelihood of preterm delivery, have been identified in a study involving more than 50,000 women. An article in the New England Journal of Medicine (NEJM) describes the scientific breakthrough that can lead to improved health and survival among children.

7 Sep 2017

Novel compounds found to be highly effective in preventing transmission of malaria parasites

Significant headway has been made in controlling malaria. However, two vexing problems remain: currently available treatments are unable to block transmission of the parasite that causes the disease, and the parasite often becomes resistant to drugs.

7 Sep 2017

Newly-discovered mutation highlights complex genetic network that underpins blood disorder

Porphyrias, a group of eight known blood disorders, affect the body's molecular machinery for making heme, which is a component of the oxygen-transporting protein, hemoglobin. When heme binds with iron, it gives blood its hallmark red color.

7 Sep 2017

New DNA sequencing technology measures effects of thousands of sequences on gene activity

When a gene is switched on, various stretches of DNA nearby act as 'control dials', influencing the level of activity and the amount of gene product that is made.

7 Sep 2017

Exploration of human genetics reveals new targets to combat heart disease

Again and again, it's the rare among humans that help the rest of us. The exploration of human genetics is revealing new targets to combat heart disease among atypical variants. Mutations in genes that play a role in heart health are the inspiration for a cluster of new heart drugs.

7 Sep 2017

Controlling zinc transporter levels could be effective plan to combat pancreatic cancer, other diseases

When trace elements rise to toxic levels, bad things happen. Patients suffering from Alzheimer's and Parkinson's disease harbor significantly higher levels of zinc and iron in their brains than healthy patients.

6 Sep 2017

Study identifies genetic alterations with potential to promote aggressiveness of astrocytomas

Among the various types of cancerous brain tumors, 70% are astrocytomas. Fatal in as many as 90% of cases, astrocytomas originate in the largest and most numerous cells in the central nervous system, called astrocytes because of their star shape.

6 Sep 2017

Breakthrough research offers novel, non-invasive test to accurately diagnose Alzheimer's disease

In the largest and most conclusive study of its kind, researchers have analysed blood samples to create a novel and non-invasive way of helping to diagnose Alzheimer's disease and distinguishing between different types of neurodegenerative disorders.

6 Sep 2017

Study reveals how changes in gene can lead to blindness in middle age

Blindness study shows how gene causes middle-age sight loss. Chemical changes in the eye that can lead to blindness have been identified by scientists, a conference has heard.

6 Sep 2017

Genetic risk for obesity influenced by lifestyle, study shows

The risk for developing obesity is influenced by our lifestyle as well as our genes. In a new study from Uppsala University, researchers show that our genetic risk for obesity is not static, but is influenced by our lifestyle. Results from the study have been published in the scientific journal PLOS Genetics.

6 Sep 2017

Split-brain study using fruit fly provides better understanding of autism

A better understanding of the cause of autism may come from an unlikely source, neurological studies of the fruit fly.

6 Sep 2017

Research provides new insights into secret life of bacteria

Bacterial infections are the number one cause of death in hospital patients in the United States, and antibiotic-resistant bacteria are on the rise, causing tens of thousands of deaths every year.

6 Sep 2017

Scientists win new funding to speed up translation of MS research into practice

An innovative multiple sclerosis Research Fellowship designed to fast-track scientific knowledge into clinical practice has been awarded to two researchers at the University of Tasmania’s Menzies Institute for Medical Research.

6 Sep 2017

Ketogenic diet prolongs life and improves memory and physical functions in aged mice find researchers

A pair of new studies find that diets termed ketogenic that are classically low in carbohydrates can prolong life in adult male laboratory mice. In addition this ketogenic diet also preserves the memory functions as well as muscle masses of the aged mice that were fed on it. The mechanism behind this could be the fact that ketogenic diet induces protein acetylation in the mice liver and muscles.

5 Sep 2017

High levels of suPAR protein shown to be likely cause of kidney damage in children

High levels of a protein known as suPAR, which has been shown to be a marker and likely cause of kidney damage, is as reliably predictive in children as in adults, according to results of a study published online today in JAMA Pediatrics, a clinical publication of the American Medical Association.

5 Sep 2017

Novel, ultra-rare damaging genetic variants may contribute to eating disorders

By combining whole exome sequencing, machine learning, and network analysis, researchers have identified new, ultra-rare gene mutations within specific biological pathways that may contribute to eating disorders.

5 Sep 2017

Largest ever genetic study paves way for potential osteoporosis treatment

Scientists are honing in on a potential treatment for osteoporosis, after performing the largest ever genetic study of the common age-related bone-thinning disease.

5 Sep 2017

Genetic News and Research

Coimbra Pediatric Hospital selects Congenica's Sapientia software platform for In2Genome project

New microfluidic device offers insights on cancer metastasis

Myriad Genetics introduces new precision medicine tool to enhance myRisk Hereditary Cancer test

Study identifies genes that regulate gestational length and likelihood of preterm delivery

Novel compounds found to be highly effective in preventing transmission of malaria parasites

Newly-discovered mutation highlights complex genetic network that underpins blood disorder

New DNA sequencing technology measures effects of thousands of sequences on gene activity

Exploration of human genetics reveals new targets to combat heart disease

Controlling zinc transporter levels could be effective plan to combat pancreatic cancer, other diseases

Study identifies genetic alterations with potential to promote aggressiveness of astrocytomas

Breakthrough research offers novel, non-invasive test to accurately diagnose Alzheimer's disease

Study reveals how changes in gene can lead to blindness in middle age

Genetic risk for obesity influenced by lifestyle, study shows

Split-brain study using fruit fly provides better understanding of autism

Research provides new insights into secret life of bacteria

Scientists win new funding to speed up translation of MS research into practice

Ketogenic diet prolongs life and improves memory and physical functions in aged mice find researchers

High levels of suPAR protein shown to be likely cause of kidney damage in children

Novel, ultra-rare damaging genetic variants may contribute to eating disorders

Largest ever genetic study paves way for potential osteoporosis treatment

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

Latest News