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New research offers crucial step towards understanding cause of myopathy

Pioneering research using the tropical zebrafish could provide new insights into the genetic basis of myopathy, a type of human muscle disease.

6 Jul 2017

Female survivors of childhood cancer have high risk for ovarian condition that causes infertility

About 11 percent of females who survive childhood cancer have an ovarian condition that leaves them at risk for infertility, weaker bones and frail health as young adults, according to research from St. Jude Children's Research Hospital.

6 Jul 2017

Study: Personalized neoantigen vaccine stimulates strong anti-tumor response in melanoma patients

A personal cancer treatment vaccine that targets distinctive "neoantigens" on tumor cells has been shown to stimulate a potent, safe, and highly specific immune anti-tumor response in melanoma patients, report scientists from Dana-Farber Cancer Institute and the Broad Institute of MIT and Harvard.

5 Jul 2017

Discovery could impact understanding, treatment of autoimmune and inflammatory diseases

Scientists from the Research Institute of the McGill University Health Centre may have cracked the code to understanding the function of special cells called regulatory T Cells.

5 Jul 2017

Study reveals link between higher BMI and increased risk of cardiometabolic diseases

Results of a new study add to the evidence of an association between higher body mass index (BMI) and increased risk of cardiometabolic diseases such as hypertension, coronary heart disease, type 2 diabetes, according to a study published by JAMA Cardiology.

5 Jul 2017

Reducing DVT and leg ulcers through personalized compression socks

Professor Charles McCollum, who heads up the vascular studies unit, is a research vascular surgeon, and he developed four-layer bandaging technique, which is the gold standard treatment for healing up leg ulcers by compression.

5 Jul 2017

Mayo Clinic study: Patients with Parkinson's have higher risk of melanoma and vice versa

People with the movement disorder Parkinson's disease have a much higher risk of the skin cancer melanoma, and vice versa, a Mayo Clinic study finds.

5 Jul 2017

UC scientists develop new computerized tool to promote shared decision-making with CF patients

Physician-researchers at the University of Cincinnati have developed a computerized decision-making model to promote shared decision-making with cystic fibrosis patients.

4 Jul 2017

Study reveals higher number of eggs as determinants of IVF success

A higher number of eggs retrieved in an IVF treatment cycle is independently associated with more chromosomally normal embryos available for transfer, according to a new Australian study.

4 Jul 2017

Emory scientists show how same enzyme spurs Alzheimer's and Parkinson's disease

Alzheimer's disease and Parkinson's disease are not the same. They affect different regions of the brain and have distinct genetic and environmental risk factors.

4 Jul 2017

First systematic genomic analysis of patients with T-ALL may aid development of new therapies

A consortium including St. Jude Children's Research Hospital and the Children's Oncology Group has performed an unprecedented genomic sequencing analysis of hundreds of patients with T-lineage acute lymphoblastic leukemia (T-ALL).

4 Jul 2017

New technique to study genetic changes could enhance cancer diagnosis

Large-scale changes to the structure of the genome are often seen in cancer cells. Scientists at the Babraham Institute in Cambridge, UK, have found a way to detect these changes, which could enhance cancer diagnosis and aid the use of targeted treatments.

4 Jul 2017

High fat diet during pregnancy increases breast cancer susceptibility in female progeny, mice study finds

Feeding pregnant female mice a diet high in fat derived from common corn oil resulted in genetic changes that substantially increased breast cancer susceptibility in three generations of female offspring, reports a team of researchers led by scientists at Georgetown Lombardi Comprehensive Cancer Center.

3 Jul 2017

Finnish mothers carry rare gene variants that protect them from pre-eclampsia, study finds

Researchers at the University of Helsinki, in cooperation with two research groups in the United States, have discovered that some Finnish mothers carry rare gene variants that protect them from pre-eclampsia, also known as toxaemia of pregnancy.

3 Jul 2017

Researchers identify link between childhood psychiatric disorders and later risk of addictions

Children's health and well-being while growing up can be indicators of the potential health issues they may encounter years later.

3 Jul 2017

Live birth outcome affected by age of male partner, study shows

Men, unlike women, do not have a menopause or a predictable and detectable decline in their fertility. Female age is thus the dominant factor in predicting (or explaining) a couple's chance of conception, whether natural or assisted.

3 Jul 2017

NEI-funded research aims to prevent or reverse progression of cataracts

Research funded by the National Eye Institute aims to reverse progression of cataracts- the most common cause of blindness worldwide- or to prevent them from forming altogether.

30 Jun 2017

SmartPractice donates $50,000 to support TGen's development of liquid biopsies

In support of efforts to find better ways of diagnosing and monitoring breast cancer patients, SmartPractice today donated $50,000 to the Translational Genomics Research Institute.

30 Jun 2017

Wayne State researchers receive NIH grant to mimic benefits of exercise in sedentary patients

A team of researchers led by Robert Wessells, Ph.D., assistant professor of physiology in the School of Medicine at Wayne State University, has received a two-year, $423,500 grant from the National Institute on Aging of the National Institutes of Health for the project, "Octopamine mediates benefits of endurance exercise in Drosophila."

30 Jun 2017

Study indicates new element involved in genome instability

Genome instability is the main risk factor in the development of tumours in humans. Understanding how, where, when and why these mutations are produced in DNA is one of the great objectives of the global scientific community.

30 Jun 2017

Genetic News and Research

New research offers crucial step towards understanding cause of myopathy

Female survivors of childhood cancer have high risk for ovarian condition that causes infertility

Study: Personalized neoantigen vaccine stimulates strong anti-tumor response in melanoma patients

Discovery could impact understanding, treatment of autoimmune and inflammatory diseases

Study reveals link between higher BMI and increased risk of cardiometabolic diseases

Reducing DVT and leg ulcers through personalized compression socks

Mayo Clinic study: Patients with Parkinson's have higher risk of melanoma and vice versa

UC scientists develop new computerized tool to promote shared decision-making with CF patients

Study reveals higher number of eggs as determinants of IVF success

Emory scientists show how same enzyme spurs Alzheimer's and Parkinson's disease

First systematic genomic analysis of patients with T-ALL may aid development of new therapies

New technique to study genetic changes could enhance cancer diagnosis

High fat diet during pregnancy increases breast cancer susceptibility in female progeny, mice study finds

Finnish mothers carry rare gene variants that protect them from pre-eclampsia, study finds

Researchers identify link between childhood psychiatric disorders and later risk of addictions

Live birth outcome affected by age of male partner, study shows

NEI-funded research aims to prevent or reverse progression of cataracts

SmartPractice donates $50,000 to support TGen's development of liquid biopsies

Wayne State researchers receive NIH grant to mimic benefits of exercise in sedentary patients

Study indicates new element involved in genome instability

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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