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New 3-D mammary gland model may pave way for better understanding of breast cancer

A team of researchers from Cardiff University and Monash Biomedicine Discovery Institute has succeeded in creating a three-dimensional mammary gland model that will pave the way for a better understanding of the mechanisms of breast cancer.

27 Oct 2016

Study sheds new light on genetics behind essential tremor

You probably know someone who has it. It is the most common movement disorder, yet most people don't even know its name.

27 Oct 2016

Researchers identify existing drugs that appear to prevent aggressive subtype of pediatric brain tumors

More than 4,000 children and teens are diagnosed with brain cancer each year and the disease kills more children than any other cancer.

27 Oct 2016

Consortium develops new approach to understand causes of common cancers

Through the development of a novel, inexpensive genotyping microarray, the OncoArray, Dartmouth investigators have led a key collaborative research study that will revolutionize our knowledge of the causes of common cancers.

27 Oct 2016

Scientists identify commonly affected genes sets among people with three mental disorders

Studying brain tissue from deceased donors, Johns Hopkins scientists have found common groups of genes disrupted among people with schizophrenia, bipolar disorder and major depression.

26 Oct 2016

Researchers take significant step forward in genetic sex reprogramming research

An international team of researchers, led by the University of Granada, has taken a significant step forward on the research on 'genetic sex reprogramming', which is closer now, although it's still an utopia.

26 Oct 2016

Researchers receive grant to investigate how gut microbiome influences breast cancer

Researchers from the University of Illinois at Chicago and the University of Chicago have received a three-year, $900,000 Defense Department grant to investigate how the gut microbiome – the trillions of bacteria, viruses and other bugs that make our digestive systems their home – influences breast cancer.

26 Oct 2016

Gene therapy may be effective method for treating Niemann-Pick disease, type C1

For the first time, National Institutes of Health researchers have demonstrated in mice that gene therapy may be the best method for correcting the single faulty gene that causes Niemann-Pick disease, type C1 (NPC1).

26 Oct 2016

Researchers identify genetic risk factor for binge eating

Researchers have identified a gene (CYFIP2) associated with binge eating. This finding represents one of the first examples of a genome-wide significant genetic factor to be identified for binge eating in model organisms or humans.

26 Oct 2016

Research findings provide clues to possible genetic causes and potential treatments for autism

As a researcher at Harvard Medical School, Christopher W. Cowan, Ph.D., used to watch autistic kids come onto campus to attend a special school.

26 Oct 2016

Novel approach to analyzing brain structures may help predict progression of Alzheimer's disease

Use of a novel approach to analyzing brain structure that focuses on the shape rather than the size of particular features may allow identification of individuals in early presymptomatic stages of Alzheimer's disease.

26 Oct 2016

CSIC project aims to study new genetic regulatory mechanisms in pathogenic bacteria

A project led by the Spanish National Research Council (CSIC) researcher, Alejandro Toledo-Arana, at the Institute of Agro biotechnology (a centre shared between CSIC, the Public University of Navarra and The Regional Government of Navarra), is studying new genetic regulatory mechanisms in pathogenic bacteria.

26 Oct 2016

Researchers use new gene-editing system to hasten quest to cure HIV+ patients

Researchers at UC San Francisco and the academically affiliated Gladstone Institutes have used a newly developed gene-editing system to find gene mutations that make human immune cells resistant to HIV infection.

26 Oct 2016

Benefit and harm of tandem mass spectrometry screening for tyrosinaemia type 1 remain unclear

Tyrosinaemia type 1 is a rare, hereditary metabolic disease that, if left untreated, can already lead to serious liver and kidney damage in infancy.

25 Oct 2016

Researchers find two new genetic risk factors for AD among African Americans

Researchers have identified two new genetic risk factors for Alzheimer's disease (AD) among African Americans.

25 Oct 2016

Study offers clues to help develop new treatments for cannabis use disorder

A new paper in Biological Psychiatry reports that chronic cannabis users have reduced levels of an enzyme called fatty acid amide hydrolase (FAAH).

25 Oct 2016

Novel C. elegans worm strain could serve as tool for testing interventions against AD

Researchers from Yale-NUS College have partnered with researchers from the National University of Singapore and SingHealth Group to develop a novel Caenorhabditis elegans (C. elegans) worm strain which expresses an amyloid beta protein fragment involved in the development of human Alzheimer's Disease (AD).

25 Oct 2016

Kent State scientists receive new NIH grants for reproductive biology research

It could be argued that no science is more valuable to us than that which helps to ensure the survival of our species by solving the problems that challenge it.

25 Oct 2016

Study finds increased risk of pregnancy-associated stroke among young women

Pregnancy was not found to raise the risk of stroke in older women, according to a study from Columbia University Medical Center and NewYork-Presbyterian. In younger women, however, the risk of stroke was significantly higher for those who were pregnant.

25 Oct 2016

Researchers design small compounds with potential to correct mitochondrial dysfunction

Charcot-Marie-Tooth disease is an inherited disorder that leads to a gradual loss of motor neurons and, eventually, paralysis. The condition is caused by genetic mutations that disrupts cells' energy factories, called mitochondria.

25 Oct 2016

Genetic News and Research

New 3-D mammary gland model may pave way for better understanding of breast cancer

Study sheds new light on genetics behind essential tremor

Researchers identify existing drugs that appear to prevent aggressive subtype of pediatric brain tumors

Consortium develops new approach to understand causes of common cancers

Scientists identify commonly affected genes sets among people with three mental disorders

Researchers take significant step forward in genetic sex reprogramming research

Researchers receive grant to investigate how gut microbiome influences breast cancer

Gene therapy may be effective method for treating Niemann-Pick disease, type C1

Researchers identify genetic risk factor for binge eating

Research findings provide clues to possible genetic causes and potential treatments for autism

Novel approach to analyzing brain structures may help predict progression of Alzheimer's disease

CSIC project aims to study new genetic regulatory mechanisms in pathogenic bacteria

Researchers use new gene-editing system to hasten quest to cure HIV+ patients

Benefit and harm of tandem mass spectrometry screening for tyrosinaemia type 1 remain unclear

Researchers find two new genetic risk factors for AD among African Americans

Study offers clues to help develop new treatments for cannabis use disorder

Novel C. elegans worm strain could serve as tool for testing interventions against AD

Kent State scientists receive new NIH grants for reproductive biology research

Study finds increased risk of pregnancy-associated stroke among young women

Researchers design small compounds with potential to correct mitochondrial dysfunction

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