Genes News and Research

RSS

UD researchers receive $1 million Keck Foundation grant to dive deep into lives of microbes

Even in sediment cores extracted more than a mile beneath the ocean floor, you'll find them. Tiny organisms only a cell in size chug along ever so slowly.

19 Jul 2017

Bone strength may be inherited, study shows

A new study indicates that bone strength may be inherited and that its genetic determinants are to some extent shared with bone mineral density.

19 Jul 2017

Researchers uncover new clues to why BRCA1 mutations cause breast and ovarian cancer

The human body holds many mysteries, and function of the BRCA1 gene is among them. Women who inherit a faulty copy of BRCA1 have up to a 65 percent chance to develop breast cancer by age 70. They also have up to a 39 percent chance to develop ovarian cancer.

19 Jul 2017

Study seeks to understand genetic synergy in cleft palate

Like all of the individual elements of fetal development, palate growth is a marvel of nature. In part of this process, ledges of tissue on the sides of the face grow downwards on each side of the tongue, then upward, fusing at the midline at the top of the mouth.

19 Jul 2017

Research shows how dietary essential fatty acids can help treat Alzheimer’s, other diseases

Understanding how dietary essential fatty acids work may lead to effective treatments for diseases and conditions such as stroke, Alzheimer's disease, age-related macular degeneration, Parkinson's disease and other retinal and neurodegenerative diseases.

18 Jul 2017

Large-scale genetic study of E. coli illustrates complexity of drug resistant 'superbugs'

The first large-scale genetic study of Escherichia coli (E. coli) cultured from patients with bloodstream infections in England showed that drug resistant 'superbugs' are not always out-competing other strains.

18 Jul 2017

Researchers discover gene mutations that worsen respiratory infections among children

Researchers funded by the Swiss National Science Foundation have discovered mutations that worsen respiratory infections among children. Their study explains the mechanism involved.

18 Jul 2017

Study provides insights into intergenerational inheritance of epigenetic information

We are more than the sum of our genes. Epigenetic mechanisms modulated by environmental cues such as diet, disease or our lifestyle take a major role in regulating the DNA by switching genes on and off.

18 Jul 2017

Study identifies potential treatment for fetal alcohol spectrum disorder

Two commonly used drugs erased the learning and memory deficits caused by fetal alcohol exposure when the drugs were given after birth, thus potentially identifying a treatment for the disorder, reports a new Northwestern Medicine study.

18 Jul 2017

New analysis compares emerging algorithms that look for cancer mutations

Sanford Burnham Prebys Medical Discovery Institute has undertaken the first-ever comparative analysis of a newly emerging category of algorithms that mine genetic information in cancer databases by focusing on internal gene structure (subgene resolution algorithms), in contrast to classical approaches that focus on genes treated as single units.

17 Jul 2017

Researchers find increased bacterial populations in Alzheimer's brains

Researchers in the UK have used DNA sequencing to examine bacteria in post-mortem brains from patients with Alzheimer's disease.

17 Jul 2017

Study identifies new gene involved in Fanconi anemia

Researchers from the group led by UAB Chair Professor Dr Jordi Surrallés at the Hospital de la Santa Creu i Sant Pau, Barcelona, the Universitat Autònoma de Barcelona and the CIBER of Rare Diseases participated in a study which has led to the identification of a new gene involved in Fanconi anemia, a rare genetic disease.

17 Jul 2017

Researchers spot two genes that influence person's risk of Alzheimer's disease

A team of researchers led by Cardiff University has identified two genes that influence a person's risk of developing Alzheimer's disease.

17 Jul 2017

Mutations arising after conception may play vital role in autism

A study of nearly 6,000 families, combining three genetic sequencing technologies, finds that mutations that occur after conception play an important role in autism.

17 Jul 2017

Scientists reveal key role of TLK2 gene in placenta development, embryo viability in mice

The placenta, a transient organ that links the developing embryo to its mother, is responsible for nutrient, waste and gas exchange between the fetus and the mother.

17 Jul 2017

'Organic gene therapy' could be effective treatment approach for serious blood disorders

Genome therapy with beneficial natural mutation could lead to new treatment for life-threatening blood disorders.

17 Jul 2017

Novel technique to study flow of liquids offers hope for tackling blood diseases

A new technique to study the flow of liquids developed by scientists from Université Paris-Saclay and the University of Amsterdam offers fresh hope for tackling blood diseases like thrombosis.

17 Jul 2017

ASU-TGen researchers find source of altered ANK1 gene expression linked to Alzheimer's disease

Researchers led by Arizona State University and the Translational Genomics Research Institute have identified altered expression of a gene called ANK1, which only recently has been associated with memory robbing Alzheimer's disease, in specific cells in the brain.

14 Jul 2017

Researchers discover new role of enzyme in promoting self-destruction of axons

Scientists in the Vollum Institute at OHSU have identified an enzyme that plays a crucial role in the degeneration of axons, the threadlike portions of a nerve cell that transmit signals within the nervous system.

14 Jul 2017

Scientists uncover new group of Treg cells and DNA features linked to juvenile idiopathic arthritis

A team of scientists and doctors from the SingHealth Duke-NUS Academic Medical Centre has uncovered a new group of regulatory T (Treg) cells and DNA features associated with juvenile idiopathic arthritis (JIA), the most common form of arthritis among children under the age of 16.

14 Jul 2017

Genes News and Research

UD researchers receive $1 million Keck Foundation grant to dive deep into lives of microbes

Bone strength may be inherited, study shows

Researchers uncover new clues to why BRCA1 mutations cause breast and ovarian cancer

Study seeks to understand genetic synergy in cleft palate

Research shows how dietary essential fatty acids can help treat Alzheimer’s, other diseases

Large-scale genetic study of E. coli illustrates complexity of drug resistant 'superbugs'

Researchers discover gene mutations that worsen respiratory infections among children

Study provides insights into intergenerational inheritance of epigenetic information

Study identifies potential treatment for fetal alcohol spectrum disorder

New analysis compares emerging algorithms that look for cancer mutations

Researchers find increased bacterial populations in Alzheimer's brains

Study identifies new gene involved in Fanconi anemia

Researchers spot two genes that influence person's risk of Alzheimer's disease

Mutations arising after conception may play vital role in autism

Scientists reveal key role of TLK2 gene in placenta development, embryo viability in mice

'Organic gene therapy' could be effective treatment approach for serious blood disorders

Novel technique to study flow of liquids offers hope for tackling blood diseases

ASU-TGen researchers find source of altered ANK1 gene expression linked to Alzheimer's disease

Researchers discover new role of enzyme in promoting self-destruction of axons

Scientists uncover new group of Treg cells and DNA features linked to juvenile idiopathic arthritis

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

Latest eBooks

Editorial Focus eBook - Spatial and single-cell omics (1st edition)

Industry Focus eBook - Analytical Chemistry (3rd edition)

Industry Focus eBook - Microbiome (1st edition)

Industry Focus eBook - Cell biology (5th edition)

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics