Genomics

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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

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

Scientists uncover new genetic markers that predispose individuals to lupus

Scientists from an international consortium have identified a large number of new genetic markers that predispose individuals to lupus.

18 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

Scientists uncover new gene therapy treatment routes for motor neurone disease

Scientists investigating the genetic causes and altered functioning of nerve cells in motor neurone disease (MND) have discovered a new mechanism that could lead to fresh treatment approaches for one of the most common forms of the disease.

14 Jul 2017

Researchers detect new gene mutation linked to Fanconi anemia

Fanconi anemia is a rare genetic disease characterized by bone marrow failure heralded by low platelet counts and unusually large red blood cells.

14 Jul 2017

CRISPR technology shows potential as a “molecular recorder” through DNA encoded movie

The researchers from Harvard University, Seth L. Shipman, Jeff Nivala, Jeffrey D. Macklis and George M. Church, believe that their study is a major step forward to a "molecular recorder" that may someday make it possible to get read-outs, has published online their proof-of-concept on July 12, 2017, in the journal Nature.

14 Jul 2017

Rise in direct-to-consumer DNA testing brings new ‘threat’ to people involved in donor conception, social scientist warns

The rise in direct-to-consumer DNA testing has increased the likelihood of individuals unexpectedly finding out they are donor-conceived, raising important ethical questions, warns social scientist Dr Marilyn Crawshaw from the University of York.

13 Jul 2017

Genetics plays major role in how infants visually explore social world, twin study reveals

New research has uncovered compelling evidence that genetics plays a major role in how children look at the world and whether they have a preference for gazing at people's eyes and faces or at objects.

12 Jul 2017

Variation in sleep patterns between age groups linked to evolutionary adaptation, study finds

A study conducted on the Hadza people in Tanzania suggests a natural variation in sleeping patterns among people living in groups, where there is rarely a moment when someone isn’t vigilant enough to raise an alarm.

12 Jul 2017

Researchers identify common genetic factors that influence muscle strength

Common genetic factors that influence muscle strength in humans have been identified for the first time in a study led by researchers from the University of Cambridge and published today in Nature Communications.

12 Jul 2017

Study shows potential of whole genome sequencing and AI to help clinicians scale precision oncology

In a study published today in the July 11, 2017 issue of Neurology Genetics, an official journal of the American Academy of Neurology, researchers at the New York Genome Center, The Rockefeller University and other NYGC member institutions, and IBM have illustrated the potential of IBM Watson for Genomics to analyze complex genomic data from state-of-the-art DNA sequencing of whole genomes.

11 Jul 2017

Genomics

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

Researchers discover gene mutations that worsen respiratory infections among children

Study provides insights into intergenerational inheritance of epigenetic information

Scientists uncover new genetic markers that predispose individuals to lupus

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

Scientists uncover new gene therapy treatment routes for motor neurone disease

Researchers detect new gene mutation linked to Fanconi anemia

CRISPR technology shows potential as a “molecular recorder” through DNA encoded movie

Rise in direct-to-consumer DNA testing brings new ‘threat’ to people involved in donor conception, social scientist warns

Genetics plays major role in how infants visually explore social world, twin study reveals

Variation in sleep patterns between age groups linked to evolutionary adaptation, study finds

Researchers identify common genetic factors that influence muscle strength

Study shows potential of whole genome sequencing and AI to help clinicians scale precision oncology

Why use light scattering to analyze proteins and viral vectors?

Changing the landscape of R&D to build clinical success from the ground up

Sensing a Healthier Future

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