Genomics

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Study finds a cellular mechanism that protects plant genes from impacts of mutation

According to a new study conducted at the University of Oxford, a cellular mechanism termed DNA mismatch repair (MMR), preferentially protects plant genes from the damaging impacts of mutation.

8 Jan 2018

Polygenic risk score predicts early-onset heart disease risk

A risk score based on multiple genetic differences, or polygenic risk score, predicted significantly more cases of early-onset heart disease than standard tests for single genetic defects, according to new research in the American Heart Association's journal Circulation: Genomic and Precision Medicine.

8 Jan 2018

Bielefeld scientists discover cause of initially unclear symptoms

The sequencing of the human genome has made it possible: nowadays scientists can discover potential disorders for which there are no known patients.

5 Jan 2018

Newly described super-silenced DNA reveals novel approach to reprogram cells

Newly described stretches of super-silenced DNA reveal a fresh approach to reprogram cell identity to use in regenerative medicine studies and one day in the clinic, according to a study in Molecular Cell last week by investigators from the Perelman School of Medicine at the University of Pennsylvania.

5 Jan 2018

Genetic differences can influence efficiency of medicines

Medicines do not follow the one size fits all principle, because genetic differences can influence their efficiency.

5 Jan 2018

Cellular mechanism protects genes from damaging effects of mutation

Researchers at the University of Oxford have discovered that a cellular mechanism preferentially protects plant genes from the damaging effects of mutation.

5 Jan 2018

Researchers use genomic technologies to better understand risk factor for stomach cancer

A research team led by National University Health System and Duke-NUS Medical School has used genomic technologies to better understand intestinal metaplasia, a known risk factor for gastric (stomach) cancer.

5 Jan 2018

Why Should We Weigh Every Protein in the Human Body?

Our mission is to advance the measurement of human proteins with greater precision, to bring to the world the benefits of absolute molecular specificity when it comes to interrogating proteins at the molecular level.

From Pittcon 5 Jan 2018

Study provides insight into how early-stage breast cancer progresses to invasive ductal carcinoma

A new genetic-based model may explain how a common form of early-stage breast cancer known as ductal carcinoma in situ progresses to a more invasive form of cancer say researchers at The University of Texas MD Anderson Cancer Center.

4 Jan 2018

Study illustrates the role of alcohol in causing damage to DNA and increased cancer risk

A new study conducted by a group of researchers at MRC Laboratory of Molecular Biology, Cambridge revealed the significant role of alcohol in causing damage to DNA in stem cells and thereby increasing cancer risks. The study was funded by Cancer Research UK and the results were published in Nature.

4 Jan 2018

Genetic labeling helps researchers track behavior of blood cells

By tagging bone marrow cells of mice with a genetic label, or barcode, researchers were able to track and describe the family tree of individual blood cells as they form in their natural environment.

4 Jan 2018

Genetic changes help mosquitoes to develop pesticide resistance

For decades, chemical pesticides have been the most important way of controlling insects like the Anopheles mosquito species that spreads malaria to humans.

4 Jan 2018

Researcher shows how rank order can be used to identify complex gene interactions

Genome sequencing has revolutionized genetics. It also requires new mathematical tools to help life scientists make sense of enormous amounts of data.

3 Jan 2018

Research sheds light on role of epigenetics in placing egg cells into stasis

Keeping egg cells in stasis during childhood is a key part of female fertility. New research published today (1st January) in Nature Structural and Molecular Biology sheds some light on the role of epigenetics in placing egg cells into stasis.

2 Jan 2018

UAB study shows missense mutations as key risk factor for severe symptoms of neurofibromatosis type 1

Research led by Ludwine Messiaen, Ph.D., professor of genetics at the University of Alabama at Birmingham, shows that missense mutations in a cluster of just five codons in the NF1 gene are an important risk factor for severe symptoms of the genetic disease neurofibromatosis type 1.

28 Dec 2017

Scientists discover five new regions of the genome that increase asthma risk

An international study led by scientists from Inserm and Paris Diderot Universit, the University of Chicago, the National Heart and Lung Institute and the University of Colorado Anschutz Medical Campus together with researchers of the Trans-National Asthma Genetics Consortium has discovered five new regions of the genome that increase the risk of asthma.

22 Dec 2017

Genomics

Study finds a cellular mechanism that protects plant genes from impacts of mutation

Polygenic risk score predicts early-onset heart disease risk

Bielefeld scientists discover cause of initially unclear symptoms

Newly described super-silenced DNA reveals novel approach to reprogram cells

Genetic differences can influence efficiency of medicines

Cellular mechanism protects genes from damaging effects of mutation

Researchers use genomic technologies to better understand risk factor for stomach cancer

Why Should We Weigh Every Protein in the Human Body?

Study provides insight into how early-stage breast cancer progresses to invasive ductal carcinoma

Study illustrates the role of alcohol in causing damage to DNA and increased cancer risk

Genetic labeling helps researchers track behavior of blood cells

Genetic changes help mosquitoes to develop pesticide resistance

Researcher shows how rank order can be used to identify complex gene interactions

Research sheds light on role of epigenetics in placing egg cells into stasis

UAB study shows missense mutations as key risk factor for severe symptoms of neurofibromatosis type 1

Scientists discover five new regions of the genome that increase asthma risk

Researchers sequence salamander genome to reveal unique features of regeneration

Salk scientists find simpler way to derive functioning cardiac cells from stem cells

Multifunctional protein also plays role in development of blood cells

Researchers use a gene-editing complex to preserve hearing in animal model of progressive deafness

Small solutions for big problems in drug discovery and delivery

Professor Nancy Ip: Pioneering New Paths in Neurodegenerative Therapy

Utilizing process Raman in optimizing cultivated meat production

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