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Fralin Life Science Institute researchers use TALENS to alter mosquito genome

Virginia Tech researchers successfully used a gene disruption technique to change the eye color of a mosquito - a critical step toward new genetic strategies aimed at disrupting the transmission of diseases such as dengue fever.

22 Mar 2013

Researchers develop new approach for HIV vaccine development

Decades of research and three large-scale clinical trials have so far failed to yield an effective HIV vaccine, in large part because the virus evolves so rapidly that it can evade any vaccine-induced immune response.

22 Mar 2013

Gene LY86 identified as likely contributor to obesity

Food and environment can chemically alter your gene function and scientists have identified a gene that is consistently altered in obesity.

22 Mar 2013

MU researchers redefine key regulatory process in defective protein responsible for cystic fibrosis

A little more than a year after the FDA approved Kalydeco (Vx-770), the first drug of its kind to treat the underlying cause of cystic fibrosis, University of Missouri researchers believe they have found exactly how this drug works and how to improve its effectiveness in the future.

22 Mar 2013

Findings provide structural basis for development of drugs to fight enterovirus 71 infection

New research findings may help scientists design drugs to treat a virus infection that causes potentially fatal brain swelling and paralysis in children.

22 Mar 2013

Genetic counseling, BRCA testing can reduce cancer incidence in black women, researchers say

Researchers at Moffitt Cancer Center and colleagues in Canada have published study results focused on black women younger than 50, a population disproportionately afflicted with and dying from early-onset breast cancer compared to their white counterparts.

22 Mar 2013

Genes play a significant role in children's eating behavior

Parents may plead, cajole or entice their children to try new foods, but some kids just won't budge. Now, new research from the University of North Carolina at Chapel Hill reveals that the reason these kids fear new foods has less to do with what's on their plate and more to do with their genes.

21 Mar 2013

TGen researcher explores latest findings about children born with limited mobility

Dr. Lisa Baumbach-Reardon, an Associate Professor at the Translational Genomics Research Institute, will lead a panel discussion about Arthrogryposis (ARGY) today at the 2013 American College of Medical Genetics Annual Clinical Genetics Meeting.

21 Mar 2013

Viewpoints: N.D. abortion law is 'repressive and extreme;' States identify 'promising' ideas to overhaul medical malpractice

Late last week, the North Dakota legislature passed a bill that would ban a woman from having an abortion as soon as the heartbeat of the fetus is detected, which can happen as early as six weeks into a pregnancy.

21 Mar 2013

Novel modification of structural protein implicated

Studying a protein that gives structure to the nucleus of cells, Johns Hopkins researchers stumbled upon mutations associated with familial partial lipodystrophy, a rare disease that disrupts normal patterns of fat distribution throughout the body.

21 Mar 2013

Online database is speeding the search for diseases caused by rogue gene

A new online database combining symptoms, family history and genetic sequencing information is speeding the search for diseases caused by a single rogue gene.

20 Mar 2013

German Research Foundation sets up eight new Research Units

The Deutsche Forschungsgemeinschaft is establishing eight new Research Units. This was decided by the DFG Senate during its 2013 March meeting in Bonn.

20 Mar 2013

Study explores new mechanism that may contribute to development of cancers

A study published today in the journal Nature Genetics explores a new mechanism that may contribute to the development of several tumours, including Chronic Lymphocytic Leukaemia, a type of cancer that affects more than a thousand new patients in Spain each year.

20 Mar 2013

Study links inherited variations in few genes to increased risk of pediatric leukemia

Humans have between 20,000 and 25,000 genes that carry instructions for assembling the proteins that do the work of cells. Work led by St. Jude Children's Research Hospital found that children who inherit certain variations in four particular genes are at much higher risk of developing acute lymphoblastic leukemia.

20 Mar 2013

Study reveals how adolescent brain matures as they sleep

New study conducted by monitoring the brain waves of sleeping adolescents has found that remarkable changes occur in the brain as it prunes away neuronal connections and makes the major transition from childhood to adulthood.

20 Mar 2013

Scientists to engineer anti-allergy genetically modified apples

Scientists are trying to engineer apples so that the most widely consumed fruit in Europe no longer triggers allergic reactions.

20 Mar 2013

New research project on systems biology of synapse proteins and ageing launched

The AgedBrainSYSBIO project on systems biology of synapse proteins & ageing was officially launched March18th in Paris, France.

20 Mar 2013

Genetic testing services for rare neurological disorders launched by Athena Diagnostics

Athena Diagnostics, a leader in neurological diagnostics, today announced the clinical availability of new genetic tests to aid the detection of several rare neurological disorders, including hereditary neuropathy, neuromuscular disease, epilepsy and certain movement disorders. The lab-developed tests are available through Athena Diagnostics, a business of Quest Diagnostics (NYSE:DGX), the world’s leading provider of diagnostic information services.

From Quest Diagnostics 19 Mar 2013

Researchers show epigenetic changes influence known genetic risk variants for type 2 diabetes

Type 2 diabetes has strong hereditary tendencies and the genes we are born with cannot be changed. However, new research from Lund University in Sweden shows that we can modify the function of the genes through the epigenetic changes that take place in the course of life.

19 Mar 2013

Study evaluates genetic predisposition in BPH patients developing prostate cancer

Patients with benign prostatic hyperplasia carrying prostate cancer a risk alleles are a potential target population for PCa screening and follow-up, according to a study, which was presented yesterday at the 28th Annual EAU Congress in Milan.

19 Mar 2013

Genetic News and Research

Fralin Life Science Institute researchers use TALENS to alter mosquito genome

Researchers develop new approach for HIV vaccine development

Gene LY86 identified as likely contributor to obesity

MU researchers redefine key regulatory process in defective protein responsible for cystic fibrosis

Findings provide structural basis for development of drugs to fight enterovirus 71 infection

Genetic counseling, BRCA testing can reduce cancer incidence in black women, researchers say

Genes play a significant role in children's eating behavior

TGen researcher explores latest findings about children born with limited mobility

Viewpoints: N.D. abortion law is 'repressive and extreme;' States identify 'promising' ideas to overhaul medical malpractice

Novel modification of structural protein implicated

Online database is speeding the search for diseases caused by rogue gene

German Research Foundation sets up eight new Research Units

Study explores new mechanism that may contribute to development of cancers

Study links inherited variations in few genes to increased risk of pediatric leukemia

Study reveals how adolescent brain matures as they sleep

Scientists to engineer anti-allergy genetically modified apples

New research project on systems biology of synapse proteins and ageing launched

Genetic testing services for rare neurological disorders launched by Athena Diagnostics

Researchers show epigenetic changes influence known genetic risk variants for type 2 diabetes

Study evaluates genetic predisposition in BPH patients developing prostate cancer

Genetics & Genomics - Second Edition 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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