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Researchers create first mouse model for common form of infant leukemia

After nearly two decades of unsuccessful attempts, researchers from the University of Chicago Medicine and the Cincinnati Children's Hospital Medical Center have created the first mouse model for the most common form of infant leukemia.

15 Nov 2016

Scientists discover link between genetic mutation and rare heart muscle disease

A strong association between a genetic mutation and a rare kind of heart muscle disease has been discovered by researchers at the University of Colorado Anschutz Medical Campus.

15 Nov 2016

Research shows workings of biochemical pathway that helps control blood glucose

Research led by a Johns Hopkins University biologist demonstrates the workings of a biochemical pathway that helps control glucose in the bloodstream, a development that could potentially lead to treatments for diabetes.

14 Nov 2016

Research shows corticotrophs in the brain can influence avoidance behavior after onset of stress

German Resilience Center presents new findings on the resistance to stress. A person exposed to stress can usually rapidly adapt the own behavior to the specific situation.

14 Nov 2016

Igenomix rewarded accreditation by CAP in Dubai for high quality of genetic testing services

Igenomix has recently been rewarded accreditation by College of American Pathologists in Dubai, given its state-of-the-art facilities and cutting-edge products in the space of advanced reproductive genetics.

14 Nov 2016

WHF’s Cholesterol Roadmap previewed at 2016 AHA Scientific Sessions

The World Heart Federation's Cholesterol Roadmap is being previewed today at the American Heart Association Scientific Sessions 2016 in New Orleans, USA.

14 Nov 2016

MGH researchers find following healthy lifestyle can mitigate genetic risk of heart disease

It is well known that following a healthy lifestyle -- not smoking, avoiding excess weight and getting regular exercise - can reduce the risk of heart disease.

13 Nov 2016

Rice University scientists uncover new clues to cause of Huntington's disease

Rice University scientists have uncovered new details about how a repeating nucleotide sequence in the gene for a mutant protein may trigger Huntington's and other neurological diseases.

11 Nov 2016

Bullied children nearly twice as likely to be overweight as young adults

Children who are bullied in primary and secondary school are nearly twice as likely to be overweight at the age of 18 than non-bullied children, according to a new study by researchers from King's College London.

11 Nov 2016

New discovery may lead to better treatment options for pancreatic cancer patients

Pancreatic cancer, the third leading cause of cancer-related deaths, is projected to be the second by the year 2030, according to a study in the journal of Cancer Research.

11 Nov 2016

Moffitt scientists show how mathematical modeling can predict patient responses to cancer drugs

Scientists have significantly improved their understanding of cancer and have developed numerous therapies that have helped to reduce patient mortality; however, the majority of drugs that make it to the clinical trial phase of development fail, despite promising data in laboratory studies.

11 Nov 2016

Technion researchers develop new diagnostic technology for improving personalized cancer treatment

Using synthetic DNA sequences as the tiniest of barcodes, Technion researchers have developed a new diagnostic technology for determining the suitability of specific anticancer drugs to a specific patient - before treatment even begins.

11 Nov 2016

Researchers start enrolling patients for Phase II gene therapy trial for choroideremia

Following on from a successful world’s first Phase I gene therapy trial for choroideremia, Professor Robert MacLaren and his team at Oxford University and the Oxford Eye Hospital at the John Radcliffe Hospital have started a Phase II trial enrolling 30 patients.

11 Nov 2016

Women with higher vitamin D levels have better long-term outcomes after breast cancer diagnosis

Women with higher vitamin D levels in their blood following a breast cancer diagnosis had significantly better long-term outcomes, according to new research from Kaiser Permanente and Roswell Park Cancer Institute.

11 Nov 2016

Irregular sleeping patterns and skipping breakfast could make children overweight

Mothers smoking in pregnancy, children skipping breakfast and not having a regular bedtime or sufficient sleep all appear to be important factors in predicting whether a child will become overweight or obese, according to new research led by UCL.

11 Nov 2016

'Sponge on a string' test could spare people with Barrett's oesophagus from endoscopies

Cancer Research UK-funded scientists have discovered that a 'sponge on a string' pill test can identify which people with a condition called Barrett's oesophagus have a low risk of developing oesophageal cancer - sparing them uncomfortable endoscopies.

11 Nov 2016

Fruit flies can be powerful model for unraveling cellular, molecular bases of damaging cold perception

The tiny fruit fly can help humans investigate the genetic and neural bases of detecting painful or harmful cold stimuli and offer intriguing, potential implications for human health, according to a new study.

10 Nov 2016

Aortic rigidity in African-Americans linked to excess risk of hypertension and cardiovascular disease

African-Americans have more rigidity of the aorta, the major artery supplying oxygen-rich blood to the body, than Caucasians and Hispanics, according to a study by UT Southwestern Medical Center cardiologists.

10 Nov 2016

Scientists identify genetic mutations in highly aggressive rhabdoid meningiomas

Meningiomas are the most common primary brain tumors, but the term encompasses over a dozen subtypes that range from benign to highly aggressive.

10 Nov 2016

Scientists uncover how common Epstein-Barr virus causes blood cancer in adults and children

Scientists at the University of Sussex, trying to uncover how the common Epstein-Barr virus causes blood cancer in adults and children, have discovered how the virus takes control of two genes involved in cancer development so it can switch them on or off.

10 Nov 2016

Genetic News and Research

Researchers create first mouse model for common form of infant leukemia

Scientists discover link between genetic mutation and rare heart muscle disease

Research shows workings of biochemical pathway that helps control blood glucose

Research shows corticotrophs in the brain can influence avoidance behavior after onset of stress

Igenomix rewarded accreditation by CAP in Dubai for high quality of genetic testing services

WHF’s Cholesterol Roadmap previewed at 2016 AHA Scientific Sessions

MGH researchers find following healthy lifestyle can mitigate genetic risk of heart disease

Rice University scientists uncover new clues to cause of Huntington's disease

Bullied children nearly twice as likely to be overweight as young adults

New discovery may lead to better treatment options for pancreatic cancer patients

Moffitt scientists show how mathematical modeling can predict patient responses to cancer drugs

Technion researchers develop new diagnostic technology for improving personalized cancer treatment

Researchers start enrolling patients for Phase II gene therapy trial for choroideremia

Women with higher vitamin D levels have better long-term outcomes after breast cancer diagnosis

Irregular sleeping patterns and skipping breakfast could make children overweight

'Sponge on a string' test could spare people with Barrett's oesophagus from endoscopies

Fruit flies can be powerful model for unraveling cellular, molecular bases of damaging cold perception

Aortic rigidity in African-Americans linked to excess risk of hypertension and cardiovascular disease

Scientists identify genetic mutations in highly aggressive rhabdoid meningiomas

Scientists uncover how common Epstein-Barr virus causes blood cancer in adults and children

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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