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Study: 52-gene risk profile accurately predicts survival for patients with severe lung disease

An international Yale-led research team has shown that a risk profile based on 52 genes accurately predicts survival for patients with a severe lung disease. If confirmed in further studies, the finding could transform the way patients are treated for the condition, which is on the rise in older adults.

20 Sep 2017

Scientists find a way to convert “bad body fat” to “good fat”

Researchers have found that the unhealthy fat in the body called “white fat” could be converted to a healthier fat by blocking a special protein. This could help fight the obesity epidemic they speculate. The report was published in the journal Cell Reports.

19 Sep 2017

UTSW receives $34 million CPRIT award for cancer research and faculty recruitment

The Cancer Prevention and Research Institute of Texas has awarded UT Southwestern researchers more than $34 million for cancer research and faculty recruitment, including support for programs in pancreatic cancer, lung cancer, breast cancer, and melanoma.

19 Sep 2017

New research identifies way to convert white fat into brown fat in mice

There's good fat and bad fat in our bodies. The good fat helps burn calories, while the bad fat hoards calories, contributing to weight gain and obesity. Now, new research at Washington University School of Medicine in St. Louis has identified a way to convert bad, white fat into good, brown fat, at least in mice.

19 Sep 2017

Scientists uncover new clues to male infertility or congenital illness

When it comes to male reproductive fertility, timing is everything. Now scientists are finding new details on how disruption of this timing may contribute to male infertility or congenital illness.

19 Sep 2017

Analytical Science in Precision Medicine

Pittcon is an analytical conference, so naturally my talk will be about analytical chemistry and how analytical chemistry will become increasingly important in delivering healthcare solutions, not only for rich people, but also, hopefully, for poor people across the world.

From Pittcon 19 Sep 2017

Gene therapy could be novel approach to treat alcoholism, research suggests

Researchers used gene transfer to block the expression of one of the two main enzymes that break down alcohol in the liver, leading to the accumulation in liver cells of acetaldehyde, a metabolic byproduct of ethanol.

19 Sep 2017

New research reveals changing aspects of teenage parenthood

The US birth rate hasn't changed for two generations of teenage girls, but other aspects of young parenthood are shifting, especially regarding young fathers, according to new Indiana University research.

19 Sep 2017

Research could lead to improvements in treating diseases caused by mutations in genes

Research carried out by academics at Northumbria University, Newcastle could lead to improvements in treating patients with diseases caused by mutations in genes, such as cancer, cystic fibrosis and potentially up to 6,000 other inherited conditions.

19 Sep 2017

Researchers discover ‘recycled’ genes in mammalian genome

One often hears about the multitude of genes we have in common with chimps, birds or other living creatures, but such comparisons are sometimes misleading. The shared percentage usually refers only to genes that encode instructions for making proteins -- while overlooking regulatory genes, which nonetheless make up a large part of the genome.

18 Sep 2017

Scientists discover markers for progressive multiple sclerosis

Scientists have uncovered two closely related cytokines -- molecules involved in cell communication and movement -- that may explain why some people develop progressive multiple sclerosis (MS), the most severe form of the disease.

18 Sep 2017

UI scientists discover gene linked to fatal renal agenesis in children

A team led by University of Iowa researchers has identified a gene linked to rare, often fatal kidney-related birth defects.

18 Sep 2017

Researchers precisely describe effects of frequent genetic mutation in congenital hyperinsulinism

Diabetes is characterized by a deficiency of insulin. The opposite is the case in congenital hyperinsulinism: patients produce the hormone too frequently and in excessive quantities, even if they haven't eaten any carbohydrates.

18 Sep 2017

Scientists genetically engineer mice that display behavioral hallmarks of human bipolar disorder

Johns Hopkins researchers report they have genetically engineered mice that display many of the behavioral hallmarks of human bipolar disorder, and that the abnormal behaviors the rodents show can be reversed using well-established drug treatments for bipolar disorder, such as lithium.

18 Sep 2017

Myriad Genetics presents positive results of new hereditary cancer test at 36th annual conference of NSGC

Myriad Genetics, Inc., a leader in molecular diagnostics and personalized medicine, today announced that two important studies will be featured in podium presentations at the 36th annual conference of the National Society of Genetic Counselors in Columbus, OH.

18 Sep 2017

Study: Genomic profiling could help identify effective treatments for pediatric gliomas

The largest genomic profiling study ever conducted into a type of brain tumor known as glioma in children has identified genetic alterations in 96% of cases. As reported in The Oncologist, this genetic information could help to identify the most effective treatments for specific cases of glioma, hopefully improving the prognosis for what is currently the leading cause of death for children with cancer in the US.

18 Sep 2017

Research unravels how stem cells in the ovaries may be harnessed to revolutionize fertility treatments

About 13 years ago, Northeastern professor Jonathan Tilly, a reproductive biologist, made a discovery that challenged everything scientists thought they knew about female reproduction. The long-held belief that mammals were born with a set number of eggs -- and no ability to create new ones -- was wrong.

15 Sep 2017

University Of Minnesota scientists describe breakthrough in research related to FSHD

A new study published in the journal Nature Communications describes a breakthrough in research related to facioscapulohumeral muscular dystrophy (FSHD). The debilitating genetic disease - which has no approved treatment - affects an estimated 38,000 Americans and causes degeneration and wasting of the skeletal muscles.

15 Sep 2017

IMB researchers make breakthrough in understanding origin of aging process

Researchers at the Institute of Molecular Biology in Mainz, Germany, have made a breakthrough in understanding the origin of the aging process. They have identified that genes belonging to a process called autophagy - one of the cells most critical survival processes - promote health and fitness in young worms but drive the process of aging later in life.

15 Sep 2017

Lesser-known gene appears to play greater role in Alzheimer's and dementia-related memory decline

The notorious genetic marker of Alzheimer's disease and other forms of dementia, ApoE4, may not be a lone wolf.

15 Sep 2017

Genetic News and Research

Study: 52-gene risk profile accurately predicts survival for patients with severe lung disease

Scientists find a way to convert “bad body fat” to “good fat”

UTSW receives $34 million CPRIT award for cancer research and faculty recruitment

New research identifies way to convert white fat into brown fat in mice

Scientists uncover new clues to male infertility or congenital illness

Analytical Science in Precision Medicine

Gene therapy could be novel approach to treat alcoholism, research suggests

New research reveals changing aspects of teenage parenthood

Research could lead to improvements in treating diseases caused by mutations in genes

Researchers discover ‘recycled’ genes in mammalian genome

Scientists discover markers for progressive multiple sclerosis

UI scientists discover gene linked to fatal renal agenesis in children

Researchers precisely describe effects of frequent genetic mutation in congenital hyperinsulinism

Scientists genetically engineer mice that display behavioral hallmarks of human bipolar disorder

Myriad Genetics presents positive results of new hereditary cancer test at 36th annual conference of NSGC

Study: Genomic profiling could help identify effective treatments for pediatric gliomas

Research unravels how stem cells in the ovaries may be harnessed to revolutionize fertility treatments

University Of Minnesota scientists describe breakthrough in research related to FSHD

IMB researchers make breakthrough in understanding origin of aging process

Lesser-known gene appears to play greater role in Alzheimer's and dementia-related memory decline

Sequencing & Genomics: Elevating Science and Healthcare 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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