Genetic News and Research

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Study explores links between genetic susceptibility and heterogeneous phenotypes of lymphedema

Each year, about 1.38 million women worldwide are diagnosed with breast cancer. Advances in diagnosis and treatment have facilitated a 90-percent, five-year survival rate, among those treated.

9 Feb 2017

Genetic variant encoded in NCF1 linked to increased risk for autoimmune diseases, study shows

Investigators at the Medical University of South Carolina report pre-clinical research showing that a genetic variant encoded in neutrophil cystolic factor 1 (NCF1) is associated with increased risk for autoimmune diseases, including systemic lupus erythematosus (SLE), rheumatoid arthritis, and Sjögren's syndrome, in the January 2017 issue of Nature Genetics.

8 Feb 2017

NIH researchers identify genes that may predict how melanoma spreads

Cancerous tumors are voracious. Once they have consumed all the oxygen and nutrients in the original tumor site, the cancer cells travel to other parts of the body (metastasize) to find more nourishment.

8 Feb 2017

Is today’s society really sleep deprived?

Sleep deprivation often hits the headlines and we are frequently told we need 8 hours a night. But how much sleep do we really need? Are we sleeping less than we used to and is today's society really sleep deprived? A recent meeting at the Royal Society of Medicine aimed to answer these questions.

8 Feb 2017

Researchers discover function of olfactory receptors in human heart muscle

Researchers have for the first time identified the function of olfactory receptors in the human heart muscle, such as are also present in the nose. One of the receptors reacts to fatty acids that occur in the blood, in patients with diabetes significantly above the normal range.

8 Feb 2017

Study sheds light on role of Armc5 protein in foetal development and T-cell immune responses

Genetic mutations of the Armc5 gene disrupt foetal development and compromise the immune response.

8 Feb 2017

Study suggests that iPSCs do not develop more mutations than subcloned cells

It's been more than 10 years since Japanese researchers Shinya Yamanaka, M.D., Ph.D., and his graduate student Kazutoshi Takahashi, Ph.D., developed the breakthrough technique to return any adult cell to its earliest stage of development (a pluripotent stem cell) and change it into different types of cells in the body.

8 Feb 2017

Research provides insights about left-right differences in embryonic neural development

Our nervous systems have left-right differences that are important for correct functioning. Handedness is probably the best known asymmetry arising from the development of the nervous system.

8 Feb 2017

Novel cell therapy may repair heart damage using modified cells from facial muscle

Researchers at the University of Cincinnati have received $2.4 million in federal funding to pursue research on a novel cell therapy that would repair heart damage using modified cells taken from the patient's own facial muscle.

8 Feb 2017

Studies open new windows into understanding untreatable group of common genetic disorders

Two Princeton University studies are opening important new windows into understanding an untreatable group of common genetic disorders known as RASopathies that are characterized by distinct facial features, developmental delays, cognitive impairment and heart problems.

7 Feb 2017

Study highlights need for increased vigilance when using GFAP, UCH-L-1 as potential biomarkers of mTBI

In patients who suffered acute orthopedic injuries, two proposed biomarkers for mild traumatic brain injury (mTBI) were not able to distinguish between patients who did or did not have mTBI.

7 Feb 2017

Mutated genes lead to tooth enamel defects that increase risk of caries

Bacteria are not the sole cause of caries; tooth resistance also plays an instrumental role. Researchers from the University of Zurich demonstrate that mutated genes lead to defects in the tooth enamel and can therefore encourage the development of caries.

7 Feb 2017

New technique efficiently separates circulating tumor cells in bloodstream

A new research, affiliated with UNIST has been highlighted on the front cover of the January 2017 issue of the prestigious journal Analytical Chemistry. The key finding of this study is the development of a new technique that seperates circulating tumor cells from whole blood at a liquid-liquid interface.

7 Feb 2017

Early menstruation linked to higher stroke risk

Women who started menstruating early in life could later face a higher risk of stroke.

7 Feb 2017

Researchers create first animal model of rare disease linked to problem of adrenal glands

The name of the gene is Armc5, for Armadillo repeat containing 5. Until now, its function was unknown. After 10 years of research, a team at the University of Montreal Hospital Research Centrehas succeeded in deleting this gene in experimental mice and discovered that its loss gives rise to a heretofore unidentified syndrome.

7 Feb 2017

Scientists use brain organoids to identify root causes of Miller-Dieker syndrome

Research led by scientists at UC San Francisco and Case Western Reserve University School of Medicine has used brain "organoids" — tiny 3D models of human organs that scientists grow in a dish to study disease — to identify root causes of Miller-Dieker Syndrome (MDS), a rare genetic disorder that causes fatal brain malformations.

7 Feb 2017

Patients with early, severe depression symptoms have increased genetic risk for psychiatric disorders

Clinical features of major depressive disorder (MDD) may help identify specific subgroups of depressed patients based on associations with genetic risk for major psychiatric disorders, reports a study in Biological Psychiatry.

7 Feb 2017

Researchers discover survival strategy that bacteria can use to outsmart human immune response

Researchers at the Hebrew University of Jerusalem have discovered a survival strategy that harmful bacteria can use to outsmart the human immune response, resulting in more severe and persistent infections and more effective spreading from person to person.

7 Feb 2017

Next-generation sequencing assay shows accuracy, sensitivity in detecting genetic mutations in tumors

One of the most promising areas of cancer research is personalized therapy using precision medicine. The National Cancer Institute's NCI-MATCH is a large, ongoing clinical trial that matches tumors to therapies based on the tumor's genetic characteristics.

7 Feb 2017

Could we really reverse aging to prolong life?

It's only a matter of time before we can reverse the aging process. It hasn't been already achieved because the human body is extremely complex and does itself a lot of different types of damage.

7 Feb 2017

Genetic News and Research

Study explores links between genetic susceptibility and heterogeneous phenotypes of lymphedema

Genetic variant encoded in NCF1 linked to increased risk for autoimmune diseases, study shows

NIH researchers identify genes that may predict how melanoma spreads

Is today’s society really sleep deprived?

Researchers discover function of olfactory receptors in human heart muscle

Study sheds light on role of Armc5 protein in foetal development and T-cell immune responses

Study suggests that iPSCs do not develop more mutations than subcloned cells

Research provides insights about left-right differences in embryonic neural development

Novel cell therapy may repair heart damage using modified cells from facial muscle

Studies open new windows into understanding untreatable group of common genetic disorders

Study highlights need for increased vigilance when using GFAP, UCH-L-1 as potential biomarkers of mTBI

Mutated genes lead to tooth enamel defects that increase risk of caries

New technique efficiently separates circulating tumor cells in bloodstream

Early menstruation linked to higher stroke risk

Researchers create first animal model of rare disease linked to problem of adrenal glands

Scientists use brain organoids to identify root causes of Miller-Dieker syndrome

Patients with early, severe depression symptoms have increased genetic risk for psychiatric disorders

Researchers discover survival strategy that bacteria can use to outsmart human immune response

Next-generation sequencing assay shows accuracy, sensitivity in detecting genetic mutations in tumors

Could we really reverse aging to prolong life?

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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