Genetics News and Research

Latest Genetics News and Research

Researchers identify gene variants linked to both type 2 diabetes and CHD risk

Type 2 diabetes (T2D) has become a global epidemic affecting more than 380 million people worldwide; yet there are knowledge gaps in understanding the etiology of type-2 diabetes.

4 Sep 2017

Genetics of circadian rhythms found to have effect on migraine

People with a specific variation in the CLOCK gene have more migraines under financial stress. This work, the first time that the genetics of circadian rhythms has been shown to have an effect on migraine, is presented at the ECNP conference in Paris.

4 Sep 2017

Existing drug may one day protect premenopausal women from infertility after cancer treatments

An existing drug may one day protect premenopausal women from life-altering infertility that commonly follows cancer treatments, according to a new study.

1 Sep 2017

Mutations altering gene function play role in development of intellectual disabilities

Intellectual disabilities are often caused by a mutation that damages a gene, preventing the associated protein from functioning properly.

1 Sep 2017

Researchers perform first-ever clinical trial involving genetic screening for Parkinson’s disease

In the first ever clinical investigation involving genetic screening for Parkinson's disease, researchers are testing whether the presence of a specific genetic mutation identifies which patients are the best candidates for deep brain stimulation surgery, and whether neurologists should perform that procedure differently based on that genetic information.

1 Sep 2017

Scientists question CRISPR human embryo editing claims

A paper published in the journal Nature on the 2nd August described how a gene editing tool CRISPR could be used to correct a genetic mutation that leads to a heart condition. This team had performed the genetic editing on the gene sequences in dozens of viable human embryos to attempt to prevent a genetic heart condition called hypertrophic cardiomyopathy.

31 Aug 2017

50% of men struggle to identify a woman’s vagina correctly on a diagram: Survey

A recent survey by a gynaecological cancer charity has shown that nearly half of the men could not identify a woman’s vagina correctly on a diagram.

31 Aug 2017

Study identifies unexpected mosaic mutations as new risk factor for developing autism

Autism spectrum disorder affects approximately one out of every 68 children in the United States. Despite expansive study, the origin and risk factors of the complex condition are not fully understood.

31 Aug 2017

Link found between fetal genes and risk of preeclampsia in mother

For the first time, a relationship has been found between fetal genes and the risk of preeclampsia in the mother.

31 Aug 2017

UAB researchers reveal key role for RSF1 protein in silencing genes

A fertilized human egg develops into multiple tissues, organs and about 200 distinct cell types. Each cell type has the same genes, but they are expressed differently during development and in mature cells.

31 Aug 2017

Human ancestors responsible for transmitting ancient strains of herpesvirus, study finds

An international study of integrated HHV-6 has discovered that a small number of human ancestors, one from about 24,000 years ago, have been responsible for transmitting ancient strains of the virus to individuals today - affecting about a million people in the UK alone.

30 Aug 2017

Genetics of digestion stayed remarkably the same from fishes to humans, research shows

Scientists have discovered a network of genes and genetic regulatory elements in the lining of the intestines that has stayed remarkably the same from fishes to humans. Many of these genes are linked to human illnesses, such as inflammatory bowel diseases, diabetes and obesity.

30 Aug 2017

Scientists identify novel role for retrotransposons in shaping embryonic chromatin landscape

Retrotransposons are repetitive elements that form almost half of the mammalian genome. Even though they are so common, they have previously been considered to be fairly insignificant.

30 Aug 2017

Research may lead to first-ever pharmacological treatment for rare genetic bone disease

Scientists at Children's Hospital of Philadelphia report that a drug candidate that blocks abnormal protein signals may lead to the first pharmacologic treatment for hereditary multiple exostoses (HME), a rare pediatric genetic disease.

29 Aug 2017

New imaging technique can help assess quality of early-stage embryos

Researchers at the ARC Centre of Excellence for Nanoscale BioPhotonics, led by the University of Adelaide, have successfully developed an advanced new imaging technique, which can help assess the quality of early-stage embryos.

29 Aug 2017

Boosting blood levels of bone-derived hormone may reverse age-related memory loss

Age-related memory loss may be reversed by boosting blood levels of osteocalcin, a hormone produced by bone cells, according to mouse studies led by Columbia University Medical Center researchers.

29 Aug 2017

Pathway from ADI to AUD symptoms influenced by ethnicity and genetics

Studies have shown that an early age of drinking initiation (ADI) increases the chance of developing an alcohol use disorder (AUD).

29 Aug 2017

Simultaneous treatment with anti-PD1 and anti-OX40 cancer therapies may have detrimental effect

Concurrent administration of the T-cell stimulating anti-OX40 antibody and the immune checkpoint inhibitor anti-PD1 antibody attenuated the effect of anti-OX40 and resulted in poor treatment outcomes in mice.

28 Aug 2017

Use of antiseptic mouthwash could put patients at risk for CVD

Nathan Bryan, Ph.D., one of the world's leading experts on the critically important role of Nitric Oxide (NO) in the health of many of the body's organs and systems, said," understanding the vital effects of bacteria in the mouth is essential for health care providers, although it is not widely understood by the public."

26 Aug 2017

Scientists develop new system to identify and characterize regulatory DNA sequences

Scientists from the Children's Medical Center Research Institute at UT Southwestern have developed an innovative system to identify and characterize the molecular components that control the activities of regulatory DNA sequences in the human genome.

24 Aug 2017

Genetics News and Research

Latest Genetics News and Research

Researchers identify gene variants linked to both type 2 diabetes and CHD risk

Genetics of circadian rhythms found to have effect on migraine

Existing drug may one day protect premenopausal women from infertility after cancer treatments

Mutations altering gene function play role in development of intellectual disabilities

Researchers perform first-ever clinical trial involving genetic screening for Parkinson’s disease

Scientists question CRISPR human embryo editing claims

50% of men struggle to identify a woman’s vagina correctly on a diagram: Survey

Study identifies unexpected mosaic mutations as new risk factor for developing autism

Link found between fetal genes and risk of preeclampsia in mother

UAB researchers reveal key role for RSF1 protein in silencing genes

Human ancestors responsible for transmitting ancient strains of herpesvirus, study finds

Genetics of digestion stayed remarkably the same from fishes to humans, research shows

Scientists identify novel role for retrotransposons in shaping embryonic chromatin landscape

Research may lead to first-ever pharmacological treatment for rare genetic bone disease

New imaging technique can help assess quality of early-stage embryos

Boosting blood levels of bone-derived hormone may reverse age-related memory loss

Pathway from ADI to AUD symptoms influenced by ethnicity and genetics

Simultaneous treatment with anti-PD1 and anti-OX40 cancer therapies may have detrimental effect

Use of antiseptic mouthwash could put patients at risk for CVD

Scientists develop new system to identify and characterize regulatory DNA sequences

Sequencing & Genomics: Elevating Science and Healthcare eBook

Real-time Raman monitoring for pharmaceutical hot melt extrusion

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