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Genetic Research

Vitamin B3 supplement reverses premature ageing in Werner Syndrome patients

There is a beacon of hope for patients with a rare genetic disorder called Werner Syndrome as researchers unveil a groundbreaking discovery: Nicotinamide riboside, a vitamin B3 derivative, reverses premature ageing.

Exosome therapy for brittle bone disease

Pascale V Guillot, Associate Professor at University College London, investigates the possibility of exosome therapy for those living with brittle bone disease.

Scientists discover 16 genes linked to ICU COVID cases

Scientists say that 16 specific genes are potentially responsible for why some people become ICU COVID cases, and others don't.

Unlocking dark matter for genome remodelling

Dr Helen Rowe, Senior Lecturer in Epigenetics, outlines the significance of research into dark matter and genome remodelling

Team discovers crucial gene in soybean, after 30 year hunt

The University of Illinois team have figured out which gene controls protein content in soybeans - a breakthrough for global food security.

Research reveals connection between high blood pressure and diabetes

Research is finally explaining the connection between patients suffering with high blood pressure (hypertension) and diabetes

New stem cell model of albinism to study related eye conditions

First patient-derived stem cell model for studying eye conditions related to oculocutaneous albinism developed by the National Eye Institute Lead author of the report, Doctor...

£2.3 million awarded to York University for sickle cell anaemia research

The Bill & Melinda Gates foundation have awarded £2.3million to the University of York, in attempt to push research into sickle cell anaemia.

‘Dark genome’ research suggests better treatment for mental disorders

Researching DNA outside of our genes, analysing the ‘dark genome’, scientists have found evolved proteins which can distinguish between schizophrenia and bipolar disorders, improving diagnosis and treatment.

Genetic disease treatment research for creatine deficiency

Professor Olivier Braissant, believes there is hope for the treatment of creatine deficiency thanks to new genetic disease research - here, he tells us all about the recent developments.

The long-term effects of exposure to nanoparticles

In toxicology & health science focus, Ken Tachibana, Sanyo-Onoda City University in Japan, walks through the long-term effects of exposure to nanoparticles

Behavioural adaptations in fish may help them adapt to Ocean warming

Virginia Tech scientists are showing the resilient nature of cold-water fish in the face of climate change and rising ocean temperatures

How to compete with COVID-19 with a computer?

Y-h. Taguchi, Professor at Chuo University in Japan, reveals how to compete with COVID-19 by using a computer.

Gene editing promises to make human industry sustainable

L. Val Giddings, PhD, Senior Fellow, Information Technology and Innovation Foundation, states that gene editing promises to make human industry sustainable*.

Whole genome sequencing increases rare disorder diagnosis by 31%

Whole Genome Sequencing from a single blood test has been found to pick up over a third more cases of rare genetic disorders than standard tests do.

What is Dandy-Walker Syndrome? – Everything you need to know

Dandy-Walker Syndrome. What is it? What are the symptoms? What are the causes? What is the prognosis? Is it treatable?

Study finds Artificial Intelligence 90% accurate in diagnosing rare diseases

A new study finds that Artificial Intelligence (AI) is 90% accurate at detecting disease causing variants in children with rare diseases.

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