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A major cause of rare mitochondrial disease found

A study from the Murdoch Children’s Research Institute (MCRI) has found a genetic cause for a rare disease that causes […]

An Eye for an Eye: A New Optic Gene Therapy

A recent paper, published in Science, explored the use of optic gene therapy to treat Leber’s Hereditary Optic Neuropathy. Surprisingly, […]

Just one base at a time

The advancements in base editing, a new genome editing approach, have generated a lot of excitement amongst scientists in recent […]

Purifying selection in T cells

A recent publication in The New England Journal of Medicine has reported observations of reduced heteroplasmy in T cells – […]

Genomics week in brief: Week ending 2nd January

Happy New Year from everyone here at Front Line Genomics! We are kicking the year off with your weekly update […]

Genomics week in brief: Week ending 12th December

The penultimate week in brief before Christmas, full of the latest research and news surrounding genomics. Top stories from the […]

Genomics week in brief: Week ending 21st November

We’ve got you covered with another round up of the top genomics news and research from around the world from […]

A year-long human spaceflight reveals circulating biomarkers

A team of researchers have profiled cfDNA isolated from plasma of an astronaut during a year-long mission on the International […]

ASHG Virtual Meeting 2020

Last week (27 – 30th October 2020), the American Society of Human Genetics (ASHG) hosted their annual meeting. The meeting […]

African genomics needed for genetic medicine

As part of the 20th anniversary of Nature Reviews Genetics, Professor Ambroise Wonkam from the University of Cape Town has […]