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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 […]

Pharma stakeholders to progress data-driven development at D4 Global

Front Line Genomics is delighted to announce the launch of D4 Global: the world’s first truly global event focusing on […]

Single Cell ONLINE – A virtual series

The human body has 40 trillion cells and roughly 200 different cell types. Amongst the diverse cell types lies incredible […]

Capture the dark genome: From repeat-expansions to CRISPR unintended mutations – Webinar Summary

Tackling Disease-Related Repeat Expansion Analysis – Marzia Rossato What is the Dark Genome? The dark genome refers to parts of […]

First Point-of-Care Test for COVID-19 using CRISPR announced

Binx Health and Sherlock Biosciences have announced a partnership to develop the world’s first point-of-care diagnostic test for COVID-19 using […]

Webinar: Capture the dark genome – From repeat-expansions to CRISPR unintended mutations

Sequenced genomes retain a surprisingly large number of “dark” regions – sections that have proven difficult to characterise via short-read […]

Base editing outcomes predicted by machine learning model

Single nucleotide variants (SNVs) are implicated in about half of all genetic diseases and so, accurately targeting and editing these […]

Study finds chemokine receptor inhibition can overcome immune hyperactivation in COVID-19 patients

A new single-cell analysis study of airway samples of COVID-19 patients has found that drugs targeting chemokine receptors may be […]

DNA Today podcast: Infertility series wrap up

DNA Today has just wrapped up their infertility series which started in April, coinciding with infertility awareness week. Over the […]

New class of precision oncology drug strips cancer of its DNA defences

Damage to the DNA in cells is the root cause of cancer, but it is also a weakness of the […]