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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 […]

Mitochondrial DNA levels may underlie human diseases

A new study, published in eLife, has identified mitochondrial DNA levels as a potential biomarker of diseases such as cancer […]

Mitochondrial DNA is released by cigarette smoke

In a recent study, researchers have discovered that mitochondrial DNA is released extracellularly upon exposure to cigarette smoke and in […]

Mitochondrial DNA genotype-phenotype interactions

A recent study has found that genetic variants in mitochondrial DNA could increase the risk of developing several common diseases, […]

Combination therapy for mitochondrial disorders

Study shows how one specific combination therapy may provide measurable benefits to patients with mitochondrial respiratory chain disorders. Mitochondrial disorders […]

Genomic Sequencing to Explain New Rare Diseases

Determining the genetic basis of rare diseases is important for counselling and for developing our understanding of disease pathogenesis. While […]

Multi-Omics ONLINE – July Series

Sequencing technologies are continuously improving, making it easier to obtain more in-depth molecular information than ever before. As such, we […]

Genomics week in brief: Week ending 1st May

We have collated all the latest genomics new and research and put it here for you to easily read! Top […]

Genomics week in brief: Week ending 27th March

Check out the latest genomics week in brief – jam-packed with all the latest genomics news and research, all in […]

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, […]