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9 天
on MSN
Decoding disease: Novel tool helps identify mutations in mitochondrial DNA
Geneticists looking inside the nuclear genome for mutations that contribute to disease have long relied on a principal known ...
生物通
1 天
生命科学学院胡家志课题组揭示线粒体DNA片段可广泛整合入核基因组
2024年11月1日,北京大学生命科学学院和北大-清华生命科学联合中心胡家志课题组及合作者在Nature Communications发表了标题为“Transfer of mitochondrial DNA into the nuclear ...
18 天
on MSN
Most patients with mitochondrial disease can be diagnosed via genomic sequencing, study says
When mitochondria are faulty due to genetic variations in key genes, cells begin to die until eventually, organ systems start ...
13 天
on MSN
Mitochondrial DNA levels impact tumor size, mouse study shows
A new collaborative study from Karolinska Institutet published in Science Advances shows that the levels of mitochondrial DNA ...
ALS News Today
5 天
Mitochondrial genome mutations linked to ALS in genetic study
Mitochondrial genome mutations may be linked to ALS, per a study, opening the door for new ways to diagnosing and treating ...
EurekAlert!
18 天
Identified 51 amyotrophic lateral sclerosis-associated mutations that could help diagnose ...
Using sequencing techniques, researchers associated 51 mutations in mitochondrial DNA with amyotrophic lateral sclerosis (ALS), an incurable degenerative ... Mutations in mtDNA can cause several ...
Labroots
14 天
Scientists Reveal 51 Mutations Linked to Changes in ALS Risk
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder in which neurons in the central nervous system that help ...
devdiscourse
3 天
Breakthrough in India: First Successful Treatment of Pearson Syndrome in Infants
Pearson Syndrome, a rare genetic condition affecting mitochondria in cells, has a global survival rate of merely one in a ...
News Medical on MSN
13 天
Researchers develop the first polymer-based therapeutic for Huntington’s disease
Breakthrough polymer-based therapy shows promise in reversing Huntington's disease symptoms by preventing toxic protein ...
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