BNIP1 identified as a risk gene for ALS
Broad data analysis points to genetic similarities between Lou Gehrig's Disease and a form of dementia...
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Broad data analysis points to genetic similarities between Lou Gehrig's Disease and a form of dementia...
An international team of researchers has identified a new gene associated with the development of amyotrophic lateral sclerosis...
Study provides a roadmap for using CRISPR to investigate neurological disorders...
Understanding how motor nerve cells respond to motor neurone disease could help researchers identify new treatment options...
A new small-molecule drug can restore brain function and memory in a mouse model of Alzheimer's disease by stopping toxic ion flow in the brain...
Scientists may have found possible targets for therapeutic interventions in the fight against Lou Gehrig’s disease.
Researchers have performed meta-analysis of neurological and neurodegenerative diseases and created an atlas of how cell characteristics are linked to their genotype...
The NIH has announced 13 two-year awards totalling $15m, to develop 3-D microphysiological system platforms that model human disease...
A new study shows that a variant in UBQLN4 gene has been associated with Lou Gehrig's disease, or amyotrophic lateral sclerosis (ALS). The study also describes how this gene variant disrupts a cellular process that drives motor neuron development. This new insight opens the door to potential treatment targets for…
BenevolentBio's CMO, Dr Patrick Keohane, says the industry is on the cusp of an artificial intelligence (AI) revolution...
Neurodegenerative diseases such as Alzheimer’s disease and Parkinson’s disease are a global health, economic and social emergency.
20 October 2016 | By Niamh Louise Marriott, Digital Content Producer
To unravel the role RNA-binding proteins play in ALS, Yeo's team gathered skin cells from ALS patients, three with a mutation in the hnRNP A2/B1 gene...
15 August 2016 | By Niamh Louise Marriott, Digital Content Producer
Targeting a single protein, SUPT4H1, reduces the levels of the three toxic entities created by the C9orf72 gene expansion, the most common genetic cause of ALS...
22 April 2016 | By Victoria White, Digital Content Producer
Researchers have developed a unique mouse model that will allow scientists to better study the genetic origins and potential treatments for ALS...
29 January 2016 | By Victoria White
Researchers have announced that they have essentially stopped the progression of amyotrophic lateral sclerosis (ALS) for nearly two years in one type of mouse model...