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          SOD1

          Image shows molecular structure of proteins.
          FeaturedGeneticsNeurologyNeuroscience Videos
          ·December 31, 2015·5 min read

          Study Opens New Doors for ALS Drug Discovery

          Researchers pin down the structure of toxic clumps of a protein associated with a large number of ALS cases. The findings could help open the door to developing new drugs to treat the disease.
          Read More
          Image shows the SOD1 protein.
          FeaturedGeneticsNeurologyOpen Neuroscience Articles
          ·May 4, 2016·3 min read

          Aggregated Protein in Neurons May Cause ALS

          A new study reports people with ALs may have a genetic mutation that causes SOD1 to aggregate motor neurons in the brain and spinal cord.
          Read More
          Diagram of SOD1.
          FeaturedNeurologyOpen Neuroscience Articles
          ·May 16, 2016·3 min read

          Second Gene Modifies Effect of Mutation in a Dog Model of ALS

          Researchers have identified a modifier gene that affects the risk of developing degenerative myelopathy, a canine disease similar to ALS in Welsh corgis.
          Read More
          Image shows the structure of SOD1.
          FeaturedNeurology
          ·September 22, 2016·6 min read

          Researchers Reverse Protein Clumping Involved in ALS

          A new study reveals stabilizing the SOD1 protein can help reverse protein clumping in neurons affected by ALS.
          Read More
          Image shows an oligodendrocyte stained green.
          FeaturedNeurology
          ·September 27, 2016·3 min read

          Oligodendrocytes Induce Motor Neuron Death in ALS

          A new study reports oligodendrocytes induce motor neuron death in ALS.
          Read More
          Image shows a schematic for MAM distribution in ALS.
          FeaturedGeneticsNeurologyOpen Neuroscience Articles
          ·November 8, 2016·3 min read

          Collapse of Mitochondria-Associated Membrane in ALS

          Researchers report a collapse of the mitochondria-associated membrane is a common halmark in two genetic forms of ALS.
          Read More
          Image shows synapses.
          FeaturedGeneticsNeurology
          ·November 19, 2016·4 min read

          Protective Molecule Sidelined in Models of ALS

          Researchers have identified a naturally occurring molecule that has the potential for preserving sites of communication between nerves and muscles in ALS.
          Read More
          Image shows a diagram explaining how amitriptyline allows drugs to pass the bbb.
          FeaturedNeurologyNeuroscience
          ·April 27, 2017·4 min read

          Antidepressants May Enhance Drug Delivery to Brain

          A new study reports an antidepressant temporarily inhibits the blood-brain barrier, allowing drugs to enter the brain. The findings could have implications for treating neurological diseases from ALS to epilepsy.
          Read More
          Image shows the structure of SOD1.
          FeaturedNeurology
          ·May 22, 2017·3 min read

          Common Protein Abnormality Pinpointed in Parkinson’s and ALS

          Study implicates abnormalities in SOD1 with Parkinson's disease and ALS.
          Read More
          Image shows a DNA strand.
          FeaturedGeneticsNeurologyOpen Neuroscience Articles
          ·June 12, 2017·4 min read

          Malaria Drug Lowers Levels of ALS Linked Biomarker

          According to researchers, a drug that has been used for decades to help treat malaria can lower levels of a biomarker associated with ALS.
          Read More
          neurons
          FeaturedGeneticsNeurologyOpen Neuroscience Articles
          ·October 17, 2017·4 min read

          Resolving Traffic Jams in Human ALS Motor Neurons

          Researchers have generated motor neurons from people with familial ALS who carry FUS mutations.
          Read More
          FeaturedGeneticsNeurologyOpen Neuroscience Articles
          ·December 20, 2017·6 min read

          First Step Toward CRISPR Cure For ALS

          UC Berkeley researchers report they have successfully used CRISPR-Cas9 gene editing to delay symptoms and extend lifespan in mouse models of ALS.
          Read More
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          Depression and Urban Deprivation: Unseen Accelerators of Biological Aging

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          Neuroscience News Weekly Roundup – June 4, 2023

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          Targeted Therapy Vorasidenib Offers Hope for Deadly Brain Tumors

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          Hitching a Ride: mRNA’s Transport System in Brain Cells Revealed

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