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Last Week’s Top-3 Most Read Posts On ALS

Read the Articles Here: Dysfunctional ALS Patient Skin-Derived Muscle Neurons Rescued by Kenpaullone ALS and Other Neurological Disorders May Benefit from Prions Created in Lab Genervon’s GM604 May Slow Disease Progression in ALS Patients…

ALS Protein Dynamics May Hold Clues for Disease Progression

Researchers at the National University of Singapore have suggested there is a fine balance between amyotrophic lateral sclerosis (ALS)-related protein TDP-43’s normal function and its potential to cause neurodegeneration. The degeneration seems to occur due to pathological factors that exaggerate the protein’s membrane association, resulting in the loss of its physiological functions as well as…

What is ALS?

“Everybody knows about the Ice Bucket Challenge. But what do you know about the disease behind this challenge, known as ALS or MND? Watch this video to learn about it.” Learn more about ALS: https://bit.ly/ALSNewsToday…

Neuronal Degeneration Linked to Decline in a Synaptic Protein

University of Bern researchers have discovered that the synaptic protein Homer-3 is linked to the death of Purkinje motor neurons in Spinocerebellar ataxia type 1 (SCA1), a motor neuron disease that, like amyotrophic lateral sclerosis (ALS), is characterized by extensive motor neuron loss. The study, titled “Impaired mTORC1-Dependent Expression of…

Phi Delta Theta Fraternity Awards $100,000 to Milton Safenowitz Postdoctoral Research Fellow Studying ALS

The ALS Association has announced the Phi Delta Theta Fraternity is contributing to support the Milton Safenowitz Postdoctoral Fellow Program by awarding $100,000 over two years to Antonia Dominguez, Ph.D., a researcher focused on finding treatments for amyotrophic lateral sclerosis (ALS). The Milton Safenowitz Postdoctoral Fellowships were founded by the Safenowitz family…