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Fungi in the digestive system of horses explored in study

AI Research Blog - The Transformer Blueprint: A Holistic Guide to the Transformer Neural Network Architecture

A deep dive into Transformer a neural network architecture that was introduced in the famous paper “attention is all you need” in 2017, its applications, impacts, challenges and future directions

National MS Society Invests $8 7M in MS Research, Clinical Trial Training

National MS Society Invests $8 7M in MS Research, Clinical Trial Training
multiplesclerosisnewstoday.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from multiplesclerosisnewstoday.com Daily Mail and Mail on Sunday newspapers.

NJ students: Flores selected as Newman Civic Fellow

NJ students: Flores selected as Newman Civic Fellow
mycentraljersey.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from mycentraljersey.com Daily Mail and Mail on Sunday newspapers.

Giving cells an appetite for viruses

 E-Mail IMAGE: A UT Southwestern study identified a gene used in the cellular recycling process called autophagy that rids cells of viruses. The above illustration breaks down the steps involved in this. view more  Credit: UT Southwestern Medical Center DALLAS - Dec. 16, 2020 - A team led by UT Southwestern researchers has identified a key gene necessary for cells to consume and destroy viruses. The findings, reported online today in Nature, could lead to ways to manipulate this process to improve the immune system s ability to combat viral infections, such as those fueling the ongoing COVID-19 pandemic. Scientists have long known that cells use a process called autophagy to rid themselves of unwanted material. Autophagy, which translates as self-eating, involves isolating cellular garbage in double-layered vesicles called autophagosomes, which are then fused with single-layered vesicles known as lysosomes to degrade the materials inside and recycle them into build

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