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Democratic presidential candidate Beto O’Rourke has revealed he was a member of a notorious decades-old hacking group.

The former congressman was a member of the Texas-based hacker group, the Cult of the Dead Cow, known for inspiring early hacktivism in the internet age and building exploits and hacks for Microsoft Windows. The group used the internet as a platform in the 1990s to protest real-world events, often to promote human rights and denouncing censorship. Among its many releases, the Cult of the Dead Cow was best known for its Back Orifice program, a remote access and administration tool.

O’Rourke went by the handle “Psychedelic Warlord,” as revealed by Reuters, which broke the story.

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For decades, we’ve thought that memories were formed in two distinct stages—short-term first, then long-term later.

We might be wrong. New research suggests that our brains make two copies of each memory in the moment they are formed. One is filed away in the hippocampus, the center of short-term memories, while the other is stored in cortex, where our long-term memories reside.

These findings, published yesterday in the journal Science, upend more than 50 years of accepted neuroscience, and they’re being hailed by other neuroscientists. Here’s James Gallagher, reporting for BBC News:

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In February, a group of 16 researchers from Harvard, MIT, and other institutions around the U.S. and Europe launched the nonprofit Academy for Health and Lifespan Research to promote future work, ease collaborations between scientists, and ensure that governments and corporations are making decisions based on the latest facts instead of rumor, speculation, or hype.


Research into extending humanity’s healthy lifespan has been progressing rapidly in recent years. In February, a group of aging and longevity scientists founded a nonprofit to foster the work and serve as a resource for governments and businesses looking to understand the potentially far-reaching implications of a population that lives significantly longer, healthier lives.

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It is often not the lack of a cure, but the lack of will. Many great strides have been made with diabetes, when people stopped trying to develop medicines, and instead focused on how to enable the body to produce insulin.


Restoration of insulin independence and normoglycemia has been the overarching goal in diabetes research and therapy. While whole-organ and islet transplantation have become gold-standard procedures in achieving glucose control in diabetic patients, the profound lack of suitable donor tissues severely hampers the broad application of these therapies. Here, we describe current efforts aimed at generating a sustainable source of functional human stem cell-derived insulin-producing islet cells for cell transplantation and present state-of-the-art efforts to protect such cells via immune modulation and encapsulation strategies.

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