A new study shows that autism symptom severity, rather than a formal diagnosis, aligns with shared brain-connectivity patterns across children diagnosed with autism or ADHD.
University of Wollongong (UOW) scientists have developed a breakthrough therapy that clears toxic proteins from nerve cells—a discovery that advances the work of the late Professor Justin Yerbury and could transform the treatment of motor neuron disease (MND).
The proof-of-concept study, published in Nature Communications and led by Dr. Christen Chisholm from UOW’s Molecular Horizons, unveils a therapeutic designer molecule, MisfoldUbL, that targets and removes toxic misfolded SOD1 (superoxide dismutase 1) proteins from cells. SOD1 is an antioxidant enzyme that plays a crucial role in protecting cells from damage caused by superoxide radicals. About 35% of people with inherited MND in Australia have SOD1 gene mutations that cause more frequent misfolding.
“In MND, proteins misfold more frequently and the cell’s degradation systems become overwhelmed and stop working properly. The misfolded protein can then accumulate, forming clumps or ‘aggregates’ and over time, this accumulation damages and eventually kills motor neurons, leading to gradual muscle weakness, paralysis and death,” Dr. Chisholm said.
This pales into comparison to ChatGPT which can effectively read and analyze tens of thousands of words per second, since I process text computationally rather than linearly.
What if there was an invention or the concept of an invention that could be created to enhance a human beings capacity to read just as quickly as ChatGPT’s? I tasked ChatGPT with a step-by-step process to create that invention:
Here’s a concrete, neuroscience-grounded invention plan to push human reading toward “machine-speed”—while keeping comprehension and recall intact.
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## 0) Core idea (one sentence)
Exploit the brain’s natural reading pipeline—VWFA → Wernicke (lexico-semantic) ↔ Broca (phonological sequencing) with eye-movement–driven coarse-to-fine vision—by timing text delivery to your saccade/ fixation cycle, suppressing unnecessary subvocalization, and entraining semantic parsing rhythms. ([PMC][1])
## 1) Hardware & sensing.
People with anxiety disorders have lower levels of choline in their brains, according to research from UC Davis Health.
The study, published in the journal Molecular Psychiatry, analyzed data from 25 studies. The researchers compared the levels of neurometabolites—chemicals produced during brain metabolism —in 370 people with anxiety disorders to 342 people without anxiety.
They found the level of choline—an essential nutrient—was about 8% lower in those with anxiety disorders. The evidence for low choline was especially consistent in the prefrontal cortex, the part of the brain that helps control thinking, emotions and behavior.
Alzheimer’s disease (AD), the leading cause of dementia, affects nearly 40 million individuals globally, resulting in a gradual loss of memory and independence. Despite extensive research over the past decades, no treatments have been found that can halt or reverse the progression of this devastating disease.
In AD, a major contributor to neuronal dysfunction is the protein tau. Tau typically plays a crucial role in keeping the internal structure of neurons stable, much like train tracks help trains stay on course. However, in some diseases, tau undergoes abnormal modifications and starts to aggregate, disrupting this transport system, thus leading to neuronal damage and subsequent memory loss.
An international team of researchers has reported a new mechanism by which boosting the natural metabolite NAD⁺ can protect the brain from the degeneration associated with AD. Their paper, titled “NAD⁺ reverses Alzheimer’s neurological deficits via regulating differential alternative RNA splicing of EVA1C,” is published in Science Advances.
Adolescence, the life stage that marks the transition between childhood and adulthood, is known to be a vital period for the brain’s development. During this critical phase, people’s mental abilities, including their problem-solving and memory skills, rapidly improve.
Past neuroscience studies have tried to link these observed cognitive improvements during adolescence to changes in the structure of the brain and the connections between different brain regions. Nonetheless, the relationship between changes in the brain and specific aspects of cognitive performance has not been fully elucidated.
Researchers at Vanderbilt University, CNRS Université de Lyon, and Wake Forest School of Medicine recently carried out a study involving monkeys that was aimed at shedding new light into the underpinnings of mental maturation during adolescence. Their findings, published in Nature Neuroscience, suggest that the cognitive development of adolescent monkeys is associated with a refined connectivity between brain regions, while changes in gray matter structure play a lesser role.
A treatment that could protect premature babies from brain damage showed promise in a recent study in Sweden. Using a first-of-its-kind prenatal brain model created with human cells, researchers observed new details about the effects of cerebral hemorrhages on stem cells during preterm birth. They also successfully tested an antidote that reduced the damage.
Publishing in Advanced Science, the researchers identified how neural stem cells in preterm infants are damaged as a result of a cerebral hemorrhage. Researchers from KTH Royal Institute of Technology, Karolinska Institutet, and Lund and Malmö Universities collaborated on the study.
The study shows that as red blood cells seep into the brain’s subventricular zone (SVZ) and break down, levels of the immune response messenger protein interleukin-1 (IL-1) become elevated. These proteins send strong signals that direct neural stem cells to stop acting like stem cells, says Professor Anna Herland, senior lecturer at the AIMES research center at KTH Royal Institute of Technology and Karolinska Institutet.
Whole-brain emulation (often called “mind uploading” in science fiction) refers to the possible future ability to scan a human brain in such detail that a digital replica could be created, capable of functioning, and perhaps even experiencing the world, like the original. While we are far away from this now (the current record is a fruit fly) an increasing number of neuroscientists and entrepreneurs are betting that we may be closer than most think. What is happening in the world of computational neuroscience, and will the world be ready for it?
A research team from the School of Engineering at The Hong Kong University of Science and Technology (HKUST) has achieved a breakthrough in brain imaging by developing the world’s first technology to capture high-resolution images of the brains of awake experimental mice in a nearly noninvasive manner.
By eliminating the need for anesthesia, this innovation enables scientists to study brain tissue in its fully functional state. The advancement promises deeper insights into human brain function in both healthy and diseased conditions, opening new frontiers in neuroscience research.
The study was recently published in Nature Communications in a paper titled “Rapid adaptive optics enabling near-noninvasive high-resolution brain imaging in awake behaving mice.”