Medical Sciences University- viewers forum

Medical Sciences University- viewers forum

Share

Founder of the University Health for All , Educate, Research, Develop Medical Sciences.

REVERSE AGING: The Nobel Prize Breakthrough 25/03/2026

Not expending on food? fasting and feasting may win you longlife and noble too.

REVERSE AGING: The Nobel Prize Breakthrough In 2016, a Japanese biologist won the Nobel Prize in Medicine for discovering how cells clean themselves. It wasn't a new drug or a superfood—it was a biolog...

19/03/2026

Mirculous cells , stem cell.

Your wisdom teeth may seem useless, but science is revealing they are a hidden biological treasure chest. These teeth contain mesenchymal stem cells, often called “master cells,” capable of transforming into different types of tissues. Researchers are exploring their potential to regenerate damaged organs, including the heart and brain, offering hope for revolutionary treatments in regenerative medicine.

Stem cells from wisdom teeth can be collected painlessly after extraction and stored for future use. Studies suggest these cells could one day help repair heart tissue after a heart attack or support brain regeneration in neurodegenerative conditions like Alzheimer’s or Parkinson’s. Unlike other stem cell sources, wisdom teeth are easy to obtain and carry fewer ethical concerns, making them an exciting area of research for cutting-edge therapies.

While these applications are still under study, the discovery highlights the untapped potential hidden in our bodies. Your wisdom teeth aren’t just leftover relics of evolution—they could be the key to life-saving treatments in the future. Preserving them might one day give you access to your own natural repair kit for some of the most critical organs in the body. Science is turning what was once considered useless into a powerful tool for health.

Follow @shadow.of_history 

A baby just became the first human to have his DNA rewritten while still alive — and it sounds like science fiction, but it’s real. Meet KJ, a nine-month-old from Philadelphia. His entire life was being threatened by something almost invisible: one single wrong letter inside his genetic code — just one mistake among nearly 3 billion DNA pairs. But that tiny error caused massive damage. Because of it, his liver couldn’t properly process ammonia. Every time he ate, toxic waste built up in his body and could flood his brain, creating a deadly cycle. Doctors knew there was only one way forward: they had to fix the problem at the source — the DNA itself. So they used CRISPR, like a GPS system for genes, to locate the broken letter, cut it out, and replace it with a healthy copy. What makes this even more unbelievable is the speed: the entire personalized treatment was designed in just six months, something never done before at this level. The therapy received approval rapidly, and KJ received the injection into his bloodstream at only six months old. The treatment traveled through his body, targeted his liver, found the defective gene, and rewrote his code from the inside. And it worked. KJ can now eat without his brain shutting down, and he’s doing what doctors once feared would never happen — sitting up, rolling over, and hitting milestones that were once considered impossible. One baby. One custom treatment. Six months from diagnosis to cure. This is not the future anymore — the future has already arrived. We post educational content daily — follow @shadow.of.history for more powerful real-life breakthroughs like this. 19/03/2026

Hope legal prectices are ethical and from trusted sources . Taking life to give life is not service , its business. so do not exchange create.

Follow @shadow.of_history A baby just became the first human to have his DNA rewritten while still alive — and it sounds like science fiction, but it’s real. Meet KJ, a nine-month-old from Philadelphia. His entire life was being threatened by something almost invisible: one single wrong letter inside his genetic code — just one mistake among nearly 3 billion DNA pairs. But that tiny error caused massive damage. Because of it, his liver couldn’t properly process ammonia. Every time he ate, toxic waste built up in his body and could flood his brain, creating a deadly cycle. Doctors knew there was only one way forward: they had to fix the problem at the source — the DNA itself. So they used CRISPR, like a GPS system for genes, to locate the broken letter, cut it out, and replace it with a healthy copy. What makes this even more unbelievable is the speed: the entire personalized treatment was designed in just six months, something never done before at this level. The therapy received approval rapidly, and KJ received the injection into his bloodstream at only six months old. The treatment traveled through his body, targeted his liver, found the defective gene, and rewrote his code from the inside. And it worked. KJ can now eat without his brain shutting down, and he’s doing what doctors once feared would never happen — sitting up, rolling over, and hitting milestones that were once considered impossible. One baby. One custom treatment. Six months from diagnosis to cure. This is not the future anymore — the future has already arrived. We post educational content daily — follow @shadow.of.history for more powerful real-life breakthroughs like this.

13/11/2025

University of Nottingham researchers have developed a protein-based gel that can regrow tooth enamel, published in Nature Communications.

The gel extracts calcium and phosphate ions from saliva to encourage mineral growth that merges with existing tooth structure.

Lead author Abshar Hasan stated the gel “promotes the growth of crystals in an integrated and organized manner.”

Lab tests on extracted human molars showed a protective layer formed within weeks, with growth happening “within a week,” according to Professor Alvaro Mata.

The regenerated enamel withstood simulated brushing, chewing, and acidic exposure. Clinical trials are scheduled for early 2026, with commercialization planned through startup Mintech-Bio.

13/11/2025

Wow..

A newly approved eye drop named VIZZ uses a drug called aceclidine to help people with presbyopia see up close clearly for up to ten hours with just one drop a day. Presbyopia is the normal age related process that often begins after age 45 when the lens inside the eye starts to stiffen and loses its ability to focus on near objects. The way VIZZ works is by gently shrinking the pupil creating a pinhole effect that increases depth of focus and sharpens near vision. Unlike older treatments it avoids pulling on the ciliary muscle which changes lens shape meaning your distance vision should stay clear without that zoomed or blurry look when you look far away.

In trials lasting tens of thousands of treatment days, users reported clearer reading vision and usually no serious side effects. Earlier drops like Vuity worked too but had some trade offs like affecting distance vision or causing discomfort because they put extra strain on muscle inside the eye. VIZZ sidesteps those issues by being selective only to the pupil so reading things close up like your phone or menus should become easier without needing reading glasses all the time. It is expected to reach people by prescription in late 2025.

Study led by researchers at LENZ Therapeutics.

Produced by 📄
LENZ Therapeutics

Stem Cells Repair Brain Damage Caused by Stroke in Mice 23/09/2025

Revealing Stem cells miracles..

Stem Cells Repair Brain Damage Caused by Stroke in Mice Brain damage caused by blocked blood vessels may be treatable using injections of stem cells, according to a new study by researchers from the University of Zurich and the University of Southern California.

Want your school to be the top-listed School/college in Jabalpur?

Click here to claim your Sponsored Listing.

Location

Address

Jabalpur