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First use of CRISPR against cancer in patients clears safety hurdles

The first attempt in the United States to use a gene editing tool called CRISPR against cancer seems safe in the three patients who have had it so far, but it’s too soon to know if it will improve survival, doctors reported Wednesday.

The doctors were able to take immune system cells from the patients’ blood and alter them genetically to help them recognize and fight cancer, with minimal and manageable side effects. The treatment deletes three genes that might have been hindering these cells’ ability to attack the disease, and adds a new, fourth feature to help them do the job.

“It’s the most complicated genetic, cellular engineering that’s been attempted so far,” said the study leader, Dr. Edward Stadtmauer of the University of Pennsylvania in Philadelphia. “This is proof that we can safely do gene editing of these cells.”

Dr. Bill Andrews Presentation & Tour of Sierra Sciences on October 11TH, 2019

Excellent lecture. Darwin’s turtle, sharks and clams 500 years old, talking about Liz Parrish at an hour and 8. And then a tour.


My mission is to drastically improve your life by helping you break bad habits, build and keep new healthy habits to make you the best version of yourself. I read the books and do all the research and share my findings with you!

This video is DR. BILL ANDREWS PRESENTATION & TOUR OF SIERRA SCIENCES ON OCTOBER 11TH, 2019. Brent Nally recorded, edited and produced this video. My apologies for the poor audio and camera work in the first few minutes. Infinite gratitude to Bill for opening up Sierra Sciences to us. Here’s a link to purchase IsaGenesis. You have to sign up first: https://getstarted.isagenix.com/VF234XXQV001

- Please consider a donation to me: My Bitcoin Cash (BCH) address: qr9gcfv92pzwfwa5hj9sqk3ptcnr5jss2g78n7w6f2 or https://paypal.me/BrentNally

SHOW NOTES:

New gene editing technology could correct 89% of genetic defects

Scientists have developed a new gene-editing technology that could potentially correct up to 89% of genetic defects, including those that cause diseases like sickle cell anemia.

The new technique is called “prime editing,” and was developed by researchers from the Broad Institute of MIT and Harvard, who published their findings Monday in the journal Nature.

Prime editing builds on powerful CRISPR gene editing, but is more precise and versatile — it “directly writes new genetic information into a specified DNA site,” according to the paper.

What is Build-A-Cell?

Cells are the fundamental “building blocks” that make up living organisms. Yet, we don’t know exactly how cells were formed in the first place. We also don’t know what all the molecules that make up any natural cell do. Finally, we can’t yet put molecules together ourselves to make new synthetic cells.

Addressing the questions and challenges posed above requires significant collaboration and cooperation. The Build-a-Cell community welcomes all who wish to learn about and cooperate in the work of fully understanding and engineering a diversity of synthetic cells.

The future of biotechnology is in realizing fully understood, lineage agnostic organisms, beginning with single cells.

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