
CEO @scribetx | at the interface of molecular and genetic engineering | designing CRISPR to be safe enough for all
Joined April 2011
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Original Article: Prevalence of Silent Atherosclerosis across Adult Life (REACT trial) nej.md/46gp1hP
Editorial: Atherosclerosis across the Adult Lifespan โ A Call to Act from REACT nej.md/4A97Ag9
#ESCCongress #Cardiology

ALT This image contains four graphs showing the prevalence of peripheral and coronary-artery silent atherosclerosis throughout adult life. Panel A shows a cross-sectional age pattern of silent atherosclerosis prevalence in men and women. Panel B shows the distribution of atherosclerosis in the three arterial vascular territories (coronary, femoral, and carotid), stratified according to age and sex. Panel C shows the prevalence of atherosclerosis among male participants in any territory and for each vascular site, and Panel D shows the same data for female participants.
Benjamin L. Oakes retweeted
Itโs Day 2 of #AHA26 and our team has new data to share on our PCSK9-targeting epigenetic silencing and LPA-targeting gene editing programs, STX-1150 and STX-1200. Stop by our scientific presentations with any questions:
๐๐ฎ๐๐ฒ-๐ฏ๐ฟ๐ฒ๐ฎ๐ธ๐ถ๐ป๐ด: ๐ฆ๐ง๐ซ-๐ญ๐ญ๐ฑ๐ฌ ๐ฃ๐ฟ๐ผ๐๐ถ๐ฑ๐ฒ๐ ๐ฃ๐ฒ๐ฟ๐๐ถ๐๐๐ฒ๐ป๐ ๐๐๐-๐ ๐๐ผ๐ป๐๐ฟ๐ผ๐น ๐ณ๐ผ๐ฟ ๐ฎ๐ ๐๐ฒ๐ฎ๐๐ ๐ง๐๐ผ ๐ฌ๐ฒ๐ฎ๐ฟ๐ ๐๐ณ๐๐ฒ๐ฟ ๐ฎ ๐ฆ๐ถ๐ป๐ด๐น๐ฒ ๐๐ผ๐๐ฒ, ๐ฎ ๐ก๐ผ๐๐ฒ๐น ๐๐ฝ๐ถ๐ด๐ฒ๐ป๐ฒ๐๐ถ๐ฐ ๐ฆ๐ถ๐น๐ฒ๐ป๐ฐ๐ถ๐ป๐ด ๐๐ฝ๐ฝ๐ฟ๐ผ๐ฎ๐ฐ๐ต
10:45 a.m. CT | Basic Science Zone
Presented by @BenjaminLOakes, co-founder and CEO
๐ ๐ฆ๐ถ๐ป๐ด๐น๐ฒ ๐๐ฑ๐บ๐ถ๐ป๐ถ๐๐๐ฟ๐ฎ๐๐ถ๐ผ๐ป ๐ผ๐ณ ๐ฆ๐ง๐ซ-๐ญ๐ฎ๐ฌ๐ฌ ๐๐ฅ๐๐ฆ๐ฃ๐ฅ-๐๐ฎ๐๐ซ ๐๐ฒ๐ป๐ฒ ๐๐ฑ๐ถ๐๐ผ๐ฟ ๐๐ฐ๐ต๐ถ๐ฒ๐๐ฒ๐ ๐ฅ๐ผ๐ฏ๐๐๐ ๐ฎ๐ป๐ฑ ๐๐๐ฟ๐ฎ๐ฏ๐น๐ฒ ๐ฅ๐ฒ๐ฑ๐๐ฐ๐๐ถ๐ผ๐ป ๐ผ๐ณ ๐๐ถ๐ฝ๐ผ๐ฝ๐ฟ๐ผ๐๐ฒ๐ถ๐ป(๐ฎ) ๐๐ฐ๐ฟ๐ผ๐๐ ๐ฃ๐ฟ๐ฒ๐ฐ๐น๐ถ๐ป๐ถ๐ฐ๐ฎ๐น ๐ ๐ผ๐ฑ๐ฒ๐น๐
11:06 a.m. CT | Basic Science Zone
Presented by Elena Smekalova, Associate Director, Discovery Biology
@American_Heart
Benjamin L. Oakes retweeted
Replying to @AHAScience
@AHAScience #sessions26 underway + joy of seeing the legends like Nanette Wenger @ Paul Dudley White Lecture; Innovation session w/leaders in tech + life science; the joy of the mentorship and young career session; and walking w AHA Leadership team. #Relentless @NancyatHeart
Benjamin L. Oakes retweeted
๐ก Today at #AHA26, @American_Heart is hosting a new Innovation Forum for clinicians, researchers, entrepreneurs, and investors to share how they turn ideas into real-world cardiovascular impact. Join our CEO @BenjaminLOakes for two featured panel discussions:
๐ง๐ต๐ฒ ๐๐ป๐๐ฟ๐ฒ๐ฝ๐ฟ๐ฒ๐ป๐ฒ๐๐ฟ'๐ ๐๐ผ๐๐ฟ๐ป๐ฒ๐: ๐๐ฟ๐ผ๐บ ๐๐ฑ๐ฒ๐ฎ ๐๐ผ ๐๐บ๐ฝ๐ฎ๐ฐ๐
8:05 a.m. CT | Room S100A
Hear candid lessons from founders and innovation leaders on turning promising ideas into scalable solutions that improve health outcomes.
๐๐ ๐ฎ๐ป๐ฑ ๐๐ต๐ฒ ๐๐๐๐๐ฟ๐ฒ ๐ผ๐ณ ๐๐ฎ๐ฟ๐ฑ๐ถ๐ผ๐๐ฎ๐๐ฐ๐๐น๐ฎ๐ฟ ๐๐ป๐ป๐ผ๐๐ฎ๐๐ถ๐ผ๐ป
11:15 a.m. CT | Room S100A
A forward-looking conversation on how artificial intelligence may reshape discovery, care delivery, clinical decision-making, and the cardiovascular innovation ecosystem.
Benjamin L. Oakes retweeted
Meet our management team at upcoming healthcare investor conferences. Details below and in our press release: globenewswire.com/news-releaโฆ
๐๐๐ด๐ด๐ฒ๐ป๐ต๐ฒ๐ถ๐บ ๐ฏ๐ฟ๐ฑ ๐๐ป๐ป๐๐ฎ๐น ๐๐ฒ๐ฎ๐น๐๐ต๐ฐ๐ฎ๐ฟ๐ฒ ๐๐ป๐ป๐ผ๐๐ฎ๐๐ถ๐ผ๐ป ๐๐ผ๐ป๐ณ๐ฒ๐ฟ๐ฒ๐ป๐ฐ๐ฒ
Fireside chat featuring our CEO @BenjaminLOakes on Tuesday, Nov. 10, 2026 at 1:00 PM ET in Boston
๐ฆ๐๐ถ๐ณ๐ฒ๐น ๐๐ฒ๐ฎ๐น๐๐ต๐ฐ๐ฎ๐ฟ๐ฒ ๐๐ผ๐ป๐ณ๐ฒ๐ฟ๐ฒ๐ป๐ฐ๐ฒ
Presentation by our CEO Benjamin Oakes on Wednesday, Nov. 11, 2026 at 3:20 PM ET in New York
๐๐ผ๐ป๐ฑ๐ผ๐ป ๐๐ถ๐ณ๐ฒ ๐ฆ๐ฐ๐ถ๐ฒ๐ป๐ฐ๐ฒ๐ ๐ช๐ฒ๐ฒ๐ธ
Management to host one-on-one meetings with investors in London between Nov. 15-20, 2026
@Stifel #LLSW2026 #BIOPartnering
Benjamin L. Oakes retweeted
#AHA26 is almost here! The Scribe team is heading to Chicago to share exciting advances on our PCSK9-targeting epigenetic silencing and LPA-targeting gene editing programs, STX-1150 and STX-1200.
If youโre attending @American_Heart Scientific Sessions this year, join our CEO @BenjaminLOakes and Associate Director of Discovery Biology Elena Smekalova for these scientific presentations and Innovation Forum panel discussions! ๐
Saturday, November 7 | Scientific Presentations
1๏ธโฃ ๐๐ฎ๐๐ฒ-๐ฏ๐ฟ๐ฒ๐ฎ๐ธ๐ถ๐ป๐ด ๐ฝ๐ฟ๐ฒ๐๐ฒ๐ป๐๐ฎ๐๐ถ๐ผ๐ป: ๐ฆ๐ง๐ซ-๐ญ๐ญ๐ฑ๐ฌ ๐ฃ๐ฟ๐ผ๐๐ถ๐ฑ๐ฒ๐ ๐ฃ๐ฒ๐ฟ๐๐ถ๐๐๐ฒ๐ป๐ ๐๐๐-๐ ๐๐ผ๐ป๐๐ฟ๐ผ๐น ๐ณ๐ผ๐ฟ ๐ฎ๐ ๐๐ฒ๐ฎ๐๐ ๐ง๐๐ผ ๐ฌ๐ฒ๐ฎ๐ฟ๐ ๐๐ณ๐๐ฒ๐ฟ ๐ฎ ๐ฆ๐ถ๐ป๐ด๐น๐ฒ ๐๐ผ๐๐ฒ, ๐ฎ ๐ก๐ผ๐๐ฒ๐น ๐๐ฝ๐ถ๐ด๐ฒ๐ป๐ฒ๐๐ถ๐ฐ ๐ฆ๐ถ๐น๐ฒ๐ป๐ฐ๐ถ๐ป๐ด ๐๐ฝ๐ฝ๐ฟ๐ผ๐ฎ๐ฐ๐ต
10:45 a.m. CT | Basic Science Zone
2๏ธโฃ ๐ฃ๐ฟ๐ฒ๐๐ฒ๐ป๐๐ฎ๐๐ถ๐ผ๐ป: ๐ ๐ฆ๐ถ๐ป๐ด๐น๐ฒ ๐๐ฑ๐บ๐ถ๐ป๐ถ๐๐๐ฟ๐ฎ๐๐ถ๐ผ๐ป ๐ผ๐ณ ๐ฆ๐ง๐ซ-๐ญ๐ฎ๐ฌ๐ฌ ๐๐ฅ๐๐ฆ๐ฃ๐ฅ-๐๐ฎ๐๐ซ ๐๐ฒ๐ป๐ฒ ๐๐ฑ๐ถ๐๐ผ๐ฟ ๐๐ฐ๐ต๐ถ๐ฒ๐๐ฒ๐ ๐ฅ๐ผ๐ฏ๐๐๐ ๐ฎ๐ป๐ฑ ๐๐๐ฟ๐ฎ๐ฏ๐น๐ฒ ๐ฅ๐ฒ๐ฑ๐๐ฐ๐๐ถ๐ผ๐ป ๐ผ๐ณ ๐๐ถ๐ฝ๐ผ๐ฝ๐ฟ๐ผ๐๐ฒ๐ถ๐ป(๐ฎ) ๐๐ฐ๐ฟ๐ผ๐๐ ๐ฃ๐ฟ๐ฒ๐ฐ๐น๐ถ๐ป๐ถ๐ฐ๐ฎ๐น ๐ ๐ผ๐ฑ๐ฒ๐น๐
11:06 a.m. CT | Basic Science Zone
In town a day early for the inaugural AHA Innovation Forum? Weโll be participating in two sessions on Friday, November 6:
3๏ธโฃ ๐ง๐ต๐ฒ ๐๐ป๐๐ฟ๐ฒ๐ฝ๐ฟ๐ฒ๐ป๐ฒ๐๐ฟ'๐ ๐๐ผ๐๐ฟ๐ป๐ฒ๐: ๐๐ฟ๐ผ๐บ ๐๐ฑ๐ฒ๐ฎ ๐๐ผ ๐๐บ๐ฝ๐ฎ๐ฐ๐
8:05 a.m. CT | Room S100A
4๏ธโฃ ๐๐ถ๐ฟ๐ฒ๐๐ถ๐ฑ๐ฒ ๐๐ผ๐ป๐๐ฒ๐ฟ๐๐ฎ๐๐ถ๐ผ๐ป: ๐๐ ๐ฎ๐ป๐ฑ ๐๐ต๐ฒ ๐๐๐๐๐ฟ๐ฒ ๐ผ๐ณ ๐๐ฎ๐ฟ๐ฑ๐ถ๐ผ๐๐ฎ๐๐ฐ๐๐น๐ฎ๐ฟ ๐๐ป๐ป๐ผ๐๐ฎ๐๐ถ๐ผ๐ป
11:15 a.m. CT | Room S100A
See you in Chicago!
Largely agree with these thoughts, and have some perhaps discordant points to add.
- Solving biological diseases in the next few years will benefit mostly from the usefulness of the language models, substantially more than molecular ML.
- Proponents of the bitter lesson for biological models (not LLM) aren't wrong, just (possibly pathologically) too early. We don't have enough data, and the data we can collect quickly is probably not the right kind (we may get lucky with biology being easy, but it's usually not).
- I think just scaling models and public (passively accumulating) data is a cost ineffective direction (it's like scaling dense NNs on the internet). Today's model outputs are as good as GPT2. A single bioinformatician with linear regression, sometimes even without any additional data, can beat these models in many applications (people rarely benchmark AI advances against a simple Potts model). The most promising approaches for molecular models are innovating heavily on architecture (e.g. Baker Lab, Alphafold, etc). This may automate/speed up with LLMs.
- Few companies (hopefully Dyno included) are betting that we've triangulated enough pieces from multiple experimental channels to predict (with scale) how things translate in humans. Having worked on translating in vitro things to primates, I'm very cautious with the idea that current models, trained on current public data, can do anything more than manipulating already working solutions, either explicitly or through implicit remixing of what has worked. It may still work, but the underlying bets offer no specific reason why there is any epistemic risk advantage other than being "made with AI".
- Short term, there is more promise in combining molecular models with LLMs rather than scaling them. The two sources of lift in AI discovery elsewhere has been (1) Breaking Silos: AI synthesizes a bunch of knowledge/expertise that is rarely present in the same room (2) Data mining : AI pushes through volumes of data, with an intelligent eye, that humans or simple algorithms simply can't scale or adapt to. I'm curious what will come out of multimodal training of LLMs and biological data, which seems to be something the big players are pursuing. I think latent reasoning in the language (or better yet, + code) domain will reveal a lot more biology than scaling on nucleotides or proteins alone.
- My view is that the next opportunity of combining lab and AI will be massive-scale hypothesis testing with LLMs. Currently a multiplexed assay generally tries to test a handful of ideas because the humans are bandwidth limited in designing properly powered experiments. LLM's can scale this very well.
I have no doubt lots of good news will come on the impact of AI in biology in the next five years. I can't tell what paradigm will win, but my prediction is that it will not be the same paradigm imported from the LLM land (which will get a ton of funding anyways, because it's easy to pattern match for tech VCs).
Thereโs a really pronounced divide between people who are on the AI side of things and people who are on the biology side of things. Even among people working in AI, the divide persists based on where theyโre focused.
The AI side, adherents of scaling laws and the bitter lesson, believe that AI getting better means AI being more capable of novel discoveries in medicine (that go beyond discovering new drugs in well understood targets or speeding up dry lab work etc).
The biology people think the idea of a bitter lesson in biology is kind of ridiculous and that regardless of AIโs capabilities itโs going to be at least 5-10 years until you could hope to reliably simulate human toxicology in silico (right now AI/ML canโt even reliably simulate in vivo studies like binding affinities or functional assays).
Even the most AI pilled of them, who will list all the areas that AI can reduce the time spent on various areas, donโt think the concept of AI discovering novel targets or generating new understanding of causal biology is realistic in the near term. Most, in fact, will readily characterize the assumption that even an โASIโ level model could find cures hidden in our current understanding (without expanding that understanding with significantly more biological data) as patently false.
This was a big part of why we wanted to experience it ourselves by using AI for a (very) small portion of what it can do in biology. It was both mind blowing and revealed some poignant insights into how different the problem of making AI better at something like coding is to the problems of biology.
Even if it unlocked the ability to generate new molecules at a stunning pace, its simulation (in silico) of binding only had 49% accuracy. And if we wanted to improve that, weโd need to feed it back the data from the lab - data that took about 30x as long to get as it took to generate the molecules. And these were tests in a test tube (turn of phrase), imagine how long it would take if we wanted to improve the model with data that required recruiting humans and monitoring their reactions.
Human biology is very complex, and adding a drug - especially a novel drug and doubly so for a novel drug acting on a novel mechanism - means mapping interactions that have nth-order-effects that we donโt have the data to predict. Virtual cells have made advancements enabled by AI, but the perturbations equate to a small fraction of the possible.
This is before you even get into curing disease, especially uniquely human diseases. Brain function involves cellular identities that are unique to humans, meaning animal studies are of little use.
How long does it take to understand what the side effects of chronic administration of a drug in humans are? AI can speed up analyzing the data, or designing the trial or even getting it approvedโฆbut it canโt make a 6 month trial complete in 3 months.
I think its important to point out that significant advancements can be made in AI that contribute to biology, while also being realistic about how much it speeds up something as complex as curing a specific cancer or diseases of the brain.
Benjamin L. Oakes retweeted
A prevention conundrum:
- LDL-C lowering is prioritized after an ASCVD event because near-term absolute risk is high.
- Yet relative benefit is greater before a first event and at younger ages.
sciencedirect.com/science/arโฆ (Burger PM et al Atherosclerosis 2024)
We need to keep moving toward improving high lifetime-risk identification before the disease declares itself.
Benjamin L. Oakes retweeted
Next week, our CEO @BenjaminLOakes will speak at the @Biocom CEO Summit in Sonoma. Industry leaders can tune in for the โCEO Perspectives: Pharma BD&Lโ session โ a real-world tutorial for biotech CEOs and executive teams โ on Friday, October 23.
This #BiocomCEOSummit panel will walk through how business development deals actually move through biotech and pharmaceutical organizations, breaking down the practical mechanics, workflows, and decision points that shape whether a deal gets done or stalls along the way.
Benjamin L. Oakes retweeted
Most clinicians & scientists donโt set out to start a company. They set out to solve a problem. At #ScientificSession26, our first-ever Innovation Forum with @AHAScience opens with The Entrepreneurโs Journey: a candid talk on getting from idea to impact. professional.heart.org/en/meโฆ
Benjamin L. Oakes retweeted
Welcome to lesson #4 of ๐ฆ๐ฐ๐ฟ๐ถ๐ฏ๐ฒ ๐ฆ๐๐น๐น๐ฎ๐ฏ๐๐, our educational series exploring how genetic medicine can tackle some of healthโs most critical challenges.
Now that weโve covered CRISPRโs surprising and unassuming origin story, weโll boil down how the technology actually works โ and itโs much easier to understand than you might expect.
Leave any questions down in the comments!
๐ ๐๐ผ๐ ๐๐ฅ๐๐ฆ๐ฃ๐ฅ ๐ช๐ผ๐ฟ๐ธ๐: ๐ฃ๐ฎ๐ฟ๐ ๐ญ
It may seem complex, but the beauty of CRISPR is that itโs a remarkably elegant tool. That simplicity is why scientists around the world keep finding new uses for it beyond its original purpose as an immune defense system.
In our last Syllabus lesson, we learned that CRISPR harnesses biological functions from bacteria that allow them to fight viruses. The entire CRISPR system has two main components: the ๐๐ฎ๐ ๐ฒ๐ป๐๐๐บ๐ฒ and the ๐ด๐๐ถ๐ฑ๐ฒ ๐ฅ๐ก๐ (โ๐ด๐ฅ๐ก๐โ).
CRISPRโs revolutionary function is its ability to recognize, attach to and edit pieces of our DNA that predispose us to disease. In order to do this, it needs to identify the problematic sequence of DNA, and then cut it so the cellโs own repair machinery can modify it. Thatโs where the gRNA and Cas come in.
The gRNA finds the target DNA, and the Cas enzyme cuts it. Read all about it in our full post on Substack, and stay tuned for a deeper dive in part 2!
๐ scribetx.substack.com/p/scriโฆ
Benjamin L. Oakes retweeted
Itโs #WorldHeartDay and #CholesterolEducationMonth. Take action against cardiovascular disease for yourself and your loved ones by knowing the numbers that make it the leading cause of death ๐
โค๏ธโ๐ฉน Every 40 seconds, someone in the US has a heart attack.
โค๏ธโ๐ฉน Americans have more than 1.5 million heart attacks and strokes each year.
โค๏ธโ๐ฉน About 1 in 5 heart attacks are silent.
โค๏ธโ๐ฉน 63 million US adults have high LDL cholesterol (LDL-C), known as โbad cholesterol.โ
โค๏ธโ๐ฉน LDL-C is one of the largest drivers of heart disease, but only 20% of US patients with high LDL-C get treated.
To protect your #HeartHealth, get your LDL-C checked and treated early. Recent studies show:
๐ก People at lower risk of heart disease may gain the most from lowering LDL-C.
๐ก The benefits build over time: Keeping LDL-C lower for longer could mean fewer procedures down the line.
Sources: @American_Heart, @CDCgov, European Journal of Preventive Cardiology, American Journal of Preventive Cardiology
Learn about our work at Scribe to develop CRISPR-based genetic medicines that are safe and potent enough to address high LDL-C โ among other major risk factors of cardiometabolic disease โ to improve heart health for all: scribetx.com
Benjamin L. Oakes retweeted
Iโll be presenting in Scribe technology platform in two venues this week. Thanks to everyone who tunes in!
This week, tune into two events where our VP of Research Sarah Denny will break down the science and engineering approach behind our CRISPR-based genetic medicines.
1๏ธโฃ 7th Genome Editing Therapeutics Summit hosted by the Cell & Gene Therapy Event Series, AKA #crispr2.0 (September 28-30, Boston)
2๏ธโฃ Tech Spotlight: AI and CRISPR Genome Editing Webinar hosted by @Tech_Networks (September 29, virtual)
Benjamin L. Oakes retweeted
This week, tune into two events where our VP of Research Sarah Denny will break down the science and engineering approach behind our CRISPR-based genetic medicines.
1๏ธโฃ 7th Genome Editing Therapeutics Summit hosted by the Cell & Gene Therapy Event Series, AKA #crispr2.0 (September 28-30, Boston)
2๏ธโฃ Tech Spotlight: AI and CRISPR Genome Editing Webinar hosted by @Tech_Networks (September 29, virtual)
Benjamin L. Oakes retweeted
Welcome to lesson #3 of ๐ฆ๐ฐ๐ฟ๐ถ๐ฏ๐ฒ ๐ฆ๐๐น๐น๐ฎ๐ฏ๐๐, our educational series exploring how genetic medicine can tackle some of healthโs most critical challenges.
We previously covered the potential of genetic medicine to restore and improve everyone's health. In this post, weโll go back in time to understand where CRISPR โ one of the most powerful technologies for genetic medicine โ came from and how itโs being used to develop breakthrough therapies today.
Have a question or a topic we should cover in a future post? Drop it in the comments.
๐ ๐๐ผ๐ ๐๐ฅ๐๐ฆ๐ฃ๐ฅ ๐๐ฎ๐ ๐ฑ๐ถ๐๐ฐ๐ผ๐๐ฒ๐ฟ๐ฒ๐ฑ
Decades before CRISPR was harnessed into a gene editing technology, scientists understood that DNA holds the natural blueprint for disease prevention. The problem was turning that knowledge into safe, reliable treatments. They lacked a tool precise enough to make efficient, accurate edits to the human genome.
The discovery of CRISPR closed that gap, and it all started with bacteria.
For the full post, head over to our Substack where we cover:
โข The origin of CRISPR as a natural defense for bacteria to fend off viruses
โข How Jennifer Doudna (one of Scribeโs co-founders) and Emmanuelle Charpentier showed that CRISPR could be engineered and reprogrammed to target any piece of DNA, not just viral DNA
โข How CRISPR is being used today to improve human health across the globe
๐ scribetx.substack.com/p/scriโฆ
โ๏ธ Image credit: IGI Glossary Icon Collection by Christine Liu of Two Photon Art for the Innovative Genomics Institute
Benjamin L. Oakes retweeted
Hear directly from our CEO @BenjaminLOakes about Scribeโs lead asset STX-1150, a clinical-stage epigenetic silencing therapy purpose-built to repress PCSK9, lower LDL cholesterol, and offer durable cardiovascular risk reduction to patients in need.
More on our cardiometabolic pipeline, engineering approach compared to first-generation CRISPR technologies, and more in his conversation with @bradloncar.
Full video is up on @BiotechTV: biotechtv.com/post/scribe-thโฆ
๐๐๐ ๐๐๐๐: @scribetx which represents the next generation of CRISPR, had its IPO in July - the first clinical program targets PCSK9. With Co-Founder & CEO @BenjaminLOakes. $SCTX
Full video: biotechtv.com/post/scribe-thโฆ
Benjamin L. Oakes retweeted
๐๐๐ ๐๐๐๐: @scribetx which represents the next generation of CRISPR, had its IPO in July - the first clinical program targets PCSK9. With Co-Founder & CEO @BenjaminLOakes. $SCTX
Full video: biotechtv.com/post/scribe-thโฆ
Benjamin L. Oakes retweeted
๐ Atherosclerosis is complex.
Its root cause is not.
โ Inflammation modifies the response.
โ Hypertension accelerates the damage.
โ Diabetes amplifies the risk.
โ Smoking fuels the process.
๐But without apoB-containing lipoproteins entering and being retained in the arterial wall, there is no atherosclerotic plaque.
๐LDL is not just another risk factor.
It is the main causal driver of atherosclerosis.
No cholesterol deposition. No plaque.
@society_eas
Benjamin L. Oakes retweeted
๐งฌ๐ We built two-factor authentication into gene silencing. Read about it in our new blog and paper โ links in the comments.
We call this approach ๐ฆ๐ฒ๐พ๐๐ฒ๐ป๐๐ถ๐ฎ๐น ๐ฃ๐ฟ๐ผ๐ผ๐ณ๐ฟ๐ฒ๐ฎ๐ฑ๐ถ๐ป๐ด. Itโs engineered into ELXR, the epigenetic silencing technology built on our CRISPR-CasX platform.
The results? ๐จ๐น๐๐ฟ๐ฎ-๐น๐ผ๐ป๐ด ๐ด๐ฒ๐ป๐ฒ ๐๐ถ๐น๐ฒ๐ป๐ฐ๐ถ๐ป๐ด ๐๐ถ๐๐ต๐ผ๐๐ ๐ฐ๐ต๐ฎ๐ป๐ด๐ถ๐ป๐ด ๐ฎ๐ป๐ ๐๐ก๐.
โ More than 10-fold greater specificity
โ More than 4-fold greater silencing activity across every target tested
โ No toxicity in stress tests, rescuing growth defects observed with Cas9-based silencers
โ Mechanism mirrors the cellโs natural regulation
Learn more about this work led by Emeric J Charles, Christie C Sze, @BenjaminLOakes, Sarah Denny, @jdf_ev, and team below.
Benjamin L. Oakes retweeted
This week, donโt miss these upcoming talks by our co-founders:
1๏ธโฃ Fireside chat with CEO @BenjaminLOakes at the @HCWCO 28th Annual Global Investment Conference. This will take place Tuesday, September 15 at 2:30 p.m. ET in New York. #HCWConference
2๏ธโฃ Panel discussion where VP of External Innovation @BStaahl will discuss โAdvances in Gene Editingโ at the Cell & Gene Therapy Symposium. The session begins Thursday, September 17 at 11:00 a.m. PT in La Jolla and is hosted by the @CALifeSciences, @CIRMnews, and Gene Therapy Initiative at @UCSanDiego.
























