Official Twitter account for David R. Liu's @davidrliu research group.

Joined February 2019
49 Photos and videos
Pinned Tweet
21 Oct 2019
Just a reminder that *all* of our lab's published papers can be freely accessed at any time on our lab webpage here: liugroup.us/publications #openscience #genomeediting #geneediting #chemtwitter

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liugroup retweeted
19 Nov 2025
Another jump for genome editing today by @davidrliu and colleagues, addressing the ~11% of nonsense mutations that lead to premature stop codons, affect protein synthesis, and suitable for disease agnostic intervention @Nature @NatureNV nature.com/articles/s41586-0… nature.com/articles/d41586-0…
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A team at the Broad Institute co-led by @Sarah_E_Pierce, @stevenerwood, and @davidrliu has developed a new genome-editing strategy that could potentially lead to a one-time treatment for multiple unrelated genetic diseases. broad.io/PERTNews
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liugroup retweeted
Single Prime Editing Platform Shows Potential vs. Multiple Diseases PERT edits the genome to permanently express a suppressor #tRNA, so that cells affected by nonsense mutations can produce functional protein @davidrliu #primeediting #geneticdiseases hubs.li/Q03Vdkqc0
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liugroup retweeted
19 Nov 2025
Today in @Nature we report a new prime editing strategy that can rescue a common cause of many genetic diseases in a disease-agnostic manner. This approach converts a redundant endogenous tRNA into an optimized suppressor tRNA, enabling a single prime edit to rescue premature stop codons across different diseases. (1/15) drive.google.com/file/d/1bSv…
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liugroup retweeted
13 Nov 2025
That @US_FDA is recognizing here the urgent need for regulatory strategies to evolve to match the pace of scientific advances in ways that streamline bringing the science safely to patients is incredibly important. I hope these new policies provide a foundation that will eventually allow certain kinds of genetic surgeries to become as routine as life-saving conventional surgeries, in which the process is robust and standardized enough to be rapidly adapted to each patient, without the need for a separate multi-year regulatory process for each surgery.
12 Nov 2025
Personalized therapies hold tremendous promise but challenge traditional models of drug and biologic development. The @US_FDA outlines a path to market entry for products where a randomized trial is not feasible. Learn more: nej.md/4nUQdcl
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liugroup retweeted
📣 Announcing the 2026 Franklin Institute Awards Laureates! Their work spans a range of scientific discoveries, from the smallest units of life to the vast expanse of the universe. Visit fi.edu/awards to learn how they are charting bold paths to the future! #FIAwards
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liugroup retweeted
10 Nov 2025
Alyssa Tapley was 13 when doctors told her she was going to die. She was diagnosed with a rare form of leukemia and had endured a year of failed treatments, including chemotherapy and a bone marrow transplant, when her doctors said they had run out of options. They were talking about end-of-life care when Tapley begged them not to give up on her. cbsn.ws/4r5E0EO
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liugroup retweeted
Tonight’s episode of @60Minutes will include a segment on the impact of federally funded science and recent cuts to science funding. Our lab’s development of base editing and prime editing and their clinical applications will be among the work described in the episode. paramountpressexpress.com/cb…
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liugroup retweeted
#NASmember David Liu is a pioneer in developing techniques to treat genetic disorders, including CRISPR. In an interview with @sciencenews, he discusses what first drew him to science, and what gives him hope for its future. Read here: ow.ly/w9BH50XcPOj #genetics
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liugroup retweeted
10 Oct 2025
An excellent interview with @davidrliu in Harvard Magazine highlighting his lab’s inventions (PACE, base editing, prime editing), his high-energy work ethic and “ceaseless” drive, his mentoring philosophy (giving freedom, emphasizing collaboration), and his motivation to translate basic research into patient impact. harvardmagazine.com/science/…
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15 Sep 2025
“Taking advantage of the ability of prime editing to do search-and-replace gene editing raises the possibility that a single composition of matter [...] might benefit many, many more patients than going after diseases one mutation at a time” -@davidrliu wired.com/story/the-next-era…
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When I first joined @GENbio in 2022, there was one name I kept hearing seemingly weekly: @davidrliu. David Liu's lab invented base and prime editing (gene editing tools now in 20 clinical trials with early wins against sickle cell, leukemia, and more). In this episode of @Inside_PM's Behind The Breakthroughs, David shares about his childhood, how he landed on the problem of engineering gene editors, and some of what he plans to reveal to the world next. Liu is a professor at @Harvard University and the @broadinstitute, co-founder of several companies, including @editasmed, @BeamTx, and @PrimeMedicine, and winner of the 2025 Life Sciences award from the @brkthroughprize. shows.acast.com/67105af84872… via @acast
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liugroup retweeted
21 Jul 2025
One-shot prime genome editing ("CRISPR 3.0") of the brain in vivo corrected AHC, a rare genetic disorder, in the mouse model. Another big step forward in the genome editing field. @CellCellPress @davidrliu and colleagues cell.com/cell/fulltext/S0092…
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liugroup retweeted
21 Jul 2025
These results represent the first use of prime editing to rescue a neurological disease in animals, establish that in vivo postnatal intervention in AHC’s pathology is possible, and suggest the potential of a one-time prime editing treatment for AHC. (Photo: hopeforannabel.org/ahc/) 9/10
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liugroup retweeted
21 Jul 2025
Today in @CellCellPress we report the use of prime editing to correct several mutations that cause alternating hemiplegia of childhood (AHC), a rare and devastating neurodevelopmental disorder, in patient-derived cells and in two mouse models. drive.google.com/file/d/1ibC… 1/10
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Partnership between @davidrliu, @jacksonlab, and rare disease group @RAREH0pe leads to first use of prime editing for a brain disease that reduced symptoms, extended lifespan in mice, offering hope for other rare genetic diseases. broad.io/Prime-AHC
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19 Jun 2025
The latest from Liu Group alum Luke Koblan? Oh, just a way to study cell state and lineage dynamics over biologically relevant spatiotemporal scales....in vivo 🧐🔬✨ Introducing PEtracer 👇🏼
1/14 On behalf of the amazing team in @JswLab, we’re excited to share PEtracer (biorxiv.org/content/10.1101/…) a prime editing-based evolving lineage recorder compatible with both scRNA-seq and high-resolution imaging readouts in intact tissue. By applying PEtracer in a syngeneic mouse model of lung metastasis, we dissect how cell-intrinsic and environmental factors coordinately shape tumor evolution in vivo.
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Researchers have developed a way to edit the genetic sequences at the root of Huntington’s disease and Friedreich’s ataxia. broad.io/GE-Huntingtons
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liugroup retweeted
27 May 2025
In @NatureGenet we report that base editing of trinucleotide repeats (TNRs) reduces somatic repeat expansions in Huntington’s disease (HD) and Friedreich’s ataxia (FRDA)—in patient-derived cells and in vivo—a collaboration with the Mouro Pinto lab. drive.google.com/file/d/1on7… 1/14
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“One of the biggest tragedies I've observed in my professional life.” @davidrliu, winner of the @brkthroughprize in Life Sciences and professor at the @broadinstitute and @Harvard, describes the cost of government cuts to science research at universities. @WalterIsaacson
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