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The CRISPR Journal Profile
The CRISPR Journal

@CRISPRjournal

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Cutting-edge peer-reviewed research and analysis on genome editing for the global CRISPR community. EIC @crisprchef | Exec Ed @kevinadavies @liebertpub

New Rochelle, NY
Joined May 2017
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@BBCBreaking
BBC Breaking News
25 days
Huntington's disease has been successfully treated for the first time, doctors tell BBC
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bbc.co.uk
One of the most devastating diseases finally has a treatment that can slow its progression and transform lives, tearful doctors tell BBC.
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@CRISPRjournal
The CRISPR Journal
25 days
Join our colleagues @GENbio for "The State of Biotech" 4-hr virtual event, today at 11 am ET/8 am PT. Highlights include a keynote interview with George Church with our Exec Editor, @KevinADavies. Registration is free:
@GENbio
Genetic Engineering & Biotechnology News
27 days
🎙️ Don’t miss @daphnezohar, @bradloncar & @cngarabedian of Biotech Hangout at #StateOfBiotech 2025 — Sept 24, 11:10 AM ET. Free summit hosted by @GENbio → https://t.co/R79K9887O8 #DrugDiscovery #LifeSciences #StateOfBiotech #BiotechHangout
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@zhangf
Feng Zhang
1 month
Deeply saddened by the loss of David Baltimore - a mentor, role model, and scientific giant who shaped so many of us. Most memorably, I was sitting next to David, a month after I started as a baby Assistant Professor, when I learned about CRISPR. His kindness and wisdom will be
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@LiebertPub
Mary Ann Liebert Inc
1 month
LAST CHANCE! TODAY, Vicky Smith, PhD, an expert in RNA biology, will provide a practical blueprint for enhancing mRNA quality using proven manufacturing strategies from TriLink’s 25+ years of expertise. REGISTER: https://t.co/iFIVmb6ZKh @TriLinkBioTech
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@nevillesanjana
Neville Sanjana
2 months
For those who read our group's lncRNA study published last year, we have recently learned that the Cas13 library included some gRNAs that were not properly filtered for potential off-targets (as described in the Methods). While this does not affect the study's main conclusions,
@nevillesanjana
Neville Sanjana
11 months
🚨🚨🚨 Thrilled to share our newest study — identifying functional long noncoding RNAs using transcriptome-scale RNA-targeting CRISPR screens. 🔎🔎🔎 We hope this scalable approach will be helpful for folks who want to connect noncoding RNAs to phenotypes & diseases.
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@KevinADavies
Kevin Davies
2 months
Can You Afford a Cure? The Gene Editing Dilemma - interview with Alta Charo https://t.co/CJrv8WWwIr via @YouTube
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@CRISPRjournal
The CRISPR Journal
2 months
The 2025 @ArrigeOrg annual meeting is being held Oct 28-29 in Strasbourg (hybrid). Speakers include: Fabiana Arzuaga, Argentina Marina Cavazzana, France Kazuto Kato, Japan Kiran Musunuru, USA Michael Pepper, SA Pawel Luckow, Poland Julian März, Switzerland https://t.co/ZA5hQ6C6U1
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@avapamini
Ava Amini
2 months
When it comes to deep learning for protein engineering, there is strength in simplicity. In a Preview piece @CellCellPress, we highlight work from @CaixiaGaoLab on using fixed-backbone sequence design to engineer genome editors with improved function. đź“„ https://t.co/NTjDMY4RP6
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@PlntTransformer
Matthew R. Willmann
2 months
Terrana Biosciences is looking to hire two Contract Research Associates to join our Delivery and Transformation team in Durham, NC.
job-boards.greenhouse.io
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@yaireinhorn
Yair Einhorn
2 months
Here’s a great interview of @davidrliu - the Co-founder of $BEAM & $PRME, in @GrinsteinJ “Behind the Breakthroughs” podcast in which they talk about CRISPR & Gene Editing & about the way that Prof. Liu’s groundbreaking modalities - Base & Prime Editing, are already saving lives!
@GrinsteinJ
Jonathan D. Grinstein, PhD
2 months
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
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@CRISPRjournal
The CRISPR Journal
2 months
Our August issue is online now: A special issue on the proceedings of the 2025 Global Observatory for Genome Editing conference, including a post-conference statement from the organizers. https://t.co/sByfaj9u2W (Full access for a limited time.)
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@GrinsteinJ
Jonathan D. Grinstein, PhD
2 months
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
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@LiebertPub
Mary Ann Liebert Inc
2 months
🚀 The State of Biotech 2025 — hosted by @GENbio. Wed, Sept 24 | 11 AM–3:30 PM ET. Free virtual summit with leaders in AI, CRISPR & biotech innovation. 🔗 https://t.co/OEEmo88D07 #Biotech #LifeSciences #Innovation #StateOfBiotech
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@CRISPRjournal
The CRISPR Journal
3 months
"A “Bare Hope of A Result”: The Second CRISPR Patent Appeal" -- Jacob Sherkow @jsherkow https://t.co/eBh6pSDziw
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@CRISPRjournal
The CRISPR Journal
3 months
"Bacterial Expression System with Deep Repression and Activation via CRISPR-Cas9" https://t.co/6l8YHGRlxb Manuvera et al.
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@CRISPRjournal
The CRISPR Journal
3 months
New online: "Implementation of an Undergraduate Laboratory-Based Mammalian Genome Editing Course" https://t.co/Fr4qJYxsuM Guerra et al.
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@CRISPRjournal
The CRISPR Journal
3 months
Malaria Transmission Blocked by One-Amino-Acid Mosquito CRISPR Edit in FREP1 - new work from Ethan Bier's group in Nature https://t.co/qLVeagiSOm via @GENbio
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genengnews.com
An allelic-drive system spreads malaria-blocking resistance in mosquitoes by altering a single amino acid in FREP1.
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@lecong
CL • Le Cong
3 months
🚀 Join CongLab @Stanford! We’re hiring postdocs to create lab-in-the-loop self-evolving AI agents, open benchmarks, to design, test & learn—advancing safer gene & cell therapies. Build on CRISPR-GPT, RNAGenesis model, Genome-Bench, for innovative medicines. #PostdocJobs
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@RLCscienceboss
Ryan Cross the Science Boss
3 months
A new #CRISPR Cures center, funded by $20M from @czi and led by @UrnovFyodor, will create 8 custom therapies for patients in the next 3 years. “Our goal is to aggressively walk the walk of CRISPR platformization,” Urnov told me. More in @endpts:
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endpoints.news
Scientists seeking to make personalized gene editing therapies a reality for more people have launched a new initiative to develop cures for the rarest of diseases left behind by drug companies.
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