|
Presenting Author |
Abstract Title |
Talk/Poster |
|
Achary, Vanpalli Mohan M |
Development of low-rancidity, shelf-stable pearl millet flour via targeted genome editing |
poster |
|
Ahn, Chul Woo |
Population-informed regulatory STRs at PITX2/PANCR nominate CRISPR-editable targets for atrial fibrillation functional genomics |
poster |
|
Ahouefa Adanho, Corynne Stephanie |
Scale up CRISPR/Cas9 and base editing of human CD34+ HSPCs using peptide-mediated RNP delivery for translating to an ex vivo therapy for sickle cell anemia |
poster |
|
Anderson, Rachel A |
Elucidating the genetic determinants of ABE editing using CRISPRi screens |
talk |
|
Aouida, Mustapha |
Enhanced cellular uptake of compact Cas proteins—A comparative study of Cas12f and Cas9 in human cells |
poster |
|
Arceneaux, Aster |
A compact, PAM-independent TasR gene-editor for single-vector exosomal-encapsulated-AAV delivery in vivo |
poster |
|
Aspiras, Ariel C |
Adapting PASSIGE for targeted insertion of CFTR Super Exons into the CFTR genomic locus |
poster |
|
Bajpai, Ruchi |
DNA barcoding measures diversity of genome edited cell pools and tracks modified alleles |
poster |
|
Barrera, Shirley |
Enhancing CRISPR-mediated HIV-1 proviral targeting through optimized SaCas9 tracrRNA design |
poster |
|
Bauer, Jackson H |
Base and prime editing to correct the most common non-deletional mutation in alpha thalassemia |
poster |
|
Blackwood, Stephanie |
Developing a therapeutic in vivo prime editing strategy for MCAD deficiency |
poster |
|
Bondy-Denomy, Joseph |
Diverse mechanisms of CRISPR-Cas evasion by bacteriophages |
talk |
|
Bonuzzi, Ilaria |
In vivo homology-independent targeted integration mediated by all-in-one AAV delivery of a novel engineered TnpB genome editor |
poster |
|
Borah, Ashir A |
PerturbAgent—An agentic framework for closed-loop discovery in perturb-seq |
poster |
|
Boros, Daniel |
Exon-sized random mutagenesis of human chromosomes using mutagenic retron elements |
talk |
|
Bouillet, Antonin |
New developments to CRISPOR for end-to-end design of genome editing experiments |
poster |
|
Brandao, Karina |
Optimizing prime editing for precise genome engineering in cancer cell models |
poster |
|
Brooks, Alan |
Targeted insertion of Factor VIII gene using a Type V CRISPR system results in dose dependent and durable Factor VIII expression in nonhuman primates |
poster |
|
Buchholz, Frank |
Gene editing platforms for innovative health solutions |
talk |
|
Buffington, Jesse D |
Engineering retron editors for robust mammalian gene editing |
poster |
|
Carbajal Contreras, Hector |
Mitigating adverse CRISPR effects in functional cell-culture studies |
poster |
|
Carnevale, Julia |
Virus-like particles enable targeted gene engineering and pooled CRISPR screening in primary human myeloid cells |
talk |
|
Chaudhry, Gautam |
Next-generation modeling of complex genetics in vivo with multiplexed, inducible prime editing |
poster |
|
Chauhan, Vikash P |
Engineered prime editors with minimal genomic errors |
talk |
|
Chen, Evelyn |
In vivo base editing screens uncover genetic modifiers of CAR-T cell therapy response in pancreatic cancer |
poster |
|
Chen, Fei |
Mapping regulators of tissue regeneration with scalable in vivo CRISPR screening |
talk |
|
Chen, Honglin |
Target RNA abundance controls the collateral activity of RfxCas13d in human cells and zebrafish embryos |
poster |
|
Chen, Wei |
De novo design of genome regulators |
talk |
|
Chi, Hongbo |
Next-generation CRISPR screens enable causal systems biology in immuno-oncology |
talk |
|
Cialek, Charlotte |
IDT custom guide RNAs and CRISPR off-target solutions—Early research to therapeutic development |
poster |
|
Conklin, Bruce |
Leveraging human genetic variation to therapeutically target hundreds of genes with dominant and dispensable disease alleles |
poster |
|
Cordes, Stefan |
Consilience—A single-cell multiomic framework for designing cis-regulatory perturbations of T-cell state |
poster |
|
Cowan, Quinn |
Manipulating DNA repair pathways to alter excision and inversion profiles in post-mitotic cells |
poster |
|
Cristian, Ana |
Efficient prime editing in vivo and in vitro using lipid nanoparticles |
talk |
|
Crosby, Kadin T |
Determining the mismatch inhibition mechanism of Cas12a2 for selective cell killing |
poster |
|
Csoma, Balazs |
Design principles and usage of alternative pegRNAs |
poster |
|
Damodaran, Arun |
Systematic single-cell exon deletions map alternative splicing-driven gene regulatory programs |
poster |
|
Daneshpajouh, Amirhossein |
A distribution-free certificate for the off-target miss-rate of clinical CRISPR guides and the limits of what can be certified |
poster |
|
Dhanjal, Soniya |
Enabling CRISPR-based functional genomics through national research infrastructure—The SciLifeLab CRISPR Functional Genomics Unit |
poster |
|
Docter, Trevor |
VIPR RNA-guided DNA recognition by noncontiguous geometric triplex formation |
talk |
|
Eid, Ayman |
Multi-component optimization of SHARC CRISPR tools in plants |
poster |
|
Eitzinger, Simon |
Molecular requirements of efficient DNA integration with evoCAST |
talk |
|
Erwood, Steven |
Engineering of compact prime editors by sequence-function mapping |
poster |
|
Eshleman, James R |
Can CRISPR-Cas9 genetically kill cancer? |
poster |
|
Fatma, Shirin |
Structure of the Type I-F3 CAST holo integration complex reveals licensing mechanisms during RNA-guided DNA integration |
talk |
|
Fayer, Shawn |
Editing stem cell genomes at scale to measure variant effects in diverse cell and genetic contexts |
talk |
|
Fuller, Mary Gracen A |
Characterization of large serine recombinases (LSRs) for genome engineering in Lactobacillus gasseri |
poster |
|
Gál, Luca |
Systematic evaluation of the effect of PBS length on editing outcome in prime editing |
poster |
|
Ganesan, Vijaydev |
Development of a high-efficiency, multiplexed CRISPR-Cas9 toolkit in non-model oleaginous yeasts for enhanced xylitol production |
poster |
|
Gao, Alex |
Beyond CRISPR—Phage protein sensing and host factor repurposing in bacterial immunity |
talk |
|
Gautier, Megan K |
In vivo corrective editing of the liver improves brain network dynamics in a mouse model of phenylketonuria |
poster |
|
Gibson, Daytan |
Base editing tiling screens with prime editing-based saturation mutagenesis as a strategy to map ligand-specific resistance |
poster |
|
Gladkov, Gregory T |
A genome-wide CRISPR loss-of-function screen in primary human CD4+ T cells identifies novel host regulators of HIV-1 Envelope biogenesis and broadly neutralizing antibody (bNAb) binding |
talk |
|
Gordan, Raluca M |
Intrinsic dCas9-DNA binding behaviors reveal mechanisms of ineffective and promiscuous guides in epigenome editing |
talk |
|
Gu, Bo |
Programmable pathway profiles reveal signaling principles of TGF-β superfamily receptors |
talk |
|
Guffy, Sharon L |
SHARC cytosine base editor optimization for agricultural applications |
talk |
|
Gupta, Nikhil |
Scarless conditional guide RNA activation enables temporal, rapid and non-leaky CRISPR perturbation |
poster |
|
Gupta, Ria |
Linking CRISPR perturbations to live-cell behavior, morphology, and paired transcriptomics in single cells |
poster |
|
Haas, Johannes |
Direct repeat engineering enables robust Cas13d multiplexing for combinatorial RNA perturbation screens |
poster |
|
Hacker, Julia |
Comparative efficacy of LNP-delivered base editing strategies in Rosa26 knock-in versus minimally humanized mouse models for multiple pathogenic variants of metabolic disease |
poster |
|
Hamilton, Jennifer R |
Programmable in vivo engineering of T cells via cell-targeted CRISPR delivery and site-specific gene integration |
talk |
|
Han, Huajun |
Perturb-seq of select Crohn’s disease candidate genes in human monocyte-derived macrophages defines cell states and fates |
poster |
|
Haupt, Amanda |
Decoupling deaminase recruitment reveals a Cas association-dependent origin of off-target base editing |
poster |
|
Held, Friederike |
Latency-resolved CRISPR perturbation of EBV+ B cells to dissect host-permissive states, EBV genomic variants, and EBV-host interactions in multiple sclerosis |
poster |
|
Hempstead, Andrew |
Fostering scientific discovery and innovation through research tool sharing |
poster |
|
Herail, Theo |
Development of a prime editing tool for the generation of protein diversity in eukaryotic cells |
poster |
|
Hernandez-Reyes, Jayvin |
Safe Harbor-enabled high-throughput screening of gene editing tools in inherited retinal disease |
poster |
|
Hess, Gaelen |
Scalable identification of function-modulating mutations using diversifying base editors |
poster |
|
Hirabayashi, Shigeki |
Functional interpretation of GATA2 variants through GenoPrime-Perturb-seq |
talk |
|
Hong, Soonwoo |
AI-guided CRISPR-based tuberculosis drug resistance detection |
poster |
|
Hsing, I-Ming |
DNA guided CRISPR Cas12a—Reprogramming the activation pathway for programmable RNA targeting |
poster |
|
Hsiung, Chris |
Higher-order combinatorial functional genomics |
talk |
|
Hu, Hannah |
Genetically modifying patient-derived induced pluripotent stem cells to rescue autosomal dominant retinal disorders for autologous transplantation therapy |
poster |
|
Iohannes, Sessen D |
A protein-responsive feedback circuit underlies transcriptional compensation in plant stem cells |
talk |
|
Jackson, Ryan N |
Molecular basis of activating Cas12a2 |
poster |
|
Jancola, Kyle |
Identification of pathogenic DNA mismatch repair variants conferring increased cancer risk |
poster |
|
Jeon, Youngkyu |
Combinatorial CRISPR screening uncovers genetic interaction networks underlying metabolic plasticity in cancer cells |
poster |
|
Jinek, Martin |
Molecular mechanisms of RNA-guided transposons and recombinases |
talk |
|
Jo, Ilhyeong |
Optimization of tomato gene promoters and regulatory elements for transgene expression and prime editing in Nicotiana benthamiana |
poster |
|
Joe, Joanna |
Modification of Easi-CRISPR knock-In protocol to create an Atm inducible mouse model of ataxia telangiectasia |
poster |
|
Jowdy, Casey C |
Enhancing T cell fitness through genome engineering using hfCas12Max delivered via mechanoporation |
poster |
|
Judge, Luke |
Mutation-specific and mutation-agnostic inactivation of a dominant-negative disease allele ameliorates spinal motor neuropathy in vivo |
poster |
|
Jung, Hyuncheol |
Virus-like particles enable targeted gene engineering and pooled CRISPR screening in primary human myeloid cells |
poster |
|
Justice, Brandon M |
Unlocking extra-hepatic therapeutics with compact gene editors |
poster |
|
Kadirkamanathan, Renuka |
Genome editing strategies for fragile DNA disorders |
poster |
|
Kahn, Elena |
Correction of a recurrent pathogenic variant in methylmalonic acidemia using adenine base editing |
poster |
|
Kennedy, Jesse G |
Don’t stop at red lights—CRISPR prime integrase for targeted knock-out and replacement in a novel traffic light assay |
poster |
|
Khan, Misbah |
A bacteria-free CRISPR–HDR workflow for editing episomal KSHV genomes directly in mammalian cells |
poster |
|
Kimihira, Tetsutaro |
Development of a novel transcriptional activation tool based on type I-E CRISPR-Cas |
poster |
|
Kinney, Kyle |
A programmable UNA guide architecture improves CRISPR genome-editing specificity across genomic loci |
poster |
|
Kipp, David W |
Quantification of early-disease biomarkers in a mouse model of IMPG2-mediated retinal degeneration |
poster |
|
Koblan, Luke W |
Comprehensive lineage tracing maps the landscape of cell fate decisions in mouse embryogenesis |
talk |
|
Komor, Alexis C |
Engineering and optimizing precision genome editing tools |
talk |
|
Kraus, Carolyn |
Myo-miR restricted muscle genome editing in mice |
poster |
|
Ku, An-Chi |
Engineered virus-like particles (eVLPs) as a versatile and safe delivery platform for advanced CRISPR genome editing |
poster |
|
Kulcsar, Peter |
In vivo genome editing of MC4R prevents and reverses obesity in mice |
poster |
|
Lai, Zheng-Sheng |
ITR-flanked single-stranded DNA is not the sole determinant of efficient CRISPR-mediated knock-in using AAV-delivered donor templates |
poster |
|
Larkin, Hailey |
Efficient large-fragment CRISPR knock-in enables a fluorescent reporter cell line for adipogenic differentiation studies |
poster |
|
Lee, Wei Ting Chelsea |
Enabling CRISPR-mediated homology-directed repair in somatic cells in vivo |
poster |
|
Li, Chaozheng |
We combine our proprietary AI-powered gene editing platform, CasN, with machine learning-driven sgRNA and ssDNA design algorithms to deliver fast, cost-effective, and high-quality gene knock-in and knockout services at scale |
poster |
|
Li, Wei |
pertTF—Context-aware AI modeling for genome-scale and cross-system perturbation prediction |
poster |
|
Li, Weilin |
Investigating the roles of cell polarity protein RACGAP1 in regulating gemcitabine resistance in pancreatic cancer |
poster |
|
Liang, Xiquan |
Vivofectamine delivery solutions—Lipid nanoparticles for in vivo gene editing in the liver |
poster |
|
Liu, Bin |
Prime assembly with linear DNA donors enables large genomic insertions |
talk |
|
Liu, David R |
Mutation-specific, mutation-agnostic, and disease-agnostic therapeutic genome editing |
poster |
|
Liu, Shawn |
Mutation-agnostic silencing of pathological alleles by CRISPR-IMPRINT |
poster |
|
Liu, Yanjing |
Combinatorial engineering identifies potent novel activators for scalable CRISPR activation |
talk |
|
Lobo, Tatiana |
FAM50A synthetic lethality in solid tumors—A biomarker-driven therapeutic opportunity |
poster |
|
Loveless, Theresa B |
Engineerable RNA Polymerase III promoters for gene editing and DNA recording |
talk |
|
Lu, Xiaona |
Brain-wide non-viral genome editing for angelman syndrome using STEP-RNP delivery in non-human primates |
talk |
|
Lucas, Julie L |
Decoupling CRISPR recognition and signal generation through binding based capture |
poster |
|
Lukarska, Maria |
Activity and specificity trade-offs in adenine base editors |
poster |
|
MacVeigh-Fierro, Daniel T |
Enhancing the purity and efficacy of click editing through chemically modified templates |
poster |
|
Manabayeva, Shuga |
Development and optimization of CRISPR/Cas9 system elements for studying drought resistance mechanisms in potatoes |
poster |
|
Maxwell, Karen L. |
Rewriting DNA repair for bacterial immunity—Widespread glycosylases target modified phage genomes |
talk |
|
McDiarmid, Troy A |
Large-scale discovery of neural enhancers for cis-regulation therapies |
poster |
|
McVicker, Graham |
Joint single-cell capture of Cas9 edits and transcriptomes reveals on- and off-target effects on gene expression |
poster |
|
Meganathan, Kesav |
A quality control framework for CRISPR-engineered iPSCs in drug discovery |
poster |
|
Mercer, Heather |
Experimentally informed model of CRISPR-CAS9 site affinity |
poster |
|
Miller, Blake |
Inhaled delivery of gene editors to the distal lung via polymer 81 |
poster |
|
Mller, Rasmus |
Endogenous microRNA logic gates for spatiotemporal control of CRISPR/Cas systems |
poster |
|
Moffat, Jason |
Integrative CRISPR approaches and annotation efforts for precision disease modeling |
talk |
|
Mondal, Indranil |
Saturation prime editing coupled to a fluorescent miRNA-activity reporter resolves DICER1 variant pathogenicity at scale |
poster |
|
Moon, Tae Seok |
CRISPR-mediated engineering of microbes and microbiota for real-world applications |
poster |
|
Mustafa, Yasmin M |
Optimization of prime editing and eePASSIGE-mediated targeted transgene integration into safe harbor locus in sheep fetal fibroblast cells |
poster |
|
Myhrvold, Cameron |
Intersegmental transfers drive target search in an RNA-targeting CRISPR system |
talk |
|
Nagatomo, Daiki |
Optimization, enhancement, and modification of PAM preference in CRISPR-Cas3-mediated gene knock-in with long DNA replacement |
poster |
|
Nakamae, Kazuki |
PtWAVE—Sanger trace deconvolution software for sensitive detection of large deletions at genome-editing target sites |
poster |
|
Napoliello, Renee |
Guide RNA and Cas9 protein structure predict CRISPR outcomes across experimental contexts |
poster |
|
Nayfach, Stephen |
Programming PAM specificity for mutation-specific base editor design |
talk |
|
Newcombe, Kevin L |
The novel recombinase Brec1 recombines HIV-1 and acts on integrated provirus |
poster |
|
Nguyen, Long T |
Engineering TIGR-TasR as a hypercompact PAMless RNA-guided genome editor for mammalian cells |
poster |
|
Noun, Tala |
Genetic interactions delineate roles of chromatin remodeling complexes in EMT |
poster |
|
Orosco, Carlos |
DNA-guided CRISPR-Cas12 for cellular RNA targeting and DNA-RNA editing |
poster |
|
Ortego, Michael S |
Investigating the impact of excess gRNA and multiplexing on RNP efficiency |
poster |
|
Osgood, Nicola |
Your New BESTIE—A high-throughput screening tool to interrogate base editing outcomes |
poster |
|
Pandala, Niharika |
A scalable computational workflow for CHANCE-seq off-target profiling of CRISPR nucleases and base editors |
poster |
|
Patel, Nikhil |
High-dimensional optical screens reveal organizing principles of biomolecular condensate assembly |
talk |
|
Patinios, Constantinos |
Natural DarT toxin diversity expands Append Editing into a modular genome editing platform |
poster |
|
Peled, Eden |
Base editing rescues survival and neurodevelopmental deficits in a mouse model of GRIN2D developmental epileptic encephalopathy |
poster |
|
Pereira, Arthur O |
Engineering CRISPR-Cas3-mediated phage resistance in Xanthomonas citri |
poster |
|
Perrotta, Ramiro M |
Engineered base editors with reduced bystander editing through directed evolution |
talk |
|
Peters, Samuel T |
Hidden structural complexity of rAAV-mediated knock-in alleles revealed by LOCK-seq |
poster |
|
Pham, Vi |
Correction of a recurrent pathogenic variant in multiple sulfatase deficiency using adenine base editing |
poster |
|
Pinello, Luca |
From long reads to personal genomes—Computational tools for measuring genome editing outcomes and predicting off-target risk across diverse populations |
talk |
|
Policastro, Bob |
Base editor genomic safety assessment: keeping pace with emerging FDA expectations |
poster |
|
Prieto Vivas, Julian |
CoMuTER 2.0: A Cas3 based platform for confined, kilobase scale in vivo mutagenesis |
talk |
|
Qasim, Waseem |
First-in-human trials of TALEN, CRISPR/Cas9 and base-edited CAR T cells |
talk |
|
Qi, Chen |
BioPrinCRISPR—A biological principle-informed framework for discovery of novel CRISPR-Cas systems |
poster |
|
Quidwai, Tooba |
A WDR35-dependent coat protein complex defines a vesicular trafficking route to cilia and a genome-edited platform for studying ciliopathies |
poster |
|
Raguram, Aditya |
Genome-wide screening reveals producer-cell modifications that improve virus-like particle production and delivery potency |
talk |
|
Rakestraw, Noah |
Programmable ligation-based genome editing with HUH endonucleases |
poster |
|
Ramirez, Josephine |
Structural insights into the mechanism of telomerase-like DNA synthesis by an antiviral reverse transcriptase |
talk |
|
Ramsden, Dale A |
Mechanisms for end-joining repair of chromosome breaks |
talk |
|
Ressnerova, Alzbeta |
Modular, self-delivering CRISPR RNP platform for in vivo genome editing across diverse tissues |
talk |
|
Riching, Andrew |
A bidirectional Dual-sgRNA system for uniform and efficient multi-gene CRISPR perturbation |
poster |
|
Rößler, Leon Marvin |
Prediction of DNA donor efficiency for effective CRISPR editing |
poster |
|
Roth, Goldie V |
Programmable surface receptor-mediated cell targeting with designer antibody-routed virus-like particles |
talk |
|
Ruis, Brian L |
The Shu complex regulates oligonucleotide-mediated, Cas9 nickase-initiated gene editing in human cells |
poster |
|
Saitova, Elizaveta |
Machine learning-guided site-specific recombinase engineering for correction of DMD duplications |
poster |
|
Sanchez, Henry |
High-throughput prime tagging of endogenous proteins for pooled imaging of protein localization |
talk |
|
Schneider, Stefan |
Megabase genome engineering toward a minimal CHO cell chassis for the production of biopharmaceuticals |
poster |
|
Shi, Honglue |
Stepwise DNA unwinding gates TnpB genome-editing activity |
talk |
|
Shi, Junwei |
Small-molecule controlled base editing for high-efficiency in vivo cancer functional genomics |
poster |
|
Shin, Jee Won Jennifer |
Spatial multiomic CRISPRi approach to map lipid metabolism gene function in MASLD |
poster |
|
Shui, Bing |
Next-generation modeling of complex genetics in vivo with multiplexed, inducible prime editing |
talk |
|
Skopintsev, Petr |
Structure and evolution-guided design of minimal RNA-guided nucleases |
poster |
|
Smith, C. I. Edvard |
Genetic and functional correction of X-linked agammaglobulinemia (XLA) by CRISPR adenine base editors |
poster |
|
Srikanth, Smriti |
Optimized CRISPR interference guide design considerations and performance in perturb-seq data |
poster |
|
Starita, Lea |
Saturation genome editing at scale—From variant effect maps to clinical evidence |
talk |
|
Sturgeon, Morgan |
Accelerated population-aware gRNA candidate selection using high-throughput nomination methods |
poster |
|
Sugiyama, Ken |
Development of a novel inducible prime editing system using split reverse transcriptases |
poster |
|
Sun, Mandy X |
A modular virus-like particle platform for transient in vivo delivery of genome and epigenome editors |
talk |
|
Talas, Andras |
In vivo rescue of a urea cycle disorder via RNA-LNP-mediated prime editing |
talk |
|
Tao, Allen |
AI-guided redesign of laboratory-evolved reverse transcriptases enhances prime editing |
talk |
|
Theva Das, Kumitaa |
Silver nanoparticle-multiplex CRISPR/Cas9 for HIV gene therapy—Blood-brain barrier protection and in vivo safety evaluation |
poster |
|
Thompson, Jared |
RNA-triggered cell elimination with CRISPR-Cas12a2 |
talk |
|
Tran, Paul M |
Rapid identification of viruses and ligands (RIVAL)—A miniaturized, multiplexed CRISPR/Cas12a platform for accelerated viral receptor discovery |
talk |
|
Tsujimoto, Eisuke |
Structural mechanism of DNA recognition by the CCA domain in an IS110 bridge recombinase |
poster |
|
Tussipkan, Dilnur |
Molecular mechanisms underlying defense responses of potato (Solanum tuberosum L.) and employing CRISPR/Cas technology for the improvement of potato |
poster |
|
Vedova, Shane A |
CRISPR screening to decode mechanisms of T cell persistence |
poster |
|
Villiger, Elina |
Prime editing of a pathogenic Scn1a allele ameliorates seizure phenotypes in a GEFS+ mouse model |
poster |
|
Walker, Sadie |
Bridging donors and NHEJ inhibitors enhance large deletions after concurrent double-strand breaks |
poster |
|
Wamsley, Jake |
Efficient HDR-mediated genome editing in primary human T cells using mbDNA™ donor templates and high-fidelity eSpOT-ON nuclease |
poster |
|
Wang, Siyuan (Steven) |
Image-based spatial transcriptomics of native and guide RNAs |
talk |
|
Wang, Xiao |
In vivo correction of pseudoxanthoma elasticum via base editing |
talk |
|
Wang, Zhaojun |
Orthologs of trans DNA-cleaving nucleases for RNA-triggered cell elimination |
poster |
|
Wasko, Kevin M |
Reprogramming T cells for intercellular delivery of genome editors |
poster |
|
Watkins, Leslie |
A pervasive quantification artifact inflates RNA knockdown by RNA-targeting CRISPR |
talk |
|
Wilkinson, Max |
Discovering new RNA-based biology in prokaryotes and their viruses |
talk |
|
Wu, Xiaolong |
DNA-guided CRISPR–Cas12a for RNA detection and intracellular RNA knockdown |
poster |
|
Zeng, Jingkun |
CRISPR-programmed chromatin shredding for disease treatment |
talk |