|
Presenting Author |
Abstract Title |
Talk/Poster |
|
Adikusuma, F. |
Frequent large deletions generated by targeted CRISPR/Cas9 cleavage indicate a novel DNA repair mechanism |
poster |
|
Aida, T. |
Cloning-free CRISPR/Cas system facilitates functional cassette knock-in in mice |
poster |
|
Akhmetov, A. |
CRISPR-mediated humanization of yeast |
poster |
|
Ali, Z. |
CRISPR/Cas9 system mediates Interference with plant DNA viruses |
talk |
|
Anand, R.P. |
Non-homologous tail differentially modulate homologous and homeologous recombination |
poster |
|
Anderson, D.G. |
Nucleic acid delivery systems for RNA therapy and gene editing |
talk |
|
Aparicio, E. |
DECKO—A simple and multiplexable CRISPR tool for targeted deletion of genomic elements including long noncoding RNAs |
poster |
|
Aryal, N.K. |
Lessons learned by targeting essential genes using CRISPR/Cas9 system |
poster |
|
Baron, G.N. |
CRISPR/Cas9-mediated gene editing in Arginase-1 deficient induced pluripotent stem cells |
poster |
|
Bauer, D.E. |
Cas9-mediated in situ saturating mutagenesis for BCL11A enhancer functional dissection. |
talk |
|
Bennett, E.P. |
Improved targeting and indel identification methodologies for genome editing |
poster |
|
Bernard, A.L. |
Use of the CRISPR/Cas9 system to generate simultaneously mutant and GFP transgenic zebrafish for the Foxo1a gene |
poster |
|
Bertier, L.D. |
Towards generating multi-disease resistant lettuce using Crispr/CAS9 genome editing |
poster |
|
Blitz, I.L. |
Leapfrogging—A method for targeting CRISPR/Cas9 genome editing to the germline in Xenopus |
talk |
|
Boel, A. |
CRISPR/Cas-mediated gene editing in zebrafish—An optimized workflow |
poster |
|
Bothmer, A.H. |
Enhancing CRISPR/Cas9 mediated DNA repair outcomes through the local recruitment of DNA repair factors |
poster |
|
Bustos, F.J. |
Use of CRISPRs to Remove of a spontaneous mouse mutation causing abnormal anxiety- /autism-like behaviors |
poster |
|
Cai, M. |
Genome editing to understand the function of CD33 in neuro-inflammation and Alzheimer's disease |
poster |
|
Carpenter, M.A. |
Editing editors with editing |
talk |
|
Charo, R. |
Germline editing of plants and non-human animals |
talk |
|
Charpentier, E. |
CRISPR-Cas9—From a bacterial immune system to a revolution in genome engineering |
talk |
|
Cheng, X. |
CRISPR/Cas9-based genome modification of a novel rat long non-coding RNA within a homologous GWAS associated locus for QT-intervals |
poster |
|
Chiang, W. |
CRISPR-Cas9D10A nickase-based genotypic and phenotypic screening to enhance efficient and accurate genome editing |
poster |
|
Church, G.M. |
Radically new genomes—E.coli, elephants, mosquitoes, pigs, humans. |
talk |
|
Cockrell, A.S. |
A CRISPR/Cas9 engineered mouse model for the middle east respiratory coronavirus (MERS-CoV) |
poster |
|
Conklin, B. |
Precision genome editing—Choosing the right nuclease for scarless point mutations in human iPS cells |
talk |
|
Corn, J. |
Cas9 asymmetrically releases one strand of target DNA, enabling rational design of templates for improved gene editing |
talk |
|
Cotta-Ramusino, C. |
Repair pathway choice in response to different types of DNA lesions mediated by different CRISPR/Cas9 variants |
talk
|
|
Courtney, D.G. |
The development of allele-specific CRISPR/Cas9 based therapeutics for corneal disorders |
poster |
|
Crist, A.B. |
A CRISPR-based mating system switch and the experimental evolution of sexual interactions in C. elegans |
poster |
|
Cuomo, E. |
CRISPR/ Cas gene editing in the study of drug resistance in EGFR- driven lung cancers |
poster |
|
Daggubati, V. |
Identifying drug resistances using genome-wide CRISPR-CAS9 libraries |
poster |
|
Davis, D.J. |
An innovative approach for analyzing the effects of stress on the kynurenine pathway in zebrafish |
poster |
|
De Rocker, N. |
Development of a myt1l knockdown zebrafish model using CRISPR-Cas9 |
poster |
|
Demozzi, M. |
Yeast-based assays for CRISPR/Cas9-mediated homologous recombination |
poster |
|
Dickel, D.E. |
Systematic deletion screens of distant-acting in vivo enhancers in mice |
talk |
|
Dillard, V. |
Making the cut—Software for designing a revolution in genome editing |
poster |
|
Ding, M. |
Proofreading the genome—Towards the development of a CRISPR/Cas9-based therapy for merosin-deficient congenital muscular dystrophy |
poster |
|
Ding, X. |
Synthetic viability by BRCA2 and PARP1 deficiency |
talk |
|
Doyon, Y. |
A scalable genome editing-based approach for mapping the human protein interactome |
poster |
|
Droguett, G. |
Creation of large, single-step homozygous humanizations of mouse genes by combining CRISPR/Cas9 cleavage with BAC-based targeting vectors |
poster |
|
Duan, J. |
Open chromatin dynamics and genetic perturbation by CRISPR editing in iPSC-derived neurons at the MIR137 schizophrenia risk locus |
talk |
|
Ehsaei, Z. |
CRISPR targeting of human induced pluripotent stem cells (hiPSCs) for lineage tracing of hiPSCs-derived neural stem cells during cortical development in vitro |
poster |
|
Eid, A. |
Viral-mediated genome editing in Arabidopsis using the CRISPR/Cas9 system |
poster |
|
Federici, F. |
Using CRISPR/Cas for morphogenetic engineering of bacterial colonies |
poster |
|
Frisch, R.L. |
A Non-conventional gene editing method in a non-conventional yeast—Using Cas9 for genome editing in Yarrowia lipolytica |
poster |
|
Frock, R.L. |
Genome-wide detection of DNA double-stranded breaks induced by engineered nucleases |
talk |
|
Fujii, H. |
Locus-specific biochemical analysis of genome functions using enChIP—An application of CRISPR/Cas to purification of specific genomic regions |
poster |
|
Greely, H. |
Human germline genome editing—Breaking out the issues |
talk |
|
Guay, D. |
Innovative protein delivery system for cell therapy |
poster |
|
Gupta, A. |
Developing a drug-inducible CRISPR/Cas9 system for precise genome editing |
poster |
|
Gurumurthy, C.B. |
Efficient insertion of sequences using longer single stranded repair DNAs at the Cas9 cut sites |
poster |
|
Guzzardo, P. |
Genome editing in haploid human cells using CRISPR/Cas9 |
poster |
|
Haber, J. |
Homologous recombination and nonhomologous end-joining of Cas9-cleaved DNA in budding yeast |
talk |
|
Hart, T. |
High-resolution detection of fitness genes and genotype-specific cancer vulnerabilities with CRISPR-Cas9 screens |
talk |
|
Hendel, A. |
Next-generation CRISPR guide RNAs with chemical modifications enhance genome editing in human primary cells |
poster |
|
Hernandez Magadan, A. |
Matching phenotypes to mutations in industrial bacterial strains by using CRISPR-Cas technology |
poster |
|
Hewitt, A. |
Public perception of human gene editing—Taking the pulse of the global community’s attitude towards CRISPR |
poster |
|
Hill, M.C. |
Complementary genome-wide CRISPR-Cas9 screens to characterize the molecular basis for Doxorubicin-induced cardiotoxicity |
poster |
|
Hoang, M. |
Creating human cellular models to investigate cardioprotective functions of GRK5 Gln41Leu single nucleotide polymorphism using CRISPR/Cas9 technology |
poster |
|
Honig, A. |
MemoGeneTM enables transient expression of CRISPR components—New possibilities for plant genome editing |
poster |
|
Horlbeck, M.A. |
Development of next-generation libraries for genome-scale control of gene repression and activation |
talk |
|
Hotta, A. |
Dual regulation of CRISPR-Cas9 for controlling cleavage activity in iPS cells |
poster |
|
Hu, Y. |
Selection of guide RNAs for generation of genetically modified mice |
poster |
|
Huang, B. |
Imaging the genome in living cells |
talk |
|
Huang, C. |
In vivo discovery of drug targets in liver cancer by RNAi in combination with CRISPR/Cas9 |
talk |
|
Huangfu, D. |
Genome editing in human pluripotent stem cells for understanding the mechanisms of pancreatic development and diabetes |
talk |
|
Jacobs, E.Z. |
CRISPR/Cas9-mediated genome editing in primed versus naïve human embryonic stem cells |
poster |
|
Jae, L.T. |
Studying genetic interactions in nuclease-engineered haploid human cells |
talk |
|
Josling, G. |
Dissecting the regulation of malaria transcription factors using CRISPR/Cas9 |
talk |
|
Joung, J. |
Defining, improving, and altering the specificities of CRISPR-Cas9 nucleases |
talk |
|
Julien, D.P. |
Identifying zebrafish somatosensory subtypes using CRISPR/Cas9-directed transgene integration |
poster |
|
KaramiNejadRanjbar, M. |
Adapting Cas9 mediated genome editing for genome wide arrayed screening in cancer cell lines |
poster |
|
Kiani, S. |
Mammalian genetic kill switches using Cas9 gRNA systems |
poster |
|
Kim, D. |
Multiplexed Digenome-seq: Genome-wide profiling of CRISPR-Cas9 off-target effects in human cells |
poster |
|
Kim, H. |
Blood group conversion using transcription activator-like effector nucleases |
poster |
|
Kim, J. |
Genome editing in stem cells, animals, and plants |
talk |
|
Kim, S. |
Generation of genome-modified mice by microinjection of CRISPR/Cas9 using sperm and egg banking |
poster |
|
Knight, S.C. |
Single-molecule dynamics of CRISPR-Cas9 genome interrogation in living cells |
talk |
|
Knowlton, M.N. |
Data integration through use of nomenclature and biological ontologies—Naming and annotating TALENs, ZFNs and CRISPR/Cas mutations in mice |
poster |
|
Koeferle, A. |
Forward epigenetics—A CRISPR-based screening method |
poster |
|
Kosicki, M. |
Generating megabase size deletions in mouse embryonic stem cells using CRISPR/Cas9 |
poster |
|
Kueh, A. |
HBO1 is essential for H3K14 acetylation in human cell lines |
poster |
|
Kumar, S. |
Highly efficient genome editing and cell engineering in stem cells using CRISPR/Cas9 |
poster |
|
Kurata, J. |
Determining microRNA function by gene knockout using TALEN or CRISPR-Cas9 based screens |
poster |
|
le Sage, C. |
CRISPR-Cas9D10A nickase-based genotypic and phenotypic screening to enhance efficient and accurate genome editing |
talk |
|
Lee, C.M. |
Optimization of CRISPR/Cas9 systems for large genomic deletions |
poster |
|
Lee, J. |
Customized site specific DNA cloning method based on type-II CRISPR/Cas bacterial immune system and isothermal assembly |
poster |
|
Lee, K. |
Gold nanoparticle-mediated delivery of CRISPR/Cas9 ribonucleoprotein and DNA donor for efficient genome editing in vitro and in vivo |
poster |
|
Lee, W. |
Construction of CRISPR/Cas DNA molecules based on microchip oligonucleotides and next-generation sequencing technology |
poster |
|
Li, W. |
Quality control, modeling and visualization of genome-wide CRISPR screens using MAGeCK-VISPR |
talk |
|
Long, C. |
Rescue of Duchenne muscular dystrophy cardiomyocyte function by myoediting |
talk |
|
Ma, H. |
Live cell interrogation of CRISPR dynamics with fluorescent sgRNAs |
poster |
|
Maizels, N. |
Genome engineering at targeted DNA nicks |
talk |
|
Mansouri, M. |
MultiPrime—A baculovirus-based multigene expression system for mammalian cells |
poster |
|
Marraffini, L. |
Tolerance during CRISPR-Cas immunity—Domesticating the virus |
talk |
|
Martens, A. |
Investigating A20’s (non-)enzymatic activities in vivo through CRISPR-Cas gene targeting |
poster |
|
Martins, N. |
Establishment of a novel model for the Nup98-HoxA9 leukemogenic translocation using CRISPR/Cas9 |
poster |
|
Mashimo, T. |
CRISPR/Cas9 with ssODNs enables gene knock-in and replacement of large genomic regions in rats |
poster |
|
Michealraj, A. |
Modelling medulloblastoma using the CRISPR/Cas9 system to generate large chromosomal deletions in mice |
poster |
|
Mohr, G. |
A reverse transcriptase-Cas1 fusion protein mediates site-specific integration of both RNA and DNA spacers into CRISPR repeats |
talk |
|
Morell Fernandez, M. |
Direct delivery of Cas9 protein via cell-derived nanovesicles |
poster |
|
Moreno-Mateos, M.A. |
CRISPRscan—Designing highly efficient sgRNAs for CRISPR/Cas9 targeting in vivo |
poster |
|
Nakanishi, T. |
Efficient DNA integration into germ line genome via programmable nucleases in Daphnia magna |
talk |
|
Natsume, T. |
A PCR-based tagging method for generation of human conditional mutants by use of the auxin-inducible degron technology |
poster |
|
Neggers, J. |
A single amino acid substitution by CRISPR/Cas9 genome editing at cysteine 528 of XPO1 confers resistance of malignant cells to SINE compounds |
poster |
|
Oliveira, R. |
Generation of Dmpk knockin mice with large CTG repeat expansions to model myotonic dystrophy |
poster |
|
Ortiz, O. |
Optimization of CRISPR/Cas9 components for gene therapy |
talk |
|
Paix, A. |
Homology-directed genome editing in C. elegans—Systematic analysis of parameters yields a high efficiency, cloning and marker-free protocol |
talk |
|
Parts, L. |
Multiplex evaluation of programmable CRISPR/Cas9 transcription factors using competitive growth assays in yeast |
talk |
|
Peterson, K.A. |
CRISPR/Cas9 mediated gene modification provides a robust platform for modeling developmental disorders |
poster |
|
Petris, G. |
CRISPR/Cas9 viral like particles for targeted genome editing in human cells |
poster |
|
Piatek, A.A. |
RNA-guided transcriptional regulation in planta via synthetic dCas9-based transcription factors |
poster |
|
Pinello, L. |
CRISPResso—Analysis of CRISPR-Cas9 genome editing outcomes from deep sequencing data |
poster |
|
Prakash, R. |
Nuclease-generated mouse mutants of homologous recombination genes |
talk |
|
Qi, L. |
CRISPR/Cas9 for transcription regulation and genome imaging |
talk |
|
Qin, L. |
CRISPR-Cas9 delivery to hard-to-transfect cells via membrane deformation |
poster |
|
Qin, W. |
Genome editing in mice mediated by the CRISPR/Cas9 nuclease with high efficiency and throughput |
poster |
|
Rahman, S.H. |
CRISPR/Cas9-mediated targeted knockout of protein S in Chinese hamster ovary (CHO) cells |
poster |
|
Ranganathan, V. |
In vivo genome editing mediated by co-delivery of SpCas9 and guide RNA through a single AAV |
poster |
|
Ratz, M. |
Live cell RESOLFT super-resolution microscopy of endogenously tagged human cells |
poster |
|
Ravinder, N. |
Rapid and highly efficient cell engineering with Cas9 ribonucleoproteins and lentiviral CRISPR systems |
poster |
|
Reha, S. |
CRISPR/Cas-based nucleases and nickases for targeted mutagenesis and HR-mediated gene targeting in plants |
poster |
|
Richie, C.T. |
Development of Cre-dependent AAV CRISPR toolkit |
poster |
|
Richter, T.R. |
The Icelandic transgenic core facility as a platform to apply the CRISPR technology |
poster |
|
Rose, J.C. |
Development and application of a chemically inducible Cas9 |
poster |
|
Rozwadowski, K.L. |
In vivo production of multicopy donor template for gene targeting using retron-mediated reverse transcription |
poster |
|
Ruiz, S. |
Cas9/RNA-based forward genetic screenings in mouse embryonic stem cells uncovered the role of genes mediating resistance to ATR inhibitors |
talk |
|
Sadhu, M.J. |
Genetics without crosses—Quantitative trait mapping with CRISPR |
poster |
|
Scaffa, A.M. |
Engineering splicing mutations in HEK 293 cells using CRISPR/Cas9 system |
poster |
|
Schmid-Burgk, J. |
CRISPaint—Ligase-4 dependent modular gene tagging |
poster |
|
Serebrenik, A.A. |
Functional interaction between the cancer genomic DNA deaminase APOBEC3B and uracil excision repair |
poster |
|
Sharma, S. |
CRISPR-Cas9 based cellular screens to identify novel low-affinity extracellular protein interactions |
poster |
|
Shi, J. |
A domain-focused CRISPR strategy for cancer drug target discovery |
talk |
|
Shirole, N. |
A rapid and tunable method to temporally control Cas9 expression enables the characterization of essential genes and the interrogation of functional gene interactions in vitro and in vivo |
poster |
|
Skarnes, W.C. |
Biallelic genome editing of human pluripotent stem cells at scale |
talk |
|
Smemo, S. |
Determining causal alleles in age-related macular degeneration |
poster |
|
Smith, A.J. |
Design considerations for highly specific and efficient synthetic crRNA molecules |
poster |
|
Sontheimer, E.J. |
Multimeric guides and tracrRNA-independent Dnase H activity for Neisseria meningitidis Cas9 |
talk |
|
Speleman, F. |
CRISPR-Cas9 modeling of cell lines and zebrafish to study the TLX1-PHF6 cooperative interrelationship in T-cell acute lymphoblastic leukemia |
talk |
|
St.Onge, B.P. |
A scalable method for isolating sequence-verified oligonucleotides from complex libraries |
poster |
|
Svitashev, S.K. |
Maize genome editing using Cas9-guideRNA technology |
talk |
|
Symington, L. |
Making the right choice at a DNA double-strand break |
talk |
|
Takeda, J. |
A combination of Bloom gene inactivation and CRISPR/Cas9-mediated DNA cleavage facilitates construction of a loss-of-heterozygosity library of the mammalian genome |
poster |
|
Thurlow, L.A. |
A fluorescently labelled dCas9 for imaging endogenous RNAs in vivo |
poster |
|
Toki, S. |
Establishment of an efficient CRISPR/Cas9 mediated genome editing system in rice |
poster |
|
Tsai, S. |
Genome-wide specificities of wild-type and engineered CRISPR-Cas9 nucleases defined by GUIDE-seq |
poster |
|
Tsang, S.H. |
CRISPR/Cas9 gene-editing of genome-wide association (GWAS) alleles in patient specific stem cell lines |
talk |
|
Turunen, M. |
Lineage-specific oncogenic transcription factors of different cancer types converge to regulate the activity of MYC and CDK4/6 |
poster |
|
Urnov, F.D. |
Genome editing in primary human cells and organs—Towards the goal of engineering genetic cures |
talk |
|
Varshney, G.K. |
High throughput gene targeting in zebrafish using CRISPR/Cas9 |
talk |
|
Vasileva, A. |
Human cell line engineering for enhanced efficiency of CRISPR/Cas9-mediated genome editing |
poster |
|
Ventura, A. |
In vivo modeling of chromosomal rearrangements using CRISPR/Cas9 |
talk |
|
Waghulde, H. |
Development of a novel Gper-1 knock out rat model using a modified CRISPR/Cas9 technology |
poster |
|
Wang, Q. |
Genome-wide identification of CRISPR/CAS9 target sites with reduced off-target effects in organisms with different genome sizes |
poster |
|
wang, X. |
Heritable gene disruption in goats with CRISPR/Cas9 results in phenotypic changes |
poster |
|
Watters, K.E. |
Structure-function design principles for CRISPR small guide RNAs |
poster |
|
Wienert, B. |
Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin |
talk |
|
Wiggins, C. |
CRISPRevolution—New opportunities in target identification and validation |
poster |
|
Willaert, A. |
Modeling the arterial tortuosity syndrome (ATS) in zebrafish using CRISPR/Cas genome editing |
poster |
|
Winters, I.P. |
Pancreatic cancer modeling with viral vectors and in vivo CRISPR/Cas9-mediated somatic genome editing |
talk |
|
Wolfe, S. |
Improving CRISPR/Cas9 Precision through tethered DNA-binding domains |
poster |
|
Wu, M. |
Type I CRISPR-Cas systems target endogenous genes to dampen host immunity |
poster |
|
Wu, Q. |
CRISPR inversion of CTCF binding sites alters genome topology and enhancer/promoter function |
talk |
|
Wu, R. |
Interactions among resistance genes lead to hybrid necrosis |
poster |
|
Wu, Y. |
Lineage-specific report lines generated by double nicking CRIPSR/Cas9 in human embryonic stem cells |
poster |
|
Xiong, K. |
Synergistic activation mediator (SAM) induced expression of reprogramming genes in porcine fibroblast |
poster |
|
Xue, W. |
CRISPR-mediated direct mutation of cancer genes in the mouse liver |
talk |
|
Yeganeh Seghalaksari, M. |
CRISPR/Cas9-mediated deletion of a SINE element within the Polr3e gene reveals a role in gene expression regulation |
poster |
|
Yuan, Y. |
Crystal structures of CRISPR-associated Csx3 reveal a manganese-dependent deadenylation exoribonuclease |
poster |
|
Yudovich, D. |
CRISPR-Cas9 mediated regulation of human hematopoietic stem and progenitor cells |
poster |
|
Yusa, K. |
A genome-wide CRISPR-Cas9 screen identifies genetic vulnerability in acute myeloid leukaemia |
talk |
|
Zerbini, F. |
Genome editing in Escherichia coli via CRISPR-Cas9 system |
poster |
|
Zhang, F. |
Genome editing using CRISPR-Cas9 |
talk |
|
Zhang, H. |
CRISPR/Cas-mediated gene editing in human iPSC-derived macrophage reveals lysosomal acid lipase function in human macrophages |
talk |
|
Zhongbao, Z. |
Isolation, structural analysis, and expression characteristics of the maize TIFY gene family |
poster |
|
Zuckermann, M. |
Somatic CRISPR/Cas9-mediated tumor suppressor disruption enables versatile brain tumor modeling |
talk |