scholarly article | Q13442814 |
P50 | author | Gregory C Finnigan | Q61156990 |
P2093 | author name string | Emily Roggenkamp | |
Madison N Schrock | |||
Megan Halloran | |||
Rachael M Giersch | |||
Emily Turnquist | |||
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A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae | Q27860636 | ||
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Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification | Q29029259 | ||
Engineering of temperature- and light-switchable Cas9 variants | Q29114084 | ||
Evolutionary dynamics of CRISPR gene drives | Q29169120 | ||
Advances in Vector Control Science: Rear-and-Release Strategies Show Promise… but Don’t Forget the Basics | Q29451751 | ||
Identification of a signal for rapid export of proteins from the nucleus | Q29547742 | ||
A short amino acid sequence able to specify nuclear location | Q29547781 | ||
Naturally Occurring Off-Switches for CRISPR-Cas9. | Q38725824 | ||
Energy biotechnology in the CRISPR-Cas9 era. | Q38732250 | ||
Structural basis of CRISPR-SpyCas9 inhibition by an anti-CRISPR protein | Q38817347 | ||
Applications of genome editing in insects | Q38902744 | ||
Guide RNA engineering for versatile Cas9 functionality | Q38979117 | ||
Harnessing the natural diversity and in vitro evolution of Cas9 to expand the genome editing toolbox | Q39394606 | ||
Inhibition Mechanism of an Anti-CRISPR Suppressor AcrIIA4 Targeting SpyCas9. | Q40164344 | ||
Inhibition of CRISPR-Cas9 with Bacteriophage Proteins | Q40389062 | ||
Manipulation of nuclear architecture through CRISPR-mediated chromosomal looping. | Q41020733 | ||
How driving endonuclease genes can be used to combat pests and disease vectors. | Q41272438 | ||
A toolbox of endogenous and heterologous nuclear localization sequences for the methylotrophic yeast Pichia pastoris. | Q41393088 | ||
CRISPR-PCS: a powerful new approach to inducing multiple chromosome splitting in Saccharomyces cerevisiae | Q41728692 | ||
Increasing the genome-targeting scope and precision of base editing with engineered Cas9-cytidine deaminase fusions | Q41960134 | ||
Multiplexed CRISPR/Cas9- and TAR-Mediated Promoter Engineering of Natural Product Biosynthetic Gene Clusters in Yeast | Q42032880 | ||
CRISPR-UnLOCK: Multipurpose Cas9-Based Strategies for Conversion of Yeast Libraries and Strains. | Q42148846 | ||
National Academies Hit the Brakes on Gene Drive-Modified Organisms | Q42994874 | ||
Generation of gene-modified mice via Cas9/RNA-mediated gene targeting | Q43179830 | ||
The creation and selection of mutations resistant to a gene drive over multiple generations in the malaria mosquito. | Q44168733 | ||
Guide RNAs: A Glimpse at the Sequences that Drive CRISPR-Cas Systems | Q44865335 | ||
Rules of the road for insect gene drive research and testing | Q44874522 | ||
Guide RNA functional modules direct Cas9 activity and orthogonality | Q44876033 | ||
Conservation demands safe gene drive | Q46260226 | ||
Evolution of Resistance Against CRISPR/Cas9 Gene Drive. | Q46447511 | ||
In-Yeast Engineering of a Bacterial Genome Using CRISPR/Cas9. | Q46985185 | ||
A CRISPR-Cas9-based gene drive platform for genetic interaction analysis in Candida albicans. | Q47418459 | ||
Safety, Security, and Policy Considerations for Plant Genome Editing. | Q47919114 | ||
Genome Engineering and Agriculture: Opportunities and Challenges. | Q47919143 | ||
Efficient genome editing by CRISPR/Cas9 with a tRNA-sgRNA fusion in the methylotrophic yeast Ogataea polymorpha | Q47969309 | ||
RICE CRISPR: Rapidly increased cut ends by an exonuclease Cas9 fusion in zebrafish | Q48218784 | ||
Using CRISPR-based gene drive for agriculture pest control. | Q48278829 | ||
The primary structure of the Saccharomyces cerevisiae gene for alcohol dehydrogenase | Q48405414 | ||
Precise base editing in rice, wheat and maize with a Cas9-cytidine deaminase fusion. | Q50453614 | ||
Dodging silver bullets: good CRISPR gene-drive design is critical for eradicating exotic vertebrates. | Q51151763 | ||
Site-specific selfish genes as tools for the control and genetic engineering of natural populations. | Q53654598 | ||
An efficient one-step site-directed and site-saturation mutagenesis protocol | Q29614689 | ||
DNA targeting specificity of RNA-guided Cas9 nucleases | Q29615793 | ||
High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells | Q29616045 | ||
Genetic screens in human cells using the CRISPR-Cas9 system | Q29617411 | ||
Push-Pull: Chemical Ecology-Based Integrated Pest Management Technology | Q31113484 | ||
Nuclear export signal consensus sequences defined using a localization-based yeast selection system | Q33371970 | ||
Budding yeast for budding geneticists: a primer on the Saccharomyces cerevisiae model system | Q33575824 | ||
Mechanisms and signals for the nuclear import of proteins | Q33635365 | ||
Efficient Recreation of t(11;22) EWSR1-FLI1+ in Human Stem Cells Using CRISPR/Cas9. | Q33659569 | ||
Complex transcriptional modulation with orthogonal and inducible dCas9 regulators. | Q33704483 | ||
CRISPR/Cas9 gene drives in genetically variable and nonrandomly mating wild populations. | Q33708101 | ||
Agricultural pest control with CRISPR-based gene drive: time for public debate: Should we use gene drive for pest control? | Q33748971 | ||
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa | Q33781297 | ||
CRISPR/Cas9 systems have off-target activity with insertions or deletions between target DNA and guide RNA sequences | Q33791286 | ||
Overcoming evolved resistance to population-suppressing homing-based gene drives. | Q33812767 | ||
Identification of an amphipathic helix important for the formation of ectopic septin spirals and axial budding in yeast axial landmark protein Bud3p | Q33847744 | ||
Disabling Cas9 by an anti-CRISPR DNA mimic | Q33898855 | ||
Vector control with driving Y chromosomes: modelling the evolution of resistance | Q33910481 | ||
Nuclear pore complex is able to transport macromolecules with diameters of about 39 nm | Q33953659 | ||
Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells | Q34093413 | ||
Optimization of ordered plasmid assembly by gap repair in Saccharomyces cerevisiae | Q34340960 | ||
Orthogonal Cas9 proteins for RNA-guided gene regulation and editing | Q34374050 | ||
A split-Cas9 architecture for inducible genome editing and transcription modulation | Q34460920 | ||
A light-inducible CRISPR-Cas9 system for control of endogenous gene activation | Q34461908 | ||
Inducible in vivo genome editing with CRISPR-Cas9 | Q34463380 | ||
Systematic analysis of CRISPR-Cas9 mismatch tolerance reveals low levels of off-target activity | Q34485743 | ||
Biology and Applications of CRISPR Systems: Harnessing Nature's Toolbox for Genome Engineering | Q34509196 | ||
Chemical and Biophysical Modulation of Cas9 for Tunable Genome Engineering | Q34512930 | ||
Diverse evolutionary roots and mechanistic variations of the CRISPR-Cas systems | Q34536517 | ||
Applications of CRISPR technologies in research and beyond | Q34539796 | ||
A chemical-inducible CRISPR-Cas9 system for rapid control of genome editing. | Q34540074 | ||
Classical nuclear localization signals: definition, function, and interaction with importin alpha | Q34591163 | ||
Genome-wide recessive genetic screening in mammalian cells with a lentiviral CRISPR-guide RNA library | Q35096218 | ||
Multicolor CRISPR labeling of chromosomal loci in human cells. | Q35190002 | ||
Dramatic enhancement of genome editing by CRISPR/Cas9 through improved guide RNA design | Q35342386 | ||
Multiplex engineering of industrial yeast genomes using CRISPRm | Q35422042 | ||
Sequence determinants of improved CRISPR sgRNA design | Q35876047 | ||
Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9. | Q35896845 | ||
Quantitative CRISPR interference screens in yeast identify chemical-genetic interactions and new rules for guide RNA design | Q35950112 | ||
mCAL: A New Approach for Versatile Multiplex Action of Cas9 Using One sgRNA and Loci Flanked by a Programmed Target Sequence. | Q36019453 | ||
Distinct patterns of Cas9 mismatch tolerance in vitro and in vivo | Q36023097 | ||
CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo | Q36109068 | ||
Homology-directed repair in rodent zygotes using Cas9 and TALEN engineered proteins | Q36128900 | ||
Highly specific epigenome editing by CRISPR-Cas9 repressors for silencing of distal regulatory elements | Q36338669 | ||
DNA-binding-domain fusions enhance the targeting range and precision of Cas9. | Q36372381 | ||
Relationships between natural enemy diversity and biological control | Q36397695 | ||
Diversity, classification and evolution of CRISPR-Cas systems | Q36399437 | ||
BIOSAFETY. Safeguarding gene drive experiments in the laboratory | Q36407747 | ||
Optimizing sgRNA structure to improve CRISPR-Cas9 knockout efficiency. | Q36425176 | ||
Roles of septins in prospore membrane morphogenesis and spore wall assembly in Saccharomyces cerevisiae | Q36574671 | ||
Two systems of glucose repression of the GAL1 promoter in Saccharomyces cerevisiae | Q36724367 | ||
Context affects nuclear protein localization in Saccharomyces cerevisiae | Q36765182 | ||
Different Effects of sgRNA Length on CRISPR-mediated Gene Knockout Efficiency | Q37035274 | ||
Coordinate action of distinct sequence elements localizes checkpoint kinase Hsl1 to the septin collar at the bud neck in Saccharomyces cerevisiae | Q37095265 | ||
CRISPR-Cas9 nuclear dynamics and target recognition in living cells. | Q37216431 | ||
An easy and efficient inducible CRISPR/Cas9 platform with improved specificity for multiple gene targeting | Q37401076 | ||
A programmable Cas9-serine recombinase fusion protein that operates on DNA sequences in mammalian cells | Q37522969 | ||
Profiling single-guide RNA specificity reveals a mismatch sensitive core sequence | Q37591346 | ||
Transcriptional reprogramming in yeast using dCas9 and combinatorial gRNA strategies | Q37704855 | ||
CRISPR-mediated adaptive immune systems in bacteria and archaea | Q38089802 | ||
Mechanisms Regulating Protein Localization. | Q38546818 | ||
Novel CRISPR/Cas9 gene drive constructs reveal insights into mechanisms of resistance allele formation and drive efficiency in genetically diverse populations. | Q38670003 | ||
Fusion of SpCas9 to E. coli Rec A protein enhances CRISPR-Cas9 mediated gene knockout in mammalian cells. | Q38713913 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 3 | |
P921 | main subject | CRISPR | Q412563 |
Saccharomyces cerevisiae | Q719725 | ||
Cas9 | Q16965677 | ||
CRISPR-Cas method | Q17310682 | ||
gene drive | Q22964789 | ||
P304 | page(s) | 999-1018 | |
P577 | publication date | 2018-03-02 | |
P1433 | published in | G3 | Q5512701 |
P1476 | title | Tuning CRISPR-Cas9 Gene Drives in Saccharomyces cerevisiae | |
P478 | volume | 8 |
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