human | Q5 |
P6178 | Dimensions author ID | 01222576301.73 |
P496 | ORCID iD | 0000-0002-5710-173X |
P69 | educated at | Gonzaga University | Q1537303 |
University of Oregon | Q766145 | ||
P108 | employer | Kansas State University | Q31249 |
University of California, Berkeley | Q168756 | ||
University of Oregon | Q766145 | ||
P735 | given name | Gregory | Q922983 |
Gregory | Q922983 | ||
P106 | occupation | researcher | Q1650915 |
Q34714955 | A genome-wide enhancer screen implicates sphingolipid composition in vacuolar ATPase function in Saccharomyces cerevisiae. |
Q99712706 | Analysis of CRISPR gene drive design in budding yeast |
Q111321874 | Analysis of a Cas12a-based gene-drive system in budding yeast |
Q42148846 | CRISPR-UnLOCK: Multipurpose Cas9-Based Strategies for Conversion of Yeast Libraries and Strains. |
Q43198208 | Complex in vivo Ligation Using Homologous Recombination and High-efficiency Plasmid Rescue from Saccharomyces cerevisiae |
Q35882356 | Comprehensive Genetic Analysis of Paralogous Terminal Septin Subunits Shs1 and Cdc11 in Saccharomyces cerevisiae |
Q88892013 | Corrigendum: Gene drive inhibition by the anti-CRISPR proteins AcrIIA2 and AcrIIA4 in Saccharomyces cerevisiae |
Q27932624 | Detection of protein-protein interactions at the septin collar in Saccharomyces cerevisiae using a tripartite split-GFP system |
Q59327062 | Development of a multi-locus CRISPR gene drive system in budding yeast |
Q52430524 | Gene drive inhibition by the anti-CRISPR proteins AcrIIA2 and AcrIIA4 in Saccharomyces cerevisiae. |
Q42615316 | Method for Multiplexing CRISPR/Cas9 in Saccharomyces cerevisiae Using Artificial Target DNA Sequences. |
Q61800190 | Modulating CRISPR gene drive activity through nucleocytoplasmic localization of Cas9 in |
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Q52429679 | Yeast Still a Beast: Diverse Applications of CRISPR/Cas Editing Technology in S. cerevisiae. |
Q36019453 | mCAL: A New Approach for Versatile Multiplex Action of Cas9 Using One sgRNA and Loci Flanked by a Programmed Target Sequence. |
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