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Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing
CRISPR/Cas9 for Cancer Therapy: Hopes and Challenges
Development Refractoriness of MLL-Rearranged Human B Cell Acute Leukemias to Reprogramming into Pluripotency
Efficient Recreation of t(11;22) EWSR1-FLI1+ in Human Stem Cells Using CRISPR/Cas9
Functional Characterization of a Dual Enhancer/Promoter Regulatory Element Leading Human CD69 Expression.
Functional characterization of two enhancers located downstream FOXP2
Gene editing of PKLR gene in human hematopoietic progenitors through 5' and 3' UTR modified TALEN mRNA
Generation and characterization of a human iPSC cell line expressing inducible Cas9 in the "safe harbor" AAVS1 locus
In vivo CRISPR/Cas9 targeting of fusion oncogenes for selective elimination of cancer cells.
Modeling mixed-lineage-rearranged leukemia initiation in CD34+ cells: a "CRISPR" solution
Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome
Robustness of Catalytically Dead Cas9 Activators in Human Pluripotent and Mesenchymal Stem Cells
Targeting OGG1 arrests cancer cell proliferation by inducing replication stress.