CRISPR-Cas12a induced DNA double-strand breaks are repaired by multiple pathways with different mutation profiles in Magnaporthe oryzae

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Polymerase Θ is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis

CRISPR/Cas9-induced mutations are generated through TMEJ. (a) Schematic

CRISPR-Cas12a ribonucleoprotein-mediated gene editing in the plant pathogenic fungus Magnaporthe oryzae

PDF) CRISPR-Cas12a ribonucleoprotein-mediated gene editing in the plant pathogenic fungus Magnaporthe oryzae

Application of CRISPR in Filamentous Fungi and Macrofungi: From Component Function to Development Potentiality

PDF] Different DNA repair pathways are involved in single-strand break- induced genomic changes in plants.

Different types and mechanisms of donor DNA integrations and

Full article: Putting CRISPR-Cas system in action: a golden window for efficient and precise genome editing for crop improvement

Mechanistic and genetic basis of single-strand templated repair at Cas12a-induced DNA breaks in Chlamydomonas reinhardtii

PDF] Different DNA repair pathways are involved in single-strand break- induced genomic changes in plants.

An in vitro CRISPR-Cas12a-mediated protocol for direct cloning of large DNA fragments

CRISPR-Cas12a ribonucleoprotein-mediated gene editing in the plant pathogenic fungus Magnaporthe oryzae

CRISPR-Based Crop Improvements: A Way Forward to Achieve Zero Hunger