Genome-wide CRISPR guide RNA design and specificity analysis with GuideScan2

RNA sequencing of TA skeletal muscle of mice with conditional ablation of dystrophin within the myofiber

The KU70-SAP domain has an overlapping function with DNA-PKcs in limiting the lateral movement of KU along DNA

In vivo CRISPR base editing for treatment of Huntington’s disease

Protective effects of red filtered light during IVF: transcriptomic analysis of murine embryos and embryo-derived EVs

SLAM/SAP signaling regulates discrete γδ T cell developmental checkpoints and shapes the innate-like γδ TCR repertoire

Targeted Amplicon Sequencing: The Interferon γ Pathway Enhances Pluripotency and X-Chromosome Reactivation in iPSC Reprogramming

Gut bacteria-derived serotonin promotes immune tolerance in early life through regulation of neonatal gut T cells II

Gut bacteria-derived serotonin promotes immune tolerance in early life through regulation of neonatal gut T cells I

Saturation genome Editing of BRCA2 variants from C-terminal DNA binding domain

The endogenous retrovirus Mtv8 which resides within the V kappa locus does not influence the mouse immunoglobulin repertoire

SPLICER: A Highly Efficient Base Editing Toolbox That Enables in vivo Exon Skipping For Targeting Alzheimer’s Disease

Sequencing-based Functional Assays for Classification of BRCA2 Variants in Mouse ES Cells

The role of SMC3 in heart development by regulating super-enhancer associated genes

Class switch recombination regulation by extracellular vesicles mediated intercellular epigenomic signaling

Acute gastrointestinal permeability after traumatic brain injury in mice precedes a bloom in Akkermansia muciniphila supported by intestinal hypoxia

Saturation genome editing of 11 codons and exon 13 of BRCA2 determines pathogenicity of variants

PI3K-Akt signaling regulates Scx-lineage tenocytes and Tppp3-lineage tendon sheath synovial cells in physiological tendon regeneration

Targeting Duchenne Muscular Dystrophy by Skipping DMD Exon 45 with Base Editors

Immunoglobulin repertoires in mice carrying a knock-in human Cµ gene downstream of the IGH 3' regulatory region