Renzhi Han

Highly efficient genome editing via 2A-coupled co-expression of two TALEN monomers.

CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx Mice.

Genetic disruption of Ano5 in mice does not recapitulate human ANO5-deficient muscular dystrophy.

Antiretroviral Therapy Normalizes Autoantibody Profile of HIV Patients by Decreasing CD33⁺CD11b⁺HLA-DR⁺ Cells: A Cross-Sectional Study.

Phylogeographical Analysis Reveals Distinct Sources of HIV-1 and HCV Transmitted to Former Blood Donors in China.

Empower multiplex cell and tissue-specific CRISPR-mediated gene manipulation with self-cleaving ribozymes and tRNA.

In Vivo Genome Editing Restores Dystrophin Expression and Cardiac Function in Dystrophic Mice.

A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptide.

Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutations.

A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9.