Jian-ping Zhang
Tianjin, China
Last Updated: 09/26/2026
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Found 26 publications
AviNP-Seq: A Blindspot-Free Single-Molecule Framework for Unmasking AAV Genome Heterogeneity and Determining Packaging Limits.
Journal: Human gene therapy
Published: June 12, 2026
A Dual-Viral Delivery Platform Enables Efficient Site-Specific Integration of Therapeutic-Length Genes in Human Primary Stem Cells.
Journal: Human gene therapy
Published: May 28, 2026
Recombinant ApoE3 corona plus sucrose vitrification endows mRNA-LNPs with Freeze-Thaw and -80 °C stability.
Journal: International journal of pharmaceutics
Published: August 01, 2025
AviTag-seq unifies nucleotide-resolution maps of CRISPR off-targets and AAV vector integrations.
Journal: Communications biology
Published: July 10, 2025
Author Correction: Efficient precise knockin with a double cut HDR donor after CRISPR/Cas9-mediated double-stranded DNA cleavage.
Journal: Genome biology
Published: May 28, 2025
Biomembrane-inspired lipid nanoparticles enhance CRISPR-Cas9 editing for hemophilia A.
Journal: Journal of controlled release : official journal of the Controlled Release Society
Published: May 23, 2025
Enhancing hemophilia A gene therapy by strategic F8 deletions in AAV vectors.
Journal: Blood science (Baltimore, Md.)
Published: July 20, 2024
A p21 reporter iPSC line for evaluating CRISPR-Cas9 and vector-induced stress responses.
Journal: Stem cells (Dayton, Ohio)
Published: May 02, 2024
Leveraging CRISPR-Cas9 for Accurate Detection of AAV-Neutralizing Antibodies: The AAV-HDR Method.
Journal: Human gene therapy
Published: December 09, 2023
Decoding the complexity of on-target integration: characterizing DNA insertions at the CRISPR-Cas9 targeted locus using nanopore sequencing.
Journal: BMC genomics
Published: June 05, 2023
OliTag-seq enhances in cellulo detection of CRISPR-Cas9 off-targets.
Journal: Communications biology
Published: May 05, 2023
Last Updated: 09/26/2026