Andrew C. Zelhof

The paper analyzes gene expression across eight tissues in Daphnia pulex and investigates selection pressures on genes in different tissues, identifying novel evolutionary patterns.

This paper establishes Drosophila intestinal cell lines derived from embryonic intestines using RasV12 expression, showing proliferation and heterogeneity, and confirms their intestinal origin through single-cell RNA sequencing.

The paper attempts to induce Cas9-dependent homologous recombination and gene drive in Tribolium castaneum but finds no evidence of homologous recombination or genetic drive.

The paper generates and tests transgenic Cas9 lines in Tribolium castaneum to improve CRISPR editing efficiency.

This paper develops a TE-based authentication protocol for Drosophila cell lines to improve reproducibility by distinguishing between different cell lines and sub-lines.

This paper uses transposable element profiles to identify and authenticate Drosophila cell lines and reveal loss of heterozygosity.

The paper describes a method to generate stable transgenic Drosophila cell lines using CRISPR-Cas9 and PhiC31 integrase systems, enabling universal cassette insertion.

This paper introduces new genetic tools for Tribolium castaneum, including GAL4 drivers, fluorescent reporters, and CRISPR-mediated markers, to enhance genetic analysis and toolkit development.