William N. Feist

This paper demonstrates efficient gene editing and phenotype generation in avian embryos using lipid nanoparticles as a delivery platform, showing successful CRISPR/Cas9 editing and long-term labeling of cranial NCC derivatives.

This paper engineers hematopoietic stem and progenitor cells to express CD4 on red blood cells, creating viral traps to neutralize HIV-1.

This study establishes a long-term culture system for rock dove primordial germ cells, enabling germline manipulation and conservation applications.

This paper describes engineering hematopoietic stem cells to produce CCR5 knockout cells and secrete HIV-1 inhibiting antibodies, aiming for a one-time cure for HIV-1.