Alignment of phylogenetically unambiguous indels for genome-wide phylogenetic analysis and detection of lateral gene transfer 

Non-viral and viral hematopoietic progenitor cell gene therapy 

Development of lentiviral vector mediated gene transfer techniques as tools to overexpress/knockdown P2X4 receptors in vitro 

Effects of a GSK-3 inhibitor on retroviral-mediated gene transfer to human CD34+ hematopoietic progenitor cells 

Gene therapy for the prevention and treatment of leukemia 

Packaging and delivery of plasmids by bacterial extracellular vesicles 

Gene delivery to pulmonary mucosa 

Supporting the transition and academic success of transfer students at a large research university 

Targeting lentivector gene delivery to hematopoietic stem and progenitor cells in vivo 

Stem cell and gene transfer-based approaches to generate insulin-producing cells 

Cell crosstalk in the healthy knee influences remodeling and inflammatory gene expression 

Engineering lentiviral vectors for gene therapy and DC-vaccine 

Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer 

Engineering lentiviral vectors for gene delivery 

Control of endogenous gene expression in the mouse 

Engineering viral vectors for gene and cell targeting 

Photo-assisted gene therapy using light-responsive catanionic vesicles 

Chorion gene amplification in Drosophila melanogaster 

Characterizing and manipulating homology-directed gene editing in human cells 

Transmission dynamics of antibiotic resistance from plant-foods to the mammalian gut microbiome 

Cell and gene therapy in the murine model of adenosine deaminase deficiency 

The role of histone H4 lysine 20 monomethylation in gene expression and differentiation 

Pseudotyped viral vectors: HIV gene therapy applications and basic studies of SARS-COV-2 

Memo, civilian paygrade advancement & transfer opportunities, 1991-04-29 

Investigating the evolution of gene networks through simulated populations