Original Article - Enabling Technologies

Improved gene delivery to adult mouse spinal cord through the use of engineered hybrid adeno-associated viral serotypes

• J J Siu
• N J Queen
• L Cao

A new plasmid-based microRNA inhibitor system that inhibits microRNA families in transgenic mice and cells: a potential new therapeutic reagent

• H Cao
• W Yu
• B A Amendt

Exosome-associated AAV vector as a robust and convenient neuroscience tool

• E Hudry
• C Martin
• C A Maguire

Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer

• C J Browne
• J L Pinyon
• G D Housley

Antithymidylate resistance enables transgene selection and cell survival for T cells in the presence of 5-fluorouracil and antifolates

• D Rushworth
• A Alpert
• L J N Cooper

Noninvasive tracking of gene transcript and neuroprotection after gene therapy

• J Ren
• Y I Chen
• P K Liu

Single-step cloning-screening method: a new tool for developing and studying high-titer viral vector producer cells

• A F Rodrigues
• A S Formas-Oliveira
• A S Coroadinha

Intra-articular delivery of anti-Hif-2α siRNA by chondrocyte-homing nanoparticles to prevent cartilage degeneration in arthritic mice

• Y Pi
• X Zhang
• Y Ao

Use of ultrasound-targeted microbubble destruction to transfect IGF-1 cDNA to enhance the regeneration of rat wounded Achilles tendon in vivo

• Y Tang
• Q Leng
• L Qiu

Chimeric rabies SADB19-VSVg-pseudotyped lentiviral vectors mediate long-range retrograde transduction from the mouse spinal cord

• L Schoderboeck
• S Riad
• S M Hughes

Replicating reoviruses with a transgene replacing the codons for the head domain of the viral spike

• D J M van den Wollenberg
• I J C Dautzenberg
• R C Hoeben

Enhanced gene disruption by programmable nucleases delivered by a minicircle vector

• A-BK Dad
• S Ramakrishna
• H Kim