D. Reay

发表

Abolishing UCHL1's hydrolase activity exacerbates TBI-induced axonal injury and neuronal death in mice

C. Dixon, S. Graham, Hao Liu, 2020, Experimental Neurology.

Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle.

S. Kochanek, A. Gambotto, E. Feingold, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene

J. Watchko, Juan Li, Xiao Xiao, 2010, Gene Therapy.

Systemic delivery of NEMO binding domain/IKKγ inhibitory peptide to young mdx mice improves dystrophic skeletal muscle histopathology

P. Robbins, J. Watchko, D. Guttridge, 2011, Neurobiology of Disease.

Development of novel NEMO-binding domain mimetics for inhibiting IKK/NF-κB activation

Simon C Watkins, G. M. Wilson, P. Robbins, 2018, PLoS biology.

Improving the identification of patients with a genetic diagnosis of familial hypercholesterolaemia in primary care: A strategy to achieve the NHS long term plan.

J. Newton, D. Neely, I. Berry, 2021, Atherosclerosis.

Effect of Nuclear Factor κB Inhibition on Serotype 9 Adeno-Associated Viral (AAV9) Minidystrophin Gene Transfer to the mdx Mouse

J. Watchko, P. Clemens, E. Raggi, 2012, Molecular medicine.

Full-length dystrophin gene transfer to the mdx mouse in utero

J. Watchko, P. Clemens, Z. Jiang, 2008, Gene Therapy.

Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero

S. Kochanek, P. Clemens, R. Bilbao, 2005, Gene Therapy.

Gene therapy for muscular dystrophy reaches human clinical trial

P. Clemens, D. Reay, S. Eghtesad, 2009, Annals of neurology.

Inhibition of the IKK/NF-κB pathway by AAV gene transfer improves muscle regeneration in older mdx mice

P. Robbins, D. Guttridge, J. Huard, 2010, Gene Therapy.

NF-κB inhibition delays DNA damage-induced senescence and aging in mice.

Simon C Watkins, D. Stolz, P. Robbins, 2012, The Journal of clinical investigation.

Binding of adenoviral fiber knob to the coxsackievirus-adenovirus receptor is crucial for transduction of fetal muscle.

T. Wickham, P. Roelvink, P. Clemens, 2003, Human gene therapy.

Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors

S. Kochanek, J. Bergelson, P. Clemens, 2003, Gene Therapy.

d-Amino Acid Substitution of Peptide-Mediated NF-κB Suppression in mdx Mice Preserves Therapeutic Benefit in Skeletal Muscle, but Causes Kidney Toxicity

K. Wack, D. Stolz, P. Robbins, 2015, Molecular medicine.

Mutation of a Ubiquitin Carboxy Terminal Hydrolase L1 Lipid Binding Site Alleviates Cell Death, Axonal Injury, and Behavioral Deficits After Traumatic Brain Injury in Mice

C. Dixon, S. Graham, Hao Liu, 2021, Neuroscience.

Role of UCHL1 in axonal injury and functional recovery after cerebral ischemia

N. Povysheva, G. Barrionuevo, Fenghua Chen, 2019, Proceedings of the National Academy of Sciences.

Patterns of gene expression from in utero delivery of adenoviral-associated vector serotype 1.

Juan Li, Xiao Xiao, P. Clemens, 2005, Human Gene Therapy.