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Beverly L. Davidson
Researcher at Children's Hospital of Philadelphia
Publications - 410
Citations - 35019
Beverly L. Davidson is an academic researcher from Children's Hospital of Philadelphia. The author has contributed to research in topics: Gene silencing & RNA interference. The author has an hindex of 94, co-authored 391 publications receiving 33041 citations. Previous affiliations of Beverly L. Davidson include United States Department of Veterans Affairs & University of California, Los Angeles.
Papers
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Journal ArticleDOI
Evolution of alternative splicing in primate brain transcriptomes
TL;DR: A genome-wide phylogenetic survey of lineage-specific splicing patterns in the primate brain is carried out, via high-density exon junction array profiling of brain transcriptomes of humans, chimpanzees and rhesus macaques, to reveal widespread human-specific changes of alternative splicing in the brain and suggest an important role of splice in the evolution of neuronal gene regulation and functions.
Journal ArticleDOI
Recombinant adenovirus: a gene transfer vector for study and treatment of CNS diseases.
TL;DR: Experiments in feasibility studies in the CNS with application to animal models of inherited disease, neurodegenerative diseases, and cerebrovascular disease have identified specific limitations and directed further research to improve vector design, formulation, and delivery.
Journal ArticleDOI
Cationic Polymer and Lipids Enhance Adenovirus-Mediated Gene Transfer to Rabbit Carotid Artery
Kazunori Toyoda,Hiroaki Ooboshi,Yi Chu,A Fasbender,Beverly L. Davidson,Michael J. Welsh,Donald D. Heistad +6 more
TL;DR: Cationic molecules improve the efficiency of adenovirus-mediated gene transfer to blood vessels by alteration of the surface charge of adnovirus and facilitation of binding to endothelium.
Patent
ALLELE-SPECIFIC siRNA-MEDIATED GENE SILENCING
TL;DR: In this paper, small interfering RNA molecules (siRNA) targeted against an allele of interest, and methods of using these siRNA molecules were presented, and the present invention was directed to small interferingRNA (siRN) targeted to small RNA molecules.
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Effects of macrophage depletion and anti-CD40 ligand on transgene expression and redosing with recombinant adenovirus.
TL;DR: It is suggested that both macrophage depletion and CD40 ligand blockade inhibit immune responses to recombinant adenovirus to slow decline of transgene expression, while only CD40ligand blockade inhibits anti-Ad antibody generation sufficiently to allow redosing to the liver.