Nanoclay-based drug delivery systems and their therapeutic potentials

N Khatoon, MQ Chu, CH Zhou - Journal of Materials Chemistry B, 2020 - pubs.rsc.org
Safe, therapeutically effective, and patient-compliant drug delivery systems are needed to
design novel tools and strategies to combat the deadliest of diseases such as cancer, SARS …

[HTML][HTML] Viral and nonviral delivery systems for gene delivery

N Nayerossadat, T Maedeh, PA Ali - Advanced biomedical …, 2012 - journals.lww.com
Gene therapy is the process of introducing foreign genomic materials into host cells to elicit
a therapeutic benefit. Although initially the main focus of gene therapy was on special …

[HTML][HTML] Current progress in gene delivery technology based on chemical methods and nano-carriers

L Jin, X Zeng, M Liu, Y Deng, N He - Theranostics, 2014 - ncbi.nlm.nih.gov
Gene transfer methods are promising in the field of gene therapy. Current methods for gene
transfer include three major groups: viral, physical and chemical methods. This review …

Targeting long non-coding RNA to therapeutically upregulate gene expression

C Wahlestedt - Nature reviews Drug discovery, 2013 - nature.com
The majority of currently available drugs and tool compounds exhibit an inhibitory
mechanism of action and there is a relative lack of pharmaceutical agents that are capable …

[HTML][HTML] Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

S Hacein-Bey-Abina, A Garrigue… - The Journal of …, 2008 - Am Soc Clin Investig
Previously, several individuals with X-linked SCID (SCID-X1) were treated by gene therapy
to restore the missing IL-2 receptor γ (IL2RG) gene to CD34+ BM precursor cells using …

Gene editing in human stem cells using zinc finger nucleases and integrase-defective lentiviral vector delivery

A Lombardo, P Genovese, CM Beausejour… - Nature …, 2007 - nature.com
Achieving the full potential of zinc-finger nucleases (ZFNs) for genome engineering in
human cells requires their efficient delivery to the relevant cell types. Here we exploited the …

Viral vectors: from virology to transgene expression

D Bouard, N Alazard‐Dany… - British journal of …, 2009 - Wiley Online Library
In the late 1970s, it was predicted that gene therapy would be applied to humans within a
decade. However, despite some success, gene therapy has still not become a routine …

Meganucleases and DNA double-strand break-induced recombination: perspectives for gene therapy

F Pâques, P Duchateau - Current gene therapy, 2007 - ingentaconnect.com
Meganucleases are sequence-specific endonucleases recognizing large (> 12 bp)
sequence sites and several laboratories have used these proteins to induce highly efficient …

Gene therapy with the sleeping beauty transposon system

P Kebriaei, Z Izsvák, SA Narayanavari, H Singh… - Trends in Genetics, 2017 - cell.com
The widespread clinical implementation of gene therapy requires the ability to stably
integrate genetic information through gene transfer vectors in a safe, effective, and …

[HTML][HTML] Mesenchymal stem cells of dental origin for inducing tissue regeneration in periodontitis: a mini-review

B Hernández-Monjaraz, E Santiago-Osorio… - International journal of …, 2018 - mdpi.com
Periodontitis is a chronic disease that begins with a period of inflammation of the supporting
tissues of the teeth table and then progresses, destroying the tissues until loss of the teeth …