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Dendrimers in gene delivery
Dendrimers have unique molecular architectures and properties that make them attractive
materials for the development of nanomedicines. Key properties such as defined …
materials for the development of nanomedicines. Key properties such as defined …
Inorganic nanoparticles as carriers of nucleic acids into cells
The transfer of nucleic acids (DNA or RNA) into living cells, that is, transfection, is a major
technique in current biochemistry and molecular biology. This process permits the selective …
technique in current biochemistry and molecular biology. This process permits the selective …
Senescence surveillance of pre-malignant hepatocytes limits liver cancer development
Upon the aberrant activation of oncogenes, normal cells can enter the cellular senescence
program, a state of stable cell-cycle arrest, which represents an important barrier against …
program, a state of stable cell-cycle arrest, which represents an important barrier against …
Hydrodynamics-based transfection in animals by systemic administration of plasmid DNA
F Liu, YK Song, D Liu - Gene therapy, 1999 - nature.com
Abstract Development of methods that allow an efficient expression of exogenous genes in
animals would provide tools for gene function studies, treatment of diseases and for …
animals would provide tools for gene function studies, treatment of diseases and for …
Nonviral gene delivery: what we know and what is next
X Gao, KS Kim, D Liu - The AAPS journal, 2007 - Springer
Gene delivery using nonviral approaches has been extensively studied as a basic tool for
intracellular gene transfer and gene therapy. In the past, the primary focus has been on …
intracellular gene transfer and gene therapy. In the past, the primary focus has been on …
The headgroup evolution of cationic lipids for gene delivery
D Zhi, S Zhang, S Cui, Y Zhao, Y Wang… - Bioconjugate …, 2013 - ACS Publications
Cationic lipids are one of the most widely used nonviral vectors for gene delivery and are
especially attractive because they can be easily synthesized and extensively characterized …
especially attractive because they can be easily synthesized and extensively characterized …
Nonviral vectors in the new millennium: delivery barriers in gene transfer
M Nishikawa, L Huang - Human gene therapy, 2001 - liebertpub.com
Development of an efficient method for introducing a therapeutic gene into target cells in
vivo is the key issue in treating genetic and acquired diseases by gene therapy. To this end …
vivo is the key issue in treating genetic and acquired diseases by gene therapy. To this end …
Nanostructured calcium phosphates for biomedical applications: novel synthesis and characterization
Materials play a key role in several biomedical applications, and it is imperative that both the
materials and biological aspects are clearly understood for attaining a successful biological …
materials and biological aspects are clearly understood for attaining a successful biological …
Advances in gene delivery systems
K Kamimura, T Suda, G Zhang, D Liu - Pharmaceutical medicine, 2011 - Springer
The transfer of genes into cells, both in vitro and in vivo, is critical for studying gene function
and conducting gene therapy. Methods that utilize viral and nonviral vectors, as well as …
and conducting gene therapy. Methods that utilize viral and nonviral vectors, as well as …
Delivery of bioactive molecules into the cell: the Trojan horse approach
In recent years, vast amounts of data on the mechanisms of neural de-and regeneration
have accumulated. However, only in disproportionally few cases has this led to efficient …
have accumulated. However, only in disproportionally few cases has this led to efficient …