Synthetic DNA-compacting peptides derived from human sequence enhance cationic lipid-mediated gene transfer in vitro and in vivo.
about
Coupling of importin beta binding peptide on plasmid DNA: transfection efficiency is increased by modification of lipoplex's physico-chemical propertiesPeptide-mediated lipofection is governed by lipoplex physical properties and the density of surface-displayed amines.Novel molecular approaches to cystic fibrosis gene therapy.Calcium phosphate nanoparticles: second-generation nonviral vectors in gene therapy.Nuclear gene delivery: the Trojan horse approach.Incorporation of histone derived recombinant protein for enhanced disassembly of core-membrane structured liposomal nanoparticles for efficient siRNA delivery.Cationic nanoparticles for cancer therapy.Peptide vectors for gene delivery: from single peptides to multifunctional peptide nanocarriers.Hydrophobic and electrostatic interactions between cell penetrating peptides and plasmid DNA are important for stable non-covalent complexation and intracellular delivery.Genetic pharmacology: progresses in siRNA delivery and therapeutic applications.Lipofection of insulin-producing RINm5F cells: methodological improvements.Nuclear localisation sequence templated nonviral gene delivery vectors: investigation of intracellular trafficking events of LMD and LD vector systems.Formulations which increase the size of lipoplexes prevent serum-associated inhibition of transfection.Vectors based on reducible polycations facilitate intracellular release of nucleic acids.An optimized amphiphilic cationic peptide as an efficient non-viral gene delivery vector.Characterisation of LMD virus-like nanoparticles self-assembled from cationic liposomes, adenovirus core peptide mu and plasmid DNA.Comparison between the interactions of adenovirus-derived peptides with plasmid DNA and their role in gene delivery mediated by liposome-peptide-DNA virus-like nanoparticles.Increased receptor-mediated gene delivery to the liver by protamine-enhanced-asialofetuin-lipoplexes.Ternary complex of plasmid DNA with NLS-Mu-Mu protein and cationic niosome for biocompatible and efficient gene delivery: a comparative study with protamine and lipofectamine.
P2860
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P2860
Synthetic DNA-compacting peptides derived from human sequence enhance cationic lipid-mediated gene transfer in vitro and in vivo.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo.
@en
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo.
@nl
type
label
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo.
@en
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo.
@nl
prefLabel
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo.
@en
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo.
@nl
P2093
P2860
P356
P1433
P1476
Synthetic DNA-compacting pepti ...... transfer in vitro and in vivo
@en
P2093
Scherman D
Schwartz B
P2860
P2888
P304
P356
10.1038/SJ.GT.3300795
P50
P577
1999-02-01T00:00:00Z
P5875
P6179
1004652565