M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

about

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

Item

http://www.wikidata.org/entity/Q39889528

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh

2009年學術文章

@zh-hant

name

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@en

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@nl

type

Item

label

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@en

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@nl

prefLabel

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@en

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@nl

P1476

M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.

@en

P2093

B Lu

http://www.w3.org/2001/XMLSchema#string

B-H Li

http://www.w3.org/2001/XMLSchema#string

D-M Xu

http://www.w3.org/2001/XMLSchema#string

H Xu

http://www.w3.org/2001/XMLSchema#string

J Gao

http://www.w3.org/2001/XMLSchema#string

J Zhao

http://www.w3.org/2001/XMLSchema#string

L Dong

http://www.w3.org/2001/XMLSchema#string

M Wu

http://www.w3.org/2001/XMLSchema#string

S-D Yao

http://www.w3.org/2001/XMLSchema#string

Y-B Liu

http://www.w3.org/2001/XMLSchema#string

P2860

Side-effects of a systemic injection of linear polyethylenimine-DNA complexes

A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine

PEGylation of poly(ethylene imine) affects stability of complexes with plasmid DNA under in vivo conditions in a dose-dependent manner after intravenous injection into mice.

Full deacylation of polyethylenimine dramatically boosts its gene delivery efficiency and specificity to mouse lung.

Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial viruses.

An overview of current delivery systems in cancer gene therapy.

Polyethylenimine-based non-viral gene delivery systems.

Polymeric nanoparticles for gene delivery.

Evidence for the role of proteoglycans in cation-mediated gene transfer.

Evaluation of hepatic antioxidant systems after intravenous administration of polymeric nanoparticles.

P2888

cgt.2009.11

P304

561-566

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/CGT.2009.11

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2009-01-30T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

23960188

http://www.w3.org/2001/XMLSchema#string

P6179

1023888512

http://www.w3.org/2001/XMLSchema#string

P698

19180143

http://www.w3.org/2001/XMLSchema#string