Enhanced intracellular delivery using arginine-rich peptides by the addition of penetration accelerating sequences (Pas).
about
Enhancing Endosomal Escape for Intracellular Delivery of Macromolecular Biologic Therapeutics.Delivery of nucleic acids and nanomaterials by cell-penetrating peptides: opportunities and challengesChemical-functional diversity in cell-penetrating peptidesHexokinase II-derived cell-penetrating peptide targets mitochondria and triggers apoptosis in cancer cellsCell-penetrating peptide-functionalized quantum dots for intracellular delivery.Endocytic Trafficking of Nanoparticles Delivered by Cell-penetrating Peptides Comprised of Nona-arginine and a Penetration Accelerating SequenceTheranostic protein targeting ErbB2 for bioluminescence imaging and therapy for cancer.Dual peptide conjugation strategy for improved cellular uptake and mitochondria targetingCellular uptake and cytotoxicity of drug-peptide conjugates regulated by conjugation siteEnhanced cellular entry and efficacy of tat conjugates by rational design of the auxiliary segment.Excipients with specialized functions for effective drug delivery.Targeting diseased tissues by pHLIP insertion at low cell surface pH.Cationic PTD/CPP-mediated macromolecular delivery: charging into the cell.Hydrophobic and electrostatic interactions between cell penetrating peptides and plasmid DNA are important for stable non-covalent complexation and intracellular delivery.Co-operative membrane disruption between cell-penetrating peptide and cargo: implications for the therapeutic use of the Bcl-2 converter peptide D-NuBCP-9-r8.Relating structure and internalization for ROMP-based protein mimics.COPA and SLC4A4 are required for cellular entry of arginine-rich peptides.Protein nanodisk assembling and intracellular trafficking powered by an arginine-rich (R9) peptide.Increased Hydrophobic Block Length of PTDMs Promotes Protein Internalization.Cell-Penetrating Peptides: Design Strategies beyond Primary Structure and Amphipathicity.Effects of N-terminal and C-terminal modification on cytotoxicity and cellular uptake of amphiphilic cell penetrating peptides.Polioviral receptor binding ligand: a novel and safe peptide drug carrier from polioviral capsid.Tat-tetanus toxin fragment C: a novel protein delivery vector and its use with photochemical internalization.
P2860
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P2860
Enhanced intracellular delivery using arginine-rich peptides by the addition of penetration accelerating sequences (Pas).
description
2009 nî lūn-bûn
@nan
2009 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@ast
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@en
type
label
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@ast
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@en
prefLabel
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@ast
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@en
P2093
P1476
Enhanced intracellular deliver ...... accelerating sequences (Pas).
@en
P2093
Hideki Matsui
Hiroyuki Michiue
Ikuhiko Nakase
Kazuhito Tomizawa
Kentaro Takayama
Shiroh Futaki
Toshihide Takeuchi
P304
P356
10.1016/J.JCONREL.2009.05.019
P407
P577
2009-05-22T00:00:00Z