|
Volumn 30, Issue 2, 2007, Pages 218-223
|
Creation of novel cell-penetrating peptides for intracellular drug delivery using systematic phage display technology originated from tat transduction domain
a b,c a,b a,b a,b a,b a,b a,b a,b a,b a,b a,b a,b b d a
c
MIE UNIVERSITY
(Japan)
|
Author keywords
Cell penetrating peptide; Phage display; Tat
|
Indexed keywords
CELL PENETRATING PEPTIDE;
CELL PENETRATING PEPTIDE PROTEIN SYNTHESIS INHIBITORY FACTOR FUSION PROTEIN;
COMPLEMENTARY DNA;
CYCLOHEXIMIDE;
DRUG CARRIER;
HYBRID PROTEIN;
PEPTIDE LIBRARY;
PROTEIN SYNTHESIS INHIBITORY FACTOR;
TRANSACTIVATOR PROTEIN;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ARTICLE;
CELL MEMBRANE;
CELLULAR DISTRIBUTION;
CHO CELL;
CLONE;
CONTROLLED STUDY;
DRUG CYTOTOXICITY;
DRUG DELIVERY SYSTEM;
DRUG IDENTIFICATION;
DRUG PENETRATION;
DRUG SCREENING;
GENETIC RECOMBINATION;
GENETIC TRANSDUCTION;
HELA CELL;
HUMAN;
HUMAN CELL;
MEMBRANE BINDING;
METHODOLOGY;
MOUSE;
NONHUMAN;
NUCLEOTIDE SEQUENCE;
PHAGE DISPLAY;
PROTEIN ANALYSIS;
PROTEIN BINDING;
PROTEIN DOMAIN;
PROTEIN EXPRESSION;
PROTEIN SYNTHESIS;
ANIMALS;
BACTERIOPHAGES;
CHO CELLS;
CRICETINAE;
CRICETULUS;
DNA, COMPLEMENTARY;
DRUG DELIVERY SYSTEMS;
ENDOCYTOSIS;
GENE PRODUCTS, TAT;
HELA CELLS;
HUMANS;
PEPTIDE LIBRARY;
PEPTIDES;
PROTEIN SYNTHESIS INHIBITORS;
RECOMBINANT FUSION PROTEINS;
TRANSDUCTION, GENETIC;
|
EID: 33846991262
PISSN: 09186158
EISSN: 13475215
Source Type: Journal
DOI: 10.1248/bpb.30.218 Document Type: Article |
Times cited : (35)
|
References (22)
|