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1 red on fibronectin than in cells cultured on polylysine.
2 s by recombinant human CKII is stimulated by polylysine.
3 lylysine and 0.22 +/- 0.12% for [99mTc] DTPA-polylysine.
4 bronectin but had no effect on attachment to polylysine.
5 A-man-PL and 0.13 +/- 0.08% for [99mTc] DTPA-polylysine.
6 asing protein (BPI or CAP57), protamine, and polylysine.
7 consisting of asialoglycoprotein coupled to polylysine.
8 r the MARCKS peptide or with the addition of polylysine.
9 y degraded protein, it bound to MDA-modified polylysine.
10 nder an electric field or in the presence of polylysine.
11 nk formation is observed with either AP-1 or polylysine.
12 approximately 15.0 MBq (99m)Tc-DTPA-succinyl-polylysine (2 microg; DTPA is diethylenetriaminepentaace
14 aximal stimulation occurs at 10 microg/ml of polylysine, a concentration which has no effect on prote
15 report the crystallographic structure of the polylysine-actin-latrunculin A complex at 3.5-A resoluti
16 was 2.84 +/- 0.83% for [99mTc]DTPA-mannosyl-polylysine and 0.22 +/- 0.12% for [99mTc] DTPA-polylysin
17 epared with either short chain or long chain polylysine and a beta-galactosidase expression plasmid.
20 mplexes were formed between the mannosylated polylysine and oligonucleotides and added to the cells i
21 tions between the charged surface-associated polylysine and phosphatidylserine are sufficient to both
23 bosylation of not only polyarginine but also polylysine and polyhistidine, and ribosylation was inhib
25 ation of coacervate microdroplets comprising polylysine and short single strands of DNA generates mem
26 ediation of the DHP receptor (e.g. caffeine, polylysine, and peptide A), induced Ca(2+) release witho
27 kinetics of inhibition by the PIP2 scavenger polylysine, and the inhibition by the phosphatidylinosit
28 ed by cross-linking polyethylene glycol with polylysine around a salt-leached polylactic-co-glycolic
29 tor, LPDII, where DNA was first complexed to polylysine at a ratio of 1:0.75 (w/w) and then entrapped
30 rowth cones also caused actin bundle loss in polylysine-attached growth cones without loss of actin m
31 lent presentation of CGP77175A on a modified polylysine backbone (degree of polymerization = 1200; 50
32 th a peptide mimetope of dsDNA on a branched polylysine backbone (DWEYSVWLSN-MAP) induces a systemic
33 anocarriers (H-Dots) are composed of epsilon-polylysine backbone for charge variations, near-infrared
35 ions using two distinct peptides on branched polylysine backbones (multiple Ag peptide)-peptides.
36 sed binding, none of the amines that inhibit polylysine binding inhibits PC binding, suggesting that
38 ine, spermine, tRNA, DNA, polyglutamic acid, polylysine, bovine serum albumin, or histone did not rel
40 s responsible for reversed galvanotropism on polylysine by growing neurons on tissue culture dishes w
43 t high mass ratios, whereas those containing polylysine-carrageenan complexes were turbid and unstabl
45 (degree of polymerization = 1200; 50% of the polylysines carry the inhibitor) greatly enhanced in viv
46 the Ad type 7 fiber and retard DNA through a polylysine chain present at the C-terminus of this linke
48 then fluorescently stained and stretched on polylysine-coated glass slides so that the positions of
52 diated endocytosis of a ribozyme-transferrin-polylysine complex, specifically reduces both cellular F
54 nd anti-IV in the form of asialoglycoprotein-polylysine complexes were administered to Huh7 cells, an
56 Under these conditions, the increase in the polylysine concentration resulted in the increase of bot
57 anodal turning were graded over the range of polylysine concentrations (0 = 0.1 < 1 < 10 = 100 microg
60 genes were complexed with asialoglycoprotein-polylysine conjugates, and 1 mg of the complexed DNA was
61 ine enkephalin, bradykinin, substance P, and polylysine-containing particles were determined with att
63 a mixture of cytochrome b5, cytochrome c and polylysine, cytochrome b5 undergoes reversible electroch
66 n techniques demonstrated that an adenovirus-polylysine-deoxyribonucleic acid (DNA) complex can be us
67 However, surprisingly, we found that epsilon-polylysine did not have a significant impact on lipid di
68 bstrates of gamma-PAK, such as histone 1 and polylysine, do not stimulate autophosphorylation or acti
69 hylenetriamine pentaacetic acid polymannosyl polylysine (DTPA-man-PL) was synthesized and tested for
70 In the presence of 1-5 mM Ca2+ (or 10 microM polylysine) ECaSt/PDI augmented the bovine pancreatic tr
71 antibody complexes and (99m)Tc-DTPA-succinyl-polylysine enabled in vivo visualization of very small a
73 gements can be blocked by positively charged polylysine, further implicating electrostatic interactio
79 influenced by the cell type tested, although polylysine homopolymers demonstrate levels of internaliz
81 ed imidazole groups to the epsilon-amines of polylysine in varying mole ratios (73.5 mol % imidazole,
82 llapse, we cultured Helisoma growth cones on polylysine in which lamellipodial collapse was prevented
83 er levels of calcium loading (>150 nmol/mg), polylysine induced monophasic Ca2+ release curves (witho
84 that inhibits actin polymerization, arrests polylysine-induced nucleation at the level of an antipar
85 sing two different systems (C167PM actin and polylysine-induced polymerization of alpha-actin) show t
87 ortant implications for the incorporation of polylysine into food systems, particularly those contain
92 tinas were removed, dissociated, plated on a polylysine/laminin substrate, and maintained in vitro fo
93 or 8-day-old Long Evans rats and cultured on polylysine/laminin-coated coverslips in serum-free mediu
94 In addition, both lysine octapeptide and polylysine ligands were accessible for binding to hepari
98 ate that formation of amphotropic retrovirus polylysine molecular conjugates (aMMLV-PL) enhanced gene
102 complexes at an optimal w/w ratio of 5:1:2 (polylysine-molossin/DNA/fusogenic peptide) resulted in 2
103 r to macromolecular acceptors (ubiquitin and polylysine) more strongly than transfer to small-molecul
104 aptotagmin interactions mediated by the C2 B polylysine motif are required to attain full synaptotagm
109 and provide evidence that a highly conserved polylysine motif in this loop supports binding to negati
111 We have demonstrated that incorporation of a polylysine motif into the pIX ectodomain results in a si
112 Together, our results demonstrate that the polylysine motif is required for efficient Ca2+-independ
113 uptake was unchanged in the mutants, and the polylysine motif mutant synaptotagmin was able to rescue
115 tagmin I (syt) transgenes harboring specific polylysine motif mutations into flies otherwise lacking
117 endent interactions mediated through the C2A polylysine motif of synaptotagmin 1 function to modulate
121 18 DTPA and 82 mannosyl groups attached to a polylysine of 100 units ([99mTc]DTPA18-man82-PL100) were
122 he adhesion of cells to an adsorbed layer of polylysine on glass plates, followed by hypotonic lysis
124 f labeled DNA the surfaces were treated with polylysine or 3-aminopropyl triethoxysilane or were coat
125 y blocking PI4K or using the PIP2 scavengers polylysine or bovine serum albumin reduced the incidence
126 comprising poly(ethylene oxide) and either a polylysine or polyester dendron were prepared and hydrop
127 an irrelevant plasmid bound to mannosylated polylysine or the expression plasmid bound to galactosyl
129 is triggered when polyphosphates bind to the polylysine patch in C2B domain and is stabilized by Mg(2
132 s, whereas carrageenan displaced pectin from polylysine-pectin complexes, which was attributed to dif
135 an amide I band of ionized polyglutamate and polylysine, peptides which adopt a polyproline II helica
136 use the arginine-glycine-aspartame (RGD) and polylysine (pK7) motifs have been shown to enhance Ad5 i
137 at is condensed by electrostatic forces with polylysine (PL) covalently linked to streptavidin (binds
138 ximately 100 different complexes of DNA with polylysine (PL) or PL covalently attached to the glycopr
139 rus protein final sigma1, when conjugated to polylysine (PL), can bind the apical surface of M cells
140 mid DNA containing the gene of interest with polylysine (PL), PL linked to a replication-incompetent
142 ay, however, where M1-4 lanes alternate with polylysine-(Plys)-only lanes, RGC axons from goldfish, z
143 on of polyplexes composed of plasmid DNA and polylysine (POL), a non-buffering polyamine, or the stro
146 ng the ED(50) values of five macromolecules: polylysine, polyarginine, protamine, low-density lipopro
148 ltivalent nature of the MAG-IgM interaction, polylysine polymers of different sizes were substituted
150 ectrolytes consisting of cyanine dye pendant polylysines ranging in number of polymer repeat units (N
151 arboxyl-terminal methionine and the upstream polylysine region are important determinants for geranyl
152 cells confirmed the importance of the K-Ras polylysine region for microtubule binding, as deletion o
154 of Ha-Ras and vice versa, we found that the polylysine region of K-Ras located immediately upstream
155 ible polycations consisting of histidine and polylysine residues (HIS RPCs) were evaluated for their
156 e expression plasmid bound to galactosylated polylysine resulted in no detectable transgene expressio
157 rted by polycations (neomycin, spermine, and polylysine) reversing the effect of PIP2 on TNP-ATP bind
158 netics observed for precursors with multiple polylysine segments support a model in which translocati
162 with polycation poly(ethylene glycol) (PEG)-polylysine (single-coat (SC) nanozyme), we introduce for
163 erol product formed in the reaction binds to polylysine SPA beads, producing a signal that is measure
165 ing sequence of a variety of genes, encoding polylysine stretches that are important for protein func
166 l root ganglion (DRG) neurite outgrowth on a polylysine substrate and that asymmetric cGMP elevation
168 which transfected neurons were replated onto polylysine substrates suggest that activation of MEK is
173 lecular conjugate consisting of mannosylated polylysine that exploits endocytosis via the macrophage
174 ecular conjugate, consisting of mannosylated polylysine that exploits endocytosis via the macrophage
175 Ca2+ release from the SR was induced by polylysine (the ryanodine receptor-specific Ca2+ release
177 rylation does not occur when cells attach to polylysine, to which cells adhere in a nonspecific fashi
178 tail, resulting in C-terminal appendage of a polylysine tract and a terminally stalled ribosome.
180 ace membranes of heat-killed neurons than on polylysine, underlining the importance of plasma membran
181 e due to the fluorescent dye, do not bind to polylysine unless hybridized to the negatively charged D
182 g lysine octapeptide, Ad vector displaying a polylysine was capable of recognizing cellular heparan s
184 , and even with HIV nucleocapsid protein and polylysine, was unacceptable; the exception was a form o
185 es with differential adhesion to immobilized polylysine, we show that neuronal colony-forming precurs
186 ing enthalpies (polyhistidine, polyarginine, polylysine), weighted by numbers of such cationic groups
189 negatively charged, but neurites growing on polylysine, which is positively charged, turned toward t
190 ce with results obtained earlier for ionized polylysine, which suggest a high polyproline II propensi
191 f (111)In-diethylenetriaminepentaacetic acid-polylysine Z2D3-F(ab')(2), and SPECT imaging was perform
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