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1 ks in formaldehyde- and chlorambucil-treated calf thymus DNA.
2 ouble-stranded nucleic acid homopolymers and calf thymus DNA.
3 ctroscopy of 160 base pair (bp) fragments of calf thymus DNA.
4 iated by adding a large excess of unlabelled calf thymus DNA.
5 evels of total uracil, U:G, and T:G pairs in calf thymus DNA.
6 unperturbed by complexation of the drug with calf thymus DNA.
7 xyuracil, compared to commercially available calf thymus DNA.
8 t interact with plasmid (pBR322) DNA or with calf thymus DNA.
9 than unimmunized mice or mice immunized with calf thymus DNA.
10 ate the ethanol-induced B to A transition in calf thymus DNA.
11  compared to heat denatured, single stranded calf thymus DNA (0.007 endotoxin/microg DNA).
12                                         With calf thymus DNA, 5-guanidino-4-nitroimidazole was dose-d
13 e formation of 8 major and at least 10 minor calf thymus DNA adducts.
14 -forming cationic lipids are able to protect calf thymus DNA against denaturation at 100 degrees C.
15 asure the binding constants between purified calf thymus DNA and a library of designed tetrapeptides
16 he ability to displace ethidium bromide from calf thymus DNA and are rapidly taken up by F98 glioma c
17 ir ability to displace ethidium bromide from calf thymus DNA and are rapidly taken up in vitro by F98
18                                              Calf thymus DNA and DNA from the livers of MNU-treated S
19 to identify BPQ adducts formed in vitro with calf thymus DNA and DNA homopolymers.
20                                              Calf thymus DNA and DNA isolated from cultured HeLa cell
21 exes exhibited moderate binding affinity for calf thymus DNA and human serum albumin.
22 vels of the alpha-anomer of dG (alpha-dG) in calf thymus DNA and in DNA isolated from mouse pancreati
23 -cdGuo and (5'S)-8,5'-cdGuo were measured in calf thymus DNA and in DNA samples isolated from three d
24 OLN had DNA polymerase activity on activated calf thymus DNA and on a singly primed template.
25 -kDa Mg(2+)-dependent nuclease that degrades calf thymus DNA and plasmid DNA.
26 nity of the compounds was also studied using calf thymus DNA and poly(dA-dT).
27  nmol/min/mg when assayed in the presence of calf thymus DNA and the four deoxyribonucleoside triphos
28 lastic glycopeptide bleomycin A2 (Fe-BLM) to calf thymus DNA and the self-complementary oligonucleoti
29 ion of the racemic syn- and anti-BgCDEs with calf thymus DNA and with purine deoxyribonucleoside-3'-p
30 r quantification of G and A concentration in calf-thymus DNA and detected ratio of G and A (i.e., [G]
31 uantum yield (approximately 0.5, bound to ds calf thymus DNA) and large molar extinction coefficient
32 intercalated DOX in isolated double-stranded calf thymus DNA, and the correlated near-field spectrosc
33                                   Binding to calf thymus DNA as assessed by differential pulse polaro
34                In the absence of polyamines, calf thymus DNA assumed a diffused, planar cholesteric p
35 tudies show that, after 18 h incubation with calf thymus DNA at a 5:1 DNA/ligand ratio, it increases
36           In fact, controls carried out with calf thymus DNA, betaNAD(+), PARP-1, and automodified PA
37  achieve when it is bound to d(CGCGCG) or to calf thymus DNA but not when bound to d(ATATAT).
38               The measurement of 8-OH-Gua in calf thymus DNA by GC/isotope-dilution MS (GC/IDMS) usin
39 ld be demonstrated that, although 3 binds to calf-thymus DNA by intercalation, the biological effects
40                  Rabbits were immunized with calf thymus DNA, chemically modified with alpha-acetoxyt
41 es but not by pUC nor Bacillus subtilis DNA; calf thymus DNA competed at higher concentrations.
42 bound to double-stranded poly(dABrdU) and to calf thymus DNA (CT DNA) and the complexes characterized
43  monostyryl derivativatives intercalate into calf thymus DNA (ct DNA), whereas photocyclization produ
44 ity are observed upon addition of 100 microM calf thymus DNA (ct-DNA).
45 ch derivative to establish interactions with calf-thymus DNA (CT-DNA) and bovine serum albumin (BSA).
46 ands regulate their ability to interact with calf thymus DNA (ctDNA) through an intercalative mode.
47 The bonding interaction between 7ESTAC01 and calf thymus DNA (ctDNA) was confirmed by UV-Vis absorpti
48             Interactions of the complex with calf thymus DNA (ctDNA) were conducted with a flow-cell
49 ost of the thymidine 5'-monophosphate (TMP), calf thymus DNA (CTDNA), and plasmid DNA (PLDNA) analyse
50              The presence of single-stranded calf thymus DNA (equimolar with duplex) eliminated the t
51 lished by derivatizing adducts isolated from calf thymus DNA exposed to AAAF.
52                       The substrate used was calf-thymus DNA exposed to gamma-radiation in N2O-satura
53 nance (NMR) studies of the interactions with calf thymus DNA for the three molecules.
54              For comparison, we also studied calf thymus DNA for which the hydration exhibits similar
55 lysis of the binding of iodoHoechst 33342 to calf thymus DNA gave an equilibrium association constant
56 3))(6)(3+), with 160 and 3000-8000 bp length calf thymus DNA has been investigated by circular dichro
57  160 base pair (bp) fragments of nucleosomal calf thymus DNA have been probed by the method of Raman
58 4-yl)diphenylporphine ions on the surface of calf thymus DNA have been studied using several spectros
59 (max)) of 632 nm, while the bound dyes (with calf thymus DNA) have electronic transitions with lambda
60 ologen (BV) with single- and double-stranded calf-thymus DNA immobilized onto gold electrodes have be
61 e betaine (GB) and urea with mononucleosomal calf thymus DNA in aqueous salt solutions are characteri
62 hydrolysis of the epoxide was accelerated by calf thymus DNA in the range of pH 6-8, with a larger en
63 -enhanced binding of the N-hydroxylamines to calf thymus DNA in vitro.
64 r 7-methylguanine (7-meG) from 3H-methylated calf thymus DNA in vitro.
65         The levels of N7-MedG and 06-MedG in calf thymus DNA increased with MNU concentration and inc
66 position of pV is reduced in the presence of calf thymus DNA, indicating that a decomposition product
67 nsfer of the electronic excitation energy in calf thymus DNA is studied by time-resolved fluorescence
68 NA interactions results in high affinity for calf thymus DNA (Kapp approximately 5 x 10(7) M(-1)).
69  the epoxide forms a reversible complex with calf thymus DNA (Kd = 0.43 mg ml-1, or 1.4 mM monomer eq
70  Further, the DNA adduction studies with the calf thymus DNA led to a mixture of dA and dG adducts fo
71 e binding to mononucleosomal (160 base-pair) calf thymus DNA of a high charge density (compact) 5-res
72 ng DPPH radical) and biocompatibility (using calf-thymus DNA) of curcumin-loaded mixed surfactant for
73  polynucleotides, of hexamine cobalt(III) to calf thymus DNA, of polyamines to T7 DNA, of oligolysine
74 the t(m) depression, whereas double-stranded calf thymus DNA only altered the t(m) of the 28-mer dupl
75                                         When calf thymus DNA or oligonucleotides were reacted with pe
76 ocytes in NZB/NZW mice injected with EC DNA, calf thymus DNA, or an immune active oligonucleotide.
77 y an excess of free aptamer but not by tRNA, calf thymus DNA, or transferrin.
78 iologically reactive metabolite and binds to calf thymus DNA (pH 5.0 or 7.0) to form the N-(deoxyguan
79 e in primer extension reactions catalyzed by calf thymus DNA polymerase (pol) alpha and human DNA pol
80 36-mer primer/template DNA by purified fetal calf thymus DNA polymerase (pol) delta was examined usin
81 catalyzed by Klenow fragment exo- (Kf exo-), calf thymus DNA polymerase alpha (pol alpha) or human DN
82 oth adducts primarily blocked replication by calf thymus DNA polymerase alpha at the modified base, w
83 t of Escherichia coli DNA polymerase I or by calf thymus DNA polymerase alpha.
84 amide gel electrophoresis, is formed between calf thymus DNA polymerase delta (pol delta) and synthet
85 ear antigen (PCNA) promotes DNA synthesis by calf thymus DNA polymerase delta (pol delta) past severa
86 e 8-oxo-7,8-dihydroguanine (8-oxoG) by fetal calf thymus DNA polymerase delta (pol delta) was examine
87  with exogenous template-primer and purified calf thymus DNA polymerase delta (pol delta).
88                                              Calf thymus DNA polymerase delta also fully restored mis
89 ypeptides were isolated with highly purified calf thymus DNA polymerase delta by conventional chromat
90 mmunoprecipitated with human p50, as well as calf thymus DNA polymerase delta heterodimer, but not wi
91  activity and to enhance the processivity of calf thymus DNA polymerase delta holoenzyme similar to c
92 lls, in contrast to the native heterodimeric calf thymus DNA polymerase delta, is not responsive to s
93  antibodies (13D5) inhibited the activity of calf thymus DNA polymerase delta.
94 le of NTP concentration in determining where calf thymus DNA primase synthesizes a primer on a DNA te
95 bacterial DNA, in comparison to 10 microg of calf thymus DNA, resulted in a fourfold increase in the
96 olution (rho(v)(90) = 0.13 at 450 nm) and on calf thymus DNA (rho(v)(90) = 0.20 at 454 nm), and chlor
97 cro-dG adducts in acrolein (10-fold)-treated calf thymus DNA showed approximately 830 lesion/10(6) DN
98 ochromate(V) with pUC19 DNA, single-stranded calf thymus DNA (ss-ctDNA), a synthetic oligonucleotide,
99 ts were formed in a dose-dependent manner in calf thymus DNA subjected to photooxidation in the prese
100 enhanced thermal denaturation temperature of calf thymus DNA ( T m), and cytotoxicity is well documen
101 -BD lesions (intrastrand and interstrand) in calf thymus DNA treated separately with S,S-, R,R-, or m
102                      In enzymatic digests of calf thymus DNA treated with 2, three adducts were ident
103 DNA upon exposure to gamma- or X-rays and in calf thymus DNA treated with Fenton reagents.
104 ation of high molecular weight and sonicated calf thymus DNA, two therapeutic oligonucleotides, and p
105 d to the analysis of etheno-dC in commercial calf thymus DNA, untreated mouse liver, and untreated ra
106 tandem MS confirmation of their formation in calf thymus DNA upon diazoacetate exposure, and the prep
107 ethylated derivatives of thymidine formed in calf thymus DNA upon exposure to diazoacetate.
108 yguanosine moiety and commercially available calf thymus DNA using this technique.
109       AP sites induced in plasmid or genomic calf thymus DNA via mild depurination or by simple incub
110 say, the rate of spontaneous depurination of calf thymus DNA was determined.
111  of small fluorescent organic molecules with calf thymus DNA was developed using two-photon absorptio
112                                              Calf thymus DNA was incubated with BaP and irradiated wi
113 he binding constant for each tetrapeptide to calf thymus DNA was obtained from the negative slope of
114                                              Calf thymus DNA was selected for the investigation, sinc
115                                         When calf thymus DNA was treated with PAH o-quinones, malondi
116                                              Calf thymus DNA was used as the substrate as well as sho
117                            Freshly dissolved calf thymus DNA was used to test the method performance.
118 nteraction of the neutral lex dipeptide with calf thymus DNA, we have prepared stable, nonmethylating
119 ) induced significant numbers of AP sites in calf thymus DNA, which were predominantly cleaved 5' to
120                                Incubation of calf-thymus DNA with MA and DTT or mercaptoethanol (MER)
121 n precipitating and resolubilizing sonicated calf thymus DNA, with N4-methyl substitution of spermidi
122  formaldehyde or chlorambucil in mixtures of calf thymus DNA, yeast RNA and proteins, and by analyzin

 
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