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1 red kinetics of RNA synthesis in an in vitro primer extension assay.
2 xonuclease to remove mispaired 3' bases in a primer extension assay.
3  rapid amplification of cDNA ends (RACE) and primer extension assay.
4 ficial array could be quantified by a simple primer extension assay.
5 avage and to highly visible stop points in a primer extension assay.
6  site was identified by RNase protection and primer extension assay.
7 cific ligation assay and a single nucleotide primer extension assay.
8  cleavage were detected and analyzed using a primer-extension assay.
9 sults were compared with those of individual primer extension assays.
10 at least in the context of reporter gene and primer extension assays.
11  of the fxbA promoter that was identified in primer extension assays.
12 substrate for nucleic acid hybridization and primer extension assays.
13 -dependent toxT transcription by time course primer extension assays.
14                                           In primer extension assays, afRFC stimulated the processivi
15                                   Using RPA, primer extension assay and 5' rapid amplification of cDN
16 iptional start point (tsp) was identified by primer extension assay and a rapid amplification of cDNA
17 t of rRNA depurination in vivo using a novel primer extension assay and show that the temporal patter
18               We established a new automated primer extension assay and successfully validated it for
19                            Using an in vitro primer extension assay and the mammalian DNA polymerase
20 osition 249, exhibits a mutator phenotype in primer extension assays and in the herpes simplex virus-
21 eir interactions using primase, helicase and primer extension assays, and a 'stripped down' reconstit
22 te that the purified O-ribosomes are pure by primer extension assays, and structurally homogenous by
23                                           By primer extension assays, cadBA expression was detected w
24                                            A primer extension assay demonstrated that the appropriate
25 e structure and function of mt-tRNA(Asp) The primer extension assay demonstrated that the m.7551A > G
26                        Iron footprinting and primer extension assays demonstrated that MK-8527-TP inh
27 of plasmid pIJ101 and, employing an in vitro primer extension assay, determined that the modification
28 ive allele-specific RT-PCR single nucleotide primer extension assays developed for two imprinted gene
29 o an agarose bead support enables repetitive primer extension assays for specific genomic DNA targets
30 chromatography (RP-HPLC) and quantified in a primer extension assay from cord blood.
31        Nucleotide-sequencing and multiplexed primer-extension assays have been used to quantitate the
32 ition, promoter consensus binding search and primer extension assay helped us to identify a new sigma
33                                              Primer extension assays identified multiple transcriptio
34                               We carried out primer extension assays in conjunction with molecular mo
35                                        Using primer extension assays in vitro, we found that a single
36  strong pause sites in reverse transcriptase primer extension assays in vitro.
37          These enzymes were characterized in primer extension assays in which the template DNA was ad
38 itatively, a strand bias was observed in the primer extension assay, in that polymerase synthesis ter
39                  Ribonuclease protection and primer extension assays indicate that alpha1aAR gene tra
40                                              Primer extension assays indicate two major transcription
41              Biochemical, reporter-based and primer-extension assays indicate that BCX4430 inhibits v
42   The results of ribonuclease protection and primer extension assays indicated that Bmp2 transcriptio
43                                 In vitro DNA primer extension assays indicated that Cl-F-ara-ATP comp
44 prtF and rofA transcripts by S1 nuclease and primer extension assays indicated that the same promoter
45                                              Primer extension assay indicates that the transcription
46 ensitive and highly reproducible multiplexed primer extension assay is described for quantitative mut
47                                            A primer extension assay is used to perform highly multipl
48                                              Primer extension assay localized the transcription initi
49 cipitated with HBV core antibody; and (iv) a primer extension assay maps the 5' end of the minus stra
50 on of Western blotting and a novel multiplex primer extension assay (MPEA), we showed that, although
51                   Using RNase protection and primer extension assays, multiple transcription initiati
52                                     Specific primer extension assays on total RNA from HeLa cells sho
53                                              Primer extension assays performed in the presence of hig
54                                              Primer extension assays performed in the presence of tra
55                                           In primer extension assays, pol eta and pol kappa replicate
56                            A simple poisoned primer extension assay readily quantified editing extent
57                                              Primer extension assay results demonstrated that both di
58                          Polymerase-mediated primer-extension assays reveal that tCfTP is efficiently
59                                              Primer extension assay revealed a transcription initiati
60                                    Moreover, primer extension assay revealed that N(4)-CMdC was a str
61                                              Primer extension assays ruled out an increase in abortiv
62                  Ribonuclease protection and primer extension assays show that each promoter is activ
63 (selective 2'-hydroxyl acylation analysed by primer extension) assays show that part of the regulated
64                      In vitro standing-start primer-extension assays show that the preferential inser
65 varying the order of reagent addition in the primer extension assay showed no distinct differences in
66                                              Primer extension assays showed that both polymerases sto
67 ng site was near dsbG, Northern blotting and primer extension assays showed that OxyR binding to the
68           Both beta-galactosidase assays and primer extension assays showed that these regions functi
69 on mutants of LAP1 by in vitro transcription-primer extension assays showed that upstream elements in
70 ata from mRNA decay studies and quantitative primer extension assays support a model in which bound C
71   To do this, we developed a high-throughput primer extension assay that allows monitoring of the kin
72 nt inhibitors of human telomerase by using a primer extension assay that does not use PCR-based ampli
73                                            A primer-extension assay that allowed determination of DNA
74                          We also developed a primer-extension assay that can monitor the methylation
75                             By employing the primer extension assay, the transcription start site of
76                          We used an in vitro primer extension assay to examine the progression of DNA
77 y (ZIBS assay); (ii) an S1 nuclease cleavage-primer extension assay to map B-Z junctions; and (iii) a
78           We used S1 nuclease protection and primer extension assays to define nucleolar dominance at
79 e seven nucleotides were analyzed by a novel primer extension assay using a mixture of one dNTP compl
80                               Interestingly, primer extension assays using human immunodeficiency vir
81                                              Primer extension assays using recombinant templates cons
82                                              Primer extension assays using substrates possessing sing
83 native substrate and RNA-chain terminator in primer-extension assays using a surrogate respiratory sy
84 etous yeast species, and the allele-specific primer extension assay was designed to identify a total
85                                            A primer extension assay was developed to assess HIV-1 RT
86                                            A primer extension assay was used for the detection of uri
87                                            A primer extension assay was used to monitor quantitativel
88                      Using a single-turnover primer extension assay, we defined two factors that dete
89                                           In primer extension assay, we found that gamma-dialkylated
90                            Using an in vitro primer extension assay, we observed sequence-specific sy
91                            In a missing base primer extension assay, we observed that the mutant enzy
92                                    Using RNA primer extension assays, we determined that the mdm-2 mR
93                                        Using primer extension assays, we mapped the transcriptional s
94 omatin immunoprecipitation-single-nucleotide primer extension assays, we measured the chromatin compo
95                           Using dot-blot and primer extension assays, we measured the susceptibility
96            Using transcriptional fusions and primer extension assays, we show here that tolC has two
97                               Using in vitro primer extension assays, we show that both G4s and stabl
98                                              Primer extension assays were used to determine the trans
99                                              Primer extension assays were used to show that individua
100 nged this notion by presenting evidence from primer extension assays which appeared to indicate that
101 y of copying both DNA and RNA templates in a primer extension assay with biased dNTP pools.
102 eloped an SNP genotyping method based on the primer extension assay with fluorescence quenching as th
103 This procedure combines the versatility of a primer extension assay with nucleotide-level resolution,
104                                   However, a primer extension assay with three dNTPs showed that F227
105                                              Primer extension assays with purified BALB/cJ and A/J pr
106                                              Primer extension assays with RNA isolated from Escherich

 
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