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1 and 10(7) to 10(8) molecules of biotinylated amplification product.
2  of energy transfer-labeled primers into the amplification product.
3 ly when the primers are incorporated into an amplification product.
4 direct sequencing and genotyping of desalted amplification products.
5 A and pgRNA by primer extension of their PCR amplification products.
6 account for signals arising from nonspecific amplification products.
7 ilies, and (iii) redundant sequencing of the amplification products.
8 mer selection, and formation of chimeric 16S amplification products.
9  by automated Web-based sequence analysis of amplification products.
10 CR and was confirmed by direct sequencing of amplification products.
11  by automated web-based sequence analysis of amplification products.
12 y (MS) analysis of base-specifically cleaved amplification products.
13  identified based on the presence/absence of amplification products.
14 ired and in improving the yield of desirable amplification products.
15 priming ability without yielding exponential amplification products.
16 y preparation and sequence analyses of these amplification products.
17 which is due to the accumulation of spurious amplification products.
18 erase chain reaction and sequencing of viral amplification products.
19                          By gel detection of amplification products, 12 of 181 culture-negative sampl
20 nin-specific polymerase chain-reaction (PCR) amplification products, 5' and 3' rapid amplification of
21 ntained within the debranched rolling-circle amplification product and map the consensus to its genom
22 chain reactions (PCR), pooling the resulting amplification products and hybridizing the mixture to a
23                                              Amplification products are detected with leuco crystal v
24                                  Second, the amplification products are used as templates in single b
25 Taq DNA polymerase by up to 150% and yielded amplification products at sample dilutions at which Taq
26                                 Detection of amplification products based on labeled probe primers wa
27 CR methodology, followed by detection of the amplification product by the hybridization protection as
28 e test strip, which detects and displays the amplification products by marker-specific hybridization
29 specific PCR with the discrimination between amplification products by their melting temperatures (Tm
30 rget nucleic acid, captures the biotinylated amplification products by using magnetic particles coate
31            Genotyping was conducted from HIV-amplification products, by automated sequencing.
32 ESI-MS) and base composition analysis of PCR amplification products can quickly and accurately identi
33 on by standard PCR and DNA sequencing of the amplification product confirmed all real-time PCR tox-po
34   DNA sequence characterization of an RT-PCR amplification product confirmed expression of tuftelin i
35 se-polymerase chain reaction, which revealed amplification products derived from PAF receptor mRNA co
36  amplified with eubacterial primers, and the amplification products derived from the fecal sample DNA
37   The other four samples failed to yield any amplification product even with a control set of primers
38                 Specifically identified were amplification products for the following NTs: NGF, BDNF,
39                                              Amplification products for the full-length Trk A and Trk
40  the conditions under which such recombinant amplification products form we monitored the exchange of
41 (STS)-PCR assay yielded the appropriate size amplification product from both total human DNA and hybr
42 e-specific primers to increase the Tm of the amplification product from the corresponding allele.
43                               The pattern of amplification products from all of the reactions, visual
44 d by gel electrophoresis, and representative amplification products from each patient were sequenced.
45                                          The amplification products from eight air samples were clone
46  labeled PCR primers are used to produce PCR amplification products from eight VNTR regions in the B.
47                  Sequence comparisons of the amplification products from four cna negative and four c
48 rometry and base composition analysis of PCR amplification products from highly conserved genomic reg
49 and high throughput, such as the checking of amplification products from many loci, from many clones,
50 escent probe hybridized to Southern blots of amplification products from Neospora DNA but not to Sout
51 or was available from 1 patient, and the IgH amplification products from plasma and tumor were sequen
52  A meiotic breakpoint strategy employing PCR amplification products from recombinant sperm was then u
53 1,000-fold difference in the quantity of the amplification products from the specific and nonspecific
54         The amplification is very sensitive; amplification products generated from as few as three ba
55                 Screening of over 2,000 cDNA amplification products identified 42 cDNAs that were pre
56       Cloning and sequencing of the purified amplification products identified a cytosine deletion in
57 AA40 allowed the generation of mixed RNA-DNA amplification products in PCR demonstrating DNA polymera
58 here can be used for detection of isothermal amplification products in the mix-and-read format as an
59                                              Amplification products increase when degraded genomic DN
60        Sequencing and cross-hybridization of amplification products indicated that at least 12 classe
61                                Sequencing of amplification products indicated that at least nine clas
62 be used to transduce isothermal nucleic acid amplification products into signals that can be readable
63  most common methods to detect the different amplification products is the use of fluorogenic probes
64 ctivity of HDA, which makes the detection of amplification products more reliable, we have developed
65                                          Two amplification products, named IL-2delta2 and IL-2delta3,
66 rimers was verified, since there were no PCR amplification products observed from heterologous nocard
67                                 Whole genome amplification products obtained by DOP-PCR proved to be
68                                              Amplification products obtained from the HCV-positive ca
69  82 degrees C product was identical with the amplification product of CEA-cDNA and cDNA from differen
70 positive staphylococci produced a single PCR amplification product of either 875, 660, 603, or 547 bp
71 oduct that was easily distinguished from the amplification product of viral RNA by agarose gel electr
72 esults obtained from unpurified COBAS TaqMan amplification products of 111 retrospectively selected c
73                 Random sequencing of the PCR amplification products of CD4+ peripheral blood T cells
74                                          PCR amplification products of ITS-1 display a approximately
75                                              Amplification products of the expected size for 15 growt
76                                              Amplification products of the expected size for HGF and
77                                              Amplification products of the expected size for NTs were
78                                              Amplification products of the expected size for the grow
79 he sequence-specific detection of unpurified amplification products of the gyrB gene of Salmonella ty
80 nd Macaca fascicularis yielded three TRIMCyp amplification products, one of which is predicted to enc
81 ers for the mur-2(ed) gene gave the expected amplification product only with E. durans strains.
82          After cloning and sequencing of the amplification products, patient-specific ABL primers wer
83  analyze up to 44 kb of diploid, color-coded amplification product per gel lane.
84 sion of the linear DNA molecules so that the amplification products remain localized near their respe
85 riction endonuclease digestions of the cpDNA amplification products resolved diagnostic restriction s
86 says, producing the expected 108- and 125-bp amplification products, respectively.
87   Stools and water samples yielded identical amplification product sequences.
88 m capillary electrophoresis for the expected amplification products showed that amplification in micr
89  capillary electrophoresis of long-range PCR amplification products significantly underestimated expa
90                  However, failure to recover amplification products spanning the nad4L-msh1 gene junc
91 ynucleotide detector probe hybridizes to the amplification product that rises in concentration during
92 m this population appears to yield two ITS-1 amplification products that match both C. bilineata and
93                  Both approaches yielded PCR amplification products that served as probes for screeni
94 on of perfect nucleic acid duplexes with the amplification products, these are enzyme-labeled and ele
95 alized because most laboratories subject the amplification products to lengthy probe hybridization pr
96                     However, the size of the amplification products used in these mRNA assays (approx
97 rmed by cloning and random sequencing of PCR amplification products using TCRBV region family-specifi
98 hain reaction; a 144 base-pair region of the amplification product was sequenced; and phylogenetic an
99 me quantitative PCR revealed that 96% of the amplification products were all within 4-fold of the ave
100                                              Amplification products were also obtained from isolates
101 f RNA from ischemic and control retinas, and amplification products were analyzed by agarose gel elec
102 uclear small-subunit rRNA gene sequence, and amplification products were confirmed by hybridization w
103 cterization of the polymerase chain reaction amplification products were determined by nucleic acid s
104  polymerase chain reaction, and the purified amplification products were directly sequenced with [35S
105                                              Amplification products were generated only from the DNAs
106                                     No cross-amplification products were observed when primers design
107                                           No amplification products were observed with template DNA f
108                                              Amplification products were obtained from 118 HCV-seropo
109                                           No amplification products were obtained from DNA extracted
110                          P. carinii-specific amplification products were obtained from samples from e
111                                              Amplification products were obtained that were similar i
112                        Different patterns of amplification products were obtained with DNA from desic
113                                              Amplification products were probed with nested oligonucl
114 results, I found that products from Mtb rRNA amplification products were processed with fluorescent r
115                                           No amplification products were produced for the full-length
116                                          The amplification products were resolved and quantified by t
117                                The resultant amplification products were used to isolate cDNAs, conta
118                      First, PCQ-PCR provided amplification products with an accurate proportion of mu
119                        These markers produce amplification products with genomic DNA from allotetrapl
120          Similarly, PCR yielded GCC-specific amplification products with specimens from normal intest

 
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