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1 tic analysis (FINS, Forensically Informative Nucleotide Sequencing).
2  transcription-polymerase chain reaction and nucleotide sequencing.
3 tive 9.4-kb clone, pUEF728, was subjected to nucleotide sequencing.
4 hybridization with a hifC gene probe, and by nucleotide sequencing.
5 sertions within the genes were determined by nucleotide sequencing.
6 , offers a rapid and accurate alternative to nucleotide sequencing.
7 followed by heteroduplex analysis and direct nucleotide sequencing.
8 ere then compared by gel electrophoresis and nucleotide sequencing.
9 ingle-base mismatches that were confirmed by nucleotide sequencing.
10 ished by genomic DNA cloning and analyzed by nucleotide sequencing.
11 on, one of these loci (ERK1) was analyzed by nucleotide sequencing.
12 analyzed by heteroduplex mobility assays and nucleotide sequencing.
13  JCV regulatory region underwent cloning and nucleotide sequencing.
14 followed by heteroduplex scanning and direct nucleotide sequencing.
15             The PCR product was subjected to nucleotide sequencing.
16 cloned, and the mutations were determined by nucleotide sequencing.
17 tein-truncation assay, followed by automated nucleotide sequencing.
18 followed by heteroduplex analysis and direct nucleotide sequencing.
19 liana has been isolated and characterised by nucleotide sequencing.
20 y heteroduplex analysis and direct automated nucleotide sequencing.
21 y heteroduplex analysis and direct automated nucleotide sequencing.
22 rose gel electrophoresis, Southern blot, and nucleotide sequencing.
23 lymerase chain reaction products, and direct nucleotide sequencing.
24 aracterized by reverse transcriptase-PCR and nucleotide sequencing.
25 A1 gene was amplified by RT-PCR, followed by nucleotide sequencing.
26 s and several of these have been analyzed by nucleotide sequencing.
27 riction mapping, Southern blot analysis, and nucleotide sequencing.
28 lassical direct immunofluorescence assay and nucleotide sequencing.
29  the presence of rhinovirus was confirmed by nucleotide sequencing.
30 ence was confirmed by biological cloning and nucleotide sequencing.
31 -transcription polymerase chain reaction and nucleotide sequencing.
32 10 times and was completely characterized by nucleotide sequencing.
33 he virus and host genetic markers by PCR and nucleotide sequencing.
34 oligonucleotide microarray hybridization and nucleotide sequencing.
35 aks (15 from one hospital) were subjected to nucleotide sequencing.
36 ned by using species-specific PCR assays and nucleotide sequencing.
37  determined by reverse transcription-PCR and nucleotide sequencing.
38  microscopy, protein profiling, and complete nucleotide sequencing.
39 ization, polymerase chain reaction (PCR) and nucleotide sequencing.
40 fish ST cDNAs were isolated and subjected to nucleotide sequencing.
41 culture results and were confirmed by direct nucleotide sequencing.
42 olymorphism (SSCP) analysis and confirmed by nucleotide sequencing.
43 nking intronic sequences, followed by direct nucleotide sequencing.
44 for alterations of MAD1L1 by RT-PCR-SSCP and nucleotide sequencing.
45              The results, from 16S rRNA gene nucleotide sequencing (1583 pb accession no HE861352) an
46 cell lines were analysed using either direct nucleotide sequencing (28 cases), denaturing gradient ge
47 romatin immunoprecipitation of OmpR:FLAG and nucleotide sequencing, 43 putative OmpR binding sites we
48                   However, Southern blot and nucleotide sequencing analyses identified intact cpb2 op
49                                              Nucleotide sequencing analysis located mutations to diff
50  significant SSCP shifts underwent automated nucleotide sequencing analysis.
51 restriction fragment length polymorphism and nucleotide sequencing analysis.
52 CA1 mutational analysis, involving automated nucleotide sequencing and a protein-truncation assay, wa
53                  Advances in high-throughput nucleotide sequencing and bioinformatics make the study
54 ng phages Gamma and Cherry was determined by nucleotide sequencing and comparative analysis.
55                                              Nucleotide sequencing and deduced amino acid sequence an
56       Here, we identified these receptors by nucleotide sequencing and demonstrate that LTD(4) recept
57 y, we subjected 11 lung cancer cell lines to nucleotide sequencing and did not detect mutations withi
58 yped in our reference laboratory by means of nucleotide sequencing and extensive phylogenetic analyse
59                                              Nucleotide sequencing and genetic complementation analys
60 y the unique challenges of working with both nucleotide sequencing and mass spectrometry proteomics d
61                                              Nucleotide sequencing and phylogenetic analyses were con
62                                              Nucleotide sequencing and phylogenetic analysis of viral
63 with those for strain characterization using nucleotide sequencing and restriction fragment length po
64 tion assays, and mutations were evaluated by nucleotide sequencing and RNA fingerprinting.
65                                              Nucleotide-sequencing and multiplexed primer-extension a
66 iption polymerase chain reaction genotyping, nucleotide sequencing, and antigenic characterization me
67                           Southern blotting, nucleotide sequencing, and detailed restriction mapping
68 lfish samples, application of nested PCR and nucleotide sequencing, and increased knowledge of NLV ge
69 in reaction-based screening of cDNA library, nucleotide sequencing, and mass spectrometry (electrospr
70 ain reaction-based screening of cDNA library/nucleotide sequencing, and mass spectrometry (reversed-p
71  followed by a competition binding assay and nucleotide sequencing, and mutants were tested for DNA-g
72 nomic DNA followed by heteroduplex analysis, nucleotide sequencing, and restriction site analysis.
73 group analysis using 3 genotyping platforms, nucleotide sequencing, and serologic evaluation was perf
74                  The results of an empirical nucleotide-sequencing approach indicate that the evoluti
75  of ENA is to support and promote the use of nucleotide sequencing as an experimental research platfo
76 ferences in human MHC molecules, revealed by nucleotide sequencing but not by serologic typing, subst
77                                    Consensus nucleotide sequencing confirmed genotype changes in 2 pa
78                      Gel electrophoresis and nucleotide sequencing confirmed the authenticity of the
79                             Recently, direct nucleotide sequencing confirmed this estimate.
80 perature stress tests in vitro combined with nucleotide sequencing, confirmed this stability but iden
81 lyses were conducted using Sanger population nucleotide sequencing data derived from blood samples fr
82                   Southern hybridization and nucleotide sequencing data have revealed apparent csrA h
83  both for deposition of, and access to, open nucleotide sequencing data.
84            The partners of the International Nucleotide Sequencing Database Collaboration, which incl
85 d by the three partners of the International Nucleotides Sequencing Database Collaboration (INSDC) (C
86 enomic DNA, heteroduplex analysis and direct nucleotide sequencing demonstrated pathogenetic COL7A1 m
87 followed by heteroduplex analysis and direct nucleotide sequencing, did not reveal sequence variants
88                     GSA correlated well with nucleotide sequencing for estimating HCV genetic diversi
89  clone was named "3pmmuc5b-1" after complete nucleotide sequencing (Genbank Accession, AF369933).
90                                              Nucleotide sequencing has become increasingly common and
91                                              Nucleotide sequencing has revealed that sid2 is located
92 termination of the number of EPIYA motifs by nucleotide sequencing, however, is a laborious and expen
93                                              Nucleotide sequencing identified a TonB-dependent recept
94    Single-stranded conformation variance and nucleotide sequencing identified all patient mutations i
95                                              Nucleotide sequencing identified an open reading frame p
96                                              Nucleotide sequencing identified atypical cpb2 genes wit
97                                              Nucleotide sequencing identified several of the clones i
98                                              Nucleotide sequencing identified three genes located dow
99 We present immune lymphocyte estimation from nucleotide sequencing (ImmuneLENS), which estimates T ce
100 and cytosine-adenine (CA) repeats in IFNG by nucleotide sequencing in 647 patients with CL caused by
101 tire coding region of CART was determined by nucleotide sequencing in 91 unrelated subjects with seve
102 rmined by methylation-specific PCR (MSP) and nucleotide sequencing in breast cancer cell lines (3/3),
103                    In five cases, beta-chain nucleotide sequencing in five selected Vbeta families sh
104   Despite the tremendous drop in the cost of nucleotide sequencing in recent years, many research pro
105      Dramatic increases in the throughput of nucleotide sequencing machines, and the promise of ever
106                                              Nucleotide sequencing of 1.2 kb of the 5' flanking regio
107                                              Nucleotide sequencing of 18 mutants enabled assignment o
108  Subcloning, complementation of trp strains, nucleotide sequencing of 5.1 kb and 1.95 kb of DNA and s
109                                      Partial nucleotide sequencing of additional clones reveals that
110                                   Additional nucleotide sequencing of both the DNA polymerase gene an
111                                              Nucleotide sequencing of BV 5.1 TCR CDR3 showed that eac
112 t the genetic level by deletion analysis and nucleotide sequencing of clones that conferred a transmi
113 tic heteroduplex analysis followed by direct nucleotide sequencing of DNA.
114                            Junctional region nucleotide sequencing of expanded TCR-Vbeta subsets was
115                                              Nucleotide sequencing of expressed Vkappas identified sh
116                                              Nucleotide sequencing of flaA, flaB, and flaC showed tha
117                                       Direct nucleotide sequencing of H CDR3s showed adult-type N-nuc
118                                              Nucleotide sequencing of H chain CDR3s of DEX-specific p
119                                 We performed nucleotide sequencing of HCV isolates from infected indi
120 ntron-exon borders, was determined by direct nucleotide sequencing of human genomic P1 clones.
121                                              Nucleotide sequencing of insert DNA revealed an open rea
122                                              Nucleotide sequencing of mobility shifts detected by sin
123 characterization of the receptor and partial nucleotide sequencing of PBR cDNA revealed that the MDA-
124                                              Nucleotide sequencing of PCR products derived from diffe
125 genotypic evidence of resistance assessed by nucleotide sequencing of protease and reverse transcript
126 e results were supported by purification and nucleotide sequencing of replicative-form DNA and by the
127                                              Nucleotide sequencing of reverse transcriptase-polymeras
128 ystem based on reverse transcription-PCR and nucleotide sequencing of the 3' half of the genomic regi
129                            Following partial nucleotide sequencing of the 4.2-kb insert, a putative o
130                                  Comparative nucleotide sequencing of the 78 loci of six M. paratuber
131                                              Nucleotide sequencing of the abnormal polymerase chain r
132 CR of readthrough transcripts and subsequent nucleotide sequencing of the amplified product revealed
133 e was analyzed by RT-PCR, spectratyping, and nucleotide sequencing of the amplified products at diffe
134                                              Nucleotide sequencing of the Arabidopsis genome is neari
135                                              Nucleotide sequencing of the AS17 topA allele and studie
136 ze the circulation patterns of HRSV strains, nucleotide sequencing of the C-terminal region of the G
137                                  Cloning and nucleotide sequencing of the C. fetus gyrA gene in the 2
138                                              Nucleotide sequencing of the dmcA gene revealed a potent
139                       The results of PCR and nucleotide sequencing of the fliD region of eight differ
140                                     Complete nucleotide sequencing of the gastrointestinal associated
141 dentified by species-specific PCR assays and nucleotide sequencing of the gene encoding ehrlichia 16S
142  the present work, we report the cloning and nucleotide sequencing of the gene kamA for C. subtermina
143  the United States and China were studied by nucleotide sequencing of the hemagglutinin and neuramini
144                                              Nucleotide sequencing of the highly conserved SMPD3 gene
145                                              Nucleotide sequencing of the inserted DNA confirmed it w
146 hering revertants thereof were identified by nucleotide sequencing of the p30 gene.
147                                  Protein and nucleotide sequencing of the paraproteins' variable regi
148                                 We performed nucleotide sequencing of the parC and gyrA genes and det
149 c DNA, followed by heteroduplex analysis and nucleotide sequencing of the PCR products demonstrating
150 nt primers that will allow amplification and nucleotide sequencing of the phylogenetically useful mat
151  gN and gB genotypes by cloning, followed by nucleotide sequencing of the plasmid DNA and/or restrict
152                                              Nucleotide sequencing of the promoter region disclosed t
153                                              Nucleotide sequencing of the promoter revealed the prese
154                                              Nucleotide sequencing of the reaper insert in virus popu
155                                              Nucleotide sequencing of the recovered PCR product indic
156 e of human metapneumovirus (HMPV), consensus nucleotide sequencing of the recovered RNA genomes provi
157           This paper reports the cloning and nucleotide sequencing of the S. typhimurium apeE gene as
158                                              Nucleotide sequencing of the topo IIalpha promoter regio
159 ute flaccid paralysis (AFP) were compared by nucleotide sequencing of the VP1 capsid region (906 nucl
160                                              Nucleotide sequencing of this cDNA fragment showed it to
161                                              Nucleotide sequencing of this complementing 1.6-kb regio
162                                              Nucleotide sequencing of this ORF revealed that the gene
163 germline of 2/60 patients analysed by direct nucleotide sequencing or DGGE, including a non-conservat
164 esolved the isolates better than either porB nucleotide sequencing or typing of the opa gene.
165 roarray, were further validated by bisulfite nucleotide sequencing (P <0.001).
166                                              Nucleotide sequencing, phenotypic analysis of mutants, a
167 were characterized by using a combination of nucleotide sequencing plus heteroduplex tracking assay o
168  house-keeping loci are assigned directly by nucleotide sequencing, rather than indirectly from the e
169 selective clones by BstNI fingerprinting and nucleotide sequencing revealed 14 distinct scFv fragment
170                                              Nucleotide sequencing revealed an open reading frame (OR
171 lowed by heteroduplex scanning and/or direct nucleotide sequencing revealed homozygous mutations in t
172                                              Nucleotide sequencing revealed that at least four unique
173                               In this study, nucleotide sequencing revealed that both ends of the ser
174                                              Nucleotide sequencing revealed that the basis for the in
175                             cDNA cloning and nucleotide sequencing revealed that the csrB gene is loc
176 ndividual exons of ITGA6, followed by direct nucleotide sequencing, revealed that the proband was hom
177            A cDNA encoding S3s was isolated, nucleotide sequencing revealing a coding region with 99.
178 , molecular cloning, Southern hybridization, nucleotide sequencing, semiquantitative RT-PCR, and ribo
179 or VLDL-receptor genes was investigated, but nucleotide sequencing showed that no sequences homologou
180                                 In addition, nucleotide sequencing studies demonstrated that PepB and
181                     We conducted mapping and nucleotide sequencing studies of extensive, multi-megaba
182                                              Nucleotide sequencing studies show that the 567 amino ac
183 s has vastly expanded through advancement in nucleotide sequencing technologies and an increasing foc
184                              High-throughput nucleotide sequencing technologies provide large amounts
185                              Next-generation nucleotide-sequencing technology has made it feasible to
186                                              Nucleotide sequencing these cDNAs revealed that the AP-2
187 gnment algorithms, the exponential growth of nucleotide sequencing throughput threatens to outpace bi
188 dition, in a subset of isolates we performed nucleotide sequencing to assess the level of conservatio
189  pig and two feral pigs and characterized by nucleotide sequencing to belong to genotype 3.
190 NA-enrichment methods and massively parallel nucleotide sequencing to comprehensively identify and ty
191 Samples positive for HCoV were submitted for nucleotide sequencing to determine the species.
192                       We used TCR beta-chain nucleotide sequencing to gain insight into the adaptive
193 ls, were molecularly cloned and subjected to nucleotide sequencing to identify the recombinant juncti
194                                              Nucleotide sequencing was performed for a small subset o
195 l sorter analysis, and TCR junctional region nucleotide sequencing was performed on expanded TCR Vbet
196           The performances of two methods of nucleotide sequencing were compared for the detection of
197          Polymerase chain reaction (PCR) and nucleotide sequencing were used to identify the specific
198                              PCR cloning and nucleotide sequencing were used to identify the specific
199 vances in molecular biology, microscopy, and nucleotide sequencing will provide the tools to test the
200    PCR assay of paraffin-embedded tissue and nucleotide sequencing with ribosomal ITS1-ITS2 universal

 
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