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1 n enzyme analysis of this gene (16S rRNA PCR-restriction fragment length polymorphism).
2 t mtDNA haplotyping by analysis with PCR and restriction fragment length polymorphism.
3 2+ ATPase gene (pfATP6) were assessed by PCR-restriction fragment length polymorphism.
4  were genotyped by polymerase chain reaction-restriction fragment length polymorphism.
5 were determined by polymerase chain reaction-restriction fragment length polymorphism.
6 ent in a White Leghorn CEF substrate pool by restriction fragment length polymorphism.
7 nalyzed with 454 pyrosequencing and terminal restriction fragment length polymorphism.
8 C2 were analyzed by pyrosequencing or by PCR restriction fragment length polymorphism.
9                   Tissue typing was based on restriction fragment length polymorphism.
10  CFH, CFB, and 10q loci were screened by PCR-restriction fragment-length polymorphism.
11 aceae), was analysed by means of chloroplast restriction fragment-length polymorphism.
12  13, and 61 were determined using engineered restriction fragment length polymorphisms.
13 d to subgroup S. aureus strains according to restriction fragment length polymorphisms.
14 ined by changes in polymerase chain reaction restriction fragment-length polymorphisms.
15 hout a region of the genome, demonstrating a restriction fragment length polymorphism among an encaps
16  mutation-specific polymerase chain reaction restriction fragment length polymorphism analyses for th
17 n alternative to conventional nested PCR and restriction fragment length polymorphism analyses for th
18                                     Terminal restriction fragment length polymorphism analyses indica
19                We have now used allozyme and restriction fragment length polymorphism analyses to con
20 ingle-strand conformational polymorphism and restriction fragment length polymorphism analyses, resul
21                            Results of IS6110 restriction fragment-length polymorphism analyses were a
22 ymes were used for polymerase chain reaction-restriction fragment length polymorphism analysis (PCR-R
23 om 15 dogs and 27 cats were typed using URA5 restriction fragment length polymorphism analysis (RFLP)
24 subtyped with a small subunit rRNA-based PCR-restriction fragment length polymorphism analysis and a
25 sinase gene correction was also confirmed by restriction fragment length polymorphism analysis and DN
26  patterns, and indistinguishable patterns on restriction fragment length polymorphism analysis and ka
27 e point, HCV genotype was determined by both restriction fragment length polymorphism analysis and ph
28 mmunity composition was assessed by terminal restriction fragment length polymorphism analysis and py
29                                              Restriction fragment length polymorphism analysis and RN
30 k of diarrhea in France were analyzed by PCR-restriction fragment length polymorphism analysis and se
31                                     Terminal restriction fragment length polymorphism analysis and se
32 mbrane protein A (ompA) gene sequencing, and restriction fragment length polymorphism analysis are cu
33 petitive units (MIRU-VNTR), and IS6110-based restriction fragment length polymorphism analysis cumula
34 morphism analysis, and sequencing as well as restriction fragment length polymorphism analysis for id
35 -based assays or a polymerase chain reaction-restriction fragment length polymorphism analysis in 160
36  were genotyped by polymerase chain reaction-restriction fragment length polymorphism analysis in 58
37  be homoplasmic by polymerase chain reaction/restriction fragment length polymorphism analysis in all
38 validated by polymerase chain reaction (PCR)-restriction fragment length polymorphism analysis of 60
39                                       B1 PCR-restriction fragment length polymorphism analysis of 8 t
40                                              Restriction fragment length polymorphism analysis of a p
41 igh rate of dissemination), according to PCR-restriction fragment length polymorphism analysis of int
42                               Sequencing and restriction fragment length polymorphism analysis of pol
43                                          PCR-restriction fragment length polymorphism analysis of rib
44 s and performed DNA sequencing and PCR-based restriction fragment length polymorphism analysis of sev
45 p1a locus in the TIGR4 genetic background by restriction fragment length polymorphism analysis of the
46     It was confirmed to be genotype 1 by PCR-restriction fragment length polymorphism analysis of the
47       Multilocus enzyme electrophoresis, PCR-restriction fragment length polymorphism analysis of the
48  polymerase chain reaction amplification and restriction fragment length polymorphism analysis of the
49                    The assay agreed with PCR-restriction fragment length polymorphism analysis of the
50 s/genotype of isolates was determined by PCR restriction fragment length polymorphism analysis of the
51                                              Restriction fragment length polymorphism analysis of Xba
52 ing differentiation without the necessity of restriction fragment length polymorphism analysis or seq
53 ining the complete rib43a coding region, and restriction fragment length polymorphism analysis placed
54                                      PCR and restriction fragment length polymorphism analysis reconf
55  of Listeria monocytogenes by serotyping and restriction fragment length polymorphism analysis using
56                                       IS6110 restriction fragment length polymorphism analysis was pe
57                                              Restriction fragment length polymorphism analysis with a
58                                              Restriction fragment length polymorphism analysis with l
59 files, monoclonal antibody binding patterns, restriction fragment length polymorphism analysis, and k
60  was assessed by ribosomal DNA (rDNA) spacer restriction fragment length polymorphism analysis, genom
61 , chromosome painting, Southern blotting and restriction fragment length polymorphism analysis, subcl
62              Isolates underwent IS6110-based restriction fragment length polymorphism analysis.
63 le nucleotide polymorphisms were detected by restriction fragment length polymorphism analysis.
64 were identified by polymerase chain reaction-restriction fragment length polymorphism analysis.
65 (38 of 59) of the IS6110 copies predicted by restriction fragment length polymorphism analysis.
66 ned by polymerase chain reaction followed by restriction fragment length polymorphism analysis.
67 ed to identify individuals with this gene by restriction fragment length polymorphism analysis.
68 acterization using nucleotide sequencing and restriction fragment length polymorphism analysis.
69  and genotyped by arbitrarily primed PCR and restriction fragment length polymorphism analysis.
70 stent with those from an independent method, restriction fragment length polymorphism analysis.
71 rs and polymerase chain reaction followed by restriction fragment length polymorphism analysis.
72 e genotypes obtained by conventional PCR and restriction fragment length polymorphism analysis.
73 d sequencing, and for RSTs by nested PCR and restriction fragment length polymorphism analysis.
74 s using group-specific LGV real-time PCR and restriction fragment length polymorphism analysis.
75 ic PCR, followed by species-specific PCR and restriction fragment length polymorphism analysis.
76 s determined by direct PCR amplification and restriction fragment length polymorphism analysis.
77 olymerase chain reaction (PCR), or PCR-based restriction fragment length polymorphism analysis.
78 s the source of T. gondii infection based on restriction fragment length polymorphism analysis.
79 med by conventional methods and confirmed by restriction fragment length polymorphism analysis.
80                                              Restriction fragment length-polymorphism analysis of vir
81 G, by means of polymerase chain reaction and restriction fragment--length polymorphism analysis.
82 morphisms by using polymerase chain reaction-restriction fragment-length polymorphism analysis in 134
83 cribed sequence (ITS) and mitochondrial cox1 Restriction fragment-length polymorphism analysis of ITS
84  On the basis of a polymerase chain reaction-restriction fragment-length polymorphism analysis of the
85  By use of a polymerase chain reaction-based restriction fragment-length polymorphism analysis techni
86          We used spoligotyping, IS6110-based restriction fragment-length polymorphism analysis, and s
87  in the YMDD motif of the polymerase gene by restriction fragment-length polymorphism analysis.
88         The Brazilian isolates were typed by restriction-fragment length polymorphism analysis and we
89                                              Restriction-fragment length polymorphism analysis of hum
90 ment was verified by cytogenetic analysis or restriction-fragment--length polymorphism analysis.
91 olates underwent insertion sequence (IS)6110 restriction-fragment-length polymorphism analysis, targe
92    Bacterial DNA was analyzed using terminal restriction fragment length polymorphism and 16S pyrotag
93 ere analyzed using polymerase chain reaction-restriction fragment length polymorphism and 5'-end [gam
94 multidrug-resistant tuberculosis cases using restriction fragment length polymorphism and by cross-ma
95 lection of clinical isolates was assessed by restriction fragment length polymorphism and confirmator
96 eumocystis control samples were genotyped by restriction fragment length polymorphism and multilocus
97                                     Combined restriction fragment length polymorphism and nucleotide
98 bovis strains had the same 16S ribosomal DNA restriction fragment length polymorphism and often had t
99                                          PCR-restriction fragment length polymorphism and partial seq
100                                 Furthermore, restriction fragment length polymorphism and pulsed-fiel
101 bs were analyzed and compared using terminal restriction fragment length polymorphism and sequence an
102 dIII-restricted DNA, Southern hybridization, restriction fragment length polymorphism and sequencing
103 3, that had insertion sequence 6110 (IS6110) restriction fragment length polymorphism and spoligotype
104 dentified by polymerase chain reaction-based restriction fragment length polymorphisms and confirmed
105 and identified, on the basis of biochemical, restriction fragment length polymorphism, and 16S rRNA g
106 -403, evaluated by polymerase chain reaction-restriction fragment length polymorphism, and CCR5Delta3
107 f the four progeny was confirmed by isozyme, restriction fragment length polymorphism, and cytologica
108 genes for toxins A, B and binary toxin using restriction fragment length polymorphism, and identifica
109 genotyped by polymerase chain reaction (PCR)-restriction fragment length polymorphism, and IL-1RN var
110 enotypically matched (by spoligotype, IS6110 restriction fragment length polymorphism, and mycobacter
111 nalytical methods, including pyrosequencing, restriction fragment length polymorphism, and sequencing
112 es underwent DNA fingerprinting using IS6110 restriction fragment length polymorphism, and those with
113 VGS is demonstrated by the identification of restriction fragment length polymorphisms, and of amplif
114                      Immunofixation, genomic restriction fragment length polymorphisms, and pulsed fi
115                      We developed a terminal restriction fragment length polymorphism assay (TRFLP) f
116 sm in NQO1 using a polymerase chain reaction-restriction fragment length polymorphism assay and for t
117 r PCR, and/or a conventional PCR method (PCR-restriction fragment length polymorphism assay), were pe
118 interaction between these variants using PCR/restriction fragment-length polymorphism assays in 454 s
119 ient isolate, there were two distinct IS1245 restriction fragment length polymorphism banding pattern
120 nt type was assigned by a combination of PCR-restriction fragment length polymorphism-based assays.
121 en demonstrated by mapping of several common restriction fragment-length polymorphism clones on both
122 and blot hybridization with three additional restriction fragment-length polymorphism clones.
123                                              Restriction fragment length polymorphism confirmed that
124                                 Ninety maize restriction fragment-length polymorphism core markers we
125             Chromosome pairing, isozyme, and restriction fragment length polymorphism data support a
126 ingle dominant locus and cosegregated with a restriction fragment length polymorphism detected by the
127  Bay, and Del Monte Beach), using multilocus restriction fragment length polymorphisms (DNA fingerpri
128 d 2008 from three humic lakes using terminal restriction fragment length polymorphism fingerprinting
129 throughput 18S rRNA tag sequencing, terminal restriction fragment length polymorphism fingerprinting,
130  were evaluated by polymerase chain reaction restriction fragment length polymorphism for polymorphis
131              We then studied the accuracy of restriction fragment length polymorphism for the -308 si
132 ed groups based on distinct ribosomal spacer restriction fragment length polymorphism genotypes (RSTs
133 We determined silk maysin concentrations and restriction fragment length polymorphism genotypes at fl
134 representing 2 distinct ribosomal DNA spacer restriction fragment-length polymorphism genotypes (RSTs
135 s genotype classification was done by IS6110 restriction fragment length polymorphism genotyping and
136 ative genetic mapping, using markers such as restriction-fragment length polymorphisms, has revealed
137 g of the -174 nucleotide variant was done by restriction fragment length polymorphism, heteroduplex a
138 ere, we describe inverse PCR-based amplified restriction fragment length polymorphism (iFLP), a new t
139  as to identify the three markers by PCR and restriction fragment length polymorphism in parallel, an
140                Analysis of 16S ribosomal DNA restriction fragment length polymorphisms indicated that
141 o population studies, were examined by using restriction fragment length polymorphism IS6110 fingerpr
142 proach of spoligotyping with IS6110-targeted restriction fragment length polymorphism (IS6110-RFLP) a
143 ne M. tuberculosis strain using IS6110-based restriction fragment length polymorphism (IS6110-RFLP) a
144 lsed-field gel electrophoresis (PFGE), IS900 restriction fragment length polymorphism (IS900-RFLP), a
145 ative in discriminating the four-band IS6110 restriction fragment length polymorphism isolates from e
146 lar organizer (Rdn1), the Smol gene, and two restriction fragment length polymorphisms linked to Smol
147    A novel method called "multiplex-terminal restriction fragment length polymorphism (M-TRFLP)" has
148 se chain reaction (qPCR), mutliplex-terminal restriction fragment length polymorphism (M-TRFLP), and
149 enitors of the major weed "johnsongrass." By restriction fragment length polymorphism mapping, variat
150 AC clone is anchored by a genetically mapped restriction fragment length polymorphism marker.
151 this approach with direct sequencing and the restriction fragment length polymorphism method indicate
152 re determined by a combination of RT-PCR and restriction fragment length polymorphism, multiplex RT-P
153 are investigated using sequence analysis and restriction fragment length polymorphism of a mitochondr
154                 We also identified a HindIII restriction fragment length polymorphism of F8A fragment
155              Molecular techniques, including restriction fragment length polymorphism of genomic DNA
156 both parental alleles were demonstrated with restriction fragment length polymorphism of polymerase c
157                                          PCR-restriction fragment length polymorphism of small subuni
158  from livestock animals were analyzed by PCR-restriction fragment length polymorphism of the Cryptosp
159                           DNA sequencing and restriction fragment length polymorphism of the PCR prod
160 he seven single-copy genes were mapped using restriction fragment length polymorphisms of recombinant
161 -phosphate dehydrogenase or to determine the restriction fragment length polymorphisms of X chromosom
162 e and suitable for PCR checking, SNP typing (restriction fragment length polymorphism or amplificatio
163 techniques have been developed, based on PCR-restriction fragment length polymorphism or sequencing a
164                                   Its IS6110 restriction fragment length polymorphism pattern was ide
165  method for the 37% of isolates displaying a restriction fragment length polymorphism pattern with <6
166        Patients whose isolates had identical restriction fragment length polymorphism patterns and sp
167                              The nonvariable restriction fragment length polymorphism patterns furthe
168  of isolates of each subgroup share the same restriction fragment length polymorphism patterns of the
169 two Nocardia patient isolates showed unusual restriction fragment length polymorphism patterns with r
170 st with HindIII, EcoRV, and AspI to generate restriction fragment length polymorphism patterns.
171 ipheral blood leukocytes and analyzed with a restriction fragment length polymorphism PCR method.
172                                          PCR-restriction fragment length polymorphism (PCR-RFLP) anal
173 TB) test, the Gen-Probe ACCUPROBE, and a PCR-restriction fragment length polymorphism (PCR-RFLP) anal
174 es of available PCV strains, a universal PCR-restriction fragment length polymorphism (PCR-RFLP) assa
175 ree controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) meth
176        These data were used to develop a PCR-restriction fragment length polymorphism (PCR-RFLP) meth
177 gment by polymerase chain reaction and HinfI restriction fragment length polymorphism (PCR/RFLP).
178 ermined on thyroid FNAB specimens by PCR and restriction fragment length polymorphism, plus direct se
179                  Genotyping was performed by restriction fragment-length polymorphism polymerase chai
180       Known methods for SNP analysis include restriction-fragment-length polymorphism polymerase chai
181 263 controls underwent CD14 genotyping using restriction fragment length polymorphism-polymerase chai
182            The progeny segregation data from restriction fragment length polymorphism, random amplifi
183  alleles, and the fourth has unique upstream restriction fragment length polymorphisms relative to cl
184 s of 420 markers (353 microsatellites and 67 restriction fragment length polymorphisms) revealed seve
185 hort tandem repeat (STR)-microsatellites and restriction fragment length polymorphism (RFLP) analyses
186 and pfdhps genes were analyzed by LDR-FM and restriction fragment length polymorphism (RFLP) analyses
187 tilocus sequence typing (MLST) and performed restriction fragment length polymorphism (RFLP) analysis
188 ng high-performance liquid chromatography or restriction fragment length polymorphism (RFLP) analysis
189 air, plasmids were sequenced or subjected to restriction fragment length polymorphism (RFLP) analysis
190                                              Restriction fragment length polymorphism (RFLP) analysis
191 In order to assess the -455G/A polymorphism, restriction fragment length polymorphism (RFLP) analysis
192                                      We used restriction fragment length polymorphism (RFLP) analysis
193 DNA dot blotting, IS1004 fingerprinting, and restriction fragment length polymorphism (RFLP) analysis
194 our nosocomial outbreaks were typed by Afut1 restriction fragment length polymorphism (RFLP) analysis
195  The isolates were genotyped by IS6110-based restriction fragment length polymorphism (RFLP) analysis
196  with culture-proven tuberculosis, combining restriction fragment length polymorphism (RFLP) analysis
197  pulsed-field gel electrophoresis (PFGE) and restriction fragment length polymorphism (RFLP) analysis
198 tuberculosis isolates were identified by PCR-restriction fragment length polymorphism (RFLP) analysis
199 l and Prevention for pncA sequencing and PCR-restriction fragment length polymorphism (RFLP) analysis
200 icobacter species isolates were subjected to restriction fragment length polymorphism (RFLP) analysis
201 R amplification of the recA gene followed by restriction fragment length polymorphism (RFLP) analysis
202 as, were identified and characterized by PCR-restriction fragment length polymorphism (RFLP) analysis
203 hods employed were somatic O serotyping, PCR-restriction fragment length polymorphism (RFLP) analysis
204 ce from genome in situ hybridization (GISH), restriction fragment length polymorphism (RFLP) analysis
205                                              Restriction fragment length polymorphism (RFLP) analysis
206                                              Restriction fragment length polymorphism (RFLP) analysis
207 peats in the acidic repeat protein gene, (2) restriction fragment length polymorphism (RFLP) analysis
208  for Pneumocystis jirovecii that is based on restriction fragment length polymorphism (RFLP) analysis
209 d voriconazole, and molecular relatedness by restriction fragment length polymorphism (RFLP) analysis
210                                              Restriction fragment length polymorphism (RFLP) analysis
211 eted for 18 paired samples (nine eyes) using restriction fragment length polymorphism (RFLP) and DNA
212                  This variation, revealed by restriction fragment length polymorphism (RFLP) and nucl
213 lymerase chain reaction and analyzed by both restriction fragment length polymorphism (RFLP) and phyl
214                       Conventional block PCR-restriction fragment length polymorphism (RFLP) and real
215  2007, 503 isolates were genotyped by IS6110 restriction fragment length polymorphism (RFLP) and spol
216 ts of the more commonly used methods, IS6110 restriction fragment length polymorphism (RFLP) and spol
217                          Two novel assays, a restriction fragment length polymorphism (RFLP) assay an
218  eight eukaryotic species, and we describe a restriction fragment length polymorphism (RFLP) assay th
219                                            A restriction fragment length polymorphism (RFLP) assay wa
220 xoplasmosis, polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP) assays w
221  of the TNFB gene encoding TNF-beta and at a restriction fragment length polymorphism (RFLP) at posit
222 cosidase activities from three H. capsulatum restriction fragment length polymorphism (RFLP) classes,
223 mparison with allozyme and mitochondrial DNA restriction fragment length polymorphism (RFLP) datasets
224 pressed sequence tag polymorphism (ESTP) and restriction fragment length polymorphism (RFLP) markers.
225 al evaluation of 479 samples was done with a restriction fragment length polymorphism (RFLP) method a
226 lts were also compared to an established PCR-restriction fragment length polymorphism (RFLP) method p
227  polymerase chain reaction amplification and restriction fragment length polymorphism (RFLP) method.
228 B. subtilis 168 isolates was demonstrated by restriction fragment length polymorphism (RFLP) of the r
229                Subjects were genotyped for a restriction fragment length polymorphism (RFLP) on the A
230 of 216 patients and all were genotyped using Restriction Fragment Length Polymorphism (RFLP) or seque
231  SmaI restriction enzymes and IS1167 and mef restriction fragment length polymorphism (RFLP) pattern
232 lates of a single serotype had a single wbiI restriction fragment length polymorphism (RFLP) pattern,
233 inks frequently demonstrate identical IS6110 restriction fragment length polymorphism (RFLP) patterns
234                                          The restriction fragment length polymorphism (RFLP) patterns
235  of the 16S rRNA gene was amplified, and PCR-restriction fragment length polymorphism (RFLP) patterns
236      Subtyping was based on subtype-specific restriction fragment length polymorphism (RFLP) patterns
237                                       Unique restriction fragment length polymorphism (RFLP) patterns
238    We identified unique HaeIII and HpaII gag restriction fragment length polymorphism (RFLP) profiles
239                                     Ribotype restriction fragment length polymorphism (RFLP) profiles
240             We have developed a combined PCR-restriction fragment length polymorphism (RFLP) techniqu
241 tly, verification of HLA-A polymorphisms and restriction fragment length polymorphism (RFLP) testing-
242 hether the system could replace conventional restriction fragment length polymorphism (RFLP) typing b
243 An evaluation of the utility of IS6110-based restriction fragment length polymorphism (RFLP) typing c
244                      The manual IS6110-based restriction fragment length polymorphism (RFLP) typing m
245                         To create artificial Restriction Fragment Length Polymorphism (RFLP), a misma
246 berculosis Hospital by spoligotyping, IS6110 restriction fragment length polymorphism (RFLP), and 24-
247 proportions to determine how pyrosequencing, restriction fragment length polymorphism (RFLP), and dir
248 al of 100 isolates were analysed with IS6110-restriction fragment length polymorphism (RFLP), spoligo
249 mal repair in muscle tissue was confirmed by restriction fragment length polymorphism (RFLP)-PCR and
250 ing 16S rRNA polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP).
251 in Francisella tularensis to type strains by restriction fragment length polymorphism (RFLP).
252 leotide sequencing of the plasmid DNA and/or restriction fragment length polymorphism (RFLP).
253 y of herpes simplex virus (HSV) isolates use restriction fragment length polymorphism (RFLP).
254 cer cases and 1,077 controls using PCR-based restriction fragment length polymorphism (RFLP-PCR) anal
255 ates had been characterized biochemically by restriction fragment length polymorphism (RFLP; AluI, Hh
256 ological studies, mainly through identifying restriction fragment length polymorphisms (RFLP).
257  tuberculosis strains associated with IS6110 restriction fragment-length polymorphism (RFLP) pattern
258 TB) during 1996-2001 were fingerprinted with restriction fragment-length polymorphism (RFLP).
259 enomic groups of C. burnetii are revealed by restriction fragment-length polymorphisms (RFLP).
260 tion inferred from mitochondrial DNA (mtDNA) restriction-fragment length polymorphism (RFLP) data and
261 and diarrhea cases were compared by means of restriction-fragment length polymorphism (RFLP), rapid a
262 ticipants for the identified polymorphism by restriction-fragment-length polymorphism (RFLP) analysis
263                Isolates were genotyped using restriction-fragment-length polymorphism (RFLP) patterns
264 e nucleotide polymorphism (SNP) (screened by restriction fragment length polymorphism [RFLP] analysis
265 thamoeba isolates, mitochondrial DNA (mtDNA) restriction fragment length polymorphisms (RFLPs) and cy
266 f N. veterana gave identical and distinctive restriction fragment length polymorphisms (RFLPs) for an
267 r DNA digested with the EcoRI enzyme and the restriction fragment length polymorphisms (RFLPs) genera
268                                              Restriction fragment length polymorphisms (RFLPs) identi
269 e often needed in order to create artificial restriction fragment length polymorphisms (RFLPs).
270 se techniques include (1) definitive genomic restriction-fragment-length polymorphisms (RFLPs) based
271                             We devised a PCR-restriction fragment length polymorphism screen for the
272                            Southern blot and restriction fragment length polymorphism segregation ana
273                                       By PCR-restriction fragment length polymorphism, sequence, and
274       Three molecular typing methods, IS6110 restriction fragment length polymorphism, spoligotyping,
275                                     Terminal restriction fragment length polymorphism (T-RFLP) analys
276 l transcribed spacer (ITS) database terminal restriction fragment length polymorphism (T-RFLP) approa
277                             We used terminal restriction fragment length polymorphism (T-RFLP) of 18S
278 isotope probing (SIP) combined with terminal restriction fragment length polymorphism (T-RFLP), high-
279 munity shifts were characterized by terminal restriction fragment length polymorphism (T-RFLP).
280          The plaque was analyzed by terminal restriction fragment length polymorphism (t-RFLP).
281  rRNA bacterial community analyses (terminal restriction fragment length polymorphism, T-RFLP) were p
282 st change in community composition (Terminal Restriction Fragment Length Polymorphism; T-RFLP).
283 ion, employing the polymerase chain reaction-restriction fragment length polymorphism technique (PCR-
284 ntional methods based on cDNA sequencing and restriction fragment length polymorphism, the microarray
285 ; 60% of the cases had clustered patterns of restriction fragment length polymorphism, thought to rep
286            We used polymerase chain reaction-restriction fragment length polymorphism to evaluate gen
287                             We used terminal restriction fragment length polymorphism (TRFLP) analysi
288 ndent techniques, quantitative PCR, terminal restriction fragment length polymorphism (TRFLP) and nex
289 ield experiment were profiled using terminal restriction fragment length polymorphism (TRFLP) and seq
290 virulence factors, ribosomal RNA gene spacer restriction fragment length polymorphism types (RSTs), o
291 jor histocompatibility complex class II DRB3 restriction fragment length polymorphism types 8/23, 3/1
292     For the SNPs, we designed a low-cost PCR-restriction fragment length polymorphism typing method.
293                                       IS6110 restriction fragment length polymorphism typing of cultu
294          Sixty strains were used to devise a restriction fragment length polymorphism typing scheme t
295 omegalovirus isolates were analyzed, both by restriction fragment-length polymorphism typing and by s
296                                              Restriction fragment-length polymorphism was used to det
297 of nirS-denitrifers (assessed using terminal restriction fragment length polymorphism) was interactiv
298 found that 4 of 46 heterozygotes analyzed by restriction fragment length polymorphism were actually G
299 genotyped for BsmI, ApaI, TaqI, and FokI VDR restriction fragment length polymorphisms were used for
300 y the presence of the A1 allele of the TaqIA restriction fragment length polymorphism, which is assoc

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