ライフサイエンスコーパス: restriction fragment length

1 a variants (at positions -238 and -308), and restriction fragment length analysis for four polymorphi

2 of the gene, using polymerase chain reaction-restriction fragment length analysis.

3 ture resulted in an increase of the terminal restriction fragment length and in the number of telomer

4 DNA damage-associated markers, mean telomere restriction fragment length, and genomic stability diffe

5 cation protocol assays and telomere terminal restriction fragment length assays were performed on poo

6 lso find that in-nucleus ligation eliminates restriction fragment length bias found with in-solution

7 of the t-loops corresponded to the telomere restriction fragment length from the ALT cell lines as d

8 We report here that the telomere restriction fragment length in senescent WRN fibroblasts

9 and aging resulted in reduction of terminal restriction fragment length paralleled by a decrease of

10 e to that of Towne-BAC, displayed an altered restriction fragment length pattern, and replicated with

11 ere, we describe inverse PCR-based amplified restriction fragment length polymorphism (iFLP), a new t

12 proach of spoligotyping with IS6110-targeted restriction fragment length polymorphism (IS6110-RFLP) a

13 ne M. tuberculosis strain using IS6110-based restriction fragment length polymorphism (IS6110-RFLP) a

14 lsed-field gel electrophoresis (PFGE), IS900 restriction fragment length polymorphism (IS900-RFLP), a

15 A novel method called "multiplex-terminal restriction fragment length polymorphism (M-TRFLP)" has

16 se chain reaction (qPCR), mutliplex-terminal restriction fragment length polymorphism (M-TRFLP), and

17 PCR-restriction fragment length polymorphism (PCR-RFLP) anal

18 TB) test, the Gen-Probe ACCUPROBE, and a PCR-restriction fragment length polymorphism (PCR-RFLP) anal

19 es of available PCV strains, a universal PCR-restriction fragment length polymorphism (PCR-RFLP) assa

20 ree controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) meth

21 These data were used to develop a PCR-restriction fragment length polymorphism (PCR-RFLP) meth

22 gment by polymerase chain reaction and HinfI restriction fragment length polymorphism (PCR/RFLP).

23 and pfdhps genes were analyzed by LDR-FM and restriction fragment length polymorphism (RFLP) analyses

24 tilocus sequence typing (MLST) and performed restriction fragment length polymorphism (RFLP) analysis

25 ng high-performance liquid chromatography or restriction fragment length polymorphism (RFLP) analysis

26 air, plasmids were sequenced or subjected to restriction fragment length polymorphism (RFLP) analysis

27 Restriction fragment length polymorphism (RFLP) analysis

28 In order to assess the -455G/A polymorphism, restriction fragment length polymorphism (RFLP) analysis

29 We used restriction fragment length polymorphism (RFLP) analysis

30 DNA dot blotting, IS1004 fingerprinting, and restriction fragment length polymorphism (RFLP) analysis

31 our nosocomial outbreaks were typed by Afut1 restriction fragment length polymorphism (RFLP) analysis

32 The isolates were genotyped by IS6110-based restriction fragment length polymorphism (RFLP) analysis

33 with culture-proven tuberculosis, combining restriction fragment length polymorphism (RFLP) analysis

34 pulsed-field gel electrophoresis (PFGE) and restriction fragment length polymorphism (RFLP) analysis

35 tuberculosis isolates were identified by PCR-restriction fragment length polymorphism (RFLP) analysis

36 l and Prevention for pncA sequencing and PCR-restriction fragment length polymorphism (RFLP) analysis

37 icobacter species isolates were subjected to restriction fragment length polymorphism (RFLP) analysis

38 R amplification of the recA gene followed by restriction fragment length polymorphism (RFLP) analysis

39 as, were identified and characterized by PCR-restriction fragment length polymorphism (RFLP) analysis

40 hods employed were somatic O serotyping, PCR-restriction fragment length polymorphism (RFLP) analysis

41 ce from genome in situ hybridization (GISH), restriction fragment length polymorphism (RFLP) analysis

42 Restriction fragment length polymorphism (RFLP) analysis

43 Restriction fragment length polymorphism (RFLP) analysis

44 peats in the acidic repeat protein gene, (2) restriction fragment length polymorphism (RFLP) analysis

45 for Pneumocystis jirovecii that is based on restriction fragment length polymorphism (RFLP) analysis

46 d voriconazole, and molecular relatedness by restriction fragment length polymorphism (RFLP) analysis

47 Restriction fragment length polymorphism (RFLP) analysis

48 eted for 18 paired samples (nine eyes) using restriction fragment length polymorphism (RFLP) and DNA

49 This variation, revealed by restriction fragment length polymorphism (RFLP) and nucl

50 lymerase chain reaction and analyzed by both restriction fragment length polymorphism (RFLP) and phyl

51 Conventional block PCR-restriction fragment length polymorphism (RFLP) and real

52 2007, 503 isolates were genotyped by IS6110 restriction fragment length polymorphism (RFLP) and spol

53 ts of the more commonly used methods, IS6110 restriction fragment length polymorphism (RFLP) and spol

54 eight eukaryotic species, and we describe a restriction fragment length polymorphism (RFLP) assay th

55 A restriction fragment length polymorphism (RFLP) assay wa

56 xoplasmosis, polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP) assays w

57 of the TNFB gene encoding TNF-beta and at a restriction fragment length polymorphism (RFLP) at posit

58 cosidase activities from three H. capsulatum restriction fragment length polymorphism (RFLP) classes,

59 pressed sequence tag polymorphism (ESTP) and restriction fragment length polymorphism (RFLP) markers.

60 al evaluation of 479 samples was done with a restriction fragment length polymorphism (RFLP) method a

61 lts were also compared to an established PCR-restriction fragment length polymorphism (RFLP) method p

62 B. subtilis 168 isolates was demonstrated by restriction fragment length polymorphism (RFLP) of the r

63 Subjects were genotyped for a restriction fragment length polymorphism (RFLP) on the A

64 of 216 patients and all were genotyped using Restriction Fragment Length Polymorphism (RFLP) or seque

65 SmaI restriction enzymes and IS1167 and mef restriction fragment length polymorphism (RFLP) pattern

66 lates of a single serotype had a single wbiI restriction fragment length polymorphism (RFLP) pattern,

67 inks frequently demonstrate identical IS6110 restriction fragment length polymorphism (RFLP) patterns

68 The restriction fragment length polymorphism (RFLP) patterns

69 of the 16S rRNA gene was amplified, and PCR-restriction fragment length polymorphism (RFLP) patterns

70 Subtyping was based on subtype-specific restriction fragment length polymorphism (RFLP) patterns

71 Unique restriction fragment length polymorphism (RFLP) patterns

72 We identified unique HaeIII and HpaII gag restriction fragment length polymorphism (RFLP) profiles

73 We have developed a combined PCR-restriction fragment length polymorphism (RFLP) techniqu

74 tly, verification of HLA-A polymorphisms and restriction fragment length polymorphism (RFLP) testing-

75 hether the system could replace conventional restriction fragment length polymorphism (RFLP) typing b

76 An evaluation of the utility of IS6110-based restriction fragment length polymorphism (RFLP) typing c

77 The manual IS6110-based restriction fragment length polymorphism (RFLP) typing m

78 To create artificial Restriction Fragment Length Polymorphism (RFLP), a misma

79 berculosis Hospital by spoligotyping, IS6110 restriction fragment length polymorphism (RFLP), and 24-

80 proportions to determine how pyrosequencing, restriction fragment length polymorphism (RFLP), and dir

81 al of 100 isolates were analysed with IS6110-restriction fragment length polymorphism (RFLP), spoligo

82 mal repair in muscle tissue was confirmed by restriction fragment length polymorphism (RFLP)-PCR and

83 ing 16S rRNA polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP).

84 in Francisella tularensis to type strains by restriction fragment length polymorphism (RFLP).

85 leotide sequencing of the plasmid DNA and/or restriction fragment length polymorphism (RFLP).

86 y of herpes simplex virus (HSV) isolates use restriction fragment length polymorphism (RFLP).

87 cer cases and 1,077 controls using PCR-based restriction fragment length polymorphism (RFLP-PCR) anal

88 ates had been characterized biochemically by restriction fragment length polymorphism (RFLP; AluI, Hh

89 Terminal restriction fragment length polymorphism (T-RFLP) analys

90 l transcribed spacer (ITS) database terminal restriction fragment length polymorphism (T-RFLP) approa

91 We used terminal restriction fragment length polymorphism (T-RFLP) of 18S

92 isotope probing (SIP) combined with terminal restriction fragment length polymorphism (T-RFLP), high-

93 munity shifts were characterized by terminal restriction fragment length polymorphism (T-RFLP).

94 The plaque was analyzed by terminal restriction fragment length polymorphism (t-RFLP).

95 We used terminal restriction fragment length polymorphism (TRFLP) analysi

96 ndent techniques, quantitative PCR, terminal restriction fragment length polymorphism (TRFLP) and nex

97 ield experiment were profiled using terminal restriction fragment length polymorphism (TRFLP) and seq

98 e nucleotide polymorphism (SNP) (screened by restriction fragment length polymorphism [RFLP] analysis

99 hout a region of the genome, demonstrating a restriction fragment length polymorphism among an encaps

100 mutation-specific polymerase chain reaction restriction fragment length polymorphism analyses for th

101 n alternative to conventional nested PCR and restriction fragment length polymorphism analyses for th

102 Terminal restriction fragment length polymorphism analyses indica

103 We have now used allozyme and restriction fragment length polymorphism analyses to con

104 ingle-strand conformational polymorphism and restriction fragment length polymorphism analyses, resul

105 ymes were used for polymerase chain reaction-restriction fragment length polymorphism analysis (PCR-R

106 om 15 dogs and 27 cats were typed using URA5 restriction fragment length polymorphism analysis (RFLP)

107 subtyped with a small subunit rRNA-based PCR-restriction fragment length polymorphism analysis and a

108 sinase gene correction was also confirmed by restriction fragment length polymorphism analysis and DN

109 patterns, and indistinguishable patterns on restriction fragment length polymorphism analysis and ka

110 e point, HCV genotype was determined by both restriction fragment length polymorphism analysis and ph

111 mmunity composition was assessed by terminal restriction fragment length polymorphism analysis and py

112 Restriction fragment length polymorphism analysis and RN

113 k of diarrhea in France were analyzed by PCR-restriction fragment length polymorphism analysis and se

114 Terminal restriction fragment length polymorphism analysis and se

115 mbrane protein A (ompA) gene sequencing, and restriction fragment length polymorphism analysis are cu

116 petitive units (MIRU-VNTR), and IS6110-based restriction fragment length polymorphism analysis cumula

117 morphism analysis, and sequencing as well as restriction fragment length polymorphism analysis for id

118 -based assays or a polymerase chain reaction-restriction fragment length polymorphism analysis in 160

119 were genotyped by polymerase chain reaction-restriction fragment length polymorphism analysis in 58

120 be homoplasmic by polymerase chain reaction/restriction fragment length polymorphism analysis in all

121 validated by polymerase chain reaction (PCR)-restriction fragment length polymorphism analysis of 60

122 B1 PCR-restriction fragment length polymorphism analysis of 8 t

123 Restriction fragment length polymorphism analysis of a p

124 igh rate of dissemination), according to PCR-restriction fragment length polymorphism analysis of int

125 Sequencing and restriction fragment length polymorphism analysis of pol

126 PCR-restriction fragment length polymorphism analysis of rib

127 s and performed DNA sequencing and PCR-based restriction fragment length polymorphism analysis of sev

128 p1a locus in the TIGR4 genetic background by restriction fragment length polymorphism analysis of the

129 It was confirmed to be genotype 1 by PCR-restriction fragment length polymorphism analysis of the

130 Multilocus enzyme electrophoresis, PCR-restriction fragment length polymorphism analysis of the

131 polymerase chain reaction amplification and restriction fragment length polymorphism analysis of the

132 The assay agreed with PCR-restriction fragment length polymorphism analysis of the

133 s/genotype of isolates was determined by PCR restriction fragment length polymorphism analysis of the

134 Restriction fragment length polymorphism analysis of Xba

135 ing differentiation without the necessity of restriction fragment length polymorphism analysis or seq

136 ining the complete rib43a coding region, and restriction fragment length polymorphism analysis placed

137 PCR and restriction fragment length polymorphism analysis reconf

138 of Listeria monocytogenes by serotyping and restriction fragment length polymorphism analysis using

139 IS6110 restriction fragment length polymorphism analysis was pe

140 Restriction fragment length polymorphism analysis with a

141 Restriction fragment length polymorphism analysis with l

142 files, monoclonal antibody binding patterns, restriction fragment length polymorphism analysis, and k

143 was assessed by ribosomal DNA (rDNA) spacer restriction fragment length polymorphism analysis, genom

144 , chromosome painting, Southern blotting and restriction fragment length polymorphism analysis, subcl

145 s the source of T. gondii infection based on restriction fragment length polymorphism analysis.

146 med by conventional methods and confirmed by restriction fragment length polymorphism analysis.

147 Isolates underwent IS6110-based restriction fragment length polymorphism analysis.

148 le nucleotide polymorphisms were detected by restriction fragment length polymorphism analysis.

149 were identified by polymerase chain reaction-restriction fragment length polymorphism analysis.

150 (38 of 59) of the IS6110 copies predicted by restriction fragment length polymorphism analysis.

151 ned by polymerase chain reaction followed by restriction fragment length polymorphism analysis.

152 ed to identify individuals with this gene by restriction fragment length polymorphism analysis.

153 acterization using nucleotide sequencing and restriction fragment length polymorphism analysis.

154 and genotyped by arbitrarily primed PCR and restriction fragment length polymorphism analysis.

155 stent with those from an independent method, restriction fragment length polymorphism analysis.

156 rs and polymerase chain reaction followed by restriction fragment length polymorphism analysis.

157 e genotypes obtained by conventional PCR and restriction fragment length polymorphism analysis.

158 d sequencing, and for RSTs by nested PCR and restriction fragment length polymorphism analysis.

159 s using group-specific LGV real-time PCR and restriction fragment length polymorphism analysis.

160 ic PCR, followed by species-specific PCR and restriction fragment length polymorphism analysis.

161 s determined by direct PCR amplification and restriction fragment length polymorphism analysis.

162 olymerase chain reaction (PCR), or PCR-based restriction fragment length polymorphism analysis.

163 Bacterial DNA was analyzed using terminal restriction fragment length polymorphism and 16S pyrotag

164 ere analyzed using polymerase chain reaction-restriction fragment length polymorphism and 5'-end [gam

165 multidrug-resistant tuberculosis cases using restriction fragment length polymorphism and by cross-ma

166 eumocystis control samples were genotyped by restriction fragment length polymorphism and multilocus

167 Combined restriction fragment length polymorphism and nucleotide

168 bovis strains had the same 16S ribosomal DNA restriction fragment length polymorphism and often had t

169 PCR-restriction fragment length polymorphism and partial seq

170 Furthermore, restriction fragment length polymorphism and pulsed-fiel

171 bs were analyzed and compared using terminal restriction fragment length polymorphism and sequence an

172 dIII-restricted DNA, Southern hybridization, restriction fragment length polymorphism and sequencing

173 3, that had insertion sequence 6110 (IS6110) restriction fragment length polymorphism and spoligotype

174 We developed a terminal restriction fragment length polymorphism assay (TRFLP) f

175 sm in NQO1 using a polymerase chain reaction-restriction fragment length polymorphism assay and for t

176 r PCR, and/or a conventional PCR method (PCR-restriction fragment length polymorphism assay), were pe

177 ient isolate, there were two distinct IS1245 restriction fragment length polymorphism banding pattern

178 Restriction fragment length polymorphism confirmed that

179 Chromosome pairing, isozyme, and restriction fragment length polymorphism data support a

180 ingle dominant locus and cosegregated with a restriction fragment length polymorphism detected by the

181 d 2008 from three humic lakes using terminal restriction fragment length polymorphism fingerprinting

182 throughput 18S rRNA tag sequencing, terminal restriction fragment length polymorphism fingerprinting,

183 were evaluated by polymerase chain reaction restriction fragment length polymorphism for polymorphis

184 We then studied the accuracy of restriction fragment length polymorphism for the -308 si

185 ed groups based on distinct ribosomal spacer restriction fragment length polymorphism genotypes (RSTs

186 We determined silk maysin concentrations and restriction fragment length polymorphism genotypes at fl

187 s genotype classification was done by IS6110 restriction fragment length polymorphism genotyping and

188 as to identify the three markers by PCR and restriction fragment length polymorphism in parallel, an

189 o population studies, were examined by using restriction fragment length polymorphism IS6110 fingerpr

190 ative in discriminating the four-band IS6110 restriction fragment length polymorphism isolates from e

191 enitors of the major weed "johnsongrass." By restriction fragment length polymorphism mapping, variat

192 AC clone is anchored by a genetically mapped restriction fragment length polymorphism marker.

193 this approach with direct sequencing and the restriction fragment length polymorphism method indicate

194 are investigated using sequence analysis and restriction fragment length polymorphism of a mitochondr

195 We also identified a HindIII restriction fragment length polymorphism of F8A fragment

196 Molecular techniques, including restriction fragment length polymorphism of genomic DNA

197 both parental alleles were demonstrated with restriction fragment length polymorphism of polymerase c

198 PCR-restriction fragment length polymorphism of small subuni

199 from livestock animals were analyzed by PCR-restriction fragment length polymorphism of the Cryptosp

200 DNA sequencing and restriction fragment length polymorphism of the PCR prod

201 e and suitable for PCR checking, SNP typing (restriction fragment length polymorphism or amplificatio

202 techniques have been developed, based on PCR-restriction fragment length polymorphism or sequencing a

203 Its IS6110 restriction fragment length polymorphism pattern was ide

204 method for the 37% of isolates displaying a restriction fragment length polymorphism pattern with <6

205 Patients whose isolates had identical restriction fragment length polymorphism patterns and sp

206 of isolates of each subgroup share the same restriction fragment length polymorphism patterns of the

207 two Nocardia patient isolates showed unusual restriction fragment length polymorphism patterns with r

208 st with HindIII, EcoRV, and AspI to generate restriction fragment length polymorphism patterns.

209 ipheral blood leukocytes and analyzed with a restriction fragment length polymorphism PCR method.

210 We devised a PCR-restriction fragment length polymorphism screen for the

211 Southern blot and restriction fragment length polymorphism segregation ana

212 ion, employing the polymerase chain reaction-restriction fragment length polymorphism technique (PCR-

213 We used polymerase chain reaction-restriction fragment length polymorphism to evaluate gen

214 virulence factors, ribosomal RNA gene spacer restriction fragment length polymorphism types (RSTs), o

215 jor histocompatibility complex class II DRB3 restriction fragment length polymorphism types 8/23, 3/1

216 For the SNPs, we designed a low-cost PCR-restriction fragment length polymorphism typing method.

217 IS6110 restriction fragment length polymorphism typing of cultu

218 Sixty strains were used to devise a restriction fragment length polymorphism typing scheme t

219 found that 4 of 46 heterozygotes analyzed by restriction fragment length polymorphism were actually G

220 of nirS-denitrifers (assessed using terminal restriction fragment length polymorphism) was interactiv

221 n enzyme analysis of this gene (16S rRNA PCR-restriction fragment length polymorphism).

222 and identified, on the basis of biochemical, restriction fragment length polymorphism, and 16S rRNA g

223 -403, evaluated by polymerase chain reaction-restriction fragment length polymorphism, and CCR5Delta3

224 f the four progeny was confirmed by isozyme, restriction fragment length polymorphism, and cytologica

225 genes for toxins A, B and binary toxin using restriction fragment length polymorphism, and identifica

226 genotyped by polymerase chain reaction (PCR)-restriction fragment length polymorphism, and IL-1RN var

227 enotypically matched (by spoligotype, IS6110 restriction fragment length polymorphism, and mycobacter

228 nalytical methods, including pyrosequencing, restriction fragment length polymorphism, and sequencing

229 es underwent DNA fingerprinting using IS6110 restriction fragment length polymorphism, and those with

230 g of the -174 nucleotide variant was done by restriction fragment length polymorphism, heteroduplex a

231 re determined by a combination of RT-PCR and restriction fragment length polymorphism, multiplex RT-P

232 ermined on thyroid FNAB specimens by PCR and restriction fragment length polymorphism, plus direct se

233 By PCR-restriction fragment length polymorphism, sequence, and

234 Three molecular typing methods, IS6110 restriction fragment length polymorphism, spoligotyping,

235 rRNA bacterial community analyses (terminal restriction fragment length polymorphism, T-RFLP) were p

236 ntional methods based on cDNA sequencing and restriction fragment length polymorphism, the microarray

237 ; 60% of the cases had clustered patterns of restriction fragment length polymorphism, thought to rep

238 y the presence of the A1 allele of the TaqIA restriction fragment length polymorphism, which is assoc

239 nt type was assigned by a combination of PCR-restriction fragment length polymorphism-based assays.

240 263 controls underwent CD14 genotyping using restriction fragment length polymorphism-polymerase chai

241 t mtDNA haplotyping by analysis with PCR and restriction fragment length polymorphism.

242 2+ ATPase gene (pfATP6) were assessed by PCR-restriction fragment length polymorphism.

243 were genotyped by polymerase chain reaction-restriction fragment length polymorphism.

244 were determined by polymerase chain reaction-restriction fragment length polymorphism.

245 ent in a White Leghorn CEF substrate pool by restriction fragment length polymorphism.

246 nalyzed with 454 pyrosequencing and terminal restriction fragment length polymorphism.

247 C2 were analyzed by pyrosequencing or by PCR restriction fragment length polymorphism.

248 Tissue typing was based on restriction fragment length polymorphism.

249 st change in community composition (Terminal Restriction Fragment Length Polymorphism; T-RFLP).

250 G, by means of polymerase chain reaction and restriction fragment--length polymorphism analysis.

251 tuberculosis strains associated with IS6110 restriction fragment-length polymorphism (RFLP) pattern

252 TB) during 1996-2001 were fingerprinted with restriction fragment-length polymorphism (RFLP).

253 Results of IS6110 restriction fragment-length polymorphism analyses were a

254 morphisms by using polymerase chain reaction-restriction fragment-length polymorphism analysis in 134

255 cribed sequence (ITS) and mitochondrial cox1 Restriction fragment-length polymorphism analysis of ITS

256 On the basis of a polymerase chain reaction-restriction fragment-length polymorphism analysis of the

257 By use of a polymerase chain reaction-based restriction fragment-length polymorphism analysis techni

258 We used spoligotyping, IS6110-based restriction fragment-length polymorphism analysis, and s

259 in the YMDD motif of the polymerase gene by restriction fragment-length polymorphism analysis.

260 interaction between these variants using PCR/restriction fragment-length polymorphism assays in 454 s

261 en demonstrated by mapping of several common restriction fragment-length polymorphism clones on both

262 and blot hybridization with three additional restriction fragment-length polymorphism clones.

263 Ninety maize restriction fragment-length polymorphism core markers we

264 representing 2 distinct ribosomal DNA spacer restriction fragment-length polymorphism genotypes (RSTs

265 Genotyping was performed by restriction fragment-length polymorphism polymerase chai

266 omegalovirus isolates were analyzed, both by restriction fragment-length polymorphism typing and by s

267 Restriction fragment-length polymorphism was used to det

268 aceae), was analysed by means of chloroplast restriction fragment-length polymorphism.

269 CFH, CFB, and 10q loci were screened by PCR-restriction fragment-length polymorphism.

270 tion inferred from mitochondrial DNA (mtDNA) restriction-fragment length polymorphism (RFLP) data and

271 and diarrhea cases were compared by means of restriction-fragment length polymorphism (RFLP), rapid a

272 The Brazilian isolates were typed by restriction-fragment length polymorphism analysis and we

273 Restriction-fragment length polymorphism analysis of hum

274 ment was verified by cytogenetic analysis or restriction-fragment--length polymorphism analysis.

275 ticipants for the identified polymorphism by restriction-fragment-length polymorphism (RFLP) analysis

276 Isolates were genotyped using restriction-fragment-length polymorphism (RFLP) patterns

277 olates underwent insertion sequence (IS)6110 restriction-fragment-length polymorphism analysis, targe

278 Known methods for SNP analysis include restriction-fragment-length polymorphism polymerase chai

279 Restriction fragment length-polymorphism analysis of vir

280 Bay, and Del Monte Beach), using multilocus restriction fragment length polymorphisms (DNA fingerpri

281 ological studies, mainly through identifying restriction fragment length polymorphisms (RFLP).

282 thamoeba isolates, mitochondrial DNA (mtDNA) restriction fragment length polymorphisms (RFLPs) and cy

283 f N. veterana gave identical and distinctive restriction fragment length polymorphisms (RFLPs) for an

284 e often needed in order to create artificial restriction fragment length polymorphisms (RFLPs).

285 dentified by polymerase chain reaction-based restriction fragment length polymorphisms and confirmed

286 Analysis of 16S ribosomal DNA restriction fragment length polymorphisms indicated that

287 lar organizer (Rdn1), the Smol gene, and two restriction fragment length polymorphisms linked to Smol

288 he seven single-copy genes were mapped using restriction fragment length polymorphisms of recombinant

289 -phosphate dehydrogenase or to determine the restriction fragment length polymorphisms of X chromosom

290 genotyped for BsmI, ApaI, TaqI, and FokI VDR restriction fragment length polymorphisms were used for

291 s of 420 markers (353 microsatellites and 67 restriction fragment length polymorphisms) revealed seve

292 VGS is demonstrated by the identification of restriction fragment length polymorphisms, and of amplif

293 Immunofixation, genomic restriction fragment length polymorphisms, and pulsed fi

294 13, and 61 were determined using engineered restriction fragment length polymorphisms.

295 d to subgroup S. aureus strains according to restriction fragment length polymorphisms.

296 enomic groups of C. burnetii are revealed by restriction fragment-length polymorphisms (RFLP).

297 ined by changes in polymerase chain reaction restriction fragment-length polymorphisms.

298 ative genetic mapping, using markers such as restriction-fragment length polymorphisms, has revealed

299 se techniques include (1) definitive genomic restriction-fragment-length polymorphisms (RFLPs) based

300 From the terminal restriction fragment length (TRFL) distribution, the aut