ライフサイエンスコーパス: amplified from

1 The fidelity of aRNA amplified from 1:10,000 to 1:100,000 of commonly used in

2 encing of polymerase-chain-reaction products amplified from 10 genetically independent patients with

3 B. henselae target DNA was amplified from 100% of samples with greater than 50 CFU/

4 (800 bp) and/or env (490 bp) sequences were amplified from 11 different individuals (eight females a

5 gments within the ureAB open reading frames, amplified from 11 independent isolates, were digested wi

6 t of detection, but orf 26 sequence was also amplified from 11 of 25 (44%) human control samples.

7 00-bp Helicobacter sp.-specific sequence was amplified from 14 liver samples.

8 p53exons 4-9 were amplified from 146 bladder tumors by PCR, screened by si

9 HCV sequences were successfully amplified from 185 patients: In the first 100, the genot

10 CMV DNA was successfully amplified from 195 of 204 eyes.

11 The IVS region was PCR-amplified from 20 Brucella isolates representing all kno

12 A 400-bp band was amplified from 26 of the 27 chicken carcasses tested by

13 A PCR product was amplified from 27 of the hybrid lines, indicating that J

14 t we identified, rpoBC, dnaK, and hsp65 were amplified from 29 ATCC reference strains and 17 clinical

15 A total of 155 exons were amplified from 35 arRP patient DNA samples, with each sa

16 A fragment of approximately 400 bp was amplified from 38 of 40 (95%) C. jejuni isolates and 5 o

17 ZIKV envelope was amplified from 4 samples.

18 The length of ITS1 region PCR products amplified from 40 species (106 clinical strains, 5 refer

19 The D18S1259 sequence was amplified from 47 TG and 30 CG samples.

20 Viral genome was amplified from 48 samples (8.7 percent) from 34 patients

21 PCR fragments were amplified from 5 to 40% of serum specimens obtained from

22 We found that (i) rdxA genes PCR amplified from 50 representative Mtz(r) strains from pre

23 Viral sequences were amplified from 8 of the 18 patients with simultaneous pl

24 on (5' UTR), VP4/VP2, VP1, and 3Dpol regions amplified from 89 HRV-C-positive respiratory samples and

25 ost variable region of the glycoprotein gene amplified from 9 patients revealed no nucleotide changes

26 The 545 bp 16 S rDNA PCR fragment was amplified from 90% of gastric biopsies from histological

27 ies, while P. carinii f. sp. carinii DNA was amplified from 98% of oral swabs.

28 suggests that an OME-derived signal could be amplified from a few nonmotile producers to act on many

29 icular ligand specificity can be selectively amplified from a million-fold larger pool of cells conta

30 Loci of interest are directly amplified from a mixed population via two rounds of PCR

31 on protein (atypical PrPres) was selectively amplified from a mixture.

32 Specifically, mKAT III cDNA was amplified from a mouse brain cDNA library, and its recom

33 A 2.4-kb cDNA was then amplified from a mouse ovarian adapter-ligated cDNA libr

34 strand conformation analysis of PCR products amplified from a panel of somatic cell hybrid lines and

35 A mouse uroguanylin complementary DNA was amplified from a partial genomic clone, and Northern ana

36 equencing polymerase chain reaction products amplified from a polymorphic sequence on chromosome 1.

37 e as PCR primers, genomic DNA fragments were amplified from a range of mammalian species that span th

38 ctedly, a subset of the SNRE elements, which amplified from a single founding SNRE element within the

39 capillary sequencing of cloned PCR products amplified from a subset of the selected regions.

40 fferent protein tyrosine kinases (PTKs) were amplified from a taste-enriched cDNA library using PCR.

41 b assay that could be reliably recovered and amplified from a variety of clinical specimens.

42 ragments encoding reverse transcriptase were amplified from a variety of isolates and were subcloned

43 idase cDNA was cloned and characterized, and amplified from affected cat fibroblasts by reverse trans

44 mples associated with PTB, bacterial DNA was amplified from all (16/16) of the culture-positive sampl

45 A PCR product was amplified from all 37 intraocular samples from eyes with

46 the OPZ19 RAPD primer a 1,264-bp product was amplified from all A. fumigatus strains initially examin

47 t 536-bp and 268-bp beta-globin targets were amplified from all aliquots.

48 DNA from Mycobacterium leprae was amplified from all nine skeletons but not from control s

49 No PCR products were amplified from all nontarget control samples.

50 PCR products suitable for sequencing were amplified from all samples tested.

51 In contrast, the 1.1-kb fragment was amplified from all serotype 5 strains only.

52 The 0.7-kb fragment was amplified from all strains of A. pleuropneumoniae tested

53 exon 9 through exon 11 of the CFTR gene was amplified from all tissues of the normal mouse.

54 In contrast, Tn5386 joints amplified from ampicillin-susceptible D344SRF revealed e

55 The 0.7-kb fragment was not amplified from any heterologous species that are also co

56 rted-repeat transposable element (mPing) has amplified from approximately 50 to approximately 1,000 c

57 PCR products (without any purification) amplified from Arabidopsis plant genomic DNA crude prepa

58 ficant and reliable signal for LAMP reaction amplified from as little as 10(-19) M virus gene.

59 Complete envelope genes were amplified from autopsy brain tissue of five individuals

60 In contrast, vlsE cassettes amplified from B. burgdorferi clones derived from a mous

61 ents covering these regulatory elements were amplified from B2 and C2 isolates to generate luciferase

62 similarity to mammalian P-glycoproteins were amplified from barley (Hordeum vulgare) root poly A+ RNA

63 A partial PDS cDNA amplified from barley was 90, 88 and 74% identical to PD

64 Genomic DNA was isolated, amplified (from base pair -527 to base pair +322) after

65 ed by phylogenetic analyses of DNA sequences amplified from baseline serum samples (n = 694).

66 eliminates the purification of PCR products amplified from bisulfite-treated DNA, use of radioisotop

67 but absent from macrophage-tropic envelopes amplified from blood and semen.

68 By applying 454 sequencing on NCCR DNA amplified from body fluid samples (urine, plasma, and ce

69 A contiguous block of 8 STSs could be amplified from both human chromosome 6 and 5.

70 CO1 and CO2 sequences amplified from both of the rho degrees cells, demonstrat

71 beta-subunits of ATP citrate lyase could be amplified from both organisms.

72 products of the C2-to-V5 region of env were amplified from both proviral DNA and virion RNA in blood

73 NA gene sequence was detected among products amplified from both the ticks and the deer blood specime

74 3' fragment of bovine GRalpha cDNA was also amplified from bovine lens.

75 ional domain of granulysin and NK-lysin were amplified from bovine PBMC mRNA.

76 The SIV env V1 region was amplified from brain and peripheral blood mononuclear ce

77 verse transcriptase PCR, and viral sequences amplified from brain tissue and serum were compared by s

78 were observed at the recombination junctions amplified from BRCA1-deficient human B cells.

79 The cDNA coding for havcr-1 was amplified from BS-C-1 and CV-1 total cellular RNA by rev

80 After RT-PCR amplification, DNAs amplified from bunyaviruses of interest were subjected t

81 tinct proviral c-myc integration events were amplified from bursas of infected 35-day-old birds, in g

82 al markers found within each group have been amplified from canine and vulpine flow-sorted, chromosom

83 RFRP and NPFF(2)R transcripts were amplified from cardiomyocytes and heart.

84 A partial HBD-3 cDNA clone was amplified from cDNA derived from IL-1beta induced fetal

85 When delta-TIP DNA fragments were amplified from cDNA of fiber 14 days after anthesis, the

86 This pseudogene is amplified from cDNA preparations contaminated with genom

87 Their Igs were amplified from cDNA using nested PCR, then cloned and se

88 t whole bacterial genomes can be effectively amplified from cells or small amounts of purified genomi

89 Two IGHJ fragments were amplified from CEMO-1 DNA and sequenced.

90 k operon, and the 51-kDa major antigen) were amplified from cercaria lysates by PCR and sequenced.

91 reverse transcription-PCR (RT-PCR) products amplified from cerebrospinal fluid.

92 tion of cDNA ends), full-length cDNA was PCR amplified from chicken brain cDNA, yielding four differe

93 Initial genomic clones were amplified from chicken genomic DNA and were used to isol

94 on of each receptor gene coding sequence was amplified from Chinese hamster genomic DNA and the resul

95 the function of E. coli FtsZ, ftsZ(Bbu) was amplified from chromosomal DNA and placed under the cont

96 e presence of human papillomavirus (HPV) DNA amplified from clinical specimens.

97 g for TLR1-9, as well as NOD1 and NOD2, were amplified from cultured and primary human intestinal myo

98 int band that is significantly less than DNA amplified from cycling cells was observed at day 15.

99 1200 by screening with a 1200 bp PCR product amplified from degenerate oligonucleotides encoding the

100 Mutant STAT3 was amplified from different tissues and sequenced, and the

101 EC cells, but Wnt-related PCR fragments were amplified from differentiating cultures, 4-14 days after

102 The E. ewingii p28 gene homologue was amplified from DNA extracted from whole blood obtained f

103 virus (LPV) archetypal regulatory region was amplified from DNA from the blood of an immunocompromise

104 the full-length Rmcf Env surface subunit was amplified from DNAs from virus-resistant backcross mice

105 The gene encoding Can f 6 was amplified from dog skin and bladder cDNA libraries.

106 and the differentiation of two DHBV isolates amplified from dried serum was demonstrated based on the

107 ne nearly full-length 16S rRNA gene could be amplified from each dog.

108 rectly sequencing the PCR products that were amplified from each exon.

109 The expected fragments were amplified from each of 60 staphylococcal isolates (13 ox

110 or variously spaced PCR fragments have been amplified from each recombinant chromosome and digested

111 Template DNAs were amplified from each T. kodakarensis strain, and transcri

112 nowledge remains restricted to a single gene amplified from environmental DNA, the 18S rRNA gene (sma

113 f cloned 5' RACE products and of products re-amplified from excised bands.

114 y direct automated sequencing of genomic DNA amplified from exonic regions and associated splice intr

115 II) clone could provirus be consistently PCR amplified from extracted PBMC DNA and quantitative compe

116 cycling Chromatiales, for which 16S rRNA was amplified from extracted RNA.

117 A PCR amplicon containing lpt3 was amplified from F62DeltaLgtA, cloned, mutagenized, and in

118 partial and full-length viral sequences were amplified from fecal RNA of 10 infected chimpanzees.

119 ragments comprising a complete provirus were amplified from fecal RNA of three wild-living chimpanzee

120 h (CP684, CP2135, and CP2139) SIVgor genomes amplified from fecal RNAs of wild-living gorillas at two

121 S. haemolyticus cap genes were amplified from four of seven clinical isolates of S. hae

122 ddition, partial pol sequences (650 bp) were amplified from four offspring of De Brazza's monkeys ori

123 Divergence among 5' sequences of DR genes amplified from G. arboreum, G. raimondii, and Gossypioid

124 oding regions were polymerase chain reaction-amplified from genomic DNA and sequenced.

125 sequence (CS-ACS1) encoding ACC synthase was amplified from genomic DNA by a polymerase chain reactio

126 ncoded mitochondrial genes were successfully amplified from genomic DNA from 63 individuals.

127 estion of polymerase chain reaction products amplified from genomic DNA indicated that affected cats

128 LAMP2 was amplified from genomic DNA isolated from peripheral lymp

129 soybean (Glycine max L. Merr.) DNA sequence amplified from genomic DNA using PCR primers designed to

130 lanin biosynthesis, a 772-bp PCR product was amplified from genomic DNA using primers based on conser

131 A conserved 200-bp gene fragment was amplified from genomic DNA with heterologous primers, an

132 xonic regions were polymerase chain reaction-amplified from genomic DNA, isolated from the above-ment

133 the percentages of productive rearrangements amplified from genomic splenic DNA.

134 globular forms of acetylcholinesterase were amplified from gingival keratinocytes (KC) by means of p

135 this sequence, a 378-bp DNA fragment was PCR amplified from H. pylori genomic DNA and used as a probe

136 c analysis was performed using HDV sequences amplified from HDV seroconverters and HDV-seropositive p

137 Although the full-length HBV genome can be amplified from high-titer blood samples by PCR using Hig

138 Restriction mapping of the products amplified from HMC and from PBL gave restriction fragmen

139 nt of the SPRR1B gene 5'-flanking region was amplified from human chromosome 1, sequentially deleted,

140 HB promoter sequence, HB569 and HB996, were amplified from human DNA, cloned into an AAV vector cass

141 PCR products were amplified from human genomic DNA and allowed to hybridiz

142 ssay, a 73-bp segment of the C6 gene was PCR-amplified from human genomic DNA, and TaqMan probes were

143 n of a sequence to a hairpin that can be PCR-amplified from human genomic DNA, exponential amplificat

144 275 amino acid open reading frame putatively amplified from human glioma cell line LN229 encodes a hu

145 Maltase-glucoamylase cDNA was amplified from human intestinal RNA using degenerate and

146 The coding region of SLC5A8 mRNA was amplified from human intestine and expressed heterologou

147 n V) coding for mature plasma factor XI were amplified from human platelet mRNA.

148 e transgenes were analyzed by sequencing DNA amplified from hypermutating Peyer's patch B cells.

149 rn of 37 nonproductively rearranged VH genes amplified from individual human B cells was analyzed.

150 nproductive VJ and V(D)J rearrangements were amplified from individual peripheral CD19+ B cells and w

151 V-1 V3-loop or gp120-envelope sequences were amplified from individually dissected cells by nested PC

152 The switches directly amplified from infected bladder and kidney tissues were

153 g-resistant virus in an infant, proviral DNA amplified from infected peripheral blood mononuclear cel

154 he fopA and tul4 genes of F. tularensis were amplified from infected spleen, lung, liver, and kidney

155 g trinucleotide or dinucleotide repeats were amplified from infected tissues, and the copy numbers we

156 ci were not observed, nor were DNA sequences amplified from intestinal tissue obtained from age-match

157 6s rRNA hypervariable regions V3 and V6 were amplified from Klebsiella pneumoniae genomic DNA with bl

158 ve differences were apparent in PCR products amplified from L. huidobrensis individuals, but the orig

159 like candidate gene in this interval was PCR amplified from Ler-0 and transformed into mutant Col-rpp

160 ction of drug resistance mutations in clones amplified from low-level plasma virus.

161 Mouse beta-defensin-4 (MBD-4) was amplified from lung cDNA using polymerase chain reaction

162 erotype 5 capsular DNA products were readily amplified from lung tissues obtained from infected swine

163 ge tropism for the majority of the envelopes amplified from lymph node, blood, and semen is striking

164 The C2-C3 coding region of HIV-1 env was PCR amplified from lysed peripheral blood mononuclear cells

165 Homologs of mdh2 were amplified from M. universalis FAM5 and strains RZ18-153

166 bouring gltB2, soxA and gsIII-like genes was amplified from M. universalis FAM5, sequenced and assemb

167 strains at the microscale are coupled to and amplified from macroscale principal strains for a majori

168 of a processed p53 pseudogene (Psip53) were amplified from many of these mice and from others collec

169 us dendritic cells (DC) transfected with RNA amplified from microdissected tumor cells are capable of

170 By PCR, ORF 4 was amplified from most isolates while ORFs 1 and 2 were amp

171 Cloning and sequencing of the cDNA amplified from mRNA isolated from VSMCs showed > 96 % am

172 bserved in a microarray analysis using cDNAs amplified from mRNA of Brca1-null mouse embryonic fibrob

173 based on Illumina sequencing of target genes amplified from multidimensionally pooled templates repre

174 hopQ and its flanking genes were PCR amplified from multiple H. pylori strains, and the nucle

175 or mutations, using complementary DNA (cDNA) amplified from muscle-biopsy specimens and genomic DNA e

176 c sequences flanking the 3'-side of L1s were amplified from neuronal DNA, and neuronal L1 libraries w

177 adaA was determined and a 59-bp fragment was amplified from Nine Mile phase I DNA by PCR.

178 The sequence of full-length NCCT cDNA amplified from normal PBMC was identical to human renal

179 HEV RNA was amplified from one farmed pig and two feral pigs and cha

180 B. burgdorferi was weakly amplified from one pool using some assays, but not other

181 d from most isolates while ORFs 1 and 2 were amplified from only some B. afzelii isolates.

182 sequence analysis of PCR fragments (271 bp) amplified from open reading frame 1 (ORF1) was performed

183 human herpesvirus-8 (HHV-8) subgenomic DNA, amplified from oral and blood samples by use of polymera

184 whereas only three or fewer DAB alleles were amplified from ornamental guppies.

185 The consensus DNA sequence, amplified from paraffin-embedded tissue and represented

186 sequences in the 297-bp HIV-1 protease gene amplified from patient PBMC.

187 ntaining multiple drug resistance mutations, amplified from patient plasma.

188 To define the molecular mechanisms, we amplified from patient platelet RNA exons 3 to 6 of core

189 rted that b12 sensitivity of HIV-1 envelopes amplified from patient tissues without culture varied co

190 Full-length E1E2 clones were PCR amplified from patient-derived serum samples, cloned int

191 ed the pattern of mutations in Nef sequences amplified from peripheral blood CD4(+) T cells and from

192 equences from 60 HIV-2-infected persons were amplified from peripheral blood lymphocytes, and nef ope

193 Provirus could be consistently PCR amplified from peripheral blood mononuclear cell (PBMC)

194 n protection, fragments of the env gene were amplified from peripheral blood mononuclear cell DNA and

195 of nuclear small-subunit rRNA gene sequences amplified from peripheral blood of a baboon chronically

196 tron-exon junctions of their FVII genes were amplified from peripheral white blood cell DNA by polyme

197 onuclear cells and reverse transcriptase-PCR amplified from plasma and pleural fluid HIV-1 virions of

198 using patient-derived gag-protease sequences amplified from plasma HIV RNA and inserted into an NL4-3

199 id mixtures and at approximately 0.1% in DNA amplified from plasma HIV-1.

200 lyze HIV-1 env genes as intact genetic units amplified from plasma virion RNA by single-genome amplif

201 B gene, which encodes the MgPa adhesin, were amplified from positive clinical specimens and evaluated

202 igated whether envelope (env) genes could be amplified from proviral DNA or RNA derived from brain ti

203 alysis of polymerase chain reaction products amplified from pulmonary samples of patients with P. car

204 No PCR product was amplified from purified DNA of Eperythrozoon suis, Mycop

205 Rabbit EP1 receptor cDNA was amplified from rabbit kidney RNA.

206 is of the RT-encoding region of the pol gene amplified from resistant viruses consistently identified

207 t least four of the centromeric repeats were amplified from retrotransposon-related sequences and wer

208 ASGP-1- and ASGP-2-specific sequences were amplified from RNA extracted from both conjunctival and

209 252 bp fragment of the putative P450scc was amplified from RNA of interrenal tissue (the adrenal cor

210 ntical to the open reading frame protein was amplified from RNA of neutrophils.

211 ycobiliprotein subunits, were differentially amplified from RNA templates derived from cells grown in

212 The iroB gene could be PCR amplified from S. enterica subsp. enterica (I), salamae

213 osomal peptide synthetase (NRPS) gene probes amplified from S. vinaceus genomic DNA.

214 We also examined sequences amplified from saliva and buffy coat samples from the sa

215 Genes encoding nitrogenase (nifH) were amplified from sediment and photosynthetic mat samples c

216 In this study, PCR and RT-PCR products were amplified from serially diluted DNA and RNA templates, r

217 tive kinase genes, CT145 and CT301, were PCR amplified from serovar L2, cloned, and sequenced.

218 HBV DNA was amplified from serum and sequenced through a conserved p

219 Coccidioides DNA was amplified from serum by a PCR using coccidioid-specific

220 We have now sequenced the HCV viral RNA amplified from serum of treated mice after the 21-day fo

221 envelope glycoprotein (E-glycoprotein) genes amplified from several other species including mosquitoe

222 nerated by inserting the env V1-to-V5 region amplified from SHIV(SF33A)-infected animals into the par

223 mutant versus wild-type HEXA gene fragments amplified from single cells without primer artifact.

224 d light-chain variable-region sequences were amplified from single IgG(4)(+) B cells.

225 anscriptome, and demonstrate that RNA can be amplified from single oocytes and embryos for analysis b

226 ce protein A (ospA) gene sequences from DNAs amplified from small mammals and ticks confirmed the pre

227 d swine, although the 1.1-kb product was not amplified from some tissues stored frozen for 6 years.

228 outer-membrane protein (OMP) P2, ompP2, was amplified from sputum samples and selected strains obtai

229 sed on sequence analysis of the flanking DNA amplified from strains that do not encode cna, the prese

230 tial pol (650 bp) SIVsyk sequences were also amplified from Sykes's monkeys (Cercopithecus albogulari

231 ganisms, small-interfering RNAs (siRNAs) are amplified from target mRNAs by RNA-dependent RNA polymer

232 ay to nonhuman samples demonstrated products amplified from template DNA extracted from Ixodes scapul

233 This report illustrates that PCR products amplified from templates differing by a single nucleotid

234 taR-I PCR product was distinct from products amplified from TGF-beta-responsive cells and was also re

235 nning was possible using phage recovered and amplified from that same patient's tumor.

236 No Helicobacter species were amplified from the 10 persistent negatives.

237 on was developed, using cDNA pools that were amplified from the anterior mesendoderm of single wild-t

238 s of the 16S rRNA gene and the groESL operon amplified from the blood of this dog matched the publish

239 this study, we characterized envelopes (Env) amplified from the brains of subtype B and C R5 SHIVE ma

240 kb fragment containing the uvrB gene was PCR amplified from the chromosomal DNA of P. gingivalis W83.

241 to a number of putative promoters that were amplified from the D. radiodurans R1 genome.

242 The ptsP gene was polymerase chain reaction amplified from the E. coli chromosome and cloned into an

243 tance mutations in cytomegalovirus (CMV) DNA amplified from the eyes of patients with AIDS and newly

244 Helicobacter species were amplified from the first stool samples of 15/26 (58%) of

245 traE2, traE3 and traE4, were identified and amplified from the genome of the leafhopper-transmitted

246 idated the approach on two long PCR products amplified from the human genome and confirmed the accura

247 ements (59 productive and 77 non-productive) amplified from the human genomic DNA of peripheral blood

248 The VDJ portion of the expressed Ig mRNA was amplified from the IgM+ a2+ and IgM+ a2- populations by

249 from analysis of PCR-generated vaa sequences amplified from the joint synovial fluid of a patient wit

250 A nearly identical VP1 sequence was amplified from the kidney of another animal.

251 rpin acceptor, one of the four loop products amplified from the LAMP is transduced to an active catal

252 Using PCR, UL81-82ast was amplified from the library.

253 patic lesions, H. hepaticus-specific DNA was amplified from the livers of 21 of 44 of the mice (47%),

254 heral blood, they are present in every clone amplified from the low levels of free virus in the plasm

255 ine survived and B. pseudomallei DNA was not amplified from the lungs or spleens of most surviving mi

256 rry stained sections, and Bartonella DNA was amplified from the lymph node (from 6 of the 13 cats), l

257 ticks harbored AP-variant 1, only AP-ha was amplified from the murine blood samples.

258 ants, and comparison of the sequence of pbp4 amplified from the mutants indicated disruption of the g

259 Bacterial DNA was amplified from the only patient with clinical intrauteri

260 er, a veillonella 16S rRNA gene sequence was amplified from the original isolation mixture, and this

261 ted NVAV strain Te34, were identical to that amplified from the original lung tissue, and phylogeneti

262 lone AF14 matched exactly with the sequences amplified from the patient's subgingival plaque.

263 iral DNA polymerase gene, a DNA fragment was amplified from the PBL or spleens of all six deer and se

264 specific exon are duplicates that have been amplified from the PCR step.

265 egrase gene (int) and gag sequences were PCR amplified from the peripheral blood lymphocytes availabl

266 However, HTLV-I tax sequence was amplified from the peripheral blood lymphocytes of 4 of

267 ndicated that P2X1-7 and P2Y1,2,6 RNA can be amplified from the pial sheet.

268 is of the RT-encoding region of the pol gene amplified from the plaque-purified mutants revealed a Pr

269 SIV(mac251) genomes were amplified from the plasma of 44 pig-tailed macaques infe

270 ified individually also can be detected when amplified from the pool.

271 162-bp vpr coding regions were successfully amplified from the respective regions of the proviral DN

272 ns, most a few hundred base pairs long, were amplified from the S. purpuratus BAC DNA by PCR, inserte

273 Helicobacter bilis was amplified from the second sample of a persistent positiv

274 EAV genomes amplified from the semen of these two stallions were com

275 kS (HlgC), a pore-forming binary toxin, were amplified from the Smith 5R strain of Staphylococcus aur

276 Rearranged IgH D(J) regions were amplified from the spleen and lymph tissue of mice immun

277 riable sites, the V4 and V8-V9 regions, were amplified from the total of eight lagoon samples and seq

278 The entire NTS was amplified from the two species by polymerase chain react

279 us 8 (HHV-8) open reading frame K1 sequences amplified from the urine of 5 of 78 (6.4%) infected peop

280 Each fragment was amplified from the variant-enriched pool and sequenced,

281 his sample in that the emm gene could not be amplified from them by PCR.

282 IRBP message was PCR amplified from these cells after microdissection.

283 Clone libraries of bacterial 16S rRNA genes amplified from these enrichments showed increased propor

284 olyketide ketosynthase (KS) domain fragments amplified from these microbiomes provide a means to eval

285 The cloning and sequencing of ITS2 DNA amplified from these same samples recovered numerically

286 Genomic DNA after bisulfite modification amplified from this region showed identical sequences be

287 med products from Ehrlichia chaffeensis were amplified from three individuals from Florida or Marylan

288 nce-confirmed products of the HGE agent were amplified from three individuals residing or having expo

289 sing 13 homologous mitochondrial gene probes amplified from three species by polymerase chain reactio

290 The 16S rRNA gene sequences amplified from tick-exposed horses showed more than 99%

291 Circle junction fragments, amplified from two-long-terminal-repeat viral DNA (vDNA)

292 b genomes (9,158 and 9227 bp in length) were amplified from uncultured blood mononuclear cell DNA of

293 A pol sequence, amplified from uncultured peripheral blood cells, is mos

294 The arp gene could not be amplified from unrelated B. burgdorferi isolates but hyb

295 Relevant segments of the CMV UL97 gene were amplified from vitreous humor, after which restriction d

296 Viral DNA was amplified from vitreous specimens and was assayed for UL

297 ingle-copy human genomic targets are readily amplified from whole blood or crude soil extract, withou

298 In vivo, miR-exon4 was most highly amplified from wild-type mouse enamel organs at the secr

299 Sequence comparison of STSs amplified from YAC clones uniquely mapped to BP2 or BP3

300 nts up to 361 bp in length were successfully amplified from Z7 fixed tissues, as demonstrated by PCR,