ライフサイエンスコーパス: hypervariable region

1 nt cells, and we mapped this activity to the hypervariable region.

2 obility analysis of the second envelope gene hypervariable region.

3 ha and Vbeta chain usage, and throughout the hypervariable region.

4 ed flanking domains and the other within the hypervariable region.

5 r more p44 species were found within the p44 hypervariable region.

6 racterized by conserved sequences flanking a hypervariable region.

7 y charged lysine at position 12 of the first hypervariable region.

8 A gene sequences by more than 80% for the V4 hypervariable region.

9 id pattern as well as a distinctive 16S rRNA hypervariable region.

10 ed except for sequence that encoded the MSP2 hypervariable region.

11 lyzed using 16S rRNA sequencing of the V3-V4 hypervariable region.

12 arnesylated-methylated KRAS4b, including the hypervariable region.

13 in the conserved positions, and GS"N in the hypervariable regions.

14 regions, including splice site acceptors and hypervariable regions.

15 S rRNA gene primer sets, targeting different hypervariable regions.

16 imilar magnitude were found in conserved and hypervariable regions.

17 have the same canonical structures in their hypervariable regions.

18 anonical structure in their first and second hypervariable regions.

19 not exclusively, directed against the hexon hypervariable regions.

20 is is further complicated by the presence of hypervariable regions.

21 of hepatitis C virus (HCV) contains several hypervariable regions.

22 Viral quasispecies in the second envelope hypervariable region 1 (E2/HVR1) and 5' untranslated reg

23 ne hypervariable region of mtDNA, designated hypervariable region 1 (HV1).

24 amino acid quasispecies complexities of the hypervariable region 1 (HVR-1) were less in the responde

25 Hypervariable region 1 (HVR1) (amino acids [aa] 384 to 4

26 edly reduced binding when amino acids within hypervariable region 1 (HVR1) and at sites approximately

27 Phylogenetic analysis of hypervariable region 1 (HVR1) and HCV genotyping were pe

28 of viral envelope glycoprotein E2, including hypervariable region 1 (HVR1) and N-linked glycans.

29 In the mild fibrosis group, intrasample hypervariable region 1 (HVR1) genetic distance and nonsy

30 HCV internal ribosomal entry site (IRES) and hypervariable region 1 (HVR1) in autopsy-derived brain,

31 Hypervariable region 1 (HVR1) is genetically diverse and

32 A hyperimmune rabbit antiserum to an E2 hypervariable region 1 (HVR1) mimotope also exhibited an

33 Interestingly, the E2 hypervariable region 1 (HVR1) mutation T385P caused (i)

34 which we find maps to a specific site within hypervariable region 1 (HVR1) of AdV5 hexon, has no appa

35 f HCV and shielding of important epitopes by hypervariable region 1 (HVR1) of E2 are believed to be m

36 The hypervariable region 1 (HVR1) of hepatitis C virus (HCV)

37 Hypervariable region 1 (HVR1) of hepatitis C virus (HCV)

38 Furthermore, replacement of hypervariable region 1 (HVR1) of the Ad capsid proteins

39 Evolutionary rates in the hypervariable region 1 (HVR1) region of the E2 gene were

40 Remarkably, sequences of hypervariable region 1 (HVR1) remained stable for up to

41 to Huh7.5 cells to produce a quasispecies of hypervariable region 1 (HVR1) that mimicked that circula

42 Hypervariable region 1 (HVR1) variability is frequently

43 Hypervariable region 1 (HVR1) within viral envelope prot

44 notype-specific epitopes of HCV core, E1, E2 hypervariable region 1 (HVR1), E2 HVR1-plus-HVR2 consens

45 of cDNA that spanned the E1 gene and the E2 hypervariable region 1 (HVR1), followed by analysis of c

46 We obtained sequences from the HCV hypervariable region 1 (HVR1), using end-point limiting-

47 Using highly NAb-sensitive hypervariable region 1 (HVR1)-deleted HCVcc, H77/JFH1(De

48 1a)/JFH1 or the highly antibody-susceptible hypervariable region 1 (HVR1)-deleted variants H77/JFH1D

49 tify AR3A resistance substitutions that have hypervariable region 1 (HVR1)-dependent effects on HCV v

50 that major outer membrane protein 1 (OMP-19) hypervariable region 1 (HVR1)-specific human monoclonal

51 s-immunoreactivity among variants of the HCV hypervariable region 1 (HVR1).

52 tensive mutations were not incorporated into hypervariable region 1 (HVR1).

53 instead of the well-known immunodominant E2 hypervariable region 1 (HVR1).

54 plotypes that had identical sequences in the hypervariable region 1 (HVR1).

55 d, ranging from high diversity (the envelope hypervariable region 1 [HVR1]) to almost no diversity (t

56 te populations, we compared mtDNA (400 bp of hypervariable region 1 and 14 restriction site polymorph

57 alizing epitopes on the E1 N-terminus and E2 hypervariable region 1 did not differ significantly.

58 h relapse were virtually identical, with the hypervariable region 1 of E2 appearing to be monoclonal,

59 on of SR-BI governed by specific residues in hypervariable region 1 of E2 leading to enhanced cell en

60 terized epitopes on E1/E2, especially to the hypervariable region 1 of E2.

61 out the envelope genes, primarily within the hypervariable region 1 of E2.

62 Next-generation sequencing data from the hypervariable region 1 of HCV were analyzed using Global

63 is virus (VSV)/HCV pseudotype model that the hypervariable region 1 of the HCV E2 envelope glycoprote

64 o 986 present-day human sequences located in hypervariable region 1 of the mitochondrion to estimate

65 Hypervariable region 1 of the second envelope gene was a

66 Most NAbs recognize hypervariable region 1 on E2, which undergoes frequent m

67 equence revealed amino acid substitutions in hypervariable region 1 that were responsible for a drama

68 yethylene glycol to a specific site in hexon hypervariable region 1 yielded vector particles that wer

69 Deletion of hypervariable region 1, a region previously proposed to

70 so generated serological responses to OMP-1g hypervariable region 1, indicating that humans and mice

71 cases, correlate also with antibodies to the hypervariable region 1, previously thought to be the pri

72 s, suggesting purifying selection, except in hypervariable region 1, where positive selection pressur

73 for immunogenicity in mice, with and without hypervariable region 1, which is an immunogenic region a

74 species diversity was analyzed by sequencing hypervariable region 1.

75 nfectivity of J6(2a) and J8(2b) with deleted hypervariable region 1.

76 lotype analysis and direct sequencing of the hypervariable regions 1 and 2 of the D-loop in muscle an

77 tes microbial communities, but sequencing of hypervariable regions 1-3 of the 16S rRNA gene provides

78 The HCV E2 hypervariable region-1 was amplified using nested revers

79 We aligned time-stamped second hypervariable region (330 bp) of G-gene sequence data (g

80 Sequencing of hypervariable region 4 poorly captures skin commensal mi

81 a single immunization of chimeric rAd5 hexon hypervariable region 48 (rAd5HVR48) vectors expressing S

82 igen (PA) as a model antigen to characterize hypervariable region 5 (HVR5) of hexon as a site for pep

83 f P. aeruginosa OprF (Epi8) in loop 1 of the hypervariable region 5 of the hexon (AdZ.Epi8).

84 l with mutations in the surface glycoprotein hypervariable regions: a previously identified variant c

85 e for viral replication, and the nsp2 middle hypervariable region (aa 324 to 813) tolerated 100-aa or

86 MiSeq and Roche454 platforms using the V3-V4 hypervariable region also showed a high level of concord

87 oximately 30 to 35 kDa consisting of several hypervariable regions alternating with conserved regions

88 ue to a mixture of P44 proteins with diverse hypervariable region amino acid sequences expressed by a

89 kines was localized to 40 amino acids in the hypervariable region (amino acids 301-340) of the protei

90 Neisserial mod alleles also contained a hypervariable region and all mod alleles exhibited varia

91 membrane but is tethered via its C-terminal hypervariable region and carboxymethylated farnesyl moie

92 Analysis of the szp gene hypervariable region and the 16S-23S rRNA intergenic spa

93 hanges both within the traditionally defined hypervariable regions and downstream, near the 3'-end of

94 sing from the crystal structure that include hypervariable regions and the epitope of a neutralizing

95 ure as determined via 18S rRNA (V4 and V8-V9 hypervariable regions) and 16S rRNA (V1-V3) gene amplico

96 creased frequency of B cells with long third hypervariable regions, and distal J(kappa) gene segment

97 r multiple markers such as the 16S rRNA gene hypervariable regions are available, MetAmp improves the

98 hout the primary amino acid sequence, with a hypervariable region at its C-terminus.

99 The hemagglutinin (H) gene and hypervariable region between the fusion and matrix genes

100 e, and -f were mapped within the nsp2 middle hypervariable region, but no conserved cleavage sites co

101 ive RNA splicing primarily in its N-terminal hypervariable region, but the functions of these isoform

102 3 million 16S rRNA sequences spanning the V4 hypervariable region by pyrosequencing.

103 n p44 conserved regions flanking the central hypervariable region by the TOPALi analysis.

104 the second constant region through the fifth hypervariable region (C2 to V5) of the surface envelope

105 While the hypervariable region CDR3 often mediates much of the spe

106 ith bNAb sensitivity, including amino acids, hypervariable region characteristics, and clade effects

107 ts and the genes from the other intraspecies hypervariable regions contributes to a better assessment

108 The hypervariable region D2 and D3 domains appear to stabili

109 The hypervariable region determined to which membrane compar

110 Only the C-terminal hypervariable regions differ significantly.

111 We propose that this hypervariable region encodes the target recognition doma

112 monella typhimurium phase 1 flagellin, this "hypervariable" region encodes two solvent-exposed domain

113 cally infected individuals by sequencing the hypervariable regions encoding TCR alpha and beta polype

114 lysis indicated that most sites outside this hypervariable region experienced strong negative selecti

115 The p44 genes include a central hypervariable region flanked by conserved regions.

116 se pseudogenes encode unique surface-exposed hypervariable regions flanked by conserved domains, whic

117 extension containing a His- and Asp/Glu-rich hypervariable region followed by a highly conserved sequ

118 identified in at least two of five examined hypervariable regions for every virus, suggesting the ev

119 d for identification of the 16S rRNA gene V3 hypervariable region from Escherichia coli genomic DNA.

120 Partial deletion of the second hypervariable region from the envelope of the primary-li

121 g it into our Ad5 vector containing all nine hypervariable regions from Ad43, Ad5.H(43m-43), increase

122 m TRUST to extract the B cell immunoglobulin hypervariable regions from bulk tumor RNA-sequencing dat

123 the specific amplification of 18s rRNA gene hypervariable regions from eukaryotic microbes: anneal-i

124 two primer pairs demonstrated that the V3-V4 hypervariable region had significantly better capture of

125 etion variants of UreG demonstrated that the hypervariable region has a minor impact on activation ef

126 by the novel gene p44-61 (p44-61/18), whose hypervariable region (hv) was a chimera of p44-20hv and

127 Second, in the two hypervariable regions HVa and HVb, thought to be involve

128 MSP2 has a central hypervariable region (HVR) flanked by highly conserved a

129 face protein 2 (MSP2), composed of a central hypervariable region (HVR) flanked by highly conserved r

130 me of the hepatitis E virus (HEV) contains a hypervariable region (HVR) in ORF1 that tolerates small

131 simulations highlight that the membrane and hypervariable region (HVR) interact with both alpha- and

132 rnesylated and positively charged C-terminal hypervariable region (HVR) is critical to its oncogenic

133 sed on chromosomal DNA fingerprints (CDF), a hypervariable region (HVR) of a 5.6-kb plasmid, the rRNA

134 Signals in the carboxy-terminal hypervariable region (HVR) of Rho and Ras GTPases target

135 man ribosomal protein S17 (RPS17) within the hypervariable region (HVR) of the HEV ORF1 protein.

136 A hypervariable region (HVR) previously identified in the

137 n, predominately against the surface-exposed hypervariable region (HVR) rather than against the invar

138 Between these two ends is a hypervariable region (HVR) that is only poorly conserved

139 Comparative sequence analysis revealed a hypervariable region (HVR) with extensive sequence varia

140 st distribution of polymorphisms occurs in a hypervariable region (HVR) within the carboxy third of t

141 cently, insertions and rearrangements of the hypervariable region (HVR) within the HEV genome, allowi

142 -Ras4B is predominantly autoinhibited by its hypervariable region (HVR), whereas the GTP-bound state

143 genetic distance and entropy were highest in hypervariable region (HVR)-1.

144 of the HCV envelope gene including the first hypervariable region (HVR-1) was reverse transcription-P

145 egments from multiple alleles to form unique hypervariable regions (HVR).

146 elatively conserved and a second, so-called 'hypervariable region' (HVR).

147 quence diversity and complexity at the first hypervariable region (HVR1) of the second envelope prote

148 Replacing hypervariable regions (HVRs) 1, 2, 4, and 5 with the equ

149 ing antibodies typically recognize M protein hypervariable regions (HVRs) and confer narrow protectio

150 at CaM preferentially binds unfolded K-Ras4B hypervariable regions (HVRs) and not alpha-helical HVRs.

151 h substantial sequence homology in the hexon hypervariable regions (HVRs) and suppressed the immunoge

152 Since hypervariable regions (HVRs) are nonconserved among hexo

153 rface-exposed regions of the capsid, such as hypervariable regions (HVRs) I to IX of VP3.

154 maeric rAd5 vectors in which the seven short hypervariable regions (HVRs) on the surface of the Ad5 h

155 us catalytic domains and flexible C-terminal hypervariable regions (HVRs) that differ across Ras isof

156 amino acid sequence variations confirms four hypervariable regions (HVRs), separated by regions under

157 (NAbs) directed primarily against the hexon hypervariable regions (HVRs).

158 FX binds to the adenovirus hexon hypervariable regions (HVRs).

159 talytic or globular domains, plus C-terminal hypervariable regions (HVRs).

160 -446 (epitope II), located downstream of the hypervariable region I within the HCV E2 protein.

161 Of 15 BDS strain clones, 1 had a hypervariable region identical to the region in a clone

162 60 million molecules) of human mitochondrial hypervariable region II amplicon was introduced into the

163 Here we show that the human mitochondrial hypervariable region II can function as a molecular fing

164 esent high-throughput sequencing analysis of hypervariable region II for spatial resolution of the co

165 the structural and physiological role of the hypervariable region in flagella assembly, stability and

166 ed sequence blocks throughout the MSP2 (P44) hypervariable region in reservoir hosts.

167 on-typeable H.influenzae isolates revealed a hypervariable region in the central portion of the mod g

168 e induction of Gal-3 expression requires the hypervariable region in the extracellular domain of beta

169 Pyrosequencing of amplicons for hypervariable regions in the 16S rRNA gene generated tax

170 oci within A. lyrata, sites corresponding to hypervariable regions in the Brassica S-loci (SLG and SR

171 16S rRNA per cells and also the presence of hypervariable regions in the genes.

172 unique, sexually dimorphic motifs in the TCR hypervariable regions in the SjS(S) mice.

173 These hypervariable regions include sites with three segregati

174 conversion of the entire (nonsegmental) p44 hypervariable region including flanking regions with a c

175 Modifications to the hypervariable region, including single-amino acid substi

176 sitive to GM-CSF, mutations within the N-Ras hypervariable region induced N-Ras mislocalization and a

177 that the P44 antigenic repertoire within the hypervariable region is restricted.

178 differences in the primary sequences of the hypervariable region manifest in different secondary str

179 genomic expression site encoding the central hypervariable region matched sequence polymorphisms in m

180 in primary structure within the immunogenic hypervariable region microdomains and tested whether the

181 QA1*0501, and DRB1 alleles sharing the first hypervariable region motif (9)EYSTS(13) were major risk

182 ted nanoclustering of H-ras helix alpha4 and hypervariable region mutants that have different bona fi

183 S ribosomal RNA amplicon sequences in the V4 hypervariable region obtained from 492 studies worldwide

184 We further identified a hypervariable region of 15 residues and a beta-hairpin s

185 .1 M bacterial pyrotag sequences from the V6 hypervariable region of 16S rRNA genes from 38 influent

186 human hepatoma cells when inserted into the hypervariable region of a genotype 1 strain, but this ch

187 g a shift from recombination of the complete hypervariable region of a given pseudogene to complex mo

188 MSP2 contains a central hypervariable region of about 100 amino acids that encod

189 s recovered, 39 recognized an amino-terminal hypervariable region of an outer membrane protein (OMP),

190 We analyzed the V4 hypervariable region of bacterial 16S rRNA genes with Il

191 plified by using primers specific for the V6 hypervariable region of bacterial 16s rRNA.

192 a crucial but commonly coded residue in the hypervariable region of CDR3 provide the basis for the s

193 anged p44Es revealed that the entire central hypervariable region of donor p44 pseudogenes or of dono

194 rough elevated signal produced to the unique hypervariable region of each - 2/114 in HL-60, 3/114 in

195 of the P28s were identified within the first hypervariable region of each P28 OMP.

196 The conservation of the hypervariable region of each p44 cDNA species of A. phag

197 oduplex tracking assay targeted to the V1/V2 hypervariable region of env.

198 The hypervariable region of K-Ras4B binds specifically to th

199 tration calorimetry, we demonstrate that the hypervariable region of K-Ras4B contributes in a major w

200 nce for four short sequential changes in the hypervariable region of msp2 coupled with the identifica

201 histocompatibility antigens, we examined one hypervariable region of mtDNA, designated hypervariable

202 recognized a linear epitope within the first hypervariable region of OMP-1g.

203 topes within the amino terminus of the first hypervariable region of OMP-1g.

204 n the conserved regions flanking the central hypervariable region of p44 genes.

205 Development of antibody to the hypervariable region of P44-18 during the rickettsemia s

206 r results show that in the murine model, the hypervariable region of PilE is required to activate imm

207 nal structure-based antigen by replacing the hypervariable region of PilE with an aspartate-glutamine

208 ly bound to the CAAX motif in the C-terminal hypervariable region of Rac1, and then inhibited Rac1 me

209 ow that elements in the known domains in the hypervariable region of Ras (amino acids 170-189) intera

210 Sequence variations within the hypervariable region of Ras isoforms underlie differenti

211 A mutation in the lysine repeat in the hypervariable region of Rsr1/Bud1 specifically abolished

212 The cDNA sequences of the central hypervariable region of several p44 genes were identical

213 Amplicons were sequenced (V3-V4 hypervariable region of the 16S rRNA gene) using MiSeq (

214 zed by bar-coded pyrosequencing of the V3-V5 hypervariable region of the 16S rRNA gene, defining 662

215 ent study, using pyrosequencing of the V1-V2 hypervariable region of the 16S rRNA gene, reported find

216 Our study included the analysis of the D1/D2 hypervariable region of the 28S ribosomal gene and the i

217 We were able to assemble the D1-D2 hypervariable region of the 28S ribosomal RNA (rRNA) of

218 This virus was unusual in that the hypervariable region of the adapted virus contained a 17

219 idase subunit 1 gene of nematodes and the V3 hypervariable region of the bacterial 16 s ribosomal RNA

220 d a tag-sequencing strategy targeting the V6 hypervariable region of the bacterial small-subunit (16S

221 ndings indicate that sequence variation in a hypervariable region of the degron affects JAZ stability

222 relatively small genomic segment, the first hypervariable region of the E2 gene, it is possible that

223 manifestations of disease are clustered in a hypervariable region of the genome termed the plasticity

224 rminants of macrophage infectivity to the V3 hypervariable region of the HIV-1 envelope glycoprotein.

225 s a 5-aa sequence motif in the third allelic hypervariable region of the HLA-DRbeta chain.

226 This residue is located in the C-terminal hypervariable region of the proteins and is not conserve

227 two attenuated viral variants differing in a hypervariable region of the spike protein.

228 ligonucleotide gold nanoprobe for one of the hypervariable regions of 16S rRNA gene.

229 nd ESPRIT-Tree, sequence data from different hypervariable regions of 16S rRNA were used and binning

230 cultures of strains NY-31, NY-36, and NY-37, hypervariable regions of 450 deduced amino acid sequence

231 serotype 5 (Ad5) vector containing the hexon hypervariable regions of Ad serotype 48 (Ad48) and expre

232 hexon-modified vector that carried the hexon hypervariable regions of Ad48, indicating that the SP mu

233 o complex mosaics with segments derived from hypervariable regions of different pseudogenes.

234 In these hybrid glycoproteins the hypervariable regions of EHV-1 gG, a vCKBP, and the clos

235 Finally, features of the first and second hypervariable regions of gp120 (V1V2) may be critical fo

236 Illumina MiSeq sequencing of the V3-V4 hypervariable regions of the 16 S rRNA gene was used to

237 oes is efficiently surveyed by sequencing of hypervariable regions of the 16s ribosomal RNA (rRNA) ge

238 lyzed by FLX+ pyrosequencing of the V1 to V4 hypervariable regions of the 16S rRNA gene and polymeras

239 Unique melt profiles generated from multiple hypervariable regions of the 16S rRNA gene for 100 clini

240 dot blot hybridization, by sequences of two hypervariable regions of the 16S rRNA gene, and by the p

241 DNA was amplified with primer pairs covering hypervariable regions of the 16S rRNA gene: primers 63F

242 iversity of sequence, primarily localized to hypervariable regions of the capsid protein, was detecte

243 The rates of evolution within hypervariable regions of the FCV capsid gene in individu

244 an interaction between the FX Gla domain and hypervariable regions of the hexon surface.

245 ensic identity testing by sequencing the two hypervariable regions of the human mtDNA control region.

246 Conventional genotyping methods target small hypervariable regions of the M. bovis genome and provide

247 is phosphorylated at sites clustered in two hypervariable regions of the protein.

248 ences between D1 domains are concentrated in hypervariable regions on the front sheet strands of the

249 bit antisera raised against either the first hypervariable region or ectodomain of E2 showed limited

250 several single-nucleotide substitutions in a hypervariable region outside the SAM-binding core can al

251 g GC and AT rich motifs correlated well with hypervariable region recombination sites across the HAdV

252 The C terminus, also known as the hypervariable region (residues 166-189), of H-, N-, and

253 terminal conserved region and P44-18 central hypervariable region, respectively.

254 quences follows the pattern of conserved and hypervariable regions seen in other S-RNases, but no reg

255 The hypervariable region sequence in the p44 expression locu

256 The K-Ras4A hypervariable region sequence is positively charged, in

257 elope protein (Env) by replacing part of its hypervariable region sequence with a sequence encoding t

258 ing more than 1.7 million bacterial 16S rRNA hypervariable region sequences from 52 to 56 samples per

259 Results obtained from the V3-V4 16S rRNA hypervariable region, sequencing on the MiSeq and Roche4

260 in the plasma membrane via lipid-tethers and hypervariable region side-chain interactions in distinct

261 ive usage of each T-cell receptor beta chain hypervariable region subfamily.

262 method also identified 18 other intraspecies hypervariable regions, such as the capsule and lipooligo

263 key changes to the lipidation pattern of the hypervariable region, suggest that dimerization is a gen

264 ermini flanking the central, surface-exposed hypervariable region that represents the variant B lymph

265 n that all serotypes have in common from the hypervariable regions that are responsible for capsid di

266 The sequences of several hypervariable regions that were > or = 97% similar to re

267 ferences between RAS isoforms lie within the hypervariable region, the additional confinement of KRAS

268 mice, suggesting that in the absence of the hypervariable region, the conserved regions of PilE alon

269 By looping out the hypervariable region, the porin structure is conserved a

270 a gonorrhoeae and contains a surface-exposed hypervariable region thought to be one feature of pili t

271 s in the mtDNA control region, including the hypervariable regions typically sequenced in a forensic

272 existence of a conserved region linked to a hypervariable region upstream of the 16S rRNA gene of H.

273 two species by pyrosequencing the 16S V1-V3 hypervariable regions using the 454 GS FLX Titanium plat

274 pected microbial profiles, sequencing of the hypervariable regions V1-V3 of the 16S ribosomal RNA gen

275 Previous studies have shown that the first hypervariable region (V1 loop) is immunogenic on soluble

276 ies (NAbs) that primarily targeted the first hypervariable region (V1 loop) of gp120, although SF162g

277 to potential N-linked glycosylation sites in hypervariable regions (V1 to V3) of the env gene of HIV

278 lope glycoproteins, the presence of all five hypervariable regions (V1 to V5) was required for optima

279 We used DNA from hypervariable regions (V1-V2) of 16S bacteria rRNA to de

280 n reaction was performed to amplify 16S rRNA hypervariable region V3-V4, and constructed libraries we

281 The 16s rRNA hypervariable regions V3 and V6 were amplified from Kleb

282 had greater accuracy than sequencing of the hypervariable region V4 in determining genus and species

283 The 16S RNA hypervariable region V4 was sequenced on Illumina MiSeq.

284 sequencing based on the bacterial 16 S rRNA hypervariable region V4.

285 The hypervariable region was subdivided into five domains, i

286 ehrlichiosis (HGE) with primers flanking the hypervariable region, we show differential expression in

287 gG variants containing the EHV-1 hypervariable region were able to bind chemokines and we

288 No significant differences in the hypervariable region were found when we compared p44 seq

289 Sequence diversities in the G protein second hypervariable region were observed in the duplicated reg

290 Complexity and diversity in the first hypervariable region were similar in the 2 groups.

291 d by genetic manipulation of the murine CC49 hypervariable regions were evaluated for their relative

292 bster strain clones were examined, 18 unique hypervariable regions were identified.

293 Substantial differences in the hexon hypervariable regions were noted between C68 and other k

294 ting phage binding were located in these two hypervariable regions, which are likely to be exposed on

295 analysis indicates that alternative 16S rRNA hypervariable regions will present similar challenges, w

296 tatic interactions of its positively charged hypervariable region with anionic lipids.

297 -DR alleles sharing amino acids at the third hypervariable region with DRB1*0401(shared epitope) are

298 he majority of their genomes but contained a hypervariable region with extensive divergence.

299 s identified as phage morons were located in hypervariable regions within individual SVMs, indicating

300 l seven HAdV species, confirmed the uniquely hypervariable regions within species.