ライフサイエンスコーパス: tandem repeat

1 f the Southwest Gulf Coast region, lack this tandem repeat.

2 ncing and strain typed using variable number tandem repeat.

3 eletion of a single repeat unit from a short tandem repeat.

4 osatellites and a genic bias in all detected tandem repeats.

5 ponding to complex insertions and long short tandem repeats.

6 with accumulation of short deletions within tandem repeats.

7 sions, complex insertions and long tracts of tandem repeats.

8 hed with various classes of interspersed and tandem repeats.

9 d of slightly polymorphic 52-nucleotide (nt) tandem repeats.

10 ides increase as a function of the number of tandem repeats.

11 loop, which consists of a variable number of tandem repeats.

12 kely to have generated this novel pattern of tandem repeats.

13 cytoma-amplified sequences with leucine-rich tandem repeats 1 (MASL1).

14 icopeptide repeat modules that contain three tandem repeats (3TPRs), we identify two classes of 3TPR

15 ding site for Srr1 and Srr2 was localized to tandem repeats 6-8 of the fibrinogen Aalpha chain.

16 f folded structures that can be generated by tandem repeating a simple helix-loop-helix-loop structur

17 trate that deleting one or more units of the tandem repeats abolished RocA production, reduced CovR p

18 copies of a minor variant ALOX5 promoter SP1 tandem repeat allele contributes to increased cysLT expo

19 redominantly homozygous for the DAT-VNTR two-tandem-repeat allele (2/2).

20 The one-tandem-repeat allele is over-represented in American MAL

21 hort interspersed element-variable number of tandem repeat-Alu (SINE-VNTR-Alu), subfamily-E retrotran

22 tial repeat), which is the largest number of tandem repeats among all the known insect mitochondrial

23 onditions, indicating the presence of shared tandem repeats among the cereals.

24 motifs, in which deletion, mutagenesis, and tandem repeat analyses of the luciferase assay identifie

25 ophoresis and multi-locus variable number of tandem repeat analyses.

26 Comparison with multi locus variable number tandem repeat analysis (MLVA) showed that although MLVA

27 irectly linked to multilocus variable-number tandem repeat analysis (MLVA) type.

28 related well with multilocus variable-number tandem repeat analysis (MLVA) typing data, with only thr

29 oresis (PFGE) and multilocus variable number tandem repeat analysis (MLVA) were conducted on all isol

30 ophoresis (PFGE), multilocus variable number tandem repeat analysis (MLVA), multilocus sequence typin

31 ) typing and with multilocus variable-number tandem repeat analysis (MLVA).

32 ism (SNP) and multiple locus variable number tandem repeat analysis (MLVA).

33 Spectral karyotyping and short tandem repeat analysis of the UISO cells matched the ori

34 notyped using multiple-locus variable-number tandem repeat analysis typing.

35 1 was genotyped using a combination of short tandem repeat analysis, triplet repeat-primed polymerase

36 Multilocus variable number of tandem repeats analysis (MLVA) is a highly discriminator

37 echnique MLVA (multiple loci variable-number tandem repeats analysis) can identify complex infections

38 ation of multiple multilocus variable-number tandem-repeat analysis (MLVA) and P1 types throughout th

39 CR-based methods, multilocus variable-number tandem-repeat analysis (MLVA) and spa typing.

40 date has compared multilocus variable-number tandem-repeat analysis (MLVA) and whole-genome sequencin

41 strains using multiple-locus variable-number tandem-repeat analysis (MLVA) compared to typing using P

42 ibotyping and multiple-locus variable-number tandem-repeat analysis (MLVA) of selected strains was pe

43 d seven different multilocus variable-number tandem-repeat analysis (MLVA) profiles.

44 ough PFGE and multiple-locus variable-number tandem-repeat analysis (MLVA) suggested that all isolate

45 In this study, multilocus variable-number tandem-repeat analysis (MLVA) was performed on C. diffic

46 protein (P1) and multilocus variable-number tandem-repeat analysis (MLVA).

47 confirmed by multiple-locus variable-number tandem-repeat analysis (MLVA).

48 ork for cell line annotation linked to short tandem repeat and single nucleotide polymorphism profile

49 PGR (RPGR(ORF15)), carrying multiple Glu-Gly tandem repeats and a C-terminal basic domain of unknown

50 A-forming motifs coverage by including short tandem repeats and adds key visualization tools to compa

51 osatellites and a genic bias in all detected tandem repeats and confirm that chimpanzee herpesvirus 1

52 Here we showed that DNA tandem repeats and double-strand breaks are necessary an

53 rther classified them into groups, including tandem repeats and Staphylococcus aureus repeat (STAR)-l

54 INS-VNTR (insulin-variable number of tandem repeats) and AIRE (autoimmune regulator) have bee

55 3 distinct domains: the amino terminal, the tandem repeat, and the carboxyl terminal domain, with ea

56 de variants, insertions and deletions, short tandem repeats, and copy number variants.

57 ear-centromeric satellite DNAs consisting of tandem repeats, and multiple species of noncoding RNAs w

58 has evolved in enhancing promoter strength, tandem repeats, and/or expression specificity, leading t

59 Long arrays of near-identical tandem repeats are a common feature of centromeric and s

60 based" approach in which modules composed of tandem repeats are aligned to identify repeat-specific f

61 Short tandem repeats are among the most polymorphic loci in th

62 Both tandem repeats are entirely contained within the transcr

63 Simple tandem repeats are highly variable genetic elements and

64 Like DXZ4, the tandem repeats are packaged into Xi-specific CTCF-bound

65 ind that cells producing a protein with many tandem repeats are relatively resistant to killing by ma

66 of repetitive DNA (transposable elements and tandem repeats) are primarily responsible for genome siz

67 Major Repeat Sequences, a class of tandem repeats, are assembled into an intermediate chrom

68 me are organised in two 4 Mbp-long arrays of tandem repeats arranged in head-to-tail fashion separate

69 Our results support the general concept that tandem repeat arrays can engage in arms-race-like strugg

70 In this study, we assess the impact of large tandem repeat arrays on the recombination rate landscape

71 and frequent expansions and contractions of tandem repeat arrays.

72 interspersed repetitive unit-variable number tandem repeat assay and other typing methods.

73 trains were genotyped according to the short tandem repeats assay.

74 ibotyped, and multiple-locus variable-number tandem-repeat assay (MLVA) subtyping was performed on cl

75 NAs, which are then redundantly encoded into tandem repeats by 'rolling-circle' reverse transcription

76 duction, the quelling pathway also maintains tandem repeats by regulating homologous recombination.

77 y rat neuronal cultures, the introduction of tandem repeats carrying the 331-369-residue Gln/Asn regi

78 A tRNA containing tandem repeat composed of at least three 7.6-kb GC-rich

79 vice for C. glabratathat targets polymorphic tandem repeat-containing loci has recently been develope

80 istance-conferring haplotypes carry up to 10 tandem repeat copies of a 31-kb DNA segment, and three d

81 ns in mammalian cells, which have dimeric or tandem-repeated CRDs enabling multivalency for various f

82 DAT) contains a 38-base pair variable number tandem repeat (DAT-VNTR); alleles have either one or two

83 interspersed repetitive-unit-variable-number tandem-repeat data.

84 olate and if the MLVA genotypes had a summed tandem-repeat difference of </= 2.

85 of single nucleotide variants (SNVs), summed tandem-repeat differences (STRDs), and locus variants (L

86 mes and are composed of long tracks of short tandem repeat DNA sequences bound by a unique set of pro

87 CAT7 contains a unique tandem repeat domain that shares high sequence similarit

88 hich bears two bacterial immunoglobulin-like tandem repeat domains and a C-terminal cell wall-anchori

89 aches primarily using antibodies against the tandem repeat domains of MUC16 (e.g., oregovomab and aba

90 ludes a modular architecture, including five tandem repeat domains, with the AIM sequence presented a

91 ribe the crystal structures of the SPRY1 and tandem-repeat domains at 1.2-1.5 A resolution, which rev

92 tors (TALEs) recognize their DNA targets via tandem repeats, each specifying a single nucleotide base

93 rain of Mmc using genome transplantation and tandem repeat endonuclease coupled cleavage (TREC) with

94 By explicitly modeling tandem repeat evolution, ClassTR helps to improve our un

95 y heterogeneous or mixed by using a model of tandem repeat evolution.

96 The increased length results from tandem repeat expansions and an unusual 13 kb IR-SSC bou

97 sertions, small indels (10-50 bp), and short tandem repeat expansions and contractions.

98 These non-coding tandem repeat expansions trigger the production of unusu

99 e methylation was particularly dramatic over tandem repeat families, including ribosomal DNA (rDNA) r

100 Moreover, Coa encompasses C-terminal tandem repeats for binding to fibrinogen, whereas vWbp h

101 otide polymorphisms and five variable number tandem repeats from 30 candidate genes in 692 available

102 Galectin-4 is a tandem-repeat galectin characterized by two carbohydrate

103 , structural characterization of full-length tandem-repeat galectins has remained elusive.

104 mechanism of carbohydrate recognition among tandem-repeat galectins.

105 ALOX5 promoter SP1 tandem repeat genotype may be a risk factor for worse as

106 rspersed repetitive units-variable number of tandem repeats genotyping to identify mycobacterial hete

107 erspersed repetitive unit-variable number of tandem repeats genotyping.

108 We did variable-number-of-tandem-repeat genotyping and whole-genome sequencing of

109 ains of multidomain proteins with homologous tandem repeats have divergent sequences, probably as a r

110 omposed primarily of two related families of tandem repeats, Human Satellites 2 and 3 (HSat2,3).

111 r than single-domain enzymes, they appear as tandem repeats in large polypeptides we refer to as CSRP

112 Subtelomeric repeats with characteristics of Tandem Repeats in Miniature (TRIM) elements were identif

113 evel the two alleles differ in the number of tandem repeats in the ORF.

114 ion signature composed of short deletions in tandem repeats; in the specific case of ribonucleotide-i

115 rprisingly, we find that during refolding of tandem repeats, independent of sequence identity, more t

116 enrichment of long arrays of near-identical tandem repeats, known as satellite DNAs, which offer a l

117 y transient interaction with lipid vesicles, tandem-repeat LBDs, often used as lipid biosensors, tend

118 uman X-linked macrosatellite DXZ4 is a large tandem repeat located at Xq23 that is packaged into hete

119 goes phase variation mediated by 7-base pair tandem repeats located within its promoter region.

120 pped or partially misaligned reads at simple tandem repeat loci.

121 robust comparison of large numbers of simple tandem repeat loci; however, analysis of their variation

122 ncy of mutation at the mouse expanded simple tandem repeat locus Ms6-hm was established in DNA sample

123 lymorphism is a one-unit deletion in a three-tandem-repeat locus upstream of the rocA gene encoding a

124 The human genome contains numerous large tandem repeats, many of which remain poorly characterize

125 ailable genotypes on approximately 400 short tandem repeat markers using a general pedigree variance

126 e shown that multidomain proteins containing tandem repeats may form stable misfolded structures.

127 erspersed repetitive unit-variable number of tandem repeat (MIRU-VNTR) typing of pairs of isolates ta

128 interspersed repetitive-unit-variable-number tandem repeat (MIRU-VNTR) typing were obtained routinely

129 erspersed repetitive units - variable number tandem repeats (MIRU-VNTR), and PyroTyping.

130 nterspersed repetitive units-variable-number tandem repeats (MIRU-VNTR).

131 interspersed repetitive-unit-variable-number tandem-repeat (MIRU-VNTR) analysis.

132 osis terminating at both ends with arrays of tandem repeats (mitochondrial telomeres) is replicated.

133 hly conserved and previously uncharacterized tandem repeat motifs at the C terminus, herein designate

134 ny one of these three drugs, expanded simple tandem repeat mutation frequencies were significantly el

135 ertions or deletions, premature termination, tandem repeat, nonstop, and missense mutations).

136 SWEETs are heptahelical proteins carrying a tandem repeat of 3-TM separated by a single TM.

137 n of the switch 2 domain of K-Ras encoding a tandem repeat of amino acids G60_A66dup in a child with

138 binds polyadenosine RNA primarily through a tandem repeat of CCCH Zn fingers.

139 The enzymatically active tandem repeat of four SN domains is crucial for targetin

140 cosylation was furthermore demonstrated on a tandem repeat of MUC16 and interferon alpha2b.

141 o half-life of an antibody Fab domain, and a tandem repeat of the monoFc further prolonged the half-l

142 To do so, we fabricate a tandem repeat of the receptor that is destabilized (unfo

143 We report the identification of a tandem repeat of the tetratricopeptide repeat (TPR) moti

144 e brain formation disorders are located on a tandem repeat of two doublecortin domains.

145 te expansion diseases are caused by unstable tandem repeats of 3-10 nucleotides that become pathogeni

146 e primates, from macaques to humans, contain tandem repeats of a 10-residue sequence, whereas Liat1 p

147 The R domain, tandem repeats of a 27-residue peptide that bind fibrino

148 s defined catalytic domains but contains two tandem repeats of a distinctive module of unknown functi

149 recursor protein that contains as many as 12 tandem repeats of alpha-hairpinin-like peptides.

150 Telomeres consist of tandem repeats of DNA sequences at the end of chromosome

151 Trinucleotide repeats (TNRs) consist of tandem repeats of Gs and As and therefore are hotspots o

152 recombinant SpA, and optimally required five tandem repeats of its Ig-binding domains.

153 ed by the fusion of fluorescence tags to the tandem repeats of ML1N.

154 WASp homology domain 2 (WH2) nucleators, use tandem repeats of monomeric actin-binding WH2 domains to

155 cell wall protein family, we show the three tandem repeats of the CWB2 motif are essential for corre

156 collapsed single-stranded DNA molecule with tandem repeats of the DNA probe.

157 TH is composed of 4 tandem repeats of the histone H2A N-terminal sequence, i

158 NGTGGV, required for germline expression and tandem repeats of the motif YAACYGY, which enhance DUO1

159 lasmids with fewer than 16 TRs or those with tandem repeats of the MREs are maintained inefficiently,

160 ies for mapping phosphorylation sites on the tandem repeats of the RNA polymerase II CTD.

161 Human telomeric DNA consists of tandem repeats of the sequence 5'-TTAGGG-3' that can fol

162 Human telomeric DNA consists of tandem repeats of the sequence 5'-TTAGGG-3', including a

163 Telomeric DNA consists of tandem repeats of the sequence d(TTAGGG) that form G-qua

164 associated protein 9 (dCas9) fused with four tandem repeats of the transcriptional activator VP16 (VP

165 In vertebrates, telomeres are composed of tandem repeats of the TTAGGG sequence that are bound by

166 hat a single copy of tTA(VP64) carrying four tandem repeats of the VP16 domain constitutively express

167 which carried long runs of degenerate short tandem repeats, often several kilobases in length, embed

168 Here we report a novel transfer RNA (tRNA) tandem repeat on human chromosome 1q23.3 that shows exte

169 The non-B DNA structures formed by short tandem repeats on the nascent strand during DNA replicat

170 red from personal genomes by profiling short tandem repeats on the Y chromosome (Y-STRs) and querying

171 Variable number of tandem repeats or VNTRs are polymorphic TR loci in which

172 R scaffold is a long, single-stranded DNA of tandem repeats, originating from the rolling circular am

173 f dopamine transporter SLC6A3 40 bp variable tandem repeat polymorphism (VNTR) and for 6/6 homozygote

174 +3A>T mutation, which extends from the short tandem repeat polymorphism D6S282 to c.1013G>A (rs434102

175 alysis, we associated the ALOX5 promoter SP1 tandem repeat polymorphism genotype (rs59439148) with as

176 Secondarily, variation at a variable number tandem repeat polymorphism in the dopamine transporter g

177 nts without the 10-repeat allele of the DAT1 tandem repeat polymorphism possess an enhanced attention

178 ought to determine if the ALOX5 promoter SP1 tandem repeat polymorphism was associated with changes i

179 whereas the thymidylate synthase rs34743033 tandem repeat polymorphism was predictive of stomatitis

180 ze the effects of the 3'-UTR variable-number-tandem-repeat polymorphism of the gene (DAT1, SLC6A3) en

181 were genotyped for two putatively functional tandem repeat polymorphisms of the dopamine transporter

182 Whereas inverted and tandem repeats predominated in alpha-herpesviruses, gamm

183 Microsatellites-simple tandem repeats present at millions of sites in the human

184 Here, we developed STR-FM, short tandem repeat profiling using flank-based mapping, a com

185 had been previously typed by variable-number tandem repeat profiling.

186 ry, immunofluorescence microscopy, and short tandem repeat profiling.

187 es a type 1 secretion (T1S) system to export tandem repeat protein (TRP) effectors and demonstrated t

188 Ehrlichia chaffeensis secretes tandem repeat protein (TRP) effectors that are involved

189 d activation was induced by three ehrlichial tandem repeat protein (TRP) effectors, with TRP120 induc

190 computational methods for de novo design of tandem repeat protein architectures driven purely by geo

191 Unlike previous approaches to tandem repeat protein engineering, our design procedure

192 The overall architecture of tandem repeat protein structures--which is dictated by t

193 mutagenesis and exploiting the simplicity of tandem-repeat protein structures, we delineate a network

194 ently we have determined that E. chaffeensis tandem repeat proteins (TRPs) are type 1 secreted effect

195 ly, molecular interactions of E. chaffeensis tandem repeat proteins 47 and 120 (TRP47 and -120) and t

196 Tandem repeat proteins, which are formed by repetition o

197 on of a gap by two Top1 cleavage events, the tandem repeat provides complementarity that promotes rea

198 ized by the presence of a 35-bp mtDNA D-loop tandem repeat proximal to the 5' end, more than 95% of s

199 organism's Vsa proteins contain an extensive tandem repeat region.

200 of the control region is made up of a large tandem-repeat region, which has a novel pattern not prev

201 The tandem-repeats region of P. albomaculatus consists of 53

202 A vaccine containing tandem repeats, region III, and thrombospondin type-I re

203 oline-rich proteins contain large regions of tandem repeats, relatively young proteins like histatins

204 Nearly single base resolution of short tandem repeats relevant to human identification is accom

205 Glycopeptide structures of the tandem repeat sequence of mucin MUC1 of epithelial tumou

206 tomate characterization of local centromeric tandem repeat sequence variation we have designed Alpha-

207 fically recognise the double-stranded TTAGGG tandem repeat sequence.

208 ecursor is glycosylated and has a 10-residue tandem repeating sequence xxCxGxYCxG, with regularly spa

209 Knobs can be made of two different tandem repeat sequences (TR-1 and 180-bp repeat), and bo

210 Large tandem repeat sequences have been poorly investigated as

211 We then examine tandem repeat sequences known for their ability to form

212 neering target RNAs with large insertions of tandem repeat sequences that are bound by protein-based

213 Microsatellites are short tandem repeat sequences that are highly prone to expansi

214 oted recruitment of the Daxx/Atrx complex to tandem repeat sequences, including retrotransposons and

215 rspersed repetitive units-variable number of tandem repeat signature) lineage 2/Beijing MDR strain im

216 h was determined by direct sequencing, short tandem repeat (STR) assay and Southern blotting.

217 tic (ME) separation for rapid forensic short tandem repeat (STR) forensic profiling in a single dispo

218 s (UAE) were typed across 15 autosomal short tandem repeat (STR) loci (D8S1179, D21S11, D7S820, CSF1P

219 Zambia and additionally genotyped four short tandem repeat (STR) loci that flank the lactase enhancer

220 with the usual cell authentication by short tandem repeat (STR) markers.

221 A short tandem repeat (STR) typing method is developed for foren

222 Short tandem repeat (STR) variants are highly polymorphic mark

223 Short tandem repeat (STR) variation has been proposed as a maj

224 microdeletion and a highly polymorphic short tandem repeat (STR) within its breakpoints.

225 Functional short tandem repeats (STR) are polymorphic in the population,

226 e authentication, but only one method (short tandem repeat [STR] profiling) has been the subject of a

227 Short tandem repeats (STRs) are found in many prokaryotic and

228 Short tandem repeats (STRs) are highly mutable genetic element

229 Short tandem repeats (STRs) are highly variable elements that

230 Short tandem repeats (STRs) are hyper-mutable sequences in the

231 Short tandem repeats (STRs) are implicated in dozens of human

232 Short tandem repeats (STRs) are mutation-prone loci that span

233 Short tandem repeats (STRs) have a wide range of applications,

234 genome-wide SNPs and the other with 13 short tandem repeats (STRs) used in forensic applications-we f

235 00 biallelic markers and 19 chromosome short tandem repeats (STRs) were genotyped to produce a high-r

236 ites are multi-allelic and composed of short tandem repeats (STRs) with individual motifs composed of

237 Short tandem repeats (STRs), also known as microsatellites, ar

238 Identifying large expansions of short tandem repeats (STRs), such as those that cause amyotrop

239 ome-wide survey of the contribution of short tandem repeats (STRs), which constitute one of the most

240 demonstrated that galectin (Gal)-8, from the tandem-repeat subgroup, exerts two well-defined effects

241 rminal p50 domain is sufficient to stimulate tandem repeat synthesis and bridge the RNP catalytic cor

242 catalytic core has a relatively low rate of tandem repeat synthesis but high processivity of repeat

243 The rate of tandem repeat synthesis is enhanced by p50-dependent rec

244 he analysis of a model protein of a spectrin tandem repeat that exemplified an intuitive stability pr

245 a concatemer containing tens to hundreds of tandem repeats that are complementary to the circular te

246 e we identified further binding sites in the tandem repeats that are found within the long TIRs.

247 Telomeres consist of DNA tandem repeats that recruit the multiprotein complex she

248 itrations, we show that binding of the FF4-6 tandem repeat to the PCTD requires simultaneous phosphor

249 Tandem repeats (TRs) are stretches of DNA that are highl

250 DNA tandem repeats (TRs) are ubiquitous genomic features whi

251 Tandem repeats (TRs) have extremely high mutation rates

252 ng an important source of genetic variation, tandem repeats (TRs) remain poorly studied due to techni

253 Short tandem repeats (TRs), or microsatellites, are often used

254 4-1BB also can bind to the tandem repeat-type lectin galectin-9 (Gal-9), and signal

255 icance of human lectins with homodimeric and tandem-repeat-type displays.

256 and to spoligotyping and variable number of tandem repeats typing before treatment and after recurre

257 rspersed repetitive units-variable number of tandem repeats typing.

258 The length of the tandem repeat unit varies from as few as 11 amino acids

259 effect of rs315952 was independent from the tandem repeat variant in IL1RN.

260 -4.90), and, repeat variants variable number tandem repeat (VNTR) 4 DRD4 (odds ratio: 1.66; confidenc

261 w that two PER3 mutations, a variable number tandem repeat (VNTR) allele and a single-nucleotide poly

262 ed repetitive-unit (MIRU-15)-variable-number tandem repeat (VNTR) analysis.

263 ions, including the promoter variable number tandem repeat (VNTR) and 2 single nucleotide polymorphis

264 Variable-number tandem repeat (VNTR) and spoligotyping analyses were use

265 nts with mutations in the variable number of tandem repeat (VNTR) domain of carboxyl ester lipase (CE

266 ified in the AKT1 gene a new variable number tandem repeat (VNTR) marker associated with baseline str

267 ation Study (GWAS) explosion Variable Number Tandem Repeat (VNTR) polymorphism exploration has seemin

268 fect of a newly characterized variant number tandem repeat (VNTR) polymorphism in AKT1 [major alleles

269 racting effects of APZ and a variable number tandem repeat (VNTR) polymorphism in DAT1/SLC6A3 (the ge

270 his region are linked with a variable number tandem repeat (VNTR) polymorphism in the first exon of A

271 nts were typed using a novel variable-number tandem repeat (VNTR) scheme and an automated repetitive-

272 5 kb), GC-rich (>80%) coding variable-number tandem repeat (VNTR) sequence in the MUC1 gene encoding

273 ndependent study reporting a variable number tandem repeat (VNTR) within the same PCSK6 locus to be a

274 me increased resolution over variable number tandem repeat (VNTR)-based clustering, it was insufficie

275 We used variable-number tandem repeats (VNTR) for fingerprinting of respiratory

276 focused on a 40-base pair variable number of tandem repeats (VNTR) polymorphism located in the 3'-unt

277 gene (3'-UTR) and intron8 variable number of tandem repeats (VNTR) polymorphisms of the DAT (SLC6A3)

278 neck region possessing a variable number of tandem repeats (VNTR).

279 ecently developed multilocus variable-number tandem-repeat (VNTR) analysis (MLVA) method for the mole

280 based methods and multilocus variable-number tandem-repeat (VNTR) analysis (MLVA) procedures.

281 (WGST), (ii) multiple-locus variable-number tandem-repeat (VNTR) analysis (MLVA), (iii) clustered re

282 e evaluated the potential of variable-number tandem-repeat (VNTR) analysis.

283 n humans, a primate-specific variable-number tandem-repeat (VNTR) polymorphism (4 or 5 repeats 54 nt

284 Variable-number tandem-repeat (VNTR) polymorphisms are ubiquitous in bac

285 and other RNAs, such as SINE/variable-number tandem-repeat (VNTR)/Alu (SVA) elements, in trans.

286 Variable number tandem repeats (VNTRs) constitute a relatively under-exa

287 MUC1 is characterized by variable number tandem repeats (VNTRs) that bind the lectin galectin-3;

288 The region of ompA containing 13 tandem repeats was sequenced, revealing only seven share

289 1B -31C/T (rs1143627) and IL1RA 86-base-pair tandem repeat were analyzed in 871 patients (DF = 384, D

290 Tandem repeats were frequently found in the intergenic r

291 Several new tandem repeats were identified and physically mapped usi

292 lite specific genotyping method, we analyzed tandem repeats, which are known to be highly variable wi

293 ic DNA of vertebrates consists of d(TTAGGG)n tandem repeats, which can form quadruplex DNA structures

294 e a specific genotype based on the number of tandem repeats within each locus.

295 h showed multiple insertions or deletions of tandem repeats within this locus for a number of specime

296 e polymorphisms (Y-SNPs) and seventeen short tandem repeat (Y-STR) loci.

297 ic pedigree searches with Y-chromosome short tandem repeat (Y-STR) profiling in large-scale crime inv

298 served open reading frame composed solely of tandem repeats, yet it is still unclear why cells utiliz

299 ene encodes a protein with a highly variable tandem-repeat zinc finger (ZF) DNA-binding domain that p

300 ion of hotspot sequence motifs by a variable tandem-repeat zinc finger domain in the protein.