ライフサイエンスコーパス: kb

1 Pol II elongation rates of 2.4-3.0 kb/min were observed, approximately twice as fast as ear

2 ates using runs of homozygosity with a 1,000-kb window (correlation = 0.94 with the estimates provide

3 ecruits PR to the CK5 promoter near the -1.1 kb essential PRE, and also to a proximal region near -13

4 estingly, RARalpha was recruited to the -1.1 kb PRE and the -130 bp PRE/RARE regions with P4, but not

5 eletion analysis, we identified a region 1.1 kb upstream of the CK5 transcriptional start site that i

6 a M25 protein, and confirmed that a late 3.1 kb mRNA encodes a 130 kDa M25 tegument protein.

7 opsin-2 (ChR2) gene under the control of a 1 kb L7/Pcp2 promoter.

8 a spliced and polyadenylated lncRNA about 1 kb in length that is found in both the nuclear and cytop

9 ker plasmids which produce both 100 bp and 1 kb DNA ladders when digested with two common restriction

10 proximately 5 bp) and long ( approximately 1 kb) genomic distances, showing that mutation drives GC c

11 A single methylation event 1 kb upstream of the DNA involved in homologous recombinat

12 pecies, and dependent on ssRNA lengths (>/=1 kb).

13 ancer class utilizing a Hi-C dataset with <1 kb resolution.

14 s telomeres from all chromosome ends from <1 kb to 18 kb using small amounts of input DNA.

15 ic exchange often incorporates regions of <1 kb, and allelic gene conversion changes the frequency of

16 Sanger sequencing of 1 kb centered on V1 was performed in the remaining 4 NCMD

17 s 550 bp upstream from the start codon, or 1 kb into the coding sequence.

18 for the two plasmids to produce 100 bp or 1 kb ladders for 1000 gels.

19 resolves repetitive structures longer than 1 kb, representing the largest repeat family and immune ge

20 atterns were predominantly observed within 1 kb from the transcription start site, where both histone

21 1-kb-long nuclear loci and sequenced them in a parallel-ta

22 The PPAR agonists also activated a 1-kb reporter containing the 863-nt deletion region.

23 We amplified four c. 1-kb-long nuclear loci and sequenced them in a parallel-ta

24 gle-nucleotide polymorphism approximately 10 kb downstream of myosin regulatory light chain interacti

25 ostly through large segmental deletions (>10 kb).

26 To examine fine-scale (order 10 kb) patterns of recombination in the DO, we overlaid put

27 ore technologies (ONT) produce reads over 10 kb in length, which have enabled high-quality genome ass

28 Rgamma2 promoter and an enhancer sequence 10 kb upstream that forms at the onset of PPARgamma2 expres

29 a specific transposable element (Tn4401, 10 kb).

30 gene from 15 kb upstream of its 5'-end to 10 kb downstream of its 3'-end to determine SOX9 interactio

31 h can provide accurate sequences of up to 10 kb, allowing us to identify rare mutations below the det

32 Linkage disequilibrium decays within 10 kb (based on the provisional genetic locations), consist

33 n for predicting crossover formation over 10-kb windows.

34 novel DREs located -70 kb upstream and +100 kb downstream from the NGB gene.

35 losely stacked consecutive approximately 100 kb loops.

36 we find that the rates of large-scale (>100 kb) de novo copy-number variants (CNVs) are significantl

37 We identified 33 hotspots of large (>100 kb) tandem duplications, a mutational signature associat

38 Large (>100 kb), rare (<1% in the population) copy number variants (

39 ations, spanning large genomic regions (>100 kb).

40 Rare CNVs with >/= 100 kb length were identified using a stringent strategy bas

41 hisms (SNPs), corresponding to 1 marker/100 kb distributed across the genome for sex-linked variatio

42 otide polymorphisms (SNPs) in the region 100 kb upstream and downstream of UBAC2.

43 g to be examined at a scale of less than 100 kb, and chromosome structures to be validated.

44 Each yielded contigs longer than 100 kb, phase blocks longer than 2.5 Mb, and scaffolds longe

45 of the primate-specific ERV-9 LTR in the 100 kb human beta-globin gene locus.

46 Three of the six genes within 100 kb of the lead SNP are expressed in the dorsolateral pre

47 The highlighted locus is a 100-kb region containing the interferon gamma-inducible prot

48 1q42.1 that encompasses a approximately 100-kb region spanning the PARP1 gene.

49 e replacement of genomic DNA with long (>100-kb) synthetic DNA, through the in vivo excision of doubl

50 also lead to a refined ERBB2 amplicon of 106 kb and show that several cases of amplifications are com

51 e with destabilized GFP, we identified an 11-kb genomic region 3' of the Nkx3.1 transcription start s

52 at the transcriptional level through the 11-kb region despite functional AR in the nucleus.

53 ugh androgen receptor (AR) binding to the 11-kb region in both normal luminal cells and CARNs and dis

54 ts per ml when vector genomes harboured a 12 kb insert, approximately twice that reported for lentivi

55 ously unidentified cis-regulatory element 12 kb upstream of HLA-G with enhancer activity, Enhancer L

56 ed cell lines at rates similar to that of 12 kb YCps.

57 Here, we analyze approximately 120 kb of exome-captured Y-chromosome DNA from a Neandertal

58 The enhancer located 135 kb upstream of the ARID5B gene locus is activated under

59 ow LD interspersed with an average LD of 139 kb.

60 mitochondrial (mt) genomes of anisakids (~14 kb) from different fish hosts in multiple countries, in

61 ty of which contained complex arrays of a 14-kb satellite repeat or its 1.2-kb subunit.

62 y chromatin immunoprecipitation with the -14-kb Pu.1 or +37-kb Cebpa enhancers after stable expressio

63 bacterial artificial chromosomes (BACs; 144 kb deletion) have been achieved by this method.

64 repair deficiencies and hyper-resection 0.15 kb from the DSB that was dependent on the nuclease activ

65 OX9 antibody, covering the Ctgf gene from 15 kb upstream of its 5'-end to 10 kb downstream of its 3'-

66 -generation sequencing at approximately 0.15-kb resolution.

67 -linked variants to sample approximately 150 kb of nuclear sequence, in addition to complete mitochon

68 n of B. turicatae genes localized on the 150 kb linear megaplasmid during the tick-mammalian transmis

69 ify association with a noncoding variant 151 kb from the gene encoding the cardiac-specific transcrip

70 adapted this method to rapidly deliver a 152 kb herpes simplex virus 1 genome cloned in yeast into ma

71 ragments comprising the HSV-1 strain KOS 152 kb genome.

72 nce that chromosomal looping, bypassing 1524 kb of linear genome, connects Auts2 to the Caln1 gene lo

73 from peak signal to prioritised gene of 153 kb.

74 METHODS AND We sequenced a approximately 158 kb region encompassing PRRX1 in 962 individuals with and

75 This process results in a 16 kb cluster that shares no sequence identity, regulation

76 e that transgenically express the entire 160-kb human C19MC locus or lentivirally express C19MC miRNA

77 position of the large-size PB transposon (17 kb) encoding the full-length DYS and green fluorescence

78 For example, expression of a 17-kb O-PS gene cluster from the highly virulent Francisell

79 Rs17518584 is located about 170 kb upstream of the transcription start site of the major

80 ling, we show that CEBPA is located in a 170-kb topological-associated domain that contains 14 potent

81 e homogenates, we assembled a contiguous 174-kb genome sequence containing 128 unique predicted open

82 es from all chromosome ends from <1 kb to 18 kb using small amounts of input DNA.

83 The 18-kb Xist long noncoding RNA (lncRNA) is essential for X-c

84 trait locus on canine chromosome 1 to a 188-kb critical interval that encompasses SMOC2.

85 ys more than 10(8) DNA fragments, each 0.2-2 kb in size, for their ability to drive transcription aut

86 7095681 at 10q25.3, intron of SHTN1 and 27.2 kb downstream of VAX1, Pmeta = 3.80E-9, OR = 0.64) in Ch

87 functional analysis of HMS1, a region of 9.2 kb in chromosome 3 of Drosophila mauritiana, which resul

88 her, we programmed 4,342 overlapping 1 and 2 kb deletions that tiled 206 kb centered on HPRT1 (includ

89 ng-strand templates at rates between 1 and 2 kb min(-1).

90 nt required for gene regulation was mapped 2 kb upstream of the 12-HETER1 transcriptional start site.

91 We determined sequences extending nearly 2 kb upstream of the transcription start site for 68 allel

92 icted to a chromatin domain extending only 2 kb either side of the DSB, and BRD2 does not spread into

93 rrays of a 14-kb satellite repeat or its 1.2-kb subunit.

94 in two variants, one consisting of a large 2-kb transcript composed of four exons and one consisting

95 After sequencing 2-kb promoter regions of 472 genes in 410 healthy adults,

96 als, meiotic recombination occurs at 1- to 2-kb genomic regions termed hotspots, whose positions and

97 AHR hotspots, PRS1 and PRS2, separated by 20 kb and located within the low-copy repeats NF1-REPa and

98 one intergenic SNP (rs11901793), which is 20 kb upstream of CXCR7 gene on chromosome 2, was associate

99 stance gene, mecA, is carried on a large (20 kb to > 60 kb) genomic island, staphylococcal cassette c

100 6 protein, is encoded by a gene located ?20 kb downstream from SLURP1.

101 of euchromatic TEs, and can extend up to 20 kb.

102 The discovery of approximately 20-kb gene clusters containing a family of paralogs of tRNA

103 01-mediated inversion of an approximately 20-kb sequence near the cps locus.

104 DNA molecules, typically between 100 and 200 kb in size and encoding circa 80-250 genes.

105 (ASTN2, DPP4 and MAST4) and one is found 200 kb upstream of SHH.

106 We recode 200 kb of the Salmonella typhimurium LT2 genome through a pr

107 A 200-kb spanning region of 1q12 previously highlighted in a g

108 r for the expression of an approximately 200-kb polycistronic transcript within the imprinted Dlk1-Di

109 Hi-C data for budding yeast and identify 200-kb scale TADs, whose boundaries are enriched for transcr

110 We traced association signals in 200-kb regions surrounding these genes in 84,813 CAD cases a

111 rlapping 1 and 2 kb deletions that tiled 206 kb centered on HPRT1 (including 87 kb upstream and 79 kb

112 t, is a major contributor of the 16p11.2 220 kb BP2-BP3 CNV-associated neurodevelopmental phenotypes.

113 plication carriers of the distal 16p11.2 220 kb BP2-BP3 interval showed that these rearrangements are

114 ad size and body weight, a second distal 220 kb BP2-BP3 CNV is likewise a potent driver of neuropsych

115 y efficient in deleting the approximately 23 kb of intervening genomic sequences.

116 s an enormous design space (1043 possible 23 kb constructs), from which an algorithm-guided 192-membe

117 onas applanata In fact, at approximately 230 kb, the ptDNA of P. uvella represents the largest plasti

118 Pathogenic meningococci have acquired a 24 kb capsule synthesis island (cps) by horizontal gene tra

119 A haplotype block across a 24-kb region within the TOX2 gene reached genome-wide signi

120 First, the entire 24-kb capsular polysaccharide biosynthesis locus, which is

121 The 240-kb SPN3US genome shares a core set of 91 genes with varp

122 ves direct iterative recombineering of 10-25 kb synthetic DNA constructs which are assembled in yeast

123 ty to the promoter-proximal approximately 25 kb is observed.

124 on complexes was blocked within the first 25 kb of genes.

125 s mouse Ebeta element and its neighboring 25 kb region by independently tethering this TF without coi

126 d the error-frequency was reduced from 14.25/kb to 0.53/kb.

127 ve earlier shown that a locus within an 250 kb haplotype block spanning the 5' untranslated region r

128 We construct a weighted network with 250-kb genomic regions as nodes and Hi-C interactions as edg

129 sms (tag-SNPs) within a region spanning 263 kb including SPINK5 ( 61 kb) in n=722 (n=367 food-allerg

130 events to intervals with a median size of 28 kb.

131 The approximately 28-kb 3' regulatory region (3'RR), which is located at the

132 ell-specific Gata3 enhancer (Tce1) lying 280 kb downstream from the structural gene and demonstrated

133 the ~48 kb risk haplotype) that spanned ~280 kb forming one risk haplotype carried by 35 % of the GSD

134 d vascular short telomere abundance (4.2-1.3 kb) 43.0 +/- 1.5 vs. 55.1 +/- 3.8%) in aged vs. young of

135 le-stranded RNA genome of approximately 13.3 kb encapsidated by multiple copies of the nucleoprotein

136 presentative M. musculus sequence (the 16.3 kb mitochondrial genome), at 100%, 100%, and 96.7% conse

137 By crossbreeding 2.3 kb Col 1a1-Cre mice with Fam20C (flox/flox) mice, we cre

138 with Fam20C (flox/flox) mice, we created 2.3 kb Col 1a1-Cre;Fam20C (foxl/flox) (cKO) mice, in which F

139 fference = 0.003), and also mapped close (~3 kb) to an ENCODE skin-specific enhancer region.

140 -0.127, p < 0.001) and directly with %LTL<3 kb (Pearson's r = 0.085; p = 0.001).

141 and the abundance of short telomeres (%LTL<3 kb).

142 plate (>300 nt) within a longer (545 bp or 3 kb) duplex.

143 GAC motifs in the upstream sequence within 3 kb of the transcription start site.

144 ority of open chromatin regions lie within 3 kb upstream of a transcription start site in all species

145 actional proviral expression of HIV RNA (1.3-kb fragment of p6, protease, and reverse transcriptase)

146 ance determinants via incorporation of a 5.3-kb mega cassette harboringmsrDandmefE Furthermore, durin

147 CFHR3 hybrid gene secondary to a de novo 6.3-kb deletion that arose through microhomology-mediated en

148 r unusually large genomes ( approximately 30 kb) associated with low mutation rates.

149 erted either in tandem or at a distance (>30 kb).

150 Large genetic deletions of 30 kb encompassing the entire DDX4 locus were also created

151 In contrast, a 30-kb deletion that eliminates APOBEC3B and creates an APOB

152 ility to resolve genomic loci spaced by <300 kb.

153 ments at approximately 80% fidelity and a 31 kb plasmid from five fragments at approximately 50% fide

154 n rates, and histone modifications) in +/-32 kb of these ERVs' integration sites and in control regio

155 mbinant inbred strains, we found that the 33-kb Ltab-Ncr3 haplotype in MHC-III was linked to the indu

156 no origin, and a homozygous approximately 34 kb deletion affecting exons 3-9 was observed in two fami

157 nome sequencing to discover a pathogenic 346 kb inversion in multiple probands, and cDNA sequencing a

158 Here, starting with the 35 kb Salmonella pathogenicity island 1 (SPI-1), we elimina

159 f the deletions revealed a approximately 350 kb critical region on chromosome 6q16.1 that encompasses

160 36% sequence identity), which is located 365 kb downstream of CAPN14.

161 sequilibrium with candidate genes within 366 kb.

162 y conserved enhancer elements at +35 and +37 kb relative to the gene.

163 unoprecipitation with the -14-kb Pu.1 or +37-kb Cebpa enhancers after stable expression in 32Dcl3 cel

164 of fired origins with an average size of 370 kb.

165 al disease in the DiGeorge syndrome to a 370-kb region containing nine genes.

166 We identified a recurrent 370-kb deletion at the 22q11.2 locus as a driver of kidney d

167 In the Ophioglossum mitogenome (372 kb), gene and intron content is slightly reduced, includ

168 tions observed at a nearby approximately 374-kb region of complete LD containing three additional can

169 321 scaffolds with L50 of 31 and N50 of 378 kb, from which 11,189 genes were predicted.

170 cus is thus refined to a shared region of 39 kb that contains DNAse hypersensitive sites active at a

171 us, which has a genome of approximately 13.4 kb and groups with aphid-transmitted viruses in the genu

172 ranscripts in two size classes (1.8 kb and 4 kb).

173 ween C. elegans and C. briggsae that span >4 kb of 5' flanking sequence.

174 a 434-nt polyadenylated lncRNA originating 4 kb 3' to the Cdkn1b gene.

175 Sequencing of LanFTc1 revealed a 1.4-kb deletion in the promoter region, which was perfectly

176 generated knockin mice that replace the 1.4-kb proximal Selp promoter with the corresponding SELP se

177 digree, we identified a complex homozygous 4-kb deletion/20-bp insertion in DSTYK (dual serine-threon

178 on when the env intron was retained in the 4-kb size class.

179 ousands of mutations across approximately 40 kb of cis-regulatory genomic space and uses knock-in gre

180 ements dispersed throughout approximately 40 kb of non-coding regions.

181 en one region-specific SNP (rs10509852), 400 kb upstream of SORCS1 gene on chromosome 10, and the glo

182 oundary was highly resilient, and only a 400-kb deletion, including the whole-gene cluster, was event

183 Of these, 1 enhancer located +42 kb from CEBPA is active and engages with the CEBPA promo

184 We conclude that a single +42-kb enhancer is essential for CEBPA expression in myeloid

185 One duplication of 43 kb was identified in nine families (with evidence for a

186 ome, we selectively excised approximately 44 kb DNA spanning promoter region, transcription start sit

187 LukPQ is encoded on a 45 kb prophage (PhiSaeq1) found in six different clonal lin

188 ancestral haplotype), and another one of 45 kb was found in a single family.

189 proximately 40 genes in an approximately 450-kb region of the QTL.

190 10(-25)), resides in an enhancer element 47 kb upstream of the transcription start site of c-Myc-int

191 19,086,778 (p = 1.4 x 10(-7)) and a rare ~48 kb risk haplotype overlapping the PKP2 gene and shared o

192 p-associated in GSDs and five within the ~48 kb risk haplotype) that spanned ~280 kb forming one risk

193 has a unique first exon (Ex1B) located 10.5 kb upstream of the first exon (Ex1A) for canonical MTP (

194 clones with an average insert size of 134.5 kb.

195 long PfKelch13 C580Y haplotype (-50 to +31.5 kb) lineage, which emerged in western Cambodia in 2008,

196 emblies of the 4.6 Mb E. coli genome, 48.5 kb lambda genome, and a representative M. musculus seque

197 convenient source of high quality long (48.5 kb) DNA.

198 e the causal variant(s) at this locus to a 5 kb region that overlaps a stretch-enhancer active in isl

199 egions and the other was the approximately 5 kb regions away from the candidate genes.

200 cs, we document seven major SV classes at 5 kb SV resolution.

201 Circular "SPHINX" DNAs <5 kb were previously isolated from nuclease-protected cyto

202 eiotic crossovers were mapped to less than 5 kb.

203 ethylation-expression relationships within 5 kb of the gene.

204 ter to modestly enhance viral pregenomic 3.5-kb RNA synthesis.

205 as9-SunTag-DNMT3A is able to methylate a 4.5-kb genomic region and repress HOXA5 gene expression.

206 tions within the cardiac myocyte genome at 5-kb resolution, enabling examination of intra- and interc

207 e pairwise interactions of over 10 million 5-kb DNA segments in the B-lymphocyte cell line GB12878.

208 ibraries with selectable insertions every 50 kb in the E. coli genome.

209 Of these 42 regions, 20 were 50 kb or less while 4 regions were larger than 0.5 Mb.

210 have been restricted to molecules of 200-500 kb.

211 The locus resides in a large (500 kb) pre-formed compartment in ESCs and activation during

212 le elements are enriched both at short (<500 kb) and longer (>1.5 Mb) genomic distances.

213 nome-wide-significance in the region (+/-500 kb of lincRNAs).

214 the centromeric regions and spans up to 500 kb.

215 They positioned predominantly around 50-500 kbs from the transcription start sites of their nearby g

216 d over six loci spanning between 30- and 500-kb chromosomal regions have been described in two Iowa S

217 error rates as low as 10(-8) and average 500-kb-long DNA fragments that can be assembled into haploty

218 lized within an evolutionarily conserved 500-kb domain in human chromosome 19q13.4 and mouse proximal

219 cantly decreased eRNAs at ESEs -428 and -525 kb upstream of the MYC oncogene transcription start site

220 s targeting STXBP4 are located within the 53 kb association signal.

221 -frequency was reduced from 14.25/kb to 0.53/kb.

222 Here we show that a 538 kb deletion of the entire MYC upstream super-enhancer re

223 of commensal Escherichia coli harbor the 54-kb clb gene cluster which codes for small molecules name

224 A 55-kb transgene encompassing the human renin locus was cros

225 f alpha-gliadin genes clustered within a 550-kb region.

226 disease/myocardial infarction revealed a 58 kb risk locus on 9p21.3.

227 18) to the chromosome and bla(VIM-1) to a 58-kb plasmid.

228 ucleotides a completely de-novo-designed, 58-kb multigene DNA.

229 design rules, and demonstrate folding of a 6-kb template by as few as 10 unique strand sequences bind

230 VSG levels could be produced from a gene 60 kb upstream of its normal telomeric location.

231 , mecA, is carried on a large (20 kb to > 60 kb) genomic island, staphylococcal cassette chromosome m

232 sed lncRNA-mRNA pairs localizing within a 60-kb region.

233 of the non-overlapping proximal 16p11.2 600 kb BP4-BP5 interval.

234 er and modifiers of the proximal 16p11.2 600 kb BP4-BP5 syndromes, respectively.

235 n of endothelin 1 (EDN1), a gene located 600 kb upstream of PHACTR1.

236 Besides the 600 kb BP4-BP5 CNV found in 0.5%-1% of individuals with auti

237 egion spanning 263 kb including SPINK5 ( 61 kb) in n=722 (n=367 food-allergic, n=199 food-sensitized

238 analysis of one such locus residing in a 610 kb gene desert on chr13q22.1 (marked by rs9543325).

239 Included in the 2.62 kb overlapping region of these duplications is an enhanc

240 The Psilotum mitogenome (628 kb) contains a rich complement of genes and introns, som

241 rescuing transgenic mouse line bearing a 662-kb Gata3 yeast artificial chromosome (YAC), and these an

242 We found that the 662-kb Gata3 YAC transgene recapitulated Gata3 expression in

243 two overlapping tandem duplications of 7.67 kb (South Africans) and 15.93 kb (Norwegians).

244 h TNFAIP3, but also with IL20RA, located 680 kb upstream.

245 estimated size of 12.6, 12.5, 13.5 and 12.7 kb, respectively.

246 ns included deletions ranging from 75 to 2.7 kb in length, most of which appear to have occurred at r

247 mbly is achieved having a contig N50 of 45.7 kb and scaffold N50 of 4.06 Mb.

248 TPA is capable of assembling a 7 kb plasmid from 10 fragments at approximately 80% fideli

249 s two canonical bipartite sites within a 0.7-kb transcriptional enhancer upstream of Mist1 that are e

250 Dengue virus, an approximately 10.7-kb positive-sense RNA virus, is the most common arthropo

251 of Boodlea composita are encoded on 1- to 7-kb DNA contigs with an exceptionally high GC content, ea

252 ure we identified two novel DREs located -70 kb upstream and +100 kb downstream from the NGB gene.

253 n immunoprecipitation suggested that the -70 kb region upstream of the NGB gene contained a neuronal-

254 e genomic distance range ( approximately 700 kb-1.5 Mb), while interactions involving actively marked

255 ble across individuals (sd: fetal LTL = 0.72 kb, MTL = 0.72 kb; children LTL = 0.81 kb, MTL = 0.82 kb

256 viduals (sd: fetal LTL = 0.72 kb, MTL = 0.72 kb; children LTL = 0.81 kb, MTL = 0.82 kb) but were high

257 and non-homologous end joining of up to 725 kb reframed the DMD gene.

258 inherited ASD and glaucoma to identify a 748-kb deletion in a gene desert that contains conserved put

259 The 1.76-kb DNA sequence (SPHINX 1.8), with an iteron before its

260 that both siblings are homozygous for a 770-kb deletion on chr22q11.1 encompassing both IL17RA and c

261 pe localize the functional variation to a 78 kb region spanning the 3'end of MLH1 and the 5'end of th

262 ed on HPRT1 (including 87 kb upstream and 79 kb downstream) with median 27-fold redundancy per base.

263 elevant transcripts in two size classes (1.8 kb and 4 kb).

264 We detected an early 2.8 kb M25 mRNA directing the synthesis of a 105 kDa M25 pro

265 ant for inhibiting long-range resection, 4.8 kb from the break, and for preventing the formation of l

266 e effect of overexpression of the entire 4.8 kb miR-183 family cluster, including the intergenic regi

267 8% of the genome with a scaffold N50 of 88.8 kb that has a high fidelity to the input data.

268 PCR amplification of fragments of at least 8 kb.

269 e novo with paired-end and long-mate-pair (8 kb) libraries were first assembled and analyzed utilizin

270 of P5CS1, containing 1.2-kB promoter and 0.8-kb transcribed regions.

271 transcript, which we detected in 0.3% of 1.8-kb RNA reads.

272 ed of four exons and one consisting of a 1.8-kb transcript lacking the second exon.

273 n from a reporter plasmid containing the 2.8-kb but not the 1.9-kb fragment.

274 PRSV) resistance in bottle gourd, to a 317.8-kb region on chromosome 1.

275 The 4.8-kb genomic RNA is needed for the formation of spherules

276 Transformation of an 8-kb genomic sequence including CNL13 into the susceptible

277 s polyembryony, a form of apomixis, to an 80-kb region containing 11 candidate genes.

278 0.72 kb, MTL = 0.72 kb; children LTL = 0.81 kb, MTL = 0.82 kb) but were highly correlated within ind

279 0.72 kb; children LTL = 0.81 kb, MTL = 0.82 kb) but were highly correlated within individuals (fetus

280 Here we report a 86-kb mosaic PAI composed of four modules that encode 80 ge

281 tiled 206 kb centered on HPRT1 (including 87 kb upstream and 79 kb downstream) with median 27-fold re

282 nctional lycopene biosynthetic pathway (11.9 kb encoding 10 genes) in Escherichia coli using a highly

283 eep windows on chromosomes were narrow ( 8.9 kb).

284 The 9 kb kawaguchipeptin (kgp) gene cluster was identified in

285 Comparison of the 1.9-kb fragment sequence to the published SULT1C3 5'-flankin

286 lasmid containing the 2.8-kb but not the 1.9-kb fragment.

287 wstonensis Each strain encodes a 9.8- to 9.9-kb linear double-stranded DNA (dsDNA) genome with large

288 e microdeletions in PWS patients define a 91-kb minimum critical deletion region encompassing 3 genes

289 ations of 7.67 kb (South Africans) and 15.93 kb (Norwegians).

290 ion of Sult1d1 at a distance of more than 95 kb but not the more proximal and silent Sult1e1 gene.

291 UNX3 through a specific element within a -97 kb super-enhancer in a manner dependent on the expressio

292 ase D (PKD) family inhibitors CRT0066101 and kb NB 142-70 prevented the increase in YAP phosphorylati

293 e estimated the Ca(2+)-binding rate constant kb ( approximately 1.8 x 10(8) M(-1) s(-1)) for mSlo1 an

294 ividual carries with the published change in kb of telomere length.

295 rustrated AFM interactions on the scale of J/kb approximately 30 K, but reveal no anomalies that woul

296 1 variant is on chromosome 10, 132 kilobase (kb) downstream from <em>CXCL12</em>, which encodes a che

297 ific segments at megabase (Mb) and kilobase (kb) resolutions of single average and ensemble structure

298 nformations at a resolution of 50 kilobases (kb).

299 ively, which resulted in 35-40 mutations per kb in each population.

300 The kb values were 5.24 x 10(5), 4.17 x 10(5) and 1.46 x 10(