ライフサイエンスコーパス: genomic organization

1 rotein levels, as well as a highly conserved genomic organization.

2 c genes in cyanophage and common patterns of genomic organization.

3 a highly conserved N-terminal domain and by genomic organization.

4 rhesus monkey (Rh-OPTN) and to determine its genomic organization.

5 t genera are distinguished by differences in genomic organization.

6 cdh alpha and gamma clusters have a striking genomic organization.

7 3, revealing a highly conserved sequence and genomic organization.

8 elated to RASSF1A, for sequence homology and genomic organization.

9 ated the mouse aif-1 gene and determined its genomic organization.

10 omic sequence allowed the elucidation of the genomic organization.

11 VR genes showed substantial conservation in genomic organization.

12 ates TbVCP to have a single-locus, two-copy, genomic organization.

13 SIGN at the nucleic acid level and a similar genomic organization.

14 or a modification that produced a single-ORF genomic organization.

15 GSC) in both sequence of the homeodomain and genomic organization.

16 express a degree of uniformity in their post-genomic organization.

17 nt genomic features, contributing to overall genomic organization.

18 eded for understanding viral replication and genomic organization.

19 and suggest a role for HR repair proteins in genomic organization.

20 mum stretch is sufficient to map large-scale genomic organization.

21 eusocial lineages share distinct features of genomic organization.

22 ghtly controlled despite complexities in its genomic organization.

23 is elements as well as the changes in global genomic organization.

24 or molecular motors and potential impacts on genomic organization.

25 ertebrates given that they possess a similar genomic organization.

26 on of gene expression and the maintenance of genomic organization.

27 ould allow a more complete analysis of their genomic organization.

28 Owing to the complexity of the genomic organization, a mouse homolog of TRIM5 has not b

29 Genomic organization also tends to be conserved between

30 Patterns of genomic organization among cats and inbred domestic cat

31 kbp) mouse Bcm gene and determination of its genomic organization, analysis of the 2 kb 5'-flanking r

32 Furthermore, knowledge of the genomic organization and alternative promoter usage in t

33 enJSRV loci cloned to date possess an intact genomic organization and are able to produce viral parti

34 In this report, we describe VCBP genomic organization and characterize adjacent and inter

35 Characterization of the genomic organization and chromosomal localization of LHX

36 bbit IKBKAP-encoded mRNAs and determined the genomic organization and chromosomal location of mouse I

37 Here, we report the genomic organization and chromosomal position of the new

38 study, we investigate the roles of tDNAs in genomic organization and chromosome function by editing

39 Because of their unique genomic organization and deep phylogenetic roots, we pro

40 As a step toward elucidating the genomic organization and distribution of gene networks r

41 s with hereditary disease, we determined its genomic organization and DNA sequence.

42 nic bacteria provided a novel perspective on genomic organization and evolution.

43 he achaete-scute genes, and to examine their genomic organization and evolution.

44 The results suggest that wild-type genomic organization and expression of nsps are required

45 We have compared the genomic organization and expression of this gene family

46 A comparison of the genomic organization and expression patterns of these Si

47 The genomic organization and expression profile of known and

48 rtant role in evolution and are important in genomic organization and function.

49 We studied the genomic organization and functional properties of the al

50 bles the alpha2 subgroup of herpesviruses in genomic organization and gene content.

51 proteins and resembles alphaherpesviruses in genomic organization and gene content.

52 so served as powerful tools in understanding genomic organization and gene regulation.

53 We describe here the genomic organization and general transcriptional control

54 some of its extraordinary traits, review its genomic organization and give insight into its diverse m

55 and transcriptional control, we examined the genomic organization and identified the promoter region

56 n, and how enhancer transcription influences genomic organization and integrity.

57 properties of human GDE1, we determined its genomic organization and its biochemical and structural

58 ividual members' phylogenetic relationships, genomic organization and life cycle expression profiles.

59 urrent study reports the upstream sequences, genomic organization and localization of the Psp and Smg

60 onservation of Atox1 structure and provide a genomic organization and localization that will aid in t

61 the study of the relationship between miRNA genomic organization and miRNA function.

62 a loss of protein function, a bidirectional genomic organization and overlapping expression patterns

63 These maps can be used to determine genomic organization and perform comparative genomics to

64 We report here the genomic organization and phylogenic relationships of CD1

65 ulating its expression, we characterized the genomic organization and promoter of mouse APEG-1.

66 ew sheds light on the likely reasons why the genomic organization and seeming redundancy of the miR-1

67 Little is known about their genomic organization and sequence diversity, and only fi

68 Based on genomic organization and sequence similarity to known pr

69 of these isoforms and the analysis of their genomic organization and structure have suggested that t

70 Characterization of the genomic organization and structure of the human ABCG1 ge

71 es exhibit significant conservation of their genomic organization and the intron 20 donor splice site

72 This manuscript reports the genomic organization and the primary sequence of the mou

73 Knowledge of the genomic organization and the promoter region of the huma

74 No apparent correlation was observed between genomic organization and transcript levels.

75 ic microarray, allowed the analysis of their genomic organizations and evolutionary relationship.

76 14 subfamilies based on sequence similarity, genomic organization, and alignments with their closest

77 to define corresponding gene families, their genomic organization, and expression patterns.

78 ing, sequence analysis, tissue distribution, genomic organization, and functional analysis of a new m

79 The Sireviruses vary greatly in their genomic organization, and many have acquired additional

80 Herein, we describe the cloning, mapping, genomic organization, and mRNA and protein expression pa

81 has moderate sequence similarity, conserved genomic organization, and near structural identity to me

82 embly, biochemical techniques to study viral genomic organization, and next-generation sequencing to

83 ir protein expression, transcript structure, genomic organization, and noncoding regions (promoter an

84 Herein we report the nucleotide sequence, genomic organization, and predicted amino acid sequence

85 These studies indicate that the structure, genomic organization, and recombination patterns of DH s

86 Here we describe the location, genomic organization, and relative ages of all human NAN

87 ted the full-length AS6 cDNA, determined its genomic organization, and sought for abnormalities in HP

88 We describe the cDNA sequence, genomic organization, and splice variants of MYO3B expre

89 s are its simplicity, both in anatomy and in genomic organization, and the elaborate methods that hav

90 expression pattern in various tissues, their genomic organization, and their homology to known genes.

91 Understanding KIR allelic diversity and genomic organization are essential prerequisites to eval

92 estor but also partial reconstruction of its genomic organization, as well as a description of two ge

93 atExplorer pipeline, and exists in a complex genomic organization at the centromere of most, or all,

94 s of the new virus genome revealed a classic genomic organization but a weak identity with known sequ

95 nts along DNA could create three-dimensional genomic organization by loop extrusion.

96 nges in five previously unreported loci with genomic organization characteristic of NAHR-mediated gai

97 e presence of genes encoding lipocalins with genomic organization, chromosomal arrangement, and orien

98 Here we report genomic organization, chromosomal localization and analy

99 of the mouse P2X(5) subunit, as well as its genomic organization, chromosomal localization and expre

100 The present study reports the genomic organization, chromosomal localization and promo

101 gned to facilitate investigations into miRNA genomic organization, co-transcription and targeting.

102 The corresponding genomic organization, coding potential, and conserved or

103 Collectively, these results describe the genomic organization, complete mRNA sequence, and sn-2-l

104 ced MNV genomes and demonstrated a conserved genomic organization consisting of four open reading fra

105 eplication timing together with higher-order genomic organization contribute to the patterns of singl

106 lation, we construct a model for macaque KIR genomic organization, defining four putative KIR3DL loci

107 The genomic organization demonstrates a high degree of conse

108 we cloned the murine UPase gene, defined its genomic organization, determined its 5'- and 3'-end flan

109 omplex rearrangement products share a common genomic organization, duplication-inverted triplication-

110 ion potential can be largely determined from genomic organization (e.g. the number, type, and placeme

111 re we report a comparison of cDNA sequences, genomic organization, editing site sequences and pattern

112 extended class II and class III regions the genomic organization, excluding several block inversions

113 biosynthetic gene clusters, which differ in genomic organization-existing either as fused domains (I

114 The study of genetic diversity, genomic organization, expression profiles, protein struc

115 This review describes the structure, genomic organization, expression, regulation, and evolut

116 We have determined the complete molecular genomic organization for both Nrv genes.

117 data demonstrate an evolutionarily conserved genomic organization for the beta-globin locus and sugge

118 elic diversity, but we find that the overall genomic organization, gene order and predicted proteomes

119 This genomic organization generates overlapping transcripts w

120 CAV shares genomic organization, genomic orientation, and common fe

121 rent genomes during the life cycle, but this genomic organization has been questioned.

122 affect multiple AIDs, or alternatively that genomic organization has resulted in the clustering of m

123 use and rat PLD1 and PLD2 and the mouse PLD2 genomic organization have recently been reported.

124 Their genomic organizations have been characterized, cDNA tran

125 HGMW-approved symbol SNAI1) and describe its genomic organization, having sequenced a region spanning

126 HBoV2 has a genomic organization identical to that of HBoV but has o

127 Genomic organization impacts accessibility and movement

128 ding discussion of their structural biology, genomic organization in pairs, developmental regulation,

129 hitecture, transcription factor binding, and genomic organization in regulation of erythrocyte membra

130 ngs advance our understanding of the role of genomic organization in the renowned ecological and phen

131 The genomic organization in this region is similar to the ne

132 Features of genomic organization including compartments, topological

133 The genomic organization, including the intron-exon borders,

134 A comprehensive comparison of the genomic organization indicates that ANKRD26 has the geno

135 Remarkable similarities in genomic organization, intron/exon boundaries, and intron

136 Its genomic organization is compared to the structures of th

137 Genomic organization is conserved between the murine and

138 Genomic organization is essentially colinear with KSHV,

139 hromosome conformations, and the large-scale genomic organization is globally unaffected by the prese

140 a single genomic locus, and this remarkable genomic organization is highly conserved from teleosts t

141 lentiviruses and, consistent with this, its genomic organization is intermediate between the nonprim

142 formation is available, the genetic context, genomic organization, mechanisms of resistance and agric

143 nd serological comparisons suggest that this genomic organization might cause var genes to diversify

144 he beta-defensins, including gene discovery, genomic organization, molecular structure, regulation of

145 e genes previously examined, established the genomic organization of 10 of these genes, and excluded

146 We determined the genomic organization of 14 clinical strains of Bordetell

147 nda paramyxovirus, with a typical Ferlavirus genomic organization of 3'-N-U-P/V/I-M-F-HN-L-5'.

148 The attempt to reconstruct the genomic organization of a tumor genome recently resulted

149 ion sequencing has advanced knowledge of the genomic organization of amphioxus; however, many aspects

150 We also report the genomic organization of both the functional gene and the

151 ly, none of the tumors showed changes in the genomic organization of c-Myc but many had one or more s

152 The genomic organization of cbl genes from a variety of mamm

153 The genomic organization of chromatin is increasingly recogn

154 tudies revealed a striking difference in the genomic organization of classic cadherin genes and one f

155 In an effort to determine the precise genomic organization of CTNS and to gain sequence-based

156 Here we report the genomic organization of DC-SIGN and map it to chromosome

157 nant brood pouch tissue and characterize the genomic organization of duplicated metalloprotease genes

158 The genomic organization of ELOVL4 and primer sets for exon

159 Genomic organization of exons and introns was nearly ide

160 We have investigated the copy numbers and genomic organization of five representative reverse tran

161 entally relevant genes and characterized the genomic organization of four genes: a hedgehog ortholog,

162 The data presented here show how the genomic organization of functionally related proteins ca

163 as begun to blur the physical boundaries and genomic organization of genic regions with noncoding tra

164 Here, we analyse the genomic organization of Hox and Hox-derived genes in 13

165 be here the complete coding sequence and the genomic organization of hSNM1B, one of at least three hu

166 The genomic organization of human, baboon, rat, and mouse ge

167 esidues, recombination signal sequences, and genomic organization of IGL genes as cladistic markers.

168 The genomic organization of IKCa1, SKCa2, and SKCa3 were def

169 The genomic organization of KSHV is similar to that of Epste

170 stance interexon PCR, we have determined the genomic organization of LRP1B and built a contiguous arr

171 us helitrons not only constantly reshape the genomic organization of maize and profoundly affect its

172 Thus, while the genomic organization of mHuA is similar to the neural-re

173 However, genomic organization of novel eukaryotic genomes is dive

174 The genomic organization of Pcdh15/PCDH15 bears similarity t

175 iate the burden of their expression, and the genomic organization of R genes into coregulatory module

176 ever, there are important differences in the genomic organization of retrotransposons in plants compa

177 The genomic organization of schistosome cathepsin D was simi

178 protocadherin genes we have investigated the genomic organization of several additional human protoca

179 This review covers the genomic organization of simple and complex constitutiona

180 We have studied the genomic organization of smarce1 and identified that it h

181 Analysis of the genomic organization of SPEC1 revealed that the coding s

182 The genomic organization of TCRbeta loci enables Vbeta-to-DJ

183 e 2 isolates, which displayed differences in genomic organization of the ACE1 duplication process.

184 Herein, we characterize the genomic organization of the AKAP12 locus, its regulatory

185 Here, we investigated the genomic organization of the amplified EPSPS copies using

186 We present the genomic organization of the BACE gene.

187 e isolated genomic clones and determined the genomic organization of the bovine mimecan gene.

188 have determined the sequence, structure and genomic organization of the cathepsin D gene locus of Sc

189 Comparison of the complexity and genomic organization of the cbl gene family and the pred

190 The genomic organization of the cbl genes from various speci

191 We took advantage of the unusual genomic organization of the ciliate Oxytricha trifallax

192 The genomic organization of the cone NCKX gene was determine

193 The genomic organization of the corresponding genes supports

194 No differences in the genomic organization of the different classes of transpo

195 In this report we (a) defined the genomic organization of the DUTT1 gene, (b) performed mu

196 the human FGFR gene family reveals that the genomic organization of the FGFRs is relatively conserve

197 We describe the genomic organization of the four lack genes in the L. ma

198 The structure and nuclear genomic organization of the gene family encoding putresc

199 The genomic organization of the gtcA region was conserved be

200 The characterization of the genomic organization of the hMRE11 gene allowed us to de

201 In this report we describe the genomic organization of the hMRE11 gene and the analysis

202 In summary, we report on the genomic organization of the human ABC1 gene and identify

203 The genomic organization of the human and mouse genes (HGMW-

204 we determine the complete cDNA sequence and genomic organization of the human BRI3 gene.

205 Reported here is the genomic organization of the human FKBP52 gene (FKBP4), w

206 We also deduced the genomic organization of the human gene VR1.

207 KLHLI genes, and have elucidated the general genomic organization of the human gene.

208 Here, we present the genomic organization of the human hairless gene (HGMW-ap

209 In this study, we characterized the cDNA and genomic organization of the human LHX5 gene and analyzed

210 ation of full-length cDNA and elucidation of genomic organization of the human MTO1 homolog.

211 the pathogenesis of ARVD, we determined the genomic organization of the human NAPOR gene including i

212 oforms of PCTAIRE 3 have been cloned and the genomic organization of the human PCTAIRE 3 gene is repo

213 The genomic organization of the human protocadherin alpha, b

214 Here we report the expression and genomic organization of the human SPEC1 gene.

215 he Sprouty2 gene, we first characterized the genomic organization of the human Sprouty2 (hSpry2) gene

216 family genes on human chromosome 2, and the genomic organization of the IL-1HY2 gene is highly conse

217 udy, we describe the cloning, expression and genomic organization of the LMX1A gene, which is compose

218 We report here the genomic organization of the Lsamp gene.

219 espite mapping to different chromosomes, the genomic organization of the macroH2A2 and macroH2A1 gene

220 s of mouse and humans were compared, and the genomic organization of the mCABYR gene was analyzed.

221 The genomic organization of the mdmx gene is identical to th

222 In many nonmammalian vertebrates, the genomic organization of the MHC class I region leads to

223 R gene expression, we have characterized the genomic organization of the mouse and human A(2A)R genes

224 in I cDNA sequence was used to determine the genomic organization of the mouse cyclin I gene which co

225 ERalpha cDNA over 15 years ago, the precise genomic organization of the mouse ERalpha gene has not y

226 re, we report the isolation, sequencing, and genomic organization of the mouse FKBP65 gene (Fkbp10) a

227 Here we report the genomic organization of the mouse orthologue of ELOVL4 a

228 hese transcripts, we first characterized the genomic organization of the NBC1 gene (SLC4A4).

229 The genomic organization of the pathway genes, syntenously p

230 we present the completed coding sequence and genomic organization of the previously published partial

231 The genomic organization of the PRKAG2 gene was determined u

232 To determine the genomic organization of the PTTG and its transcriptional

233 Details of the genomic organization of the recently isolated maize (Zea

234 cular pathology of SCA8, we have defined the genomic organization of the SCA8 RNA transcripts and ass

235 effort to gain a better understanding of the genomic organization of the skeletal MyHC genes and its

236 izing clones were sequenced to determine the genomic organization of the SLC24A2 gene.

237 The genomic organization of the ste3 locus bears significant

238 he sequences, phylogenetic distribution, and genomic organization of the SurE family reveal examples

239 angements focuses on characterization of the genomic organization of the TCRB locus.

240 We have characterized the genomic organization of the three zebrafish L chain isot

241 The genomic organization of the transposable DNA elements in

242 The complete genomic organization of the two mucin genes MUC2 and MUC

243 Finally, we show that the genomic organization of the universal ribosomal componen

244 nsion of odorant receptor genes and the role genomic organization of these genes might have in their

245 Using gene-specific primers to explore the genomic organization of these two genes, it was determin

246 The presence and genomic organization of these two pairs of duplicated ge

247 The genomic organization of this chromosomal region is diffe

248 tGPX7 in Arabidopsis was identified, and the genomic organization of this family was reported.

249 Comparison of the genomic organization of this locus among several insect

250 and Rv1812c are cotranscribed, and that the genomic organization of this operon is specific to M. tu

251 Accordingly, we identified the complete genomic organization of this putative phospholipase A(2)

252 Despite a significant expansion, genomic organizations of BdAP2/EREBPs were monotonous as

253 The genomic organizations of many other frameshifting viruse

254 The genomic organizations of some AgR loci permit the assemb

255 The divergent genomic organizations of two FeSOD genes in the same org

256 ow that all EGF-CFC genes share an identical genomic organization over the entire coding region.

257 ty between mouse and human CABYR, the common genomic organization, presence of similar testis-specifi

258 hcg pair is distinct in chromosome location, genomic organization, promoter structure, and tissue-spe

259 This genomic organization promotes translocation breakpoints

260 ogeny, gene structure, evolutionary history, genomic organization, protein topology, and expression p

261 Here, the phylogeny, genomic organization, protein topology, expression, and

262 Therefore, this variable and constant genomic organization provides a genetic mechanism for di

263 biting HDACs leads to significant changes in genomic organization, recruiting regions of transcriptio

264 e implications of recent data about parkin's genomic organization, regulation and function.

265 nd explored their functional categorization, genomic organization, regulatory motifs, and association

266 mbination to assemble both V exons and has a genomic organization resembling the likely ancestral for

267 Complete nucleotide sequence and genomic organization revealed that the mouse sTnT gene s

268 It consists of 11 exons with a genomic organization similar to that of GLUT3 and likely

269 e of representative cDNAs reveals a striking genomic organization similar to that of immunoglobulin a

270 evelopment and the characterization of their genomic organization, spatiotemporal activities and sequ

271 elements that generate two stripes and their genomic organization suggest that single-stripe elements

272 arison between Galliformes and Passeriformes genomic organization suggests an origin of the second TC

273 e single copy F3galtase gene has a different genomic organization than Bz1.

274 jejuni strain 81-176 revealed a less complex genomic organization than the corresponding region in th

275 Hox clusters display a much higher level of genomic organization than their invertebrate counterpart

276 ions that the nucleus encounters can perturb genomic organization that in turn influences cellular be

277 st-transcriptional processes and features of genomic organization that safeguard cell identity in the

278 as made recently in our understanding of the genomic organization, the obligate requirements, and the

279 Consistent with their genomic organization, these miRNAs have a similar expres

280 gue with 70% amino acid identity and similar genomic organization to human PSCA has also been identif

281 While similar in genomic organization to other complex retroviruses, foam

282 ic islands (GIs) share similarities in their genomic organization to pathogenicity islands from other

283 intron organization and were also similar in genomic organization to the 5' exons for the CSPG core p

284 uratus) with similarity in both sequence and genomic organization to the vertebrate Rag1 and Rag2 gen

285 the formation of an International Structural Genomics Organization to formulate policy and foster coo

286 alpha-gliadin genes were obtained from their genomic organization, transcription patterns, transposab

287 Here we present the first description of the genomic organization, transcriptional regulatory sequenc

288 stool samples from dogs with diarrhea, has a genomic organization typical of a picornavirus and encod

289 In a genomic organization unique to trypanosomes, there are a

290 Moreover, its genomic organization was almost identical to that of hum

291 The genomic organization was found to be conserved between m

292 The genomic organization was most similar to those of vitivi

293 This type of modular genomic organization was similar to several other phages

294 hages each gave rise to a plasmid form whose genomic organization was very similar to that of the CTX

295 ARHGAP8 shares an identical genomic organization with ARHGAP1/CDC42GAP/p50RHOGAP and

296 ion to conserved cellular, developmental and genomic organization with mammals.

297 Comparison of the B3 genomic organization with that of Mu revealed evidence o

298 Comparison of mouse genomic organization with the Human Genome Database pred

299 ading to a better understanding of genes and genomic organization within the kingdom.

300 We identified novel genomic organizations within functional cps loci, consis