ライフサイエンスコーパス: gene locus

1 100 homolog in Myxococcus xanthus (MXAN_4832 gene locus).

2 ncer disorder caused by mutations at the NF2 gene locus.

3 action has been uncovered within the Igkappa gene locus.

4 ent and proliferation and rearranged the IgH gene locus.

5 s-triggered epigenetic regulation of the KOR gene locus.

6 n of DNA methylation of this X chromosome AR gene locus.

7 cetylation at specific regions near the IFNG gene locus.

8 me3 mark of active chromatin at the receptor gene locus.

9 ic ERV-9 LTR in the 100 kb human beta-globin gene locus.

10 l, chromosomally translocated, and amplified gene locus.

11 ct to the organization of the alpha-defensin gene locus.

12 ed for linkage to the phospholipase C-beta 1 gene locus.

13 creased MLL and menin occupancy in the HOXA9 gene locus.

14 F therapy and an RA risk allele at the PTPRC gene locus.

15 chromosomal proteins present within the pgm gene locus.

16 changes attributable to the chromosomal pgm gene locus.

17 ata in a sample of DNA sequences at the APOE gene locus.

18 cteristic epigenetic imprinting at the Foxp3 gene locus.

19 of a RNA polymerase II transcribed reporter gene locus.

20 f transcription complexes to the beta-globin gene locus.

21 mplementation group within the MHV replicase gene locus.

22 functionally distinct isoforms from a single gene locus.

23 tion of the immunoglobulin heavy chain (IgH) gene locus.

24 with regulatory elements of the beta-globin gene locus.

25 ent of transcription complexes to the globin gene locus.

26 of patients carrying a mutation in the HPC1 gene locus.

27 s driven by the endogenous mouse alpha(2A)AR gene locus.

28 iption of the symbiosis polysaccharide (syp) gene locus.

29 elated deregulated methylation of the HUMARA gene locus.

30 ncer disorder caused by mutations at the NF2 gene locus.

31 of RNA Polymerase II (Pol II) clusters at a gene locus.

32 hancers and promoters positioned within each gene locus.

33 romatin structure throughout the beta-globin gene locus.

34 B is invariably colocalized with the histone gene locus.

35 antisense strands across the IIa-IIx-IIb MHC gene locus.

36 erated by polymorphism within each penaeidin gene locus.

37 duction to homozygosity of the mutant COL7A1 gene locus.

38 ects of two insertion mutations at the AtSS3 gene locus.

39 iced mRNA and protein isoforms from a single gene locus.

40 ity to the X inactivation center or the Xist gene locus.

41 te histones 3 and 4 at the human beta-globin gene locus.

42 ross the genomic region encompassing the CRP gene locus.

43 timulate the transcription of the downstream gene locus.

44 with loss-of-function mutations in the DPPI gene locus.

45 r matrix (ECM), is associated with the LOXL1 gene locus.

46 T2) expressed under the control of the Mist1 gene locus.

47 ety of mRNA processing events from the PRTN3 gene locus.

48 ng on STAT binding sites within the IL-17A/F gene locus.

49 suggest chromatin interactions with the KLF4 gene locus.

50 nthesis at the replication-dependent histone gene locus.

51 involved association of SMCR8 with the ULK1 gene locus.

52 transcriptional regulation of ANG and RNASE4 gene locus.

53 stone locus body (HLB) forms at each histone gene locus.

54 . burgdorferi clone that lacked only the arp gene locus.

55 nd variation at the vitamin D receptor (VDR) gene locus.

56 tion on the proximal promoter region of this gene locus.

57 roRNAs (miRNAs) located within the EBV BHRF1 gene locus.

58 ring drug treatment, and variants at the LPA gene locus.

59 Four SNPs across the PRF1 gene locus, 5 for GZMB, 7 for UNC13D, and 11 for Rab27a

60 (4) determination of tprD allele in the tprD gene locus, (5) the presence of a 51-bp insertion betwee

61 One of these is a newly identified gene locus, AKR1B15, which clusters on chromosome 7 with

62 m triplication of the alpha-synuclein (SNCA) gene locus allows unprecedented opportunities to explore

63 ere, we show that SAP, encoded by the SH2D1A gene locus, also has a crucial role during the developme

64 tion between common variation at the SLC23A1 gene locus and circulating concentrations of L-ascorbic

65 es the genetic association between the SORT1 gene locus and coronary artery calcification.

66 a functional NRF2 binding site in the HIPK2 gene locus and demonstrating for the first time a transc

67 We found LOH of the ERCC5 gene locus and downregulation of ERCC5 gene expression t

68 er-order chromatin structure throughout this gene locus and found that expression of the reprogrammin

69 etween Bifidobacterium and the lactase (LCT) gene locus and identify an association between the host

70 on memory in RAG1-deficient mice to the RAG1 gene locus and implicate RAG1 in memory formation.

71 te resulted in hypermethylation of the Foxp3 gene locus and inhibited Foxp3 transcription, which is e

72 scribed from the opposite strand of the HAS2 gene locus and is represented by several independent exp

73 CTCF and Scc3/SA1 at the imprinted IGF2/H19 gene locus and our analyses of human DM1 alleles contain

74 f transcription complexes in the beta-globin gene locus and play important roles in restricting beta-

75 quilibrium between marker D85261 in the PCM1 gene locus and schizophrenia.

76 identify a new cistron in the MHV replicase gene locus and show that nsp3 has an essential role in t

77 osome 21, the human lipoprotein lipase (LPL) gene locus and the multi-locus genotypes of coral popula

78 e disequilibrium throughout the entire OPRM1 gene locus and thus affects the functional contribution

79 te changes in chromatin structure at the FXN gene locus, and assessed the effect of nicotinamide trea

80 yglutarate, reduced methylation of the Foxp3 gene locus, and increased Foxp3 expression.

81 ciates at many locations throughout the rRNA gene locus, and it is important for processing of rRNA i

82 ing list of elements in the interferon-gamma gene locus, and maps of their three-dimensional interact

83 ocated close to the previously reported Rag2 gene locus, and QTL_13_2 was close to the rag4 locus.

84 anonical GATA binding sites within the Gpr49 gene locus, and show by EMSAs that GATA-6 can bind to th

85 factor FOXP3 and demethylation of the FOXP3 gene locus, and T cells from at least some of these pati

86 encompassing the GAD1 GABA synthesis enzyme gene locus, and we describe a loop formation involving t

87 two novel transcripts arising from the UL117 gene locus, and we reported that the UL117 open reading

88 solute carrier family 39 member 8 (SLC39A8) gene locus are associated with the regulation of whole-b

89 Forkhead Box transcription factor F1 (FOXF1) gene locus are frequently found in patients with alveola

90 Mice with a targeted disruption of Scd1 gene locus are lean and display increased insulin sensit

91 cate that certain CpG sites within the Fgf-1 gene locus are preferentially methylated by Dnmt3a but n

92 nimals carrying the entire human beta-globin gene locus as a transgene.

93 hromatin segment containing the alpha globin gene locus as it changes from a poised, silent state in

94 -to-chromosome-17 ratio by using the eusomic gene locus as the reference.

95 binds to the proximal promoter of the Olig2 gene locus, as well as to the K23 enhancer, which drives

96 inesin family member 3A, is a susceptibility gene locus associated with asthma; however, mechanisms b

97 vides powerful opportunities for identifying gene locus associations with potentially any nuclear sub

98 ay which tiled across the entire mouse RankL gene locus at a 50-bp resolution using chromatin immunop

99 are associated with genomic gains of the FIR gene locus at chromosome 8q24.3 in human HCC specimens.

100 The mouse TCRalpha/TCRdelta/Dad1 gene locus bears a locus control region (LCR) that drive

101 -cyclin increases CDK8 occupancy at the EGR1 gene locus before and after serum stimulation.

102 processing of transcription factors and via gene locus binding, but few targets of proteasomal regul

103 e chromosomal segment including the CHRFAM7A gene locus, but not the CHRNA7 locus, is deleted in some

104 otes produce multiple products from a single gene locus by alternative splicing, translation or promo

105 es were also tested for serotype 19A capsule gene locus by PCR.

106 eveals histone H3 lysine-27 acetylation at a gene locus can alter downstream transcription kinetics b

107 multiple cis-regulatory modules (CRMs) of a gene locus can be active concurrently to support similar

108 ' end processing mechanism by which a single gene locus can yield both a stable nuclear-retained nonc

109 encoding CD4 proteins in the endogenous Cd8 gene locus caused major histocompatibility complex class

110 Our findings also confirm GGCX as the second gene locus causing PXE.

111 ction, we now report that the Cd8 coreceptor gene locus co-opts any coreceptor protein encoded within

112 The mouse TCR alpha-chain gene locus contains a cis-acting locus control region (L

113 The processes of Ig gene locus contraction and looping during V(D)J-recombin

114 n, with loss of heterozygosity of the TGFBR3 gene locus correlating with decreased TbetaRIII expressi

115 ng this transcriptomic data, we identified a gene locus, designated here as hps, that appears to enco

116 There was no evidence of gene conversion, gene locus duplication, or natural selection from malari

117 idence that H3K4me2 bookmarks the active var gene locus during later developmental stages for express

118 amic interplay of CBs with a U2 snRNA target gene locus during transcriptional activation in living c

119 Furthermore, the same IGFBP3 gene locus (e.g. rs11977526) that was associated with IG

120 was inserted by gene targeting into the apoE gene locus (EGFPapoE) immediately after the translation

121 ion factor was first retroposed into another gene locus encoding a protease and survived with differe

122 We found a unique gene locus encoding an amylase-binding adhesin AbpA and

123 The gene locus encoding protein-tyrosine phosphatase non-rec

124 onas genomes and identified a conserved four-gene locus encoding the enzymes involved in its complete

125 udies have revealed that variations near the gene locus encoding the transcription factor Kruppel-lik

126 nalyses have implicated the MS4A2-containing gene locus (encoding FcepsilonRIbeta) as a candidate for

127 lysine 4 methyltransferases to the IFN-gamma gene locus, enhancing IFN-gamma expression in key T cell

128 Encoded by the gene locus fimQ-fimP-srtC1, the type 1 fimbria is compri

129 These data support a new gene locus for familial FSGS on chromosome 2p15.

130 d a genetic polymorphism associated with the gene locus for interleukin 28B (IL28B), a type III inter

131 e pathogenic role of a mutant interrupted at gene locus FTL_0325, which encodes an OmpA-like protein.

132 ovel regulatory elements in the IL-10 family gene locus function via an intermediate regulatory RNA.

133 c transcription factor COLORLESS NONRIPENING gene locus, further clarifying the relationship between

134 occupying novel binding sites within the AR gene locus, GATA2 positively regulates AR expression bef

135 We show that a single gene locus gives rise to two fully processed and functio

136 s DISC1 (disrupted in schizophrenia 1) whose gene locus has been associated with many psychiatric con

137 No gene locus has been confirmed; the pathophysiology may i

138 However, alteration of the PTCH gene locus has been poorly studied in squamous cell carc

139 The Th2 cytokine gene locus has emerged as a remarkable example of coordi

140 The mouse Igkappa gene locus has three known transcriptional enhancers: an

141 The mouse Igkappa gene locus has three known transcriptional enhancers: an

142 loped for MLHE-1 and used to show that arxA (gene locus ID mlg_0216) was required for chemoautotrophi

143 tion of polymorphisms within the human OPRM1 gene locus identified strong association between single

144 , P = 2.76 x 10(-21)] and rs6759676, closest gene locus IL1F10 [n = 13,994, P = 1.73 x 10(-17)]).

145 n could be achieved by activating the native gene locus in a human salivary ductal cell line and prim

146 e 2 (ERK2) directly to chromatin at the ESR1 gene locus in a process that was dependent upon activati

147 we demonstrate amplification at the STAT5A/B gene locus in a significant fraction of clinical PCa spe

148 Here we demonstrate that a single, complex gene locus in Bacteroides ovatus confers XyG catabolism

149 methylation or by homozygous deletion of the gene locus in certain cancers, whereas their expression

150 ibed from the antisense strand of homeobox C gene locus in chromosome 12.

151 DNA methylation specifically to the targeted gene locus in human cells.

152 identified VDR-binding sites across the Vdr gene locus in kidney and intestine using ChIP-sequencing

153 of Speg gene isoforms, we disrupted the Speg gene locus in mice by replacing common exons 8, 9, and 1

154 reviously showed that disruption of the Speg gene locus in mice leads to a dilated cardiomyopathy wit

155 By targeting tau-lacZ to the melanopsin gene locus in mice, ganglion cells that would normally e

156 understood because of quadruplication of its gene locus in mice, hindering conventional knockout stud

157 ood because of quadruplication of the Bcl2a1 gene locus in mice, hindering conventional knockout stud

158 t increase of mutations at the Aprt reporter gene locus in mouse T cells.

159 e addressed chromatin-remodeling of the Oct4 gene locus in retinoic acid (RA)-treated embryonal carci

160 ikingly, altered splicing of the Nogo (Rtn4) gene locus in skeletal muscle of Zfp106 knockout mice re

161 to conserved regulatory regions of the Il10 gene locus in Th2 cells, supporting a direct role for Ik

162 roportional to the methylation levels of the gene locus in the presence of hydrogen peroxide.

163 the epitope tag into the native chromosomal gene locus in vertebrate cells, embryonic stem cells and

164 eracts with the regulatory elements of Olig2 gene locus in vivo and it is critical for proper Olig2 t

165 ntified, and linkage studies have placed the gene locus in Xq13.2.

166 ere the complete sequence of the marmoset GH gene locus, including the intergenic regions and 5' and

167 genomic locus should be assigned to a single gene locus, including those that fail to share promoters

168 Noncoding variants in the human MIR137 gene locus increase schizophrenia risk with genome-wide

169 Multiplication of the alpha-synuclein gene locus increases alpha-synuclein expression and caus

170 cooperates with loss of the tumor suppressor gene locus Ink4a;Arf to produce glioblastomas in the mou

171 genome transposon mutagenesis revealed a 19-gene locus, involved in LPS O-antigen polysaccharide syn

172 The beta-globin gene locus is a paradigm of cell- and developmental stag

173 hancer located 135 kb upstream of the ARID5B gene locus is activated under a superenhancer in T-ALL c

174 of one 6C isolate showed that the 6C capsule gene locus is almost identical (>98% homologous) to that

175 cular disease, and the angiotensinogen (AGT) gene locus is associated with human essential hypertensi

176 The SEC62 gene locus is at 3q26.2, and 3q amplification is reporte

177 The MLF1IP gene locus is at chromosome 4q35.1 and is composed of 14

178 e excision repair at an actively transcribed gene locus is decreased, whereas UV-induced RNAPII degra

179 by different protein isoforms from a single gene locus is dependent on the combination of differenti

180 Here, we show that the htrA gene locus is highly conserved in worldwide strains.

181 wn that the mouse adenosine deaminase (MADA) gene locus is packaged into an exceptionally regular nuc

182 The PAT biosynthetic gene locus is similar to that of another trehalose glyco

183 at a state of haploinsufficiency for the Il4 gene locus is specifically relevant for IL-4-dependent I

184 The activation of a silent gene locus is thought to involve pioneering transcriptio

185 aintain each other's effects at a particular gene locus is unknown.

186 It is becoming apparent that each gene/locus is heterogeneous and that multiple rare indep

187 the variable region of immunoglobulin (V(H)) gene locus, leading to hypermutation in the V(H) genes o

188 its toxicity, because multiplication of its gene locus leads to autosomal dominant PD, and transgeni

189 this analysis which empirically adjusts for gene locus length (the length of the gene body and its s

190 Adjustment for gene locus length is necessary because it is often posit

191 hIP-Enrich can account for the wide range of gene locus length-to-peak presence relationships (observ

192 ve an excess of genes with longer or shorter gene locus lengths.

193 ut sequencing technologies have allowed many gene locus-level molecular biology assays to become geno

194 We describe a method, differential gene locus mapping (DIGMAP), which aligns the known chro

195 tions in TP53 and amplification of the CXCR4 gene locus may be early events in the development of HGS

196 tions or mutations affecting the PLSCR3(-/-) gene locus may contribute to the risk for lipid-related

197 s that the Z-DNA-forming sequence in the DM2 gene locus may have a protective effect of reducing the

198 This RNA binds to DNMT1 and prevents CEBPA gene locus methylation.

199 Although they map to the same gene locus, MHCII proteins exhibit a high degree of poly

200 mechanisms that integrate such information, gene locus modeling is a more challenging task than mode

201 y of YY1 that has been inserted into another gene locus named Mbtps2 (membrane-bound transcription fa

202 scribed from the opposite strand of a coding gene locus, NATs are proving to be a heterogeneous group

203 ci were genome-wide significant, a candidate gene locus NPPB (rs198389, P=1.18x10(-09)) and a novel m

204 the HDR/NHEJ ratios were highly dependent on gene locus, nuclease platform, and cell type.

205 duced histone modifications across the JMJD3 gene locus occur upon ATF4 binding.

206 on by polyols, we have cloned the human MIOX gene locus of 10 kb containing 5.6 kb of the 5' upstream

207 The major immediate-early (MIE) gene locus of human cytomegalovirus (HCMV) is the master

208 tive trait loci (eQTL) associations within a gene locus of interest in real time.

209 knocked the FFAA Fen1 mutation into the Fen1 gene locus of mice.

210 on of the DNA sequence of the entire capsule gene locus of one 6C isolate showed that the 6C capsule

211 and genomic organization of the cathepsin D gene locus of Schistosoma mansoni.

212 ls because methylation analysis of the Foxp3 gene locus of transferred and reisolated Treg cells duri

213 ents in 56R(+) B cells tend to involve the D gene locus on both alleles and the most J(H)-proximal V(

214 l polymorphic markers, we identified a novel gene locus on chromosome 3q in this PRRT2-mutation-negat

215 ygosity mapping that identified a second IIH gene locus on chromosome 5q35 with a maximum logarithm o

216 the epidermal growth factor receptor (EGFR) gene locus on chromosome 7, an association for which the

217 tion at the miR-106b-25 polycistron and MCM7 gene locus on chromosome 7q22.1.

218 ORM (yeast)-like protein isoform 3 (ORMDL3) gene locus on human chromosome 17q to be a highly signif

219 mplex (EDC), a keratinocyte lineage-specific gene locus on mouse chromosome 3, occurs during epiderma

220 rated by variation at the mu-opioid receptor gene locus (OPRM1).

221 is thaliana and is conferred by the dominant gene LOCUS ORCHESTRATING VICTORIN EFFECTS1 (LOV1), which

222 The ATP13A2 gene (locus PARK9) encodes the protein ATP13A2, a lysoso

223 are, low-frequency and common alleles at one gene locus, phospholipase B1 (PLB1), might contribute to

224 that mechanisms independent of the Ink4a-Arf gene locus play a dominant role in HSC loss during condi

225 Although the DMPK gene locus positions precisely at the outer edge of a fa

226 ctive chromatin remodeling in the Il17-Il17f gene locus, possibly because of effects on CNS2-mediated

227 nst MapViewer data successfully identify the gene locus predicted.

228 19563 RA susceptibility variant at the PTPRC gene locus predicts improved response to anti-TNF biolog

229 A functional polymorphism of the MHC2TA gene locus previously associated with RA in a European p

230 tion at the immunoglobulin heavy chain (IgH) gene locus prior to and during V(D)J recombination.

231 ew risk factors are known aside from the PrP gene locus (PRNP).

232 st resistance Phytophthora sojae-susceptible gene locus, PSS1 In this study, we identified six candid

233 On RA treatment, the Nanog gene locus remodels specifically in the CR1 region of it

234 n of the Drosophila third chromosome chorion gene locus requires multiple chromosomal elements.

235 studies of the newly identified cholinergic gene locus resolve the neurotransmitter identity of the

236 procal chromosomal translocations at the MLL gene locus result in expression of novel fusion proteins

237 Disruption of the Grik4 gene locus resulted in a significant reduction in synapt

238 nsertion of Pol III genes into a non-Pol III gene locus results in the centromeric localization of th

239 les, a SNP at the PTPRC (also known as CD45) gene locus (rs10919563) was associated with the primary

240 We also identified association at the CCL21 gene locus (rs2812378, P = 0.00097 replication, P = 2.8

241 We identified a common variant at the CD40 gene locus (rs4810485, P = 0.0032 replication, P = 8.2 x

242 At the EGR1 gene locus, RV-cyclin increases and maintains RNA polyme

243 ed by Cre recombinase knocked into the Foxp3 gene locus showed that although IL-10 production by Treg

244 a polymorphism in the serotonin transporter gene (locus, SLC6A4; variant, serotonin 5-HTTLPR) modera

245 A damage repair from ionizing radiation at a gene locus-specific and genome-wide level.

246 imed to characterize the relationships among gene-locus-specific methylation alterations, disease sta

247 n genes serve as excellent models of complex gene locus structure and function, but their study has b

248 loss of CTCF binding at the immediate early gene locus, suggesting that cohesins may be a direct tar

249 d noncoding sequences within the human IL17A gene locus suggests an accessible chromatin structure (H

250 The cblT and cblS genes (locus tags lin1153 and lin1110) of L. innocua enc

251 identified common polymorphisms at the LMO1 gene locus that are highly associated with neuroblastoma

252 tion start site within intron 1 of the PRTN3 gene locus that coincided with active disease (odds rati

253 th, suggesting that the products of the Lgn1 gene locus that control intracellular growth in macropha

254 Cjj81176_1038 is the first gene of a six-gene locus that encodes homologous components of the E.

255 Functional polymorphisms of the OCTN gene locus that have previously been associated with RA

256 clease genes in that they maintain a complex gene locus that is conserved across species with transcr

257 identify a novel RNA arising from the CEBPA gene locus that is critical in regulating the local DNA

258 iption factor CREB activates expression of a gene locus that produces two microRNAs, miR-132 and miR-

259 The mutations map within a six-gene locus that we term ids for identification of self.

260 or using virus completely lacking the EBNA3 gene locus, that-after a phase of rapid proliferation-in

261 In the human epsilon-globin gene locus, the HS2 enhancer in the Locus Control Region

262 including the human lipoprotein lipase (LPL) gene locus, the human Y-chromosome in several population

263 In this gene locus, the nucleoprotein filament cis-spreads towar

264 iparum can both maintain a single active var gene locus through many erythrocytic cycles and also ach

265 intron structure and the organization of the gene locus to be conserved between the mouse and the hum

266 viously mapped the DMS-MFH tumor-suppressing-gene locus to chromosomal region 9p21-22 but failed to i

267 r regions, as it takes advantage of the full gene locus to conduct the search.

268 a conditional null mutation in the Stat5a/b gene locus to determine the requirement for STAT5 in MPN

269 icing at the human glucuronosyltransferase 1 gene locus (UGT1) produces alternate isoforms UGT1A_i2s

270 f linear genome, connects Auts2 to the Caln1 gene locus under baseline conditions.

271 The immunoglobulin heavy-chain (IgH) gene locus undergoes radial repositioning within the nuc

272 associates with a stably integrated reporter gene locus upon transcriptional down-regulation and its

273 n-DNA interactions in the murine beta-globin gene locus using the methyltransferase accessibility pro

274 while the pre-mRNA is still tethered to the gene locus via RNA polymerase.

275 n was regulated by several mechanisms: EPHB4 gene locus was amplified in 27% tumor specimens and 33%

276 ion in the 3'-protein-phosphatase-1G (PPM1G) gene locus was associated with alcohol use disorder.

277 The deletion of the ure gene locus was constructed in STEC strain 88-0643, and t

278 The vasa gene locus was duplicated from the original site and int

279 Although the Ifng gene locus was epigenetically repressed in naive Ag-inex

280 The disrupted in schizophrenia 1 (DISC1) gene locus was originally identified in a Scottish pedig

281 hose subjects, and a portion of the 16S rRNA gene locus was PCR amplified by using universal primers.

282 The Abcc6 gene locus was recently found to mediate DCC; however, a

283 Furthermore, on a stably integrated reporter gene locus, we demonstrate the role of SRSF1 in RNA poly

284 For each gene locus, we first generate the K best candidate gene

285 gh the discovery of a duplicated cholinergic gene locus, we now show that choline acetyltransferase a

286 ithin a BAC containing the DHFR housekeeping gene locus, we obtain copy-number-dependent, position-in

287 everal missense variants at the alpha-globin gene locus were associated with lower hemoglobin.

288 he endogenous p21 promoter within the Cdkn1a gene locus were generated.

289 Nine polymorphisms across the SLC26A2 gene locus were investigated using MassArray genotyping

290 ted with glycerol, strains carrying the pocR gene locus were potent reuterin producers, with L. reute

291 represent the conserved region of the Vgamma gene locus whereas the remaining Vgamma genes have been

292 on which connexin was expressed on the Cx50 gene locus, whereas homeostasis of central fibers and no

293 increases transcription throughout the ATF3 gene locus which requires TFII-I and correlates with inc

294 examined two CRMs from the Drosophila snail gene locus, which are both active in the ventral region

295 ion in macrophages is controlled by the Lgn1 gene locus, which expresses the nonpermissive phenotype

296 te gene-trap reporter driven from the STOML1 gene locus, which indicated that STOML1 is expressed in

297 tiologically links amplification of the HER2 gene locus with human cancer pathogenesis.

298 for the existence of an expanded human OPRM1 gene locus with new promoters, alternative exons and reg

299 entified significant associations at the ABO gene locus with risk of pancreatic cancer, but the influ

300 eling to ask how the association of a single gene locus with the nuclear envelope influences the surr