ライフサイエンスコーパス: ectopic

1 ed GFP, and cause localized accumulations of ectopic 53BP1-a DNA repair protein.

2 i-mediated ABHD5 silencing promotes, whereas ectopic ABHD5 overexpression inhibits, the invasion and

3 ects in axonal transport of SVPs, leading to ectopic accumulation of synaptic vesicles in the proxima

4 unstable MTs act as cargo traps, leading to ectopic accumulations of cargo and reduced availability

5 This should lead to its ectopic activation in vivo and thereby disrupt membrane

6 These observations suggest that ectopic activation of a Y-located SRY gene could exert m

7 ng Stat1, in adipocytes in vitro and in vivo Ectopic activation of type I IFN signaling in brown adip

8 mains incomplete, fasciculations derive from ectopic activity generated in the motor system.

9 f coupled myofibroblasts and by cessation of ectopic activity of cardiomyocytes coupled to myofibrobl

10 lly compartmentalize or prevent premature or ectopic activity of pleiotropic, soluble cytokines such

11 brosis models exhibiting slow conduction and ectopic activity, block of TGF-beta1 signaling completel

12 Ectopic ACTL6A/p63 expression promotes tumorigenesis, wh

13 sly described the unstacking of Golgi by the ectopic adhesion of Golgi cisternae to mitochondria.

14 Aging and obesity induce ectopic adipocyte accumulation in bone marrow cavities.

15 rt the idea that dietary fat per se promotes ectopic adiposity and cardiometabolic syndrome in humans

16 ps with the binding site of some allosteric, ectopic and bitopic ligands.

17 Both ectopic and endogenous hG9a augmented p53-dependent tran

18 etention of Wolffian ducts was not caused by ectopic androgen production or action.

19 ward the IPN and, when disrupted, results in ectopic, anteriorly directed axonal projections.

20 DNA synthesis and DNA damage without much of ectopic apoptosis.

21 ethylene glycol (PEG)-based nanoporous human ectopic artificial livers (HEALs), implanted them in mic

22 of ventricular cells, and the appearance of ectopic atrial gene expression within the ventricle.

23 g functions upstream of Nkx genes to inhibit ectopic atrial gene expression.

24 We conclude that Munc18c's role in mediating ectopic basolateral membrane fusion of ZGs contributes t

25 lecular mechanisms alters the probability of ectopic beats is not understood.

26 mally helps protect against the formation of ectopic beats.

27 Adjustment for demographic, behavioral, and ectopic body fat measures did not explain racial/ethnic

28 rates of membrane exposure and a noteworthy, ectopic bone formation above the mesh in 72% of sites.

29 ystemic administration of PTHrP1-17 augments ectopic bone formation in vivo.

30 ion in non-osteogenic C4-2b PCa cells led to ectopic bone formation under subcutaneous implantation.

31 Ectopic bone formation was monitored by micro-computed t

32 nuation of 1) total new bone and soft tissue ectopic bone with 0.5 mg/kg (38.5% and 14.7%) and 2.5 mg

33 plasticity of fibroblasts in contributing to ectopic calcification and identify pharmacological targe

34 Chondrocyte apoptosis, synovitis, and ectopic calcification appear to be targets for potential

35 5, synovitis present at day 14, osteophytes, ectopic calcification, and meniscus pathology.

36 ys, initiates a molecular pathway inhibiting ectopic calcification.

37 in the body and may represent precursors of ectopic calcification.

38 ted into pyrophosphate, a major inhibitor of ectopic calcification.

39 Ectopic cAMP signaling is pathologic in polycystic kidne

40 ans including the liver, bowel loops and the ectopic cardia.

41 e possible therapeutic strategies to prevent ectopic cartilage calcification and some forms of congen

42 into the defect but transdifferentiate into ectopic cartilage; in the absence of tenogenic cells, ex

43 ults are reproduced by hepatic expression of ectopic CCDC3 in mice on HFD.

44 Accordingly, ectopic Cdk1 activation results in immediate Nuf dispers

45 tissue, while utilizing both endogenous and ectopic cellular behaviours to dismantle the aberrant st

46 ly divergent, resembling the terminals from "ectopic" centrifugal neurons in Neognathae.

47 rly events in centromere establishment at an ectopic chromosomal locus, and maintain centromere funct

48 Deletion of WHI5, CDC55 and ectopic CLN2 expression suppress the START delay of igo1

49 These ectopic clocks also require cyc, yet CYC expression is r

50 Ectopic clocks also require the blue light photoreceptor

51 overexpression in wild-type cortices led to ectopic clustering of Pcdh19-positive neurons.

52 l assay to assess functionality reveals that ectopic compound eyes can rescue the ability to respond

53 gnals are observed in motile and stabilized "ectopic" contacts.

54 f tRNA genes, were rescued by introducing an ectopic copy of a single tRNA gene.

55 In contrast, ectopic Cyclin E overproduction uncouples short G1 from

56 /-) embryos, together with the appearance of ectopic cystic duct-like epithelia in their gallbladders

57 Genetic experiments show that ectopic dATM is sufficient to promote DNA synthesis in w

58 Ectopic delivery of miR-194 stimulated migration, invasi

59 on during neuroepithelium formation leads to ectopic determination of RNE cells and consequently impa

60 in the ovary after sex determination caused ectopic development of steroidogenic cells at the embryo

61 Our results demonstrate that hilar ectopic DGCs preferentially synapse onto adult-born DGCs

62 a double knockdown of Mcm10 and HP1a induced ectopic DNA synthesis and DNA damage without much of ect

63 IT form a positive regulatory loop, in which ectopic DNMT1 expression increases, whereas targeted DNM

64 Genetic inactivation of ectopic EFNA3 restores a wild-type cortico-collicular ma

65 d that embryogenesis is remarkably robust to ectopic Erk signaling, except from 1 to 4 hr post-fertil

66 Ectopic Etv5 expression in Th2 cells that lack Etv5 rest

67 ely controls mGlu5 receptor activity both in ectopic expressing systems and in striatal primary neuro

68 Although ectopic expression experiments have suggested an inhibit

69 inhibiting TNF-alpha-induced apoptosis upon ectopic expression in HeLa cells, the percentage of infe

70 Upon ectopic expression in primary human articular chondrocyt

71 In the cells negative for active p53, NPRL2 ectopic expression leads to activation of CHK1 or CHK2 k

72 Here, we show that the ectopic expression of a truncated RocA derivative, harbo

73 Ectopic expression of APC, but not its familial adenomat

74 Conversely, ectopic expression of beta1 integrin was sufficient to i

75 ther regulatory cell types simply by loss or ectopic expression of bHLH genes, and male-to-female and

76 Ectopic expression of BRD7, but not its mutants defectiv

77 Notably, ectopic expression of catalytically-inactive RICE1 not o

78 Ectopic expression of Cdh1 leads to premature differenti

79 On ectopic expression of CDX2, these transitional basal pro

80 rentiate, their plasticity is restricted and ectopic expression of CHE-1 no longer results in activat

81 In undifferentiated cells, ectopic expression of CHE-1 results in activation of ASE

82 Defects upon RetSat depletion are rescued by ectopic expression of ChREBP but not by its putative enz

83 Ectopic expression of cmo-miR156, using a virus-based mi

84 Conversely, ectopic expression of CSDE1 impairs neural differentiati

85 Most importantly, the ectopic expression of CX45 significantly enhanced the re

86 rogrammed into pluripotent stem cells by the ectopic expression of defined transcriptional factors.

87 lation and gene expression levels, featuring ectopic expression of developmental transcription factor

88 the major Glut4 PAT, based on evidence that ectopic expression of DHHC7 increased Glut4 palmitoylati

89 Ectopic expression of different members of the RAS super

90 Conversely, ectopic expression of Dmrt1 led to largely masculinized

91 hd-knockdown defects, which were reversed by ectopic expression of EcR.B2 but not by EcR.A or EcR.B1

92 Ectopic expression of EgWRI1-1 in plant produced dramati

93 Ectopic expression of EP300-ZNF384 and CREBBP-ZNF384 fus

94 In a new mouse model, ectopic expression of ephrin-A3 (Efna3) in a subset of r

95 Bacterial infection and/or ectopic expression of EspL leads to rapid inactivation o

96 Ectopic expression of EspW results in formation of uniqu

97 inhibited by EZH2 depletion, was rescued by ectopic expression of EZH2 but not by TRIM28 expression

98 ollagen-induced arthritis (CIA) model, while ectopic expression of FGF2 in vivo exacerbated tissue in

99 iation of Gene 33 with histone H2AX and that ectopic expression of Gene 33 promotes the interaction b

100 Here we show that ectopic expression of Gene 33 triggers DDR in an ATM ser

101 Here, we show that ectopic expression of GPR124 promotes cell adhesion, add

102 x2 proteins are enhanced during infection or ectopic expression of HCV core protein.IMPORTANCE Endogl

103 Finally, the ectopic expression of HD5 in tumor cells diminished the

104 Ectopic expression of HLH-2 and HLH-3 together promoted

105 Although ectopic expression of HRAS increased statin sensitivity,

106 rant receptors (HsOrs) responds to CHCs, and ectopic expression of HsOrs in Drosophila neurons impart

107 Likewise, ectopic expression of human THOR in zebrafish accelerate

108 Third, ectopic expression of IFITMs, known to potently block in

109 The ectopic expression of ILT3 in CLL was a distinctive feat

110 UB aggregates, which are resolved following ectopic expression of individual GABARAPs.

111 In this study, we demonstrate that ectopic expression of insulin epitope B:9-23 (InsB9-23)

112 xpression and mouse HL-1 cardiomyocytes with ectopic expression of K2P1 channels recapitulate two lev

113 ced in Lck/Hck/Fgr triple knockout cells and ectopic expression of Lck/Hck/Fgr dampened the antiviral

114 g defects in lefty mutants can be rescued by ectopic expression of lefty far from its normal expressi

115 ch in mesenchymal nephron progenitors causes ectopic expression of Lhx1 and Hnf1b and that these cell

116 Ectopic expression of lineage master regulators induces

117 Knockdown of LKB1 increased and ectopic expression of LKB1 decreased glycolysis, anchora

118 Finally, we observed that ectopic expression of LmPRL-1 in L. major led to an incr

119 Ectopic expression of LRRC25 impaired NF-kappaB activati

120 Impaired CSR can be rescued by ectopic expression of Mbd4 Mbd4 deficiency yields a defi

121 moxifen (TAM)-resistant breast cancer cells, ectopic expression of miR-29b-1/a did not drive TAM-resi

122 Ectopic expression of miR-383 inhibited tumor-initiating

123 Ectopic expression of miR-K6-5p specifically inhibited t

124 Modulation of AKT or HSF1 activity via the ectopic expression of mutant alleles support the ability

125 sites on target proteins typically requires ectopic expression of mutant SUMOs with introduced trypt

126 found reduction of ERalpha expression, while ectopic expression of MYST3 had the reversed effect.

127 In contrast, ectopic expression of NFI-A in myeloid progenitors from

128 bal profile of arginine GlcNAcylation during ectopic expression of NleB1, EPEC infection in vitro, or

129 Ectopic expression of non-phosphorylated SNAP-23 mutant

130 onstrate that, in the cells with active p53, ectopic expression of NPRL2 induces NOX2-dependent produ

131 Consistent with this, we found that ectopic expression of oncogenic KRas and HRas in cells r

132 Ectopic expression of OPN4 using a ubiquitous promoter r

133 Mechanistically, we demonstrated that ectopic expression of OSBPL3 facilitates SREBP-1 process

134 involve dedifferentiation of beta-cells and ectopic expression of other islet hormones, including so

135 Ectopic expression of p205 induced expression of an Asc

136 We demonstrate that the ectopic expression of Pax4 in delta cells is sufficient

137 ated and converted into beta-like cells upon ectopic expression of Pax4 opened new avenues of researc

138 Ectopic expression of pdgfaa interferes with cardiac fus

139 Ectopic expression of PGBD5 in primary immortalized huma

140 the EKLF/KLF1 transcription factor leads to ectopic expression of proteins that are not normally exp

141 We also found that ectopic expression of PS improves Arabidopsis resistance

142 Furthermore, ectopic expression of Pt-Ets4 is sufficient to induce ce

143 eclinical models of experimental metastasis, ectopic expression of RAGE on human prostate cancer cell

144 Importantly, ectopic expression of RPL10L prevents the death of cultu

145 Blocking of FGF8 caused ectopic expression of SEMA3C and a migration defect of c

146 ey SHF transcription factor, resulted in the ectopic expression of Sema3c in the pharyngeal arch regi

147 and SinR antagonist slrR Deletion of sinR or ectopic expression of slrR in the spermidine-deficient D

148 Ectopic expression of Snail in cancer cell lines lacking

149 Ectopic expression of SNHG6-003 in HCC cells promoted ce

150 pre-B cells into macrophages induced by the ectopic expression of specific transcription factors.

151 keratin 5-positive (Krt5(+)) basal cells and ectopic expression of squamous-like differentiation mark

152 Consistent with a gain-of-function effect, ectopic expression of the 2 identified SAMD9L mutants de

153 Ectopic expression of the EMT-activating transcription f

154 dies with patient lymphoblasts and following ectopic expression of the mutant in HEK293 cells.

155 ells associated with collagen deposition and ectopic expression of the myofibroblastic markers viment

156 Removing an intronic PAS results in ectopic expression of the neuronal ankyrin isoform in no

157 In contrast, ectopic expression of the same chicken Ntn1 in the mouse

158 ectopically expressing wild-type (WT) Brg1, ectopic expression of the SE-Brg1 mutant reduced prolife

159 ockout cells could be restored completely by ectopic expression of TIM-1 but not TIM-3 or TIM-4.

160 ion of autoreactive T cells by promoting the ectopic expression of tissue-specific genes in the thymi

161 Ectopic expression of TRAF6 promoted the K63-linked ubiq

162 microfluidic peptide array and confirmed by ectopic expression of TRP120 lysine mutants in cells.

163 channels and mouse HL-1 cardiomyocytes with ectopic expression of two pore-domain K(+) channel isofo

164 Remarkably, although ectopic expression of wild-type Beclin1 promoted cardiom

165 Ectopic expression of wild-type Pdcd4 and Pdcd4(157-469)

166 e also required for necroptosis triggered by ectopic expression of ZBP1 and caspase blockade, and ZBP

167 In contrast, ectopic expression of ZFP521 in HSCs led to a robust mai

168 Following ectopic expression, SCL contributes to oncogenesis in T-

169 achieved through rescue of MRP RNA levels by ectopic expression.

170 unctional developmental outcomes, and render ectopic eye formation a widely accessible paradigm to st

171 Here, we use ectopic eye formation as a paradigm to investigate the e

172 nature of the middorsal head-the location of ectopic eye induction-converges onto that of regular com

173 ratification, for six traits associated with ectopic fat (hereinafter referred to as ectopic-fat trai

174 Age-dependent ectopic fat accumulation (EFA) in animals contributes to

175 DPP4 expression is elevated in subjects with ectopic fat accumulation in the liver.

176 The MED/LC diet mobilizes specific ectopic fat depots, and exercise has an independent cont

177 not explained by demographic, behavioral, or ectopic fat measures.

178 we identified seven new loci associated with ectopic-fat traits (ATXN1, UBE2E2, EBF1, RREB1, GSDMB, G

179 with ectopic fat (hereinafter referred to as ectopic-fat traits).

180 altered lymphocyte recirculation and display ectopic formation of lymphocyte aggregates within mucosa

181 Ectopic FOXM1 rescues the proliferative capacity of MYC-

182 The ectopic GATA1 expression repressed Gata2 transcription a

183 of loop domains does not lead to widespread ectopic gene activation but does affect a significant mi

184 G) is prevalent in women and associates with ectopic germinal centers (GCs) development and inflammat

185 factors, and disruption of the formation of ectopic germinal centers are considered the main therape

186 striatum.SIGNIFICANCE STATEMENT Delivery of ectopic glial cell line-derived neurotrophic factor (GDN

187 eological methods were used to measure hilar ectopic granule cells, mossy cells, mossy fiber sproutin

188 ntly correlated with the generation of hilar ectopic granule cells, the number of mossy cells, the ex

189 Ectopic heartbeats can trigger reentrant arrhythmias, le

190 the loss of matrix Gla protein (MGP), causes ectopic hepatic differentiation in the pulmonary epithel

191 e tumour pO2 levels (p<0.05) in mice bearing ectopic human xenograft MIA PaCa-2 pancreatic tumours wi

192 hypoxic heart tube or following induction of ectopic hypoxic responses.

193 To describe the presence of continuous ectopic inner foveal layers associated with epiretinal m

194 26.3%) ERMs were associated with continuous ectopic inner foveal layers crossing the entire foveal a

195 The presence of continuous ectopic inner foveal layers was identified in 63 out of

196 The presence of ectopic inner foveal layers was negatively correlated wi

197 %) were thick and associated with continuous ectopic inner foveal layers.

198 Furthermore, ectopic integration of ASAR6 or ASAR15 transgenes into m

199 Ectopic IRF5 increases the expression of LMP1, while kno

200 corticosterone concentrations, and decreased ectopic lipid (triacylglycerol/diacylglycerol) content i

201 ltered cardiac energy metabolism, leading to ectopic lipid accumulation and glucose overload, the exa

202 Dietary fat composition can affect ectopic lipid accumulation and, thereby, insulin resista

203 ong mitochondrial dysfunction with increased ectopic lipid deposition, insulin resistance, and type 2

204 itochondrial activity and is associated with ectopic lipid-induced insulin resistance.

205 Ectopic LKB1 reduced HK-II along with glycolysis.

206 Furthermore, ectopic M1L expression decreased staurosporine-induced (

207 By counteracting ectopic microtubule assembly and disorganization of the

208 sin-13 protein MCAK (KIF2C) also resulted in ectopic microtubule asters during mitosis in C. elegans

209 Ectopic midline vascularisation in endothelial Nrp1 and

210 ogress in pseudoxanthoma elasticum and other ectopic mineralization disorders, as presented in the sy

211 ma elasticum (PXE), a prototype of heritable ectopic mineralization disorders, is caused in most case

212 nthoma elasticum is a prototype of heritable ectopic mineralization disorders, with phenotypic overla

213 target of molecular correction to counteract ectopic mineralization in pseudoxanthoma elasticum.

214 models of pseudoxanthoma elasticum depicting ectopic mineralization in the skin, eyes, and the arteri

215 Plasma levels of PPi and the degree of ectopic mineralization were determined.

216 mice and, consequently, completely prevented ectopic mineralization.

217 Also, 'anti-metastatic' effects of ectopic miR-383 expression were observed in a PCa experi

218 SPR-edited MRP loci loses this activity, and ectopic MRP RNA expression restores cleavage activity.

219 Ectopic muscle islands, each composed of myofibers of un

220 lastoma cell growth and tumor formation, and ectopic MYCN partially reversed the effects of MDM2 depl

221 ith severe tissue disorganization, including ectopic neural spheroids containing differentiated neuro

222 enotype, namely an increase from two to four ectopic neural tubes, corresponding to the switch in NMP

223 or surface, increase MT stability, and cause ectopic neurite growth.

224 ion of hyperstable MTs and the generation of ectopic neurites; the lack of potential sites for polyam

225 n and abnormal cell junctions, generating an ectopic neuronal layer that resembles cerebral cortex ab

226 ines involved in inflammatory responses, and ectopic NOSTRIN overexpression functionally restricted e

227 Ectopic Notch expression causes a significant increase i

228 support a model in which NMC is dependent on ectopic NUT-mediated interactions between EP300 and comp

229 s cerevisiae Replication stresses induced by ectopic oncogenic expression of cyclin E, G-quadruplexes

230 ve barrier is compromised in the presence of ectopic OPCs.

231 ses are mostly unaffected in the presence of ectopic OPCs.

232 Ectopic or intrinsic high expression of TRIB2 induces dr

233 6-1 mutant demonstrated that NEK6 suppresses ectopic outgrowth and promotes cell elongation in differ

234 MiR-181b-1 ectopic overexpression further diminishes Bcl-2 expressi

235 RAGE ectopic overexpression in breast cancer cells increased

236 By ectopic overexpression of ARR10, Arabidopsis lines hyper

237 Ectopic overexpression of miR-503 promotes cell growth a

238 ediated protection was not observed, whereas ectopic overexpression of Notch1 diminished TNFalpha-ind

239 er anchorage-independent conditions, whereas ectopic overexpression of p62 enhanced the self-renewal

240 Ectopic overexpression of the newly cloned AA-enriched v

241 eal maize plant architecture originated from ectopic overexpression of tru1 in axillary branches, a c

242 Ectopic overexpression results in the development of ect

243 Frs2alpha(Fl/Fl) mice, a renal cystic model, ectopic p-Creb stained proximal tubule-derived cystic se

244 Ectopic (p)ppGpp synthesis restored biofilm dispersal in

245 Ectopic p53 stimulates endogenous LMP1 expression.

246 ance monitoring was developed to treat mouse ectopic pancreatic cancer.

247 , and its heterozygosity strongly suppresses ectopic peripheral nervous system neurons in mir-279/996

248 splay reductions in the ITC marker Foxp2 and ectopic persistence of the dorsal lateral ganglionic emi

249 if found in IGT genes was required for these ectopic phenotypes.

250 ion toward an SDF1alpha gradient, leading to ectopic platelet release within the bone marrow.

251 1 - became abnormally enriched and spread to ectopic positions on the sperm's chromatin before entry

252 ultrasound features of uncommon locations of ectopic pregnancies such as an ectopic scar is crucial f

253 o before reaching the uterus could result in ectopic pregnancy and lead to maternal death.

254 preterm birth, tubal factor infertility, and ectopic pregnancy in women.

255 evated B-Hcg levels, the possibility of scar ectopic pregnancy should be considered.

256 ID) is an important cause of infertility and ectopic pregnancy, and Chlamydia trachomatis and Neisser

257 Scar pregnancy is an extremely rare type of ectopic pregnancy, where there is implantation of the ge

258 teratoma, meconium peritonitis and abdominal ectopic pregnancy.

259 In mutants, we observed ectopic production of DA neurons derived from the Dbx1 m

260 d the suppressive effect of p53 and enhanced ectopic progenitor proliferation after genotoxic injury,

261 monstrate that elevated levels of E2F3 drive ectopic proliferation in multiple tissues.

262 insulator led to premature activation of the ectopic promoter.

263 I3 repressor in Ptch1-deficient mice rescued ectopic Ptch2 expression and obstructive hydronephrosis.

264 ormalized on RNaseH1-mediated suppression of ectopic R-loops, inversely correlates with disease sever

265 f repeated sequences exacerbates the risk of ectopic recombination and chromosome rearrangements.

266 Immunohistochemistry for NKCC1, KCC2, and ectopic recurrent mossy fiber (rMF) sprouting as well as

267 ly expressed in preimplantation embryos, and ectopic removal of H3K27me3 induces maternal allele expr

268 overexpression results in the development of ectopic root hair cells.

269 nsive and severe dysgenetic areas, with more ectopic SC and germ cells (GC) than DBP-FW treatment; DB

270 Our findings demonstrate that ectopic SC do not differentiate de novo, but result from

271 We aim on developing a polymeric ectopic scaffold in a readily accessible site under the

272 locations of ectopic pregnancies such as an ectopic scar is crucial for a correct diagnosis and earl

273 ing as focal aggregation of Leydig cells and ectopic Sertoli cells (SC).

274 Later in development, the effects of ectopic signaling are buffered, at least in part, by com

275 cus and TH17 cell differentiation via SMAD4: ectopic SKI expression inhibits H3K9 acetylation of the

276 Ectopic SMAD4 expression suppresses RORgammat expression

277 These effects are rescued by ectopic Snail1 expression.

278 Co-expressing ectopic SoxN with svb rescued diverse denticle morpholog

279 n of nonphosphorylatable H3.3S10A results in ectopic spreading of H3K9me2 into adjacent euchromatic r

280 ically enhancing WAT lipolysis could produce ectopic steatosis because of an overflow of lipids from

281 lular responses that arise from long-term or ectopic stimulation, especially in neuronal compartments

282 e head patterning gene-orthodenticle-induces ectopic structures externally resembling compound eyes a

283 ding enzyme in the mutants revealed that the ectopic suberization at the endodermal cells limits Ca t

284 p formation [9], disrupted Casparian strips, ectopic suberization of endodermal cells, and low accumu

285 is JIL-1 dependent, we provide evidence that ectopic tethering of JIL-1 and subsequent H3S10 phosphor

286 Although ectopic TpnC4 in TDT muscles was able to maintain jumpin

287 NA-binding specificity in vivo, resulting in ectopic transcription and anemia in the Nan mouse model.

288 egies of engineering resistant crops through ectopic transcription of plants' own defence genes, such

289 aberrant DNA-binding events genome wide and ectopic transcriptional consequences of this binding.

290 ly remodeled into vascularized bone using an ectopic transplantation model.

291 a potential cause of proarrhythmic cellular ectopic (triggered) activity in AF.

292 ited growth of both lung and colon carcinoma ectopic tumors, whereas blockade of miR-24 in tumor cell

293 The gene ectopic viral integration site 1 (EVI) and its variant m

294 line-dependent shrinking, glycogen loss, and ectopic vitellogenin expression, utilizes distinct molec

295 get genes and impairs mitotic entry, whereas ectopic VprBP expression strongly activates a FoxM1 tran

296 Expressing ectopic VSG117 from different genomic locations showed t

297 y high levels of VSG expression by inserting ectopic VSG117 into VSG221 expressing T. brucei.

298 We regenerated cells stably expressing ectopic wild-type and mutant phosphatidylinositol-3,4,5-

299 and afferent innervation on E6 suggests that ectopic Wnt9a expands the neural-side fate, possibly by

300 Ectopic ZEB1 is sufficient for IRF1 silencing, whereas Z