ライフサイエンスコーパス: be ablated

1 base pair in the hairpin (otherwise priming is ablated).

2 om patients with HGD, all areas of BE should be ablated.

3 enic mouse in which FAP-expressing cells can be ablated.

4 potential in vivo of shL5 cells was found to be ablated.

5 e gene cabeza (caz), the fly homolog of FUS, is ablated.

6 cell receptor-activated tyrosine kinase Lck is ablated.

7 ouse strains in which the eosinophil lineage is ablated.

8 to inhibit tRNA gene transcription when p53 is ablated.

9 ated to alanine, the binding of D1D2 to LRP1 is ablated.

10 munodeficiency patients where TACI signaling is ablated.

11 insensitive mutant SIK is introduced or LKB1 is ablated.

12 opment, which is partially rescued when PTEN is ablated.

13 rotects against starvation when AgRP neurons are ablated.

14 resholds at which phenotype and transmission are ablated.

15 ersists even when recurrent inputs from LMAN are ablated.

16 lt mice whose agouti-related peptide neurons are ablated.

17 ody extremities, including ear and forepaws, was ablated.

18 osomes, we constructed a mutant in which NES was ablated.

19 were maintained at control levels when Cx36 was ablated.

20 ti-IL-17A mAb, the anti-tumor effect of APCP was ablated.

21 hich the CaMKII phosphorylation site on RyR2 was ablated.

22 We characterized mice in which the bi-1 gene was ablated.

23 hich the CaMKII site on ryanodine receptor 2 was ablated.

24 s with other mouse models in which Dicer has been ablated.

25 ynthase (iNOS) or endothelial NOS (eNOS) had been ablated.

26 the binding sites of TFs whose activity has been ablated.

27 in-repeat region with or without KASH domain were ablated.

28 ve advantage in nuclear layers where neurons were ablated.

29 rf tumor-suppressor gene and the gammac gene were ablated.

30 ding leucine of AT1aR, binding and signaling were ablated.

31 tachycardias/premature ventricular complexes were ablated.

32 When the hem is ablated a necessary balance is perturbed, and cerebra

33 al for maintaining the sAHP when hippocalcin is ablated, a condition that likely impairs PIP2 generat

34 was normal during embryonic development but was ablated after birth (alphaMHC-Cre x GRK2 fl/fl) or o

35 grown in 11 rats, but only one of the tumors was ablated after intravenous administration of (99m)Tc-

36 n II or thapsigargin-induced store depletion is ablated, although the mechanisms are not understood.

37 red" MGN, in which normal auditory afferents are ablated and novel retinal inputs innervate the MGN.

38 Large volumes of tissue may be ablated and large vessels coagulated with multiple-an

39 ination with rapamycin, mTOR kinase activity is ablated and apoptosis induced.

40 s result, transcription of full-length corin is ablated and W(sh) mice develop symptoms of cardiomega

41 ly induced when UCP1-dependent thermogenesis is ablated, and creatine reduction in Ucp1-deficient mic

42 s were ablated, intermediate if some sources were ablated, and lowest if no sources were ablated (p <

43 ogenitor cells that co-express Sox2 and Bmi1 are ablated, as we observed that ageing in mice started

44 ng from the ostium of the left ventricle may be ablated at the base of the aortic cusps.

45 ty of patients with atrial fibrillation will be ablated at the time of their mitral valve surgery.

46 Phosphorylated dynein was ablated at kinetochores after inhibiting Plk1 with a

47 ude, but not frequency, was reduced when SCs were ablated at E15.5, suggesting that postsynaptic alte

48 In addition, 18 of the low-risk patients were ablated based on patient/parental decision.

49 ich the expression of full-length SH protein was ablated because it provided a modest selective advan

50 e neurons or descending serotonergic neurons were ablated before hyperalgesic priming, IL-6- and carr

51 When Kupffer cells were ablated before the onset of bacteremia, there was a

52 isted when BM-resident dendritic cells (DCs) were ablated but failed when all phagocytic cells were d

53 F was absent in 80.3% of patients if sources were ablated but in only 18.2% of patients if sources we

54 rt failure, where ISO-induced nuclear import is ablated, but G(q)-agonist mediated export is preserve

55 f the CD4-binding site on the agonist ligand is ablated, but the same mutation on an endogenous ligan

56 CMs observed in mef2ca;mef2cb double mutants are ablated by a morpholino capable of knocking down oth

57 However, when melanocyte stem cells (MSCs) are ablated by early treatment with the erbB3 inhibitor

58 As expected, RNA foci are ablated by RNase treatment.

59 es in liver and plasma F2-isoprostanes could be ablated by 1-aminobenztriazole, implicating the PB-in

60 Orthograde coupling was previously shown to be ablated by a glycine for glutamate substitution at Ry

61 ](cyt) induced by nucleotide derivatives can be ablated by Ca(2+)-channel blocking agents and by the

62 his restraint of innate immune signaling can be ablated by inhibition of proteasome function.

63 , forms part of a secondary lineage that can be ablated by larval HU application.

64 ccurs during mitosis and cytokinesis and can be ablated by SETD2 deletion, which causes mitotic spind

65 of CHD1 and Mediator from cell extracts can be ablated by shRNA knockdown of a specific Mediator sub

66 ary cells even when its CD4 binding site had been ablated by deletion of a highly conserved aspartic

67 ompetent even after its CD4 binding site had been ablated by mutagenesis.

68 use model in which the V2a interneurons have been ablated by targeted expression of diphtheria toxin

69 d to be dependent on its enzymatic activity, being ablated by mutation of its phosphatase domain and

70 ulum stress, and that this modulatory effect is ablated by 37W and 607F.

71 e hypoxic extension of replicative life span is ablated by a dominant negative HIF.

72 th cyclooxygenase-2 (COX-2) upregulation and is ablated by COX-2 inhibitors.

73 l3 in HEK293T cells in which Cul3 expression is ablated by either siRNA or by CRISPR-Cas9 genome edit

74 onstrate that neuronal TRKB trophic function is ablated by MMP9-mediated degradation in the diabetic

75 In contrast, IL-1beta secretion is ablated by potassium, scavenging mitochondrial ROS, a

76 lation and monoubiquitylation of H2AX, which is ablated by siRNA suppression of MDC1.

77 on, is selectively denervated of LC input or is ablated by the cell-specific neurotoxin ibotenic acid

78 [Ca2+]i) transient in endothelial cells that was ablated by a combination of superoxide dismutase and

79 cular ejection fraction, 58+/-10%), only AFL was ablated by achieving bidirectional isthmus conductio

80 Rats in which the sympathoadrenal axis was ablated by adrenal medullectomy showed normal durati

81 associated with elevations in the microbiota was ablated by antibiotic pretreatment and correlated wi

82 appaB pathway in the presence of VP16, which was ablated by Bay11, suggesting that AAV transduction a

83 in response to histamine in vitro, but this was ablated by blockade of H1R but not H2R.

84 issue and bone marrow norepinephrine content was ablated by chemical sympathectomy with 6-hydroxydopa

85 The effect of CO2/HCO3(-) was ablated by connexin43 inhibition or knockdown.

86 A small amount of sample material was ablated by focusing 266 nm laser light onto a spot.

87 nic mutant derivative in which Chk1 function was ablated by gene targeting.

88 ure senescence in H9C2 myoblasts, the effect was ablated by MIF replenishment.

89 IL-10 promoter activity was ablated by mutating two nonpolymorphic binding sites

90 This NO-induced inhibition was ablated by mutation of the Cys-273 site.

91 dent down-regulation of GluR1 AMPAR currents was ablated by overexpression of SAP97-I2I5 (which does

92 This effect was ablated by pharmacological and genetic inhibition of

93 d to prevent apoptosis when endogenous SfIAP was ablated by RNA silencing.

94 Human cells in which RNF4 expression was ablated by siRNA or chicken DT40 cells with a homozy

95 This effect was ablated by the mutation H267A in the beta subunit.

96 izing anti-IFN-gamma monoclonal antibody but was ablated by the neutralization of tumor necrosis fact

97 ized hES-RPE showed enhanced survival, which was ablated by the presence of anti-PEDF antibody.

98 owth factor-mediated induction of HIF-1alpha was ablated by transient expression of a dominant negati

99 AT activation exhibited delayed kinetics and was ablated by treatment with cycloheximide.

100 izer induction: the primary dorsal organizer was ablated by UV irradiation, and a new organizer was i

101 Both of these effects were ablated by a F170S substitution in the HPIV1 C prot

102 Both effects were ablated by angiotensin II type 1a (AT(1a)) receptor

103 results in increased telomere fusions, which were ablated by Ctip knockdown.

104 d VV-induced CD4 T-cell IFN-gamma production were ablated by cyclosporine A, which inhibits signaling

105 emias induced by the rag2-EGFP-Myc transgene were ablated by irradiation, whereas leukemias in double

106 and most of the perifovea of the treated eye were ablated by laser photocoagulation at the start of t

107 e fovea and most of the perifovea in one eye were ablated by laser photocoagulation.

108 Importantly, these effects of FGF2 were ablated by PD173074, a small molecule inhibitor of

109 ced P-S6 levels by Western blot, and effects were ablated by pretreatment of cells with mTOR-specific

110 Nitric oxide donor-related effects were ablated by pretreatment of myocytes or isolated hea

111 but was abolished if either ORF45 or RSK1/2 were ablated by siRNA, a pattern that is correlated with

112 While GEPCOT NICs were ablated by temozolomide, pre-GEPCOT cells survived

113 d luciferase activity, whereas these effects were ablated by the mutation of the seed region of the m

114 Importantly, all of these associations were ablated by the PAK inhibitor IPA3, suggesting that

115 of the assays was confirmed, as the signals were ablated by the Scurfy mutation of the FoxP3 gene.

116 Aortic aneurysms in these LDS mice were ablated by treatment with the Ang II type 1 (AT1) r

117 eedlelike cryoprobes were placed and lesions were ablated by using real-time MR imaging for intraproc

118 levels and increased ROS productions, which were ablated by XMJ in concentration-dependent manner.

119 but not if both germ line and somatic gonad were ablated, by a precursor of the DAF-12 ligand, dafac

120 lation of Spry1, Pten, and Pdcd4 when miR-21 was ablated coincided with reduced phosphorylation of ER

121 or wild-type explants in which HS expression was ablated could extend axons in response to netrin-1.

122 Transgenic mice in which CX3CR1 signaling was ablated (CX3CR1(GFP/GFP)/CX3CR1(-/-)) and preserved

123 receptor mice in which CD11b-positive cells were ablated, decreased tumor cell survival without alte

124 AF sources were ablated directly in 100% of FIRM cases and coincide

125 misregulation, and Aurora A(S361*) activity is ablated due to loss of structural integrity.

126 F/YF)) in which the PI3K binding site in Cbl is ablated due to the mutation in the regulatory tyrosin

127 nt was severely disrupted when Lhx2 function was ablated during embryonic development.

128 lly affected when radial glial primary cilia were ablated earlier in development.

129 e synapse formation in mutants in which TrkB is ablated either in presynaptic or in both presynaptic

130 imprinted control region when transcription is ablated, establishing a connection between transcript

131 Embryos in which Ovol2 is ablated exhibit lethality by E10.5, prior to which th

132 When these neurons are ablated, fish failed to rotate their eyes following

133 When successive steps in folate biosynthesis were ablated, folE (lacking pterins and folates) and fol

134 regions with an interval confidence level >7 were ablated followed by pulmonary vein isolation (PVI).

135 CFAE sites with continuous electric activity were ablated followed by PVI.

136 In mice, mutant Ad5 vectors that are ablated for FX-binding become detargeted from hepato

137 advantageous in creating animal models that are ablated for specific cells and in other targeted cel

138 s were predominantly men (68%); the majority were ablated for the first time (71%); left atrium was 4

139 In LAAPPI the analytes are ablated from water-rich solid samples or from aqueou

140 ents have been reported in whom VT could not be ablated from the right or left ventricular endocardiu

141 her the nsp2 protein antagonist function can be ablated from the virus, we introduced point mutations

142 mouse model in which androgen receptor (AR) is ablated from approximately 75% of adult Leydig stem c

143 absence of Pax3, the enteric nervous system is ablated from its inception.

144 Mice in which the Ttf1 gene was ablated from differentiated neurons grew normally an

145 When PMNs were ablated from mice, DeltayopM Y. pestis grew as well

146 When the subtype was ablated, ganglion cells tuned toward low spatial fre

147 When Wnt and Eda were intact but Shh was ablated, germ induction and subsequent duct formatio

148 Flies in which Leuc or Lkr neurons are ablated have defects identical to those of leucokini

149 dominant and GC functionality and phenotype are ablated, i.e., EBV infection is not consistent with

150 rtantly, the anticancer effects of the drugs are ablated if CLU expression is blunted by RNA interfer

151 e report that LPS-mediated Ca2+ oscillations are ablated in ECs deficient in Nox2, Stim1, and type II

152 SF and neutrophilia, whereas these responses are ablated in G-CSF- or TLR2-deficient mice.

153 al TRPC3 channels; intriguingly, these cells are ablated in moonwalker mice by 1 month of age.

154 not apoptosis, all three of these processes are ablated in p53(3KR/3KR) cells.

155 and Ago2, but not either Ago1 or Ago2 alone, are ablated in the skin, the global expression of microR

156 ine in which the Notch1-expressing cells can be ablated in a controlled manner.

157 TgPEPCKnet can also be ablated in a glycolysis-deficient mutant, while TgPEP

158 provide evidence that aromatase activity can be ablated in a signaling pathway- and cell-specific fas

159 g a mouse model in which the T1IFNR gene can be ablated in vivo, specifically in cardiomyocytes.

160 Dmp1Cre.Socs3 (f/f) mice, in which SOCS3 has been ablated in osteocytes, have high trabecular bone vo

161 urthermore, such DNs are abrogated when RTN3 is ablated in aging and AD mouse models.

162 xoviruses and arenaviruses, where resistance is ablated in animals depleted of microbiota.

163 pression of neuronal differentiation markers is ablated in both KIF1Bbeta-deficient mouse neuroblasts

164 flox); Osx-Cre mice, in which the Smpd3 gene is ablated in both late-stage chondrocytes and osteoblas

165 )17-dependent autoimmunity occurs when STAT3 is ablated in CD4 cells.

166 Prion protein-mediated zinc uptake is ablated in cells expressing familial associated mutan

167 that leukocyte rolling on P- and L-selectin is ablated in cells lacking O-glycans, with N-glycan tru

168 Moreover, when the Smad4 gene is ablated in combination with its DNA binding cofactor

169 Post-anoxia MEND is ablated in DHHC5-deficient hearts, inhibited by cyclo

170 ta), in response to inflammasome activation, is ablated in FABP4/aP2(-/-) macrophages, as well as in

171 ten conditional knockout mice, in which Pten is ablated in granule cells of the dentate gyrus and pyr

172 equires functional Foxq1 as their expression is ablated in hair follicles of satin mice.

173 e developed a model in which SHIP expression is ablated in HSCs while they are resident in a SHIP-com

174 a mouse neuronal model of TSC in which Tsc1 is ablated in most neurons during cortical development.

175 rated and studied a mouse model in which S1P is ablated in postnatal chondrocytes.

176 Concordantly, reovirus infection is ablated in primary cortical neurons derived from NgR1

177 ly increased in rho0 cells but this increase is ablated in rho0 rsb1Delta cells.

178 ur with high penetrance in mice in which Nf1 is ablated in Schwann cells in the context of a heterozy

179 knock-out model in which the Miz1 POZ domain is ablated in Schwann cells.

180 enerating a novel mouse model in which PTH1R is ablated in the limb mesenchyme using Prx1Cre transgen

181 we generated mice in which Ikbkap expression is ablated in the peripheral nervous system and identify

182 This response is ablated in Tlr4(-/-) mice or when co-administered wit

183 VT was ablated in 19 patients by use of focal and/or linear

184 The VLPO was ablated in 25 rats by bilateral local injection of o

185 When NgR2 was ablated in AD transgenic mice expressing Swedish APP

186 and were markedly reduced when dystroglycan was ablated in adult mice, suggesting a role for dystrog

187 Moreover, activation of MAPK pathway was ablated in APRIL-stimulated XID cells.

188 atRA signaling was ablated in beta-cells by overexpressing a dominant-n

189 e desensitizing effect of McTnT1-44 on pCa50 was ablated in beta-Tm fibres.

190 rate-docking site of the PDK1 protein kinase was ablated in Cre-expressing tissues in a way that prev

191 within the peritoneal cavity, a pattern that was ablated in CXCR3-deficient mice.

192 MCC expression was ablated in each case, enabling oncogenic beta-cateni

193 assay confirmed that de novo heme synthesis was ablated in FC knock-out parasites.

194 This subset was ablated in huLangerin-DTA mice, resulting in reduced

195 dependent phosphorylation of IRS-1 and IRS-2 was ablated in IGFRKO cells but not in IRKO cells.

196 P generation, with the IP agonist cicaprost, was ablated in IP-deficient cells and was independent of

197 of C. pneumoniae to increase the ATP content was ablated in macrophages deficient in expression of ei

198 noid-mediated long-term depression (eCB-LTD) was ablated in mBACtgDyrk1a mice.

199 ansfer into Rag1(-/-) hosts, but this effect was ablated in mice that lacked fully functional B cells

200 o the skin following cutaneous OVA challenge was ablated in mice that lacked lymph nodes.

201 I(h) was ablated in most large neurons in HCN1(-/-) mice.

202 ependent, as Hib-OMPC-induced TNF production was ablated in MyD88 knockout (KO) mice.

203 n of corneal clarity; however, this response was ablated in MyD88(-/-) mice, which were not significa

204 in the eye caused CNV, irrespectively if it was ablated in newborn or 3-week-old mice.

205 Increased IFN-induced gene expression was ablated in NOD.IFNAR1(-/-) islets.

206 e generation were p53-dependent; this effect was ablated in p53-null cells.

207 Megakaryocyte and platelet FAK expression was ablated in Pf4-Cre/FAK-floxed mice without affecting

208 The HDC/HA/HR axis was ablated in sham and BDL Kit(W-sh) mice.

209 le repair was severely perturbed when Ptpn11 was ablated in stem cells due to a deficit in stem cell

210 In contrast, mice in which SHP2 was ablated in the Col10alpha1-Cre-expressing cells appe

211 Mouse embryos were generated in which Hnf4a was ablated in the epithelial cells of the fetal colon b

212 ptor-mediated ERK activation, a pathway that was ablated in the l/l mouse through a mutation of the t

213 v-erbalpha at these sites was lost when HNF6 was ablated in the liver.

214 ation and visualization system, the gap area was ablated in the MR scanner.

215 Interestingly, STAT2 degradation activity was ablated in the NS2 ubiquitin mutant rRSV.

216 hen cultured with LPS or CpG, and production was ablated in the presence of anti-IL-18R Ab.

217 K (Thr-172) and ACC (Ser-79), but the effect was ablated in the S399A mutant.

218 of IFN-gamma and IL-12 caused by LPS priming was ablated in the spleens, but not blood, of IL-10 knoc

219 l LC patterning in neonates, but not when LC were ablated in adults and replaced by bone marrow-deriv

220 Vdelta2 T cells were ablated in blood and tissue from CD patients receiv

221 These therapeutic effects were ablated in both CD4(+)- and CD8(+)-depleted mice an

222 These responses to flagellin were ablated in DCs from NLRC4(-/-) mice but not Toll-li

223 The cardioprotective effects of metformin were ablated in mice lacking functional AMPK or eNOS.

224 These increases were ablated in MyD88-/- mice, and NF-kappaB p65 was pho

225 n of innate immunity in that these responses were ablated in MyD88-deficient mice and that flagellin

226 Group IV afferent fibers were ablated in neonatal Sprague-Dawley rats by subcutan

227 ptotic effects of IL-11 on DCs, whereas they were ablated in Stat1(-/-) cultures.

228 MyoD expressing cells were ablated in the epiblast by labeling them with the G

229 the ASE chemosensory neurons (ASEL and ASER) are ablated, indicating that this pair has a dominant ro

230 covered in which expression of M2-1 and M2-2 was ablated individually or together [rdeltaM2-1, rdelta

231 Freedom from AF was highest if all sources were ablated, intermediate if some sources were ablated,

232 ouse strains in which the eosinophil lineage is ablated, large numbers of T. spiralis larvae are kill

233 /-) mice, and mice in which IL-12 production was ablated only from CD8alpha(+) DCs failed to control

234 increased AP duration by 67% only when Kv2.1 is ablated or inhibited and enhanced GSIS by 2.7-fold.

235 he discriminatory salivary biomarker profile was ablated or disrupted.

236 adaptor MyD88, or transcription factor IRF7 was ablated or pDCs were depleted.

237 R Ca2+ stores was absent when NKCC1 activity was ablated or pharmacologically inhibited.

238 ent RFA every 3 months until all areas of BE were ablated or cancer developed.

239 in embryos where specific founder cells have been ablated, or where zygotic transcription has been in

240 urces were ablated, and lowest if no sources were ablated (p < 0.001).

241 ic CD8 T cells was impaired when CD4 T cells were ablated prior to infection but not at 4 days postin

242 on of GSK-3beta by phosphorylation at Ser(9) was ablated providing a molecular basis for these findin

243 owever, adenovirally encoded gene expression is ablated rapidly by CD8+ T-cell-dependent mechanisms.

244 When cells are ablated rather than wounded, Rho GTPase activation a

245 late Sp1 interactions with the CDK4 promoter was ablated, rendering the CDK4 promoter unresponsive to

246 F-beta1 injection into mice in which MKs had been ablated restored HSC quiescence, and conditional de

247 e vesicular glutamate transporter 2 (VGLUT2) is ablated selectively from DRG neurons.

248 onal Nurr1 gene-targeted mice in which Nurr1 is ablated selectively in mature DA neurons by treatment

249 g by engineering mice in which the Jnk1 gene was ablated selectively in adipose tissue.

250 tants in which this ParG temporal regulation is ablated show partition deficient phenotypes as a resu

251 randomly chosen obstacles in a regular array is ablated; single-file diffusion in pores; transient an

252 are increased in mice in which MHC class II is ablated specifically in LC suggesting that direct cog

253 ally null mice, in which expression of CTIP2 was ablated specifically in epidermal keratinocytes, sug

254 When canonical NF-kappaB signaling was ablated specifically in mature B cells, the differen

255 Therefore, we generated mice in which Snf5 was ablated specifically in nestin-positive and/or glial

256 ction in the prostate, the Frs2alpha alleles were ablated specifically in the prostatic epithelial pr

257 When both NM II-C and II-B are ablated the B-C-/B-C- cardiac myocytes show major de

258 When 2d and 4d were ablated the embryo developed into a rounded cell ma

259 erm line, endoderm or mesoderm founder cells are ablated, the remaining cells do not alter their clea

260 Thus, when FANCJ binding to BRCA1 is ablated, the molecular mechanism chosen for the repai

261 yD88 in DCs, the early IL-12 response by DCs was ablated, the IFN-gamma response by natural killer ce

262 e critical for protection: when PMNs in mice were ablated, the mice lost all ability to be protected

263 f the larval heart to serotonin when the CNS was ablated, thus suggesting a direct neural input.

264 gradation in ADAMTS-4/5-double-knockout mice was ablated, to a level comparable with that in ADAMTS-5

265 When the gene encoding 4E-BP1 was ablated together with Mtor, marked improvements were

266 ation, we find that when IFN-gamma signaling is ablated, type I IFNs drive inflammation, resulting in

267 tion in this model and the activity of IL-13 was ablated under conditions leading to expression of th

268 on of MLC (serine 19) through a pathway that was ablated under conditions that blocked CD36 ligation

269 nged activation of MAPK (p38 and ERK1/2) and was ablated under MAPK inhibition.

270 ges in transcription and locus repositioning are ablated upon transformation with v-Abl, which render

271 acellular parasitism observed in TP-null ECs was ablated upon restoration of TP expression.

272 ane positions, micrometer-diameter pores can be ablated upstream of desired cellular targets.

273 Ets-1 and Runx2 protein expression in CT26 was ablated using antisense oligonucleotides and resulte

274 l lines, in which the function of KILLER/DR5 was ablated using inducible RNA interference.

275 -4.6 cm; mean SUVmax, 22.7; range, 9.5-77.1) were ablated using radiofrequency (n = 16) or microwave

276 Patients were ablated using single-tip ablation with conventional

277 actions of many antidepressants at SERT have been ablated via knock-in substitution (SERT Met172) wit

278 The microbiota was ablated via germ-free or antibiotic approaches.

279 When these neurons are ablated, we found that the behavioral response is sh

280 adult mice in which hippocampal neurogenesis was ablated, we found specific impairments in spatial di

281 Using mice in which cone photoreceptors were ablated, we found that rods signal through cones at

282 for the BH3-only molecules Bim and Puma had been ablated were studied on a high-fat diet.

283 rs or transgenic mice wherein the JNK-1 gene was ablated were subjected to 5 or 20 min of ischemia fo

284 However, beta(2)AR-Nedd4 interaction is ablated when beta-arrestin2 expression is knocked dow

285 Similarly, long-term survival induced by DST was ablated when HO-1 activity was blocked by zinc proto

286 in mTORC2 activity in Gpat1(-/-) hepatocytes was ablated when rictor was knocked down.

287 In addition, we demonstrate that degradation was ablated when the proteasome was inhibited, whereas a

288 es to guide treatment so lesions of interest are ablated whereas sparing surrounding healthy tissues,

289 ell as the increased activity of TAp63gamma, is ablated with the expression of a ubiquitin-deficient

290 t not in cytosol/nonraft membrane fractions, was ablated with cyclodextrin.

291 Rather, the tumor vasculature was ablated with high-dose intratumoral IFN-beta, and co

292 Phosphorylation of this Akt subspecies was ablated with methyl-beta-cyclodextrin, a cholesterol

293 which the expression of endogenous perforin was ablated with miR30-based short hairpin (sh) RNAs.

294 The tumor in each animal was ablated with RF (1-cm active size ablation catheter,

295 Porcine corneas were ablated with a free-electron laser tuned to 2.77 or

296 Rabbit corneas were ablated with an excimer laser and were observed and

297 Seventy-three patients were ablated with MN and 72 with a standard manual appro

298 Focal atrial tachycardias were ablated with point lesions that targeted the earlie

299 d 164 with ICM, presenting with sustained VT were ablated with radiofrequency catheter ablation.

300 These effects were ablated with selective siRNA silencing of these pro